TIMOTHYLOTZETIMOTHY LOTZE29.70508570000000-95.401808700000002118LOTZE, TIMOTHYProfessorprns:coAuthorOfcoauthor ofFaculty Rankprns:fullNamefull nameprns:hasAuthorListauthor listprns:hasFacultyRankhas faculty rankprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns:latitudelatitudeprns:longitudelongitudeprns:mainImagephotoprns:maxWeightmaximum weightprns:medlineTAjournal title abbreviationprns:meshDescriptorUIMeSH DescriptorUIprns:meshSemanticGroupNameMeSH semantic group nameprns:minWeightminimum weightprns:numberOfAuthorsnumber of authorsprns:numberOfConnectionsnumber of connectionsprns:numberOfPublicationsnumber of publicationsprns:personIdPerson IDprns:personInPrimaryPositionperson in primary positionprns:physicalNeighborOfphysical neighborprns:positionInDepartmentposition in departmentprns:positionInDivisionposition in divisionprns:predicateNodepredicate nodeprns:publicationDatepublication dateprns:similarTosimilar toprns:sortOrdersort orderprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed IdentifierAddressvivo:address1address line 1vivo:addressCitycityvivo:addressPostalCodepostal codevivo:addressStatestate or provincevivo:authorInAuthorshipselected publicationsvivo:authorRankauthor rank in publicationAuthorshipDepartmentDivisionvivo:hasResearchArearesearch areasvivo:hrJobTitleHR job titleInformation Resourcevivo:linkedAuthorlinked authorvivo:linkedInformationResourcelinked information resourcevivo:mailingAddressmailing addressvivo:personInPositionpositionsPositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlerdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPerson25339213Graves J, Grandhe S, Weinfurtner K, Krupp L, Belman A, Chitnis T, Ness J, Weinstock-Guttman B, Gorman M, Patterson M, Rodriguez M, Lotze T, Aaen G, Mowry EM, Rose JW, Simmons T, Casper TC, James J, Waubant E, US Network of Pediatric Multiple Sclerosis CentersNeurologyProtective environmental factors for neuromyelitis optica. Neurology. 2014 Nov 18; 83(21):1923-9.Neurology2014-10-22T00:00:002014Protective environmental factors for neuromyelitis optica.Authorship 826969Authorship 835722Pharmaceutical Health Outcomes and PolicyAuthorship 901724Authorship 956761Authorship 1193053Authorship 55638326805781Lalani SR, Liu P, Rosenfeld JA, Watkin LB, Chiang T, Leduc MS, Zhu W, Ding Y, Pan S, Vetrini F, Miyake CY, Shinawi M, Gambin T, Eldomery MK, Akdemir ZH, Emrick L, Wilnai Y, Schelley S, Koenig MK, Memon N, Farach LS, Coe BP, Azamian M, Hernandez P, Zapata G, Jhangiani SN, Muzny DM, Lotze T, Clark G, Wilfong A, Northrup H, Adesina A, Bacino CA, Scaglia F, Bonnen PE, Crosson J, Duis J, Maegawa GH, Coman D, Inwood A, McGill J, Boerwinkle E, Graham B, Beaudet A, Eng CM, Hanchard NA, Xia F, Orange JS, Gibbs RA, Lupski JR, Yang YAmerican journal of human geneticsRecurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations. Am J Hum Genet. 2016 Feb 04; 98(2):347-57.Am J Hum Genet2016-01-21T00:00:002016Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations.6621 FANNINHouston, 77030TXAuthorship 29212310Authorship 2942729Authorship 3024608Authorship 304067225270659Casper TC, Rose JW, Roalstad S, Waubant E, Aaen G, Belman A, Chitnis T, Gorman M, Krupp L, Lotze TE, Ness J, Patterson M, Rodriguez M, Weinstock-Guttman B, Browning B, Graves J, Tillema JM, Benson L, Harris Y, US Network of Pediatric Multiple Sclerosis CentersJournal of child neurologyThe US Network of Pediatric Multiple Sclerosis Centers: Development, Progress, and Next Steps. J Child Neurol. 2015 Sep; 30(10):1381-7.J Child Neurol2014-09-30T00:00:002014The US Network of Pediatric Multiple Sclerosis Centers: Development, Progress, and Next Steps.25906753Spurney CF, McCaffrey FM, Cnaan A, Morgenroth LP, Ghelani SJ, Gordish-Dressman H, Arrieta A, Connolly AM, Lotze TE, McDonald CM, Leshner RT, Clemens PRJournal of the American Society of Echocardiography : official publication of the American Society of EchocardiographyFeasibility and Reproducibility of Echocardiographic Measures in Children with Muscular Dystrophies. J Am Soc Echocardiogr. 2015 Aug; 28(8):999-1008.J Am Soc Echocardiogr2015-04-21T00:00:002015Feasibility and Reproducibility of Echocardiographic Measures in Children with Muscular Dystrophies.26060307Pena JA, Lotze T, Yang Y, Umana L, Walkiewicz M, Hunter JV, Scaglia FJournal of child neurologyMethionyl-tRNA Formyltransferase (MTFMT) Deficiency Mimicking Acquired Demyelinating Disease. J Child Neurol. 2016 Feb; 31(2):215-9.J Child Neurol2015-06-09T00:00:002015Methionyl-tRNA Formyltransferase (MTFMT) Deficiency Mimicking Acquired Demyelinating Disease.26683648Chitnis T, Ness J, Krupp L, Waubant E, Hunt T, Olsen CS, Rodriguez M, Lotze T, Gorman M, Benson L, Belman A, Weinstock-Guttman B, Aaen G, Graves J, Patterson M, Rose JW, Casper TCNeurologyClinical features of neuromyelitis optica in children: US Network of Pediatric MS Centers report. Neurology. 2016 Jan 19; 86(3):245-52.Neurology2015-12-18T00:00:002015Clinical features of neuromyelitis optica in children: US Network of Pediatric MS Centers report.26952271Chiang DY, Allen HD, Kim JJ, Valdes SO, Wang Y, Pignatelli RH, Lotze TE, Miyake CYThe American journal of cardiologyRelation of Cardiac Dysfunction to Rhythm Abnormalities in Patients With Duchenne or Becker Muscular Dystrophies. Am J Cardiol. 2016 Apr 15; 117(8):1349-54.Am J Cardiol2016-01-28T00:00:002016Relation of Cardiac Dysfunction to Rhythm Abnormalities in Patients With Duchenne or Becker Muscular Dystrophies.Authorship 316224Authorship 3162257Authorship 3162264Authorship 31622728Authorship 3162287McDonald J, Graves J, Waldman A, Lotze T, Schreiner T, Belman A, Greenberg B, Weinstock-Guttman B, Aaen G, Tillema JM, Hart J, Lulu S, Ness J, Harris Y, Rubin J, Candee M, Krupp LB, Gorman M, Benson L, Rodriguez M, Chitnis T, Mar S, Barcellos LF, Laraia B, Rose J, Roalstad S, Simmons T, Casper TC, Waubant EMult Scler Relat Disord.A case-control study of dietary salt intake in pediatric-onset multiple sclerosis. Mult Scler Relat Disord. 2016; 6:87-92.2016-03-01T00:00:002016A case-control study of dietary salt intake in pediatric-onset multiple sclerosis26870756Bacino C, Chao YH, Seto E, Lotze T, Xia F, Jones RO, Moser A, Wangler MFData in briefDataset for a case report of a homozygous PEX16 F332del mutation. Data Brief. 2016 Mar; 6:722-7.Data Brief2015-12-17T00:00:002015Dataset for a case report of a homozygous PEX16 F332del mutation.26788680Agarwal S, Potocki L, Collier TR, Woodbury SL, Adesina AM, Jones J, Lotze TEMuscle & nerveUtility of whole exome sequencing in evaluation of juvenile motor neuron disease. Muscle Nerve. 2016 Apr; 53(4):648-52.Muscle Nerve2016-02-22T00:00:002016Utility of whole exome sequencing in evaluation of juvenile motor neuron disease.74Professor10Assistant Professor54Instructor14Associate Professor46Distinguished Emeritus Professor78Professor Emeritus6Adjunct ProfessorAuthorship 3248411127358474Belman AL, Krupp LB, Olsen CS, Rose JW, Aaen G, Benson L, Chitnis T, Gorman M, Graves J, Harris Y, Lotze T, Ness J, Rodriguez M, Tillema JM, Waubant E, Weinstock-Guttman B, Casper TC, US Network of Pediatric MS CentersPediatricsCharacteristics of Children and Adolescents With Multiple Sclerosis. Pediatrics. 2016 07; 138(1).Pediatrics2016-07-01T00:00:002016Characteristics of Children and Adolescents With Multiple Sclerosis.Authorship 326437427572861Absoud M, Greenberg BM, Lim M, Lotze T, Thomas T, Deiva KNeurologyPediatric transverse myelitis. Neurology. 2016 Aug 30; 87(9 Suppl 2):S46-52.Neurology2016-08-30T00:00:002016Pediatric transverse myelitis.14745073Lotze TE, Wilfong AANeurologyZonisamide treatment for symptomatic infantile spasms. Neurology. 