DANIEL GLAZE

TitleDistinguished Emeritus Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Pediatrics
Address
vCardDownload vCard
    Other Positions
    TitleDistinguished Emeritus Professor
    InstitutionBaylor College of Medicine
    DepartmentDepartment of Neurology
    DivisionNeurology


    Collapse Research 
    Collapse research activities and funding
    R01HL062404     (GLAZE, DANIEL G.)Sep 20, 1999 - Jul 31, 2005
    NIH
    OBSTRUCTIVE SLEEP APNEA IN CHILDREN
    Role: Principal Investigator

    P01HD024234     (GLAZE, DANIEL G.)May 1, 1988 - Aug 31, 1999
    NIH
    RETT SYNDROME: PROGRAM PROJECT
    Role: Principal Investigator

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Ak M, Suter B, Akturk Z, Harris H, Bowyer K, Mignon L, Pasupuleti S, Glaze DG, Pehlivan D, Ak M, Suter B, Akturk Z, Harris H, Bowyer K, Mignon L, Pasupuleti S, Glaze DG, Pehlivan D. Exploring the characteristics and most bothersome symptoms in MECP2 duplication syndrome to pave the path toward developing parent-oriented outcome measures. Mol Genet Genomic Med. 2022 08; 10(8):e1989. PMID: 35702943; PMCID: PMC9356562.
      Citations:    Fields:    
    2. Duis J, Pullen LC, Picone M, Friedman N, Hawkins S, Sannar E, Pfalzer AC, Shelton AR, Singh D, Zee PC, Glaze DG, Revana A, Duis J, Pullen LC, Picone M, Friedman N, Hawkins S, Sannar E, Pfalzer AC, Shelton AR, Singh D, Zee PC, Glaze DG, Revana A. Diagnosis and management of sleep disorders in Prader-Willi syndrome. J Clin Sleep Med. 2022 06 01; 18(6):1687-1696. PMID: 35172921; PMCID: PMC9163612.
      Citations:    Fields:    Translation:Humans
    3. Ak M, Akturk Z, Bowyer K, Mignon L, Pasupuleti S, Glaze DG, Suter B, Pehlivan D, Ak M, Akturk Z, Bowyer K, Mignon L, Pasupuleti S, Glaze DG, Suter B, Pehlivan D. Assessing the Burden on Caregivers of MECP2 Duplication Syndrome. Pediatr Neurol. 2022 08; 133:1-8. PMID: 35716604.
      Citations:    Fields:    Translation:Humans
    4. Buchanan CB, Stallworth JL, Joy AE, Dixon RE, Scott AE, Beisang AA, Benke TA, Glaze DG, Haas RH, Heydemann PT, Jones MD, Lane JB, Lieberman DN, Marsh ED, Neul JL, Peters SU, Ryther RC, Skinner SA, Standridge SM, Kaufmann WE, Percy AK, Buchanan CB, Stallworth JL, Joy AE, Dixon RE, Scott AE, Beisang AA, Benke TA, Glaze DG, Haas RH, Heydemann PT, Jones MD, Lane JB, Lieberman DN, Marsh ED, Neul JL, Peters SU, Ryther RC, Skinner SA, Standridge SM, Kaufmann WE, Percy AK. Anxiety-like behavior and anxiolytic treatment in the Rett syndrome natural history study. J Neurodev Disord. 2022 05 14; 14(1):31. PMID: 35568815; PMCID: PMC9107202.
      Citations:    Fields:    Translation:Humans
    5. Duis J, Nespeca M, Summers J, Bird L, Bindels-de Heus KGCB, Valstar MJ, de Wit MY, Navis C, Ten Hooven-Radstaake M, van Iperen-Kolk BM, Ernst S, Dendrinos M, Katz T, Diaz-Medina G, Katyayan A, Nangia S, Thibert R, Glaze D, Keary C, Pelc K, Simon N, Sadhwani A, Heussler H, Wheeler A, Woeber C, DeRamus M, Thomas A, Kertcher E, DeValk L, Kalemeris K, Arps K, Baym C, Harris N, Gorham JP, Bohnsack BL, Chambers RC, Harris S, Chambers HG, Okoniewski K, Jalazo ER, Berent A, Bacino CA, Williams C, Anderson A, Duis J, Nespeca M, Summers J, Bird L, Bindels-de Heus KGCB, Valstar MJ, de Wit MY, Navis C, Ten Hooven-Radstaake M, van Iperen-Kolk BM, Ernst S, Dendrinos M, Katz T, Diaz-Medina G, Katyayan A, Nangia S, Thibert R, Glaze D, Keary C, Pelc K, Simon N, Sadhwani A, Heussler H, Wheeler A, Woeber C, DeRamus M, Thomas A, Kertcher E, DeValk L, Kalemeris K, Arps K, Baym C, Harris N, Gorham JP, Bohnsack BL, Chambers RC, Harris S, Chambers HG, Okoniewski K, Jalazo ER, Berent A, Bacino CA, Williams C, Anderson A. A multidisciplinary approach and consensus statement to establish standards of care for Angelman syndrome. Mol Genet Genomic Med. 2022 03; 10(3):e1843. PMID: 35150089; PMCID: PMC8922964.
      Citations: 1     Fields:    Translation:Humans
    6. Neul JL, Percy AK, Benke TA, Berry-Kravis EM, Glaze DG, Peters SU, Jones NE, Youakim JM, Neul JL, Percy AK, Benke TA, Berry-Kravis EM, Glaze DG, Peters SU, Jones NE, Youakim JM. Design and outcome measures of LAVENDER, a phase 3 study of trofinetide for Rett syndrome. Contemp Clin Trials. 2022 03; 114:106704. PMID: 35149233.
      Citations:    Fields:    Translation:HumansCTClinical Trials
    7. Patel VP, Patroneva A, Glaze DG, Davis Ms K, Merikle E, Revana A, Patel VP, Patroneva A, Glaze DG, Davis Ms K, Merikle E, Revana A. Establishing the content validity of the Epworth Sleepiness Scale for Children and Adolescents in Prader-Willi syndrome. J Clin Sleep Med. 2022 Feb 01; 18(2):485-496. PMID: 34437052; PMCID: PMC8804999.
      Citations:    Fields:    Translation:Humans
    8. Revana A, Vecchio J, Guffey D, Minard CG, Glaze DG, Revana A, Vecchio J, Guffey D, Minard CG, Glaze DG. Clinical application of home sleep apnea testing in children: a prospective pilot study. J Clin Sleep Med. 2022 Feb 01; 18(2):533-540. PMID: 34534072; PMCID: PMC8805000.
      Citations:    Fields:    Translation:Humans
    9. Motil KJ, Geerts S, Annese F, Neul JL, Benke T, Marsh E, Lieberman D, Skinner SA, Glaze DG, Heydemann P, Beisang A, Standridge S, Ryther R, Lane JB, Edwards L, Percy AK, Motil KJ, Geerts S, Annese F, Neul JL, Benke T, Marsh E, Lieberman D, Skinner SA, Glaze DG, Heydemann P, Beisang A, Standridge S, Ryther R, Lane JB, Edwards L, Percy AK. Anthropometric Measures Correspond with Functional Motor Outcomes in Females with Rett Syndrome. J Pediatr. 2022 05; 244:169-177.e3. PMID: 35063470; PMCID: PMC9086122.
      Citations:    Fields:    Translation:Humans
    10. Vakharia M, Pehlivan D, Hoyos-Martinez A, Glaze DG, Tosur M. New-Onset Diabetes Presenting With Hyperosmolar Hyperglycemic State in a Lean Adolescent With Atypical Rett Syndrome Using Antipsychotics. Clin Diabetes. 2022; 40(4):503-507. PMID: 36385977; PMCID: PMC9606562.
      Citations:    
    11. Veatch OJ, Malow BA, Lee HS, Knight A, Barrish JO, Neul JL, Lane JB, Skinner SA, Kaufmann WE, Miller JL, Driscoll DJ, Bird