2004 Jan 27; 62(2):296-8.Neurology2004-01-27T00:00:002004Zonisamide treatment for symptomatic infantile spasms.15520093Maricich SM, Neul JL, Lotze TE, Cazacu AC, Uyeki TM, Demmler GJ, Clark GDPediatricsNeurologic complications associated with influenza A in children during the 2003-2004 influenza season in Houston, Texas. Pediatrics. 2004 Nov; 114(5):e626-33.Pediatrics2004-11-01T00:00:002004Neurologic complications associated with influenza A in children during the 2003-2004 influenza season in Houston, Texas.19027335Dhar SU, Scaglia F, Li FY, Smith L, Barshop BA, Eng CM, Haas RH, Hunter JV, Lotze T, Maranda B, Willis M, Abdenur JE, Chen E, O'Brien W, Wong LJMolecular genetics and metabolismExpanded clinical and molecular spectrum of guanidinoacetate methyltransferase (GAMT) deficiency. Mol Genet Metab. 2009 Jan; 96(1):38-43.Mol Genet Metab2008-11-21T00:00:002008Expanded clinical and molecular spectrum of guanidinoacetate methyltransferase (GAMT) deficiency.19029900Brunetti-Pierri N, Berg JS, Scaglia F, Belmont J, Bacino CA, Sahoo T, Lalani SR, Graham B, Lee B, Shinawi M, Shen J, Kang SH, Pursley A, Lotze T, Kennedy G, Lansky-Shafer S, Weaver C, Roeder ER, Grebe TA, Arnold GL, Hutchison T, Reimschisel T, Amato S, Geragthy MT, Innis JW, Obersztyn E, Nowakowska B, Rosengren SS, Bader PI, Grange DK, Naqvi S, Garnica AD, Bernes SM, Fong CT, Summers A, Walters WD, Lupski JR, Stankiewicz P, Cheung SW, Patel ANature geneticsRecurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities. Nat Genet. 2008 Dec; 40(12):1466-71.Nat Genet2008-12-01T00:00:002008Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.19038852Callen DJ, Shroff MM, Branson HM, Lotze T, Li DK, Stephens D, Banwell BLNeurologyMRI in the diagnosis of pediatric multiple sclerosis. Neurology. 2009 Mar 17; 72(11):961-7.Neurology2008-11-26T00:00:002008MRI in the diagnosis of pediatric multiple sclerosis.Authorship 3281393727640307Harel T, Yoon WH, Garone C, Gu S, Coban-Akdemir Z, Eldomery MK, Posey JE, Jhangiani SN, Rosenfeld JA, Cho MT, Fox S, Withers M, Brooks SM, Chiang T, Duraine L, Erdin S, Yuan B, Shao Y, Moussallem E, Lamperti C, Donati MA, Smith JD, McLaughlin HM, Eng CM, Walkiewicz M, Xia F, Pippucci T, Magini P, Seri M, Zeviani M, Hirano M, Hunter JV, Srour M, Zanigni S, Lewis RA, Muzny DM, Lotze TE, Boerwinkle E, Baylor-Hopkins Center for Mendelian Genomics, University of Washington Center for Mendelian Genomics, Gibbs RA, Hickey SE, Graham BH, Yang Y, Buhas D, Martin DM, Potocki L, Graziano C, Bellen HJ, Lupski JRAmerican journal of human geneticsRecurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes. Am J Hum Genet. 2016 Oct 06; 99(4):831-845.Am J Hum Genet2016-09-15T00:00:002016Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes.15710863Lalani SR, Vladutiu GD, Plunkett K, Lotze TE, Adesina AM, Scaglia FArchives of neurologyIsolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiency. Arch Neurol. 2005 Feb; 62(2):317-20.Arch Neurol2005-02-01T00:00:002005Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiency.23045520Coorg R, Lotze TENeurologyChild Neurology: a case of PMM2-CDG (CDG 1a) presenting with unusual eye movements. Neurology. 2012 Oct 09; 79(15):e131-3.Neurology2012-10-09T00:00:002012Child Neurology: a case of PMM2-CDG (CDG 1a) presenting with unusual eye movements.17712245Treadwell-Deering D, Evankovich K, Lotze TJournal of the American Academy of Child and Adolescent PsychiatryCase report: "Purely" psychiatric presentation of multiple sclerosis in an adolescent boy. J Am Acad Child Adolesc Psychiatry. 2007 Sep; 46(9):1213-1217.J Am Acad Child Adolesc Psychiatry2007-09-01T00:00:002007Case report: "Purely" psychiatric presentation of multiple sclerosis in an adolescent boy.18509092McKeon A, Lennon VA, Lotze T, Tenenbaum S, Ness JM, Rensel M, Kuntz NL, Fryer JP, Homburger H, Hunter J, Weinshenker BG, Krecke K, Lucchinetti CF, Pittock SJNeurologyCNS aquaporin-4 autoimmunity in children. Neurology. 2008 Jul 08; 71(2):93-100.Neurology2008-05-28T00:00:002008CNS aquaporin-4 autoimmunity in children.18838462Lotze TE, Northrop JL, Hutton GJ, Ross B, Schiffman JS, Hunter JVPediatricsSpectrum of pediatric neuromyelitis optica. Pediatrics. 2008 Nov; 122(5):e1039-47.Pediatrics2008-10-06T00:00:002008Spectrum of pediatric neuromyelitis optica.Authorship 652560426644994Bacino C, Chao YH, Seto E, Lotze T, Xia F, Jones RO, Moser A, Wangler MFMolecular genetics and metabolism reportsA homozygous mutation in PEX16 identified by whole-exome sequencing ending a diagnostic odyssey. Mol Genet Metab Rep. 2015 Dec 01; 5:15-18.Mol Genet Metab Rep2015-12-01T00:00:002015A homozygous mutation in PEX16 identified by whole-exome sequencing ending a diagnostic odyssey.21753160Escolar DM, Hache LP, Clemens PR, Cnaan A, McDonald CM, Viswanathan V, Kornberg AJ, Bertorini TE, Nevo Y, Lotze T, Pestronk A, Ryan MM, Monasterio E, Day JW, Zimmerman A, Arrieta A, Henricson E, Mayhew J, Florence J, Hu F, Connolly AMNeurologyRandomized, blinded trial of weekend vs daily prednisone in Duchenne muscular dystrophy. Neurology. 2011 Aug 02; 77(5):444-52.Neurology2011-07-13T00:00:002011Randomized, blinded trial of weekend vs daily prednisone in Duchenne muscular dystrophy.22488736Holder JL, Lotze TE, Bacino C, Cheung SWAmerican journal of medical genetics. Part AA child with an inherited 0.31?Mb microdeletion of chromosome 14q32.33: further delineation of a critical region for the 14q32 deletion syndrome. Am J Med Genet A. 2012 Aug; 158A(8):1962-6.Am J Med Genet A2012-04-09T00:00:002012A child with an inherited 0.31?Mb microdeletion of chromosome 14q32.33: further delineation of a critical region for the 14q32 deletion syndrome.Authorship 8685081528320170Bourne T, Waltz M, Casper TC, Kavak K, Aaen G, Belman A, Benson L, Candee M, Chitnis T, Graves J, Greenberg B, Gorman M, Harris Y, Krupp L, Lotze T, Mar S, Ness J, Olsen C, Roalstad S, Rodriguez M, Rose J, Rubin J, Schreiner T, Tillema JM, Kahn I, Waldman A, Barcellos L, Waubant E, Weinstock-Guttman B, US Network of Pediatric MS CentersJournal of the neurological sciencesEvaluating the association of allergies with multiple sclerosis susceptibility risk and disease activity in a pediatric population. J Neurol Sci. 2017 Apr 15; 375:371-375.J Neurol Sci2017-02-20T00:00:002017Evaluating the association of allergies with multiple sclerosis susceptibility risk and disease activity in a pediatric population.Authorship 868672928356466Gianfrancesco MA, Stridh P, Rhead B, Shao X, Xu E, Graves JS, Chitnis T, Waldman A, Lotze T, Schreiner T, Belman A, Greenberg B, Weinstock-Guttman B, Aaen G, Tillema JM, Hart J, Caillier S, Ness J, Harris Y, Rubin J, Candee M, Krupp L, Gorman M, Benson L, Rodriguez M, Mar S, Kahn I, Rose J, Roalstad S, Casper TC, Shen L, Quach H, Quach D, Hillert J, B??rnhielm M, Hedstrom A, Olsson T, Kockum I, Alfredsson L, Metayer C, Schaefer C, Barcellos LF, Waubant E, Network of Pediatric Multiple Sclerosis CentersNeurologyEvidence for a causal relationship between low vitamin D, high BMI, and pediatric-onset MS. Neurology. 2017 Apr 25; 88(17):1623-1629.Neurology2017-03-29T00:00:002017Evidence for a causal relationship between low vitamin D, high BMI, and pediatric-onset MS.Authorship 869167928393317Yeh EA, Grover SA, Powell VE, Alper G, Banwell BL, Edwards K, Gorman M, Graves J, Lotze TE, Mah JK, Mednick L, Ness J, Obadia M, Slater R, Waldman A, Waubant E, Schwartz CE, Pediatric MS Adherence Study GroupQuality of life research : an international journal of quality of life aspects of treatment, care and rehabilitationImpact of an electronic monitoring device and behavioral feedback on adherence to multiple sclerosis therapies in youth: results of a randomized trial. Qual Life Res. 2017 09; 26(9):2333-2349.Qual Life Res2017-04-09T00:00:002017Impact of an electronic monitoring device and behavioral feedback on adherence to multiple sclerosis therapies in youth: results of a randomized trial.Authorship 8699811028457522Burrage LC, Guillerman RP, Das S, Singh S, Schady DA, Morris SA, Walkiewicz M, Schecter MG, Heinle JS, Lotze TE, Lalani SR, Mallory GBThe Journal of pediatricsLung Transplantation for FLNA-Associated Progressive Lung Disease. J Pediatr. 2017 07; 186:118-123.e6.J Pediatr2017-04-28T00:00:002017Lung Transplantation for FLNA-Associated Progressive Lung Disease.Authorship 8722474Authorship 8723901327063630McDonald J, Graves J, Waldman A, Lotze T, Schreiner T, Belman A, Greenberg B, Weinstock-Guttman B, Aaen G, Tillema JM, Hart J, Lulu S, Ness J, Harris Y, Rubin J, Candee M, Krupp LB, Gorman M, Benson L, Rodriguez M, Chitnis T, Mar S, Barcellos LF, Laraia B, Rose J, Roalstad S, Simmons T, Casper TC, Waubant EMultiple sclerosis and related disordersA case-control study of dietary salt intake in pediatric-onset multiple sclerosis. Mult Scler Relat Disord. 2016 Mar; 6:87-92.Mult Scler Relat Disord2016-02-12T00:00:002016A case-control study of dietary salt intake in pediatric-onset multiple sclerosis.28097202Chitnis T, Graves J, Weinstock-Guttman B, Belman A, Olsen C, Misra M, Aaen G, Benson L, Candee M, Gorman M, Greenberg B, Krupp L, Lotze T, Mar S, Ness J, Rose J, Rubin J, Schreiner T, Tillema J, Waldman A, Rodriguez M, Casper C, Waubant E, U.S. Network of Pediatric MS CentersAnnals of clinical and translational neurologyDistinct effects of obesity and puberty on risk and age at onset of pediatric MS. Ann Clin Transl Neurol. 2016 12; 3(12):897-907.Ann Clin Transl Neurol2016-11-04T00:00:002016Distinct effects of obesity and puberty on risk and age at onset of pediatric MS.Authorship 872884628608728Pakpoor J, Seminatore B, Graves JS, Schreiner T, Waldman AT, Lotze TE, Belman A, Greenberg BM, Weinstock-Guttman B, Aaen G, Tillema JM, McDonald JC, Hart J, Ness JM, Harris Y, Rubin J, Candee M, Krupp L, Gorman M, Benson L, Rodriguez M, Chitnis T, Mar S, Kahn I, Rose J, Carmichael SL, Roalstad S, Waltz M, Casper TC, Waubant E, US Network of Pediatric Multiple Sclerosis CentersMultiple sclerosis (Houndmills, Basingstoke, England)Dietary factors and pediatric multiple sclerosis: A case-control study. Mult Scler. 2018 07; 24(8):1067-1076.Mult Scler2017-06-13T00:00:002017Dietary factors and pediatric multiple sclerosis: A case-control study.28671037Murrell DV, Lotze TE, Farber HJ, Crawford CA, Wiemann CMJournal of child neurologyThe Experience of Families With Children With Spinal Muscular Atrophy Type I Across Health Care Systems. J Child Neurol. 2017 Oct; 32(11):917-923.J Child Neurol2017-07-03T00:00:002017The Experience of Families With Children With Spinal Muscular Atrophy Type I Across Health Care Systems.11063085Lotze TE, Paolicchi JJournal of child neurologyVertebral artery dissection and migraine headaches in children. J Child Neurol. 2000 Oct; 15(10):694-6.J Child Neurol2000-10-01T00:00:002000Vertebral artery dissection and migraine headaches in children.Authorship 875349212785750Lotze T, Jankovic JSeminars in pediatric neurologyParoxysmal kinesigenic dyskinesias. Semin Pediatr Neurol. 2003 Mar; 10(1):68-79.Semin Pediatr Neurol2003-03-01T00:00:002003Paroxysmal kinesigenic dyskinesias.28742085Luo X, Rosenfeld JA, Yamamoto S, Harel T, Zuo Z, Hall M, Wierenga KJ, Pastore MT, Bartholomew D, Delgado MR, Rotenberg J, Lewis RA, Emrick L, Bacino CA, Eldomery MK, Coban Akdemir Z, Xia F, Yang Y, Lalani SR, Lotze T, Lupski JR, Lee B, Bellen HJ, Wangler MF, Members of the UDNPLoS geneticsClinically severe CACNA1A alleles affect synaptic function and neurodegeneration differentially. PLoS Genet. 2017 Jul; 13(7):e1006905.PLoS Genet2017-07-24T00:00:002017Clinically severe CACNA1A alleles affect synaptic function and neurodegeneration differentially.15791925Johnsen SD, Bodensteiner JB, Lotze TEJournal of child neurologyFrequency and nature of cerebellar injury in the extremely premature survivor with cerebral palsy. J Child Neurol. 2005 Jan; 20(1):60-4.J Child Neurol2005-01-01T00:00:002005Frequency and nature of cerebellar injury in the extremely premature survivor with cerebral palsy.19038851Callen DJ, Shroff MM, Branson HM, Li DK, Lotze T, Stephens D, Banwell BLNeurologyRole of MRI in the differentiation of ADEM from MS in children. Neurology. 2009 Mar 17; 72(11):968-73.Neurology2008-11-26T00:00:002008Role of MRI in the differentiation of ADEM from MS in children.Authorship 8777107Authorship 8777119Authorship 87771224Authorship 8777135Authorship 87771420Authorship 8777158Authorship 8777162021414825Fruhman G, Landsverk ML, Lotze TE, Hunter JV, Wangler MF, Adesina AM, Wong LJ, Scaglia FMolecular genetics and metabolismAtypical presentation of Leigh syndrome associated with a Leber hereditary optic neuropathy primary mitochondrial DNA mutation. Mol Genet Metab. 2011 Jun; 103(2):153-60.Mol Genet Metab2011-02-26T00:00:002011Atypical presentation of Leigh syndrome associated with a Leber hereditary optic neuropathy primary mitochondrial DNA mutation.22585439Shah S, Freeman E, Wolf V, Murthy S, Lotze TNeurologyIntracranial optic nerve enlargement in infantile Krabbe disease. Neurology. 2012 May 15; 78(20):e126.Neurology2012-05-15T00:00:002012Intracranial optic nerve enlargement in infantile Krabbe disease.22914370Wolf VL, Lupo PJ, Lotze TEJournal of child neurologyPediatric acute transverse myelitis overview and differential diagnosis. J Child Neurol. 2012 Nov; 27(11):1426-36.J Child Neurol2012-08-21T00:00:002012Pediatric acute transverse myelitis overview and differential diagnosis.29334853Agarwal S, Keller JR, Nunneley CE, Muscal E, Braun MC, Srivaths P, Lotze TEJournal of child neurologyTherapeutic Plasma Exchange Use in Pediatric Neurologic Disorders at a Tertiary Care Center: A 10-Year Review. J Child Neurol. 2018 02; 33(2):140-145.J Child Neurol2018-02-01T00:00:002018Therapeutic Plasma Exchange Use in Pediatric Neurologic Disorders at a Tertiary Care Center: A 10-Year Review.29274015Yeh EA, Grover SA, Powell VE, Alper G, Banwell BL, Edwards K, Gorman M, Graves J, Lotze TE, Mah JK, Mednick L, Ness J, Obadia M, Slater R, Waldman A, Waubant E, Schwartz CE, Pediatric MS Adherence Study GroupQuality of life research : an international journal of quality of life aspects of treatment, care and rehabilitationCorrection to: Impact of an electronic monitoring device and behavioural feedback on adherence to multiple sclerosis therapies in youth: results of a randomized trial. Qual Life Res. 2018 04; 27(4):1117.Qual Life Res2018-04-01T00:00:002018Correction to: Impact of an electronic monitoring device and behavioural feedback on adherence to multiple sclerosis therapies in youth: results of a randomized trial.29141802Lavery AM, Waldman AT, Charles Casper T, Roalstad S, Candee M, Rose J, Belman A, Weinstock-Guttman B, Aaen G, Tillema JM, Rodriguez M, Ness J, Harris Y, Graves J, Krupp L, Benson L, Gorman M, Moodley M, Rensel M, Goyal M, Mar S, Chitnis T, Schreiner T, Lotze T, Greenberg B, Kahn I, Rubin J, Waubant E, U.S. Network of Pediatric MS CentersMultiple sclerosis and related disordersExamining the contributions of environmental quality to pediatric multiple sclerosis. Mult Scler Relat Disord. 2017 Nov; 18:164-169.Mult Scler Relat Disord2017-09-07T00:00:002017Examining the contributions of environmental quality to pediatric multiple sclerosis.29049805Self MM, Fobian A, Cutitta K, Wallace A, Lotze TEJournal of pediatric psychologyHealth-Related Quality of Life in Pediatric Patients With Demyelinating Diseases: Relevance of Disability, Relapsing Presentation, and Fatigue. J Pediatr Psychol. 2018 03 01; 43(2):133-142.J Pediatr Psychol2018-03-01T00:00:002018Health-Related Quality of Life in Pediatric Patients With Demyelinating Diseases: Relevance of Disability, Relapsing Presentation, and Fatigue.28993476Azary S, Schreiner T, Graves J, Waldman A, Belman A, Guttman BW, Aaen G, Tillema JM, Mar S, Hart J, Ness J, Harris Y, Krupp L, Gorman M, Benson L, Rodriguez M, Chitnis T, Rose J, Barcellos LF, Lotze T, Carmichael SL, Roalstad S, Casper CT, Waubant EJournal of neurology, neurosurgery, and psychiatryContribution of dietary intake to relapse rate in early paediatric multiple sclerosis. J Neurol Neurosurg Psychiatry. 2018 01; 89(1):28-33.J Neurol Neurosurg Psychiatry2017-10-09T00:00:002017Contribution of dietary intake to relapse rate in early paediatric multiple sclerosis.28980494Gianfrancesco MA, Stridh P, Shao X, Rhead B, Graves JS, Chitnis T, Waldman A, Lotze T, Schreiner T, Belman A, Greenberg B, Weinstock-Guttman B, Aaen G, Tillema JM, Hart J, Caillier S, Ness J, Harris Y, Rubin J, Candee M, Krupp L, Gorman M, Benson L, Rodriguez M, Mar S, Kahn I, Rose J, Roalstad S, Casper TC, Shen L, Quach H, Quach D, Hillert J, Hedstrom A, Olsson T, Kockum I, Alfredsson L, Schaefer C, Barcellos LF, Waubant E, Network of Pediatric Multiple Sclerosis CentersMultiple sclerosis (Houndmills, Basingstoke, England)Genetic risk factors for pediatric-onset multiple sclerosis. Mult Scler. 2018 12; 24(14):1825-1834.Mult Scler2017-10-05T00:00:002017Genetic risk factors for pediatric-onset multiple sclerosis.Authorship 8856391529653437Suleiman L, Waubant E, Aaen G, Belman A, Benson L, Candee M, Chitnis T, Gorman M, Goyal M, Greenberg B, Harris Y, Hart J, Kahn I, Krupp L, Lotze T, Mar S, Moodley M, Ness J, Nourbakhsh B, Rensel M, Rodriguez M, Rose J, Rubin J, Schreiner T, Tillema JM, Waldman A, Weinstock-Guttman B, Casper TC, Waltz M, Graves JS, Network of Pediatric Multiple Sclerosis Centers.Multiple sclerosis and related disordersEarly infectious exposures are not associated with increased risk of pediatric-onset multiple sclerosis. Mult Scler Relat Disord. 2018 May; 22:103-107.Mult Scler Relat Disord2018-03-26T00:00:002018Early infectious exposures are not associated with increased risk of pediatric-onset multiple sclerosis.true1ProfessorProfessortrue1Assistant ProfessorAssistant Professortrue1ProfessorProfessortrue1ProfessorProfessortrue1Assistant ProfessorAssistant ProfessorAuthorship 891052Emmanuell Waubant, TImothy Lotze (Eds.)Pediatric Demyelinating Diseases of the Central Nervous System and Their Mimics
A Case-Based Clinical GuidePediatric Demyelinating Diseases of the Central Nervous System and Their Mimics
A Case-Based Clinical Guide. 2017.2017-10-01T00:00:002017Pediatric Demyelinating Diseases of the Central Nervous System and Their Mimics
A Case-Based Clinical GuideD009462Occupations691120.855001NeurologyD014897Disorders14210.974869Spinal Muscular Atrophies of ChildhoodD009103Disorders1243480.753802Multiple SclerosisD009422Disorders3234970.699843Nervous System DiseasesAuthorship 10952410Authorship 9164923Authorship 93221221Authorship 9334154Authorship 93574614Authorship 9398109Authorship 9401432530266528Murrell DV, Crawford CA, Jackson CT, Lotze TE, Wiemann CMJournal of pediatric nursingIdentifying Opportunities to Provide Family-centered Care for Families With Children With Type 1 Spinal Muscular Atrophy. J Pediatr Nurs. 2018 Nov - Dec; 43:111-119.J Pediatr Nurs2018-09-25T00:00:002018Identifying Opportunities to Provide Family-centered Care for Families With Children With Type 1 Spinal Muscular Atrophy.30167764Ortiz CB, Kukreja KU, Lotze TE, Chau APediatric radiologyUltrasound-guided cervical puncture for nusinersen administration in adolescents. Pediatr Radiol. 2019 01; 49(1):136-140.Pediatr Radiol2018-08-30T00:00:002018Ultrasound-guided cervical puncture for nusinersen administration in adolescents.30349849Lavery AM, Waubant E, Casper TC, Roalstad S, Candee M, Rose J, Belman A, Weinstock-Guttman B, Aaen G, Tillema JM, Rodriguez M, Ness J, Harris Y, Graves J, Krupp L, Charvet L, Benson L, Gorman M, Moodley M, Rensel M, Goyal M, Mar S, Chitnis T, Schreiner T, Lotze T, Greenberg B, Kahn I, Rubin J, Waldman ATAnnals of clinical and translational neurologyUrban air quality and associations with pediatric multiple sclerosis. Ann Clin Transl Neurol. 2018 Oct; 5(10):1146-1153.Ann Clin Transl Neurol2018-09-27T00:00:002018Urban air quality and associations with pediatric multiple sclerosis.30653506Chi C, Shao X, Rhead B, Gonzales E, Smith JB, Xiang AH, Graves J, Waldman A, Lotze T, Schreiner T, Weinstock-Guttman B, Aaen G, Tillema JM, Ness J, Candee M, Krupp L, Gorman M, Benson L, Chitnis T, Mar S, Belman A, Casper TC, Rose J, Moodley M, Rensel M, Rodriguez M, Greenberg B, Kahn L, Rubin J, Schaefer C, Waubant E, Langer-Gould A, Barcellos LFPLoS geneticsAdmixture mapping reveals evidence of differential multiple sclerosis risk by genetic ancestry. PLoS Genet. 2019 01; 15(1):e1007808.PLoS Genet2019-01-17T00:00:002019Admixture mapping reveals evidence of differential multiple sclerosis risk by genetic ancestry.30556452Aaen G, Waltz M, Vargas W, Makhani N, Ness J, Harris Y, Casper TC, Benson L, Candee M, Chitnis T, Gorman M, Graves J, Greenberg B, Lotze T, Mar S, Tillema JM, Rensel M, Rodriguez M, Rose J, Rubin J, Schreiner T, Waldman A, Weinstock-Guttman B, Belman A, Waubant E, Krupp LJournal of child neurologyAcquisition of Early Developmental Milestones and Need for Special Education Services in Pediatric Multiple Sclerosis. J Child Neurol. 2019 03; 34(3):148-152.J Child Neurol2018-12-17T00:00:002018Acquisition of Early Developmental Milestones and Need for Special Education Services in Pediatric Multiple Sclerosis.30564618Mar S, Liang S, Waltz M, Casper TC, Goyal M, Greenberg B, Weinstock-Guttman B, Rodriguez M, Aaen G, Belman A, Barcellos LF, Rose J, Gorman M, Benson L, Candee M, Chitnis T, Harris Y, Kahn I, Roalsted S, Hart J, Lotze T, Moodley M, Ness J, Rensel M, Rubin J, Schreiner T, Tillema JM, Waldman A, Krupp L, Graves JS, Waubant E, U.S. Network of Pediatric Multiple Sclerosis CentersAnnals of clinical and translational neurologySeveral household chemical exposures are associated with pediatric-onset multiple sclerosis. Ann Clin Transl Neurol. 2018 Dec; 5(12):1513-1521.Ann Clin Transl Neurol2018-10-09T00:00:002018Several household chemical exposures are associated with pediatric-onset multiple sclerosis.D009471Disorders13260.960581Neuromyelitis OpticaDepartment of NeurologyDepartment of OphthalmologyDepartment of PediatricsDepartment of Molecular & Human GeneticsMolecular & Human GeneticsNeurologyOphthalmologyPediatrics-NeurologyPediatrics-PsychologyBaylor College of MedicineUniversity of Houston College of PharmacyANDREWLEEANDREW LEE0.000000000000000.000000000000001958LEE, ANDREWAdjunct Professor4.771920.00723457439research areas1.764320.021610897coauthor of49.86469.6566460similar to11112selected publicationsMICHELLEHOLICKMICHELLE HOLICK29.70508570000000-95.401808700000003855HOLICK, MICHELLEAssistant ProfessorJOSEPHJANKOVICJOSEPH JANKOVIC0.000000000000000.000000000000002398JANKOVIC, JOSEPHProfessorROBERTZELLERROBERT ZELLER29.70508570000000-95.401808700000002565ZELLER, ROBERTProfessor EmeritusMARIELLASELFMARIELLA SELF0.000000000000000.00000000000000793SELF, MARIELLAProfessorMARVINFISHMANMARVIN FISHMAN29.70508570000000-95.401808700000002815FISHMAN, MARVINProfessor EmeritusJAMESLUPSKIJAMES LUPSKI29.71073630000000-95.396604500000003140LUPSKI, JAMESProfessorGARYCLARKGARY CLARK29.70508570000000-95.401808700000003440CLARK, GARYProfessorVICTORRIVERAVICTOR RIVERA0.000000000000000.000000000000003455RIVERA, VICTORDistinguished Emeritus ProfessorBERNHARDSUTERBERNHARD SUTER29.70508570000000-95.401808700000003873SUTER, BERNHARDAssociate ProfessorRAJENDERAPARASURAJENDER R. APARASU29.70508570000000-95.401808700000004604APARASU, RAJENDERProfessorAuthorship 9436161130333163Krysko KM, Graves J, Rensel M, Weinstock-Guttman B, Aaen G, Benson L, Chitnis T, Gorman M, Goyal M, Krupp L, Lotze T, Mar S, Rodriguez M, Rose J, Waltz M, Charles Casper T, Waubant E, US Network of Pediatric MS CentersNeurologyUse of newer disease-modifying therapies in pediatric multiple sclerosis in the US. Neurology. 2018 11 06; 91(19):e1778-e1787.Neurology2018-10-17T00:00:002018Use of newer disease-modifying therapies in pediatric multiple sclerosis in the US.Authorship 945005530966859Jimenez-Gomez A, Stowe RC, Balasa A, Castillo J, Lotze TEJournal of child neurologyGlobal Health Education in Child Neurology and Neurodevelopmental Disabilities Training Programs in the United States: A National Survey. J Child Neurol. 2019 07; 34(8):452-457.J Child Neurol2019-04-09T00:00:002019Global Health Education in Child Neurology and Neurodevelopmental Disabilities Training Programs in the United States: A National Survey.Authorship 1114933Authorship 9469561431081484Graves JS, Barcellos LF, Krupp L, Belman A, Shao X, Quach H, Hart J, Chitnis T, Weinstock-Guttman B, Aaen G, Benson L, Gorman M, Greenberg B, Lotze T, Soe M, Ness J, Rodriguez M, Rose J, Schreiner T, Tillema JM, Waldman A, Casper TC, Waubant EMultiple sclerosis (Houndmills, Basingstoke, England)Vitamin D genes influence MS relapses in children. Mult Scler. 2020 07; 26(8):894-901.Mult Scler2019-05-13T00:00:002019Vitamin D genes influence MS relapses in children.Authorship 950128631211169Rhead B, Shao X, Graves JS, Chitnis T, Waldman AT, Lotze T, Schreiner T, Belman A, Krupp L, Greenberg BM, Weinstock-Guttman B, Aaen G, Tillema JM, Rodriguez M, Hart J, Caillier S, Ness J, Harris Y, Rubin J, Candee MS, Gorman M, Benson L, Mar S, Kahn I, Rose J, Casper TC, Quach H, Quach D, Schaefer C, Waubant E, Barcellos LF, US Network of Pediatric MS CentersAnnals of clinical and translational neurologymiRNA contributions to pediatric-onset multiple sclerosis inferred from GWAS. Ann Clin Transl Neurol. 2019 Jun; 6(6):1053-1061.Ann Clin Transl Neurol2019-05-15T00:00:002019miRNA contributions to pediatric-onset multiple sclerosis inferred from GWAS.Authorship 951678331294820Hsieh DT, Faux BM, Lotze TEHeadacheHeadache and Hypoglossal Nerve Palsy in a Child With Idiopathic Hypertrophic Pachymeningitis. Headache. 2019 09; 59(8):1390-1391.Headache2019-07-11T00:00:002019Headache and Hypoglossal Nerve Palsy in a Child With Idiopathic Hypertrophic Pachymeningitis.true1ProfessorProfessorAuthorship 1087532Authorship 9617621131775571Wallach AI, Waltz M, Casper TC, Aaen G, Belman A, Benson L, Chitnis T, Gorman M, Graves J, Harris Y, Lotze TE, Mar S, Moodley M, Ness JM, Rensel M, Rodriguez M, Rose JW, Schreiner T, Tillema JM, Waubant E, Weinstock-Guttman B, Charvet LE, Krupp LBMultiple sclerosis (Houndmills, Basingstoke, England)Cognitive processing speed in pediatric-onset multiple sclerosis: Baseline characteristics of impairment and prediction of decline. Mult Scler. 2020 12; 26(14):1938-1947.Mult Scler2019-11-28T00:00:002019Cognitive processing speed in pediatric-onset multiple sclerosis: Baseline characteristics of impairment and prediction of decline.Authorship 9792901632181591Markovitz R, Ghosh R, Kuo ME, Hong W, Lim J, Bernes S, Manberg S, Crosby K, Tanpaiboon P, Bharucha-Goebel D, Bonnemann C, Mohila CA, Mizerik E, Woodbury S, Bi W, Lotze T, Antonellis A, Xiao R, Potocki LAmerican journal of medical genetics. Part AGARS-related disease in infantile spinal muscular atrophy: Implications for diagnosis and treatment. Am J Med Genet A. 2020 05; 182(5):1167-1176.Am J Med Genet A2020-03-17T00:00:002020GARS-related disease in infantile spinal muscular atrophy: Implications for diagnosis and treatment.true1Distinguished Emeritus ProfessorDistinguished Emeritus Professortrue1Adjunct ProfessorAdjunct ProfessorAuthorship 9867101432267005Krysko KM, Graves JS, Rensel M, Weinstock-Guttman B, Rutatangwa A, Aaen G, Belman A, Benson L, Chitnis T, Gorman M, Goyal MS, Harris Y, Krupp L, Lotze T, Mar S, Moodley M, Ness J, Rodriguez M, Rose J, Schreiner T, Tillema JM, Waltz M, Casper TC, Waubant E, US Network of Pediatric MS CentersAnnals of neurologyReal-World Effectiveness of Initial Disease-Modifying Therapies in Pediatric Multiple Sclerosis. Ann Neurol. 2020 07; 88(1):42-55.Ann Neurol2020-05-14T00:00:002020Real-World Effectiveness of Initial Disease-Modifying Therapies in Pediatric Multiple Sclerosis.Authorship 988468432358069Erickson TA, Muscal E, Munoz FM, Lotze T, Hasbun R, Brown E, Murray KOPediatricsInfectious and Autoimmune Causes of Encephalitis in Children. Pediatrics. 2020 06; 145(6).Pediatrics2020-05-01T00:00:002020Infectious and Autoimmune Causes of Encephalitis in Children.Authorship 9949521132690790Santoro JD, Waltz M, Aaen G, Belman A, Benson L, Gorman M, Goyal MS, Graves JS, Harris Y, Krupp L, Lotze T, Mar S, Moodley M, Ness J, Rensel M, Rodriguez M, Schreiner T, Tillema JM, Waubant E, Weinstock-Guttman B, Hurtubise BF, Roalstad S, Rose J, Casper TC, Chitnis T, US Network of Pediatric MS CentersNeurologyPediatric Multiple Sclerosis Severity Score in a large US cohort. Neurology. 2020 09 29; 95(13):e1844-e1853.Neurology2020-07-20T00:00:002020Pediatric Multiple Sclerosis Severity Score in a large US cohort.Authorship 9973691032810215Chitnis T, Aaen G, Belman A, Benson L, Gorman M, Goyal MS, Graves JS, Harris Y, Krupp L, Lotze T, Mar S, Ness J, Rensel M, Schreiner T, Tillema JM, Waubant E, Weinstock-Guttman B, Roalstad S, Rose J, Weiner HL, Casper TC, Rodriguez M, US Network of Paediatric Multiple Sclerosis CentersBrain : a journal of neurologyImproved relapse recovery in paediatric compared to adult multiple sclerosis. Brain. 2020 09 01; 143(9):2733-2741.Brain2020-09-01T00:00:002020Improved relapse recovery in paediatric compared to adult multiple sclerosis.true1ProfessorProfessor2ProfessorProfessorAuthorship 10044357Authorship 1005315833146414Herman I, Lopez MA, Marafi D, Pehlivan D, Calame DG, Abid F, Lotze TEMuscle & nerveClinical exome sequencing in the diagnosis of pediatric neuromuscular disease. Muscle Nerve. 2021 03; 63(3):304-310.Muscle Nerve2020-11-13T00:00:002020Clinical exome sequencing in the diagnosis of pediatric neuromuscular disease.33212335Albert DVF, Bass N, Bodensteiner J, Draconi C, Duke ES, Felker M, Gropman A, Lotze T, Mink JW, Reese JJ, Spiciarich M, Urion DK, Edgar LPediatric neurologyDeveloping a New Set of ACGME Milestones for Child Neurology Residency. Pediatr Neurol. 2021 01; 114:47-52.Pediatr Neurol2020-10-24T00:00:002020Developing a New Set of ACGME Milestones for Child Neurology Residency.Authorship 1010473833533931McAtee CL, Lubega J, Underbrink K, Curry K, Msaouel P, Barrow M, Muscal E, Lotze T, Srivaths P, Forbes LR, Allen C, Bernhardt MBJAMA network openAssociation of Rituximab Use With Adverse Events in Children, Adolescents, and Young Adults. JAMA Netw Open. 2021 02 01; 4(2):e2036321.JAMA Netw Open2021-02-01T00:00:002021Association of Rituximab Use With Adverse Events in Children, Adolescents, and Young Adults.Authorship 1011286333578253Calame DG, Houck K, Lotze T, Emrick L, Parnes MEuropean journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology SocietyA novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients. Eur J Paediatr Neurol. 2021 Mar; 31:21-26.Eur J Paediatr Neurol2021-01-16T00:00:002021A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients.Authorship 1012299233630777Pareek AV, Lotze TE, Demmler G, Mohila CA, Tran B, Shah VSJournal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology SocietyDouble Vision and Gait Ataxia in an Immunocompetent 9-Year-Old Girl With Intracranial Phaeohyphomycosis. J Neuroophthalmol. 2021 09 01; 41(3):399-403.J Neuroophthalmol2021-09-01T00:00:002021Double Vision and Gait Ataxia in an Immunocompetent 9-Year-Old Girl With Intracranial Phaeohyphomycosis.Authorship 1013454733684630Fisher KS, Gill J, Todd HF, Yang MB, Lopez MA, Abid F, Lotze T, Shah VSPediatric neurologyPediatric Autoimmune Ocular Myasthenia Gravis: Evaluation of Presentation and Treatment Outcomes in a Large Cohort. Pediatr Neurol. 2021 05; 118:12-19.Pediatr Neurol2021-02-05T00:00:002021Pediatric Autoimmune Ocular Myasthenia Gravis: Evaluation of Presentation and Treatment Outcomes in a Large Cohort.Authorship 10166416033874999Gillentine MA, Wang T, Hoekzema K, Rosenfeld J, Liu P, Guo H, Kim CN, De Vries BBA, Vissers LELM, Nordenskjold M, Kvarnung M, Lindstrand A, Nordgren A, Gecz J, Iascone M, Cereda A, Scatigno A, Maitz S, Zanni G, Bertini E, Zweier C, Schuhmann S, Wiesener A, Pepper M, Panjwani H, Torti E, Abid F, Anselm I, Srivastava S, Atwal P, Bacino CA, Bhat G, Cobian K, Bird LM, Friedman J, Wright MS, Callewaert B, Petit F, Mathieu S, Afenjar A, Christensen CK, White KM, Elpeleg O, Berger I, Espineli EJ, Fagerberg C, Brasch-Andersen C, Hansen LK, Feyma T, Hughes S, Thiffault I, Sullivan B, Yan S, Keller K, Keren B, Mignot C, Kooy F, Meuwissen M, Basinger A, Kukolich M, Philips M, Ortega L, Drummond-Borg M, Lauridsen M, Sorensen K, Lehman A, CAUSES Study, Lopez-Rangel E, Levy P, Lessel D, Lotze T, Madan-Khetarpal S, Sebastian J, Vento J, Vats D, Benman LM, Mckee S, Mirzaa GM, Muss C, Pappas J, Peeters H, Romano C, Elia M, Galesi O, Simon MEH, van Gassen KLI, Simpson K, Stratton R, Syed S, Thevenon J, Palafoll IV, Vitobello A, Bournez M, Faivre L, Xia K, SPARK Consortium, Earl RK, Nowakowski T, Bernier RA, Eichler EEGenome medicineRare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders. Genome Med. 2021 04 19; 13(1):63.Genome Med2021-04-19T00:00:002021Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.Authorship 10177111233949769Keehan L, Jiang MM, Li X, Marom R, Dai H, Murdock D, Liu P, Hunter JV, Heaney JD, Robak L, Emrick L, Lotze T, Blieden LS, Undiagnosed Diseases Network, Lewis RA, Levin AV, Capasso J, Craigen WJ, Rosenfeld JA, Lee B, Burrage LCAmerican journal of medical genetics. Part AA novel de novo intronic variant in ITPR1 causes Gillespie syndrome. Am J Med Genet A. 2021 08; 185(8):2315-2324.Am J Med Genet A2021-05-05T00:00:002021A novel de novo intronic variant in ITPR1 causes Gillespie syndrome.Authorship 10183031133977145Calame DG, Fatih J, Herman I, Akdemir ZC, Du H, Jhangiani SN, Gibbs RA, Marafi D, Pehlivan D, Posey JE, Lotze T, Mancias P, Bhattacharjee MB, Lupski JRNeurology. GeneticsBiallelic Pathogenic Variants in TNNT3 Associated With Congenital Myopathy. Neurol Genet. 2021 Jun; 7(3):e589.Neurol Genet2021-04-26T00:00:002021Biallelic Pathogenic Variants in TNNT3 Associated With Congenital Myopathy.DANIELCALAMEDANIEL CALAME16788CALAME, DANIELInstructorAuthorship 10243762Authorship 10243802Authorship 1024390234215381Clark GD, Lotze TENeurologic clinicsNeurology in a Pandemic. Neurol Clin. 2021 08; 39(3):699-704.Neurol Clin2021-08-01T00:00:002021Neurology in a Pandemic.34215383Clark GD, Lotze TENeurologic clinicsNovel Treatments and Clinical Research in Child Neurology. Neurol Clin. 2021 08; 39(3):719-722.Neurol Clin2021-08-01T00:00:002021Novel Treatments and Clinical Research in Child Neurology.34215388Malani Shukla N, Lotze TE, Muscal ENeurologic clinicsInflammatory Diseases of the Central Nervous System. Neurol Clin. 2021 08; 39(3):811-828.Neurol Clin2021-06-09T00:00:002021Inflammatory Diseases of the Central Nervous System.Authorship 10268222234353894Greenberg BM, Casper TC, Mar SS, Ness JM, Plumb P, Liang S, Goyal M, Weinstock-Guttman B, Rodriguez M, Aaen GS, Belman A, Barcellos LF, Rose JW, Gorman MP, Benson LA, Candee M, Chitnis T, Harris YC, Kahn IL, Roalstad S, Hart J, Lotze TE, Rensel M, Rubin JP, Schreiner TL, Tillema JM, Waldman AT, Krupp L, Graves J, Drake K, Waubant ENeurology(R) neuroimmunology & neuroinflammationFamilial History of Autoimmune Disorders Among Patients With Pediatric Multiple Sclerosis. Neurol Neuroimmunol Neuroinflamm. 2021 09; 8(5).Neurol Neuroimmunol Neuroinflamm2021-08-05T00:00:002021Familial History of Autoimmune Disorders Among Patients With Pediatric Multiple Sclerosis.Authorship 10297961434524739Calame DG, Fatih JM, Herman I, Coban-Akdemir Z, Du H, Mitani T, Jhangiani SN, Marafi D, Gibbs RA, Posey JE, Mehta VP, Mohila CA, Abid F, Lotze TE, Pehlivan D, Adesina AM, Lupski JRAnnals of clinical and translational neurologyDeep clinicopathological phenotyping identifies a previously unrecognized pathogenic EMD splice variant. Ann Clin Transl Neurol. 2021 10; 8(10):2052-2058.Ann Clin Transl Neurol2021-09-15T00:00:002021Deep clinicopathological phenotyping identifies a previously unrecognized pathogenic EMD splice variant.Authorship 1030091534541304Mandel LA, O'Donnell E, Canenguez K, Castro-Mendoza PB, Lotze T, Waubant E, Weinstock-Guttmann B, Chitnis TJournal of patient experienceFamily Perspectives on Clinical Research for Pediatric Multiple Sclerosis: Enhancing Equity. J Patient Exp. 2021; 8:23743735211039319.J Patient Exp2021-09-15T00:00:002021Family Perspectives on Clinical Research for Pediatric Multiple Sclerosis: Enhancing Equity.Authorship 10370471635000467Ziaei A, Lavery AM, Shao XM, Adams C, Casper TC, Rose J, Candee M, Weinstock-Guttman B, Aaen G, Harris Y, Graves J, Benson L, Gorman M, Rensel M, Mar S, Lotze T, Greenberg B, Chitnis T, Hart J, Waldman AT, Barcellos LF, Waubant EMultiple sclerosis (Houndmills, Basingstoke, England)Gene-environment interactions increase the risk of pediatric-onset multiple sclerosis associated with ozone pollution. Mult Scler. 2022 08; 28(9):1330-1339.Mult Scler2022-01-08T00:00:002022Gene-environment interactions increase the risk of pediatric-onset multiple sclerosis associated with ozone pollution.true1InstructorInstructorAuthorship 1038008935260471Rossor T, Yeh EA, Khakoo Y, Angelini P, Hemingway C, Irani SR, Schleiermacher G, Santosh P, Lotze T, Dale RC, Deiva K, Hero B, Klein A, de Alarcon P, Gorman MP, Mitchell WG, Lim M, OMS Study GroupNeurology(R) neuroimmunology & neuroinflammationDiagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International Perspective. Neurol Neuroimmunol Neuroinflamm. 2022 05; 9(3).Neurol Neuroimmunol Neuroinflamm2022-03-08T00:00:002022Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International Perspective.Authorship 10446142835477763Brown GJ, Ca?ete PF, Wang H, Medhavy A, Bones J, Roco JA, He Y, Qin Y, Cappello J, Ellyard JI, Bassett K, Shen Q, Burgio G, Zhang Y, Turnbull C, Meng X, Wu P, Cho E, Miosge LA, Andrews TD, Field MA, Tvorogov D, Lopez AF, Babon JJ, L?pez CA, G?nzalez-Murillo ?, Garulo DC, Pascual V, Levy T, Mallack EJ, Calame DG, Lotze T, Lupski JR, Ding H, Ullah TR, Walters GD, Koina ME, Cook MC, Shen N, de Lucas Collantes C, Corry B, Gantier MP, Athanasopoulos V, Vinuesa CGNatureTLR7 gain-of-function genetic variation causes human lupus. Nature. 2022 05; 605(7909):349-356.Nature2022-04-27T00:00:002022TLR7 gain-of-function genetic variation causes human lupus.Authorship 138193224294520Pena JA, Lotze TEAutoimmune diseasesPediatric multiple sclerosis: current concepts and consensus definitions. Autoimmune Dis. 2013; 2013:673947.Autoimmune Dis2013-11-02T00:00:002013Pediatric multiple sclerosis: current concepts and consensus definitions.Authorship 1046609435616550Ferrante L, Melendez-Zaidi A, Lindsey W, Lotze TMuscle & nerveNovel use of nusinersen as a therapeutic bridge to onasemnogene abeparvovec-xioi in a premature neonate with type 1 spinal muscular atrophy. Muscle Nerve. 2022 08; 66(2):E8-E10.Muscle Nerve2022-06-09T00:00:002022Novel use of nusinersen as a therapeutic bridge to onasemnogene abeparvovec-xioi in a premature neonate with type 1 spinal muscular atrophy.Authorship 169433Authorship 10597503Authorship 105691317Authorship 105637410Authorship 10603654Authorship 10619201636102704Boguniewicz J, Demmler-Harrison GJ, Lotze TE, Jarjour IT, Whitehead WE, Frontiero J, Dutta A, Fogarty T, Hunter JV, Ogunbona OB, Pareek AV, Cameron LHThe Pediatric infectious disease journalManagement of Extensive Central Nervous System Cladophialophora bantiana Infection in a 9-Year-Old Child. Pediatr Infect Dis J. 2022 11 01; 41(11):e481-e486.Pediatr Infect Dis J2022-08-31T00:00:002022Management of Extensive Central Nervous System Cladophialophora bantiana Infection in a 9-Year-Old Child.36088544Gaudioso CM, Mar S, Casper TC, Codden R, Nguyen A, Aaen G, Benson L, Chitnis T, Francisco C, Gorman MP, Goyal MS, Graves J, Greenberg BM, Hart J, Krupp L, Lotze T, Narula S, Pittock SJ, Rensel M, Rodriguez M, Rose J, Schreiner T, Tillema JM, Waldman A, Weinstock-Guttman B, Wheeler Y, Waubant E, Flanagan EP, United States Network of Pediatric Multiple Sclerosis CentersAnnals of neurologyMOG and AQP4 Antibodies among Children with Multiple Sclerosis and Controls. Ann Neurol. 2023 02; 93(2):271-284.Ann Neurol2022-10-04T00:00:002022MOG and AQP4 Antibodies among Children with Multiple Sclerosis and Controls.36607927Silverstein RS, Wang DD, Haruno LS, Lotze TE, Scott AC, Rosenfeld SBJournal of pediatric orthopedicsBethlem Myopathy (Collagen VI-Related Dystrophies): A Retrospective Cohort Study on Musculoskeletal Pathologies and Clinical Course. J Pediatr Orthop. 2023 Feb 01; 43(2):e163-e167.J Pediatr Orthop2022-10-26T00:00:002022Bethlem Myopathy (Collagen VI-Related Dystrophies): A Retrospective Cohort Study on Musculoskeletal Pathologies and Clinical Course.36460473Pizzolato Umeton R, Waltz M, Aaen GS, Benson L, Gorman M, Goyal M, Graves JS, Harris Y, Krupp L, Lotze TE, Shukla NM, Mar S, Ness J, Rensel M, Schreiner T, Tillema JM, Roalstad S, Rodriguez M, Rose J, Waubant E, Weinstock-Guttman B, Casper C, Chitnis T, US Network of Pediatric MS CentersNeurologyTherapeutic Response in Pediatric Neuromyelitis Optica Spectrum Disorder. Neurology. 2023 02 28; 100(9):e985-e994.Neurology2022-12-02T00:00:002022Therapeutic Response in Pediatric Neuromyelitis Optica Spectrum Disorder.36189711Krupp LB, Waubant E, Waltz M, Casper TC, Belman A, Wheeler Y, Ness J, Graves J, Gorman M, Benson L, Mar S, Goyal M, Schreiner T, Weinstock-Guttman B, Rodriguez M, Tillema JM, Lotze T, Aaen G, Rensel M, Rose J, Chitinis T, George A, Charvet LE, US Network of Pediatric MS CentersMultiple sclerosis (Houndmills, Basingstoke, England)A new look at cognitive functioning in pediatric MS. Mult Scler. 2023 01; 29(1):140-149.Mult Scler2022-10-01T00:00:002022A new look at cognitive functioning in pediatric MS.Authorship 10633621836725329Nasr Z, Schoeps VA, Ziaei A, Virupakshaiah A, Adams C, Casper TC, Waltz M, Rose J, Rodriguez M, Tillema JM, Chitnis T, Graves JS, Benson L, Rensel M, Krupp L, Waldman AT, Weinstock-Guttman B, Lotze T, Greenberg B, Aaen G, Mar S, Schreiner T, Hart J, Simpson-Yap S, Mesaros C, Barcellos LF, Waubant EJournal of neurology, neurosurgery, and psychiatryGene-environment interactions increase the risk of paediatric-onset multiple sclerosis associated with household chemical exposures. J Neurol Neurosurg Psychiatry. 2023 07; 94(7):518-525.J Neurol Neurosurg Psychiatry2023-02-01T00:00:002023Gene-environment interactions increase the risk of paediatric-onset multiple sclerosis associated with household chemical exposures.Authorship 10653401036871372Bhise V, Waltz M, Casper TC, Aaen G, Benson L, Chitnis T, Gorman M, Goyal MS, Wheeler Y, Lotze T, Mar S, Rensel M, Abrams A, Rodriguez M, Rose J, Schreiner T, Shukla N, Waubant E, Weinstock-Guttman B, Ness J, Krupp L, Mendelt-Tillema J, U.S. Network of Pediatric Multiple Sclerosis CentersMultiple sclerosis and related disordersSilent findings: Examination of asymptomatic demyelination in a pediatric US cohort. Mult Scler Relat Disord. 2023 Mar; 71:104573.Mult Scler Relat Disord2023-02-18T00:00:002023Silent findings: Examination of asymptomatic demyelination in a pediatric US cohort.true1Associate ProfessorAssociate ProfessorAuthorship 10662811036960480Schreiner T, Wilson-Murphy M, Mendelt-Tillema J, Waltz M, Codden R, Benson L, Gorman M, Goyal M, Krupp L, Lotze T, Mar S, Ness J, Rensel M, Roalstad S, Rodriguez M, Rose J, Shukla N, Waubant E, Wheeler Y, Casper TC, Chitnis TMultiple sclerosis (Houndmills, Basingstoke, England)Characteristics of pediatric patients with multiple sclerosis and related disorders infected with SARS-CoV-2. Mult Scler. 2023 04; 29(4-5):576-584.Mult Scler2023-03-23T00:00:002023Characteristics of pediatric patients with multiple sclerosis and related disorders infected with SARS-CoV-2.Authorship 1068803937043503Calame DG, Moreno Vadillo C, Berger S, Lotze T, Shinawi M, Poupak J, Heller C, Cohen J, Person R, Telegrafi A, Phitsanuwong C, Fiala K, Thiffault I, Del Viso F, Zhou D, Fleming EA, Pastinen T, Fatemi A, Thomas S, Pascual SI, Torres RJ, Prior C, G?mez-Gonz?lez C, Biskup S, Lupski JR, Maric D, Holmgren M, Regier D, Yano STBrain : a journal of neurologyCation leak through the ATP1A3 pump causes spasticity and intellectual disability. Brain. 2023 08 01; 146(8):3162-3171.Brain2023-08-01T00:00:002023Cation leak through the ATP1A3 pump causes spasticity and intellectual disability.true1Professor EmeritusProfessor Emeritustrue1Professor EmeritusProfessor EmeritusAuthorship 10697205Authorship 10697121237167966Morales-Rosado JA, Schwab TL, Macklin-Mantia SK, Foley AR, Pinto E Vairo F, Pehlivan D, Donkervoort S, Rosenfeld JA, Boyum GE, Hu Y, Cong ATQ, Lotze TE, Mohila CA, Saade D, Bharucha-Goebel D, Chao KR, Grunseich C, Bruels CC, Littel HR, Estrella EA, Pais L, Kang PB, Zimmermann MT, Lupski JR, Lee B, Schellenberg MJ, Clark KJ, Wierenga KJ, B?nnemann CG, Klee EWAmerican journal of human geneticsBi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy. Am J Hum Genet. 2023 06 01; 110(6):989-997.Am J Hum Genet2023-05-10T00:00:002023Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy.37168752Shah KP, Ramachandran V, Nicholas SK, Hanson IC, Lotze TE, Martinez CA, Fishman DSJPGN reportsSevere Combined Immunodeficiency with De Novo Duchenne Muscular Dystrophy Mutation. JPGN Rep. 2022 Feb; 3(1):e135.JPGN Rep2021-11-29T00:00:002021Severe Combined Immunodeficiency with De Novo Duchenne Muscular Dystrophy Mutation.Authorship 1073322637348193Malani Shukla N, Casper TC, Ness J, Wheeler Y, Chitnis T, Lotze T, Gorman M, Benson L, Weinstock-Guttmann B, Aaen G, Rodriguez M, Tillema JM, Krupp L, Schreiner T, Mar S, Goyal M, Rensel M, Abrams A, Rose J, Waltz M, Liu T, Manlius C, Waubant E, U.S. Network of Pediatric Multiple Sclerosis CentersPediatric neurologyDemographic Features and Clinical Course of Patients With Pediatric-Onset Multiple Sclerosis on Newer Disease-Modifying Treatments. Pediatr Neurol. 2023 Aug; 145:125-131.Pediatr Neurol2023-04-28T00:00:002023Demographic Features and Clinical Course of Patients With Pediatric-Onset Multiple Sclerosis on Newer Disease-Modifying Treatments.37544084Kannan V, Sandweiss AJ, Erickson TA, Yarimi JM, Ankar A, Hardwick VA, Shukla NM, Lotze TE, Risen SR, Riviello JJ, Lai YC, Moeller KK, Fisher KPediatric neurologyFulminant Anti-Myelin Oligodendrocyte Glycoprotein-Associated Cerebral Cortical Encephalitis: Case Series of a Severe Pediatric Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Phenotype. Pediatr Neurol. 2023 10; 147:36-43.Pediatr Neurol2023-07-11T00:00:002023Fulminant Anti-Myelin Oligodendrocyte Glycoprotein-Associated Cerebral Cortical Encephalitis: Case Series of a Severe Pediatric Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Phenotype.Authorship 107851813Authorship 1078653837716108Kerr LM, Ryan ME, Lim M, Hearn S, Klein A, Deiva K, Hopkins SE, Bacchus MK, Sokol EA, Waanders AJ, Mitchell WG, Khakoo Y, Lotze TE, Zhang B, Gorman MPPediatric neurologyAn International Pediatric-Onset Opsoclonus-Myoclonus Ataxia Syndrome Registry and Clinical Research Network: Development, Progress, and Vision. Pediatr Neurol. 2023 11; 148:145-147.Pediatr Neurol2023-05-16T00:00:002023An International Pediatric-Onset Opsoclonus-Myoclonus Ataxia Syndrome Registry and Clinical Research Network: Development, Progress, and Vision.Authorship 1082769337895210Hentrich L, Parnes M, Lotze TE, Coorg R, de Koning TJ, Nguyen KM, Yip CK, Jungbluth H, Koy A, Dafsari HSGenesNovel Genetic and Phenotypic Expansion in GOSR2-Related Progressive Myoclonus Epilepsy. Genes (Basel). 2023 09 25; 14(10).Genes (Basel)2023-09-25T00:00:002023Novel Genetic and Phenotypic Expansion in GOSR2-Related Progressive Myoclonus Epilepsy.Authorship 108591416Authorship 1085810338154238Gambrah-Lyles C, Kannan V, Lotze T, Abrams A, Schreiner T, Rodriguez M, Casper TC, Rose JW, Gorman MP, Chitnis T, Loud S, Wheeler Y, Mar S, US Network of Pediatric MS CentersPediatric neurologyAssessing Needs and Perceptions of Research Participation in Pediatric-Onset Multiple Sclerosis: A Multistakeholder Survey. Pediatr Neurol. 2024 Feb; 151:115-120.Pediatr Neurol2023-12-04T00:00:002023Assessing Needs and Perceptions of Research Participation in Pediatric-Onset Multiple Sclerosis: A Multistakeholder Survey.38141560Nasr Z, Virupakshaiah A, Schoeps VA, Cherbuin N, Casper TC, Waltz M, Hart J, Rodriguez M, Gorman MP, Benson LA, Chitnis T, Rensel M, Abrams A, Krupp L, Waldman AT, Lotze T, Aaen GS, Mar S, Schreiner T, Wheeler Y, Rose J, Shukla NM, Barcellos LF, Lucas R, Waubant EMultiple sclerosis and related disordersGene-environment interactions and risk of pediatric-onset multiple sclerosis associated with time spent outdoors. Mult Scler Relat Disord. 2024 Feb; 82:105351.Mult Scler Relat Disord2023-12-08T00:00:002023Gene-environment interactions and risk of pediatric-onset multiple sclerosis associated with time spent outdoors.Authorship 1087049538231402Prablek M, Reyes G, Kannan V, Gay CT, Lotze TE, Donoho DA, Bauer DFChild's nervous system : ChNS : official journal of the International Society for Pediatric NeurosurgeryAnterior cervical discectomy and fusion for the treatment of pediatric Hirayama disease. Childs Nerv Syst. 2024 Jan 17.Childs Nerv Syst2024-01-17T00:00:002024Anterior cervical discectomy and fusion for the treatment of pediatric Hirayama disease.Authorship 10885231338332747Ziaei A, Solomon O, Casper TC, Waltz M, Weinstock-Guttman B, Aaen G, Wheeler Y, Graves J, Benson L, Gorman M, Rensel M, Mar S, Lotze T, Greenberg B, Chitnis T, Waldman AT, Krupp L, James JA, Hart J, Barcellos LF, Waubant EMultiple sclerosis (Houndmills, Basingstoke, England)Gene-environment interactions: Epstein-Barr virus infection and risk of pediatric-onset multiple sclerosis. Mult Scler. 2024 Mar; 30(3):308-315.Mult Scler2024-02-09T00:00:002024Gene-environment interactions: Epstein-Barr virus infection and risk of pediatric-onset multiple sclerosis.Authorship 10898301638405817Calame DG, Wong JH, Panda P, Nguyen DT, Leong NCP, Sangermano R, Patankar SG, Abdel-Hamid M, AlAbdi L, Safwat S, Flannery KP, Dardas Z, Fatih JM, Murali C, Kannan V, Lotze TE, Herman I, Ammouri F, Rezich B, Efthymiou S, Alavi S, Murphy D, Firoozfar Z, Nasab ME, Bahreini A, Ghasemi M, Haridy NA, Goldouzi HR, Eghbal F, Karimiani EG, Srinivasan VM, Gowda VK, Du H, Jhangiani SN, Coban-Akdemir Z, Marafi D, Rodan L, Isikay S, Rosenfeld JA, Ramanathan S, Staton M, Clark RD, Wenman C, Loughlin S, Saad R, Ashraf T, Male A, Tadros S, Boostani R, Abdel-Salam GMH, Zaki M, Abdalla E, Manzini MC, Pehlivan D, Posey JE, Gibbs RA, Houlden H, Alkuraya FS, Bujakowska K, Maroofian R, Lupski JR, Nguyen LNmedRxiv : the preprint server for health sciencesBiallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a pleiotropic disease spectrum from adult neurodegeneration to severe developmental disorders. medRxiv. 2024 Feb 13.medRxiv2024-02-13T00:00:002024Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a pleiotropic disease spectrum from adult neurodegeneration to severe developmental disorders.true1ProfessorProfessorAuthorship 308325Authorship 1409225Authorship 140974224002165Martinez HR, Craigen WJ, Ummat M, Adesina AM, Lotze TE, Jefferies JLEuropean journal of human genetics : EJHGNovel cardiovascular findings in association with a POMT2 mutation: three siblings with a-dystroglycanopathy. Eur J Hum Genet. 2014 Apr; 22(4):486-91.Eur J Hum Genet2013-09-04T00:00:002013Novel cardiovascular findings in association with a POMT2 mutation: three siblings with a-dystroglycanopathy.24126608Gonzaga-Jauregui C, Lotze T, Jamal L, Penney S, Campbell IM, Pehlivan D, Hunter JV, Woodbury SL, Raymond G, Adesina AM, Jhangiani SN, Reid JG, Muzny DM, Boerwinkle E, Lupski JR, Gibbs RA, Wiszniewski WJAMA neurologyMutations in VRK1 associated with complex motor and sensory axonal neuropathy plus microcephaly. JAMA Neurol. 2013 Dec; 70(12):1491-8.JAMA Neurol2013-12-01T00:00:002013Mutations in VRK1 associated with complex motor and sensory axonal neuropathy plus microcephaly.Authorship 483183Authorship 688921Authorship 520501Authorship 541124Authorship 564523ROHINICOORGROHINI COORG7888COORG, ROHINIAssistant ProfessorAuthorship 8182914Authorship 603591Authorship 1514782Authorship 151668325149941Agarwal S, Lotze TE, Woodbury SLSeminars in pediatric neurologyA 7-year-old child with chronic droopy eyes, weakness in head-neck control, and an abnormal gait. Semin Pediatr Neurol. 2014 Jun; 21(2):111-3.Semin Pediatr Neurol2014-04-18T00:00:002014A 7-year-old child with chronic droopy eyes, weakness in head-neck control, and an abnormal gait.25266625Pena JA, Birchansky S, Lotze TEPediatric neurologyLymphocytic hypophysitis associated with pediatric multiple sclerosis. Pediatr Neurol. 2014 Oct; 51(4):580-2.Pediatr Neurol2014-06-25T00:00:002014Lymphocytic hypophysitis associated with pediatric multiple sclerosis.Authorship 707575Authorship 1536951825439098Lalani SR, Zhang J, Schaaf CP, Brown CW, Magoulas P, Tsai AC, El-Gharbawy A, Wierenga KJ, Bartholomew D, Fong CT, Barbaro-Dieber T, Kukolich MK, Burrage LC, Austin E, Keller K, Pastore M, Fernandez F, Lotze T, Wilfong A, Purcarin G, Zhu W, Craigen WJ, McGuire M, Jain M, Cooney E, Azamian M, Bainbridge MN, Muzny DM, Boerwinkle E, Person RE, Niu Z, Eng CM, Lupski JR, Gibbs RA, Beaudet AL, Yang Y, Wang MC, Xia FAmerican journal of human geneticsMutations in PURA cause profound neonatal hypotonia, seizures, and encephalopathy in 5q31.3 microdeletion syndrome. Am J Hum Genet. 2014 Nov 06; 95(5):579-83.Am J Hum Genet2014-10-16T00:00:002014Mutations in PURA cause profound neonatal hypotonia, seizures, and encephalopathy in 5q31.3 microdeletion syndrome.Authorship 15549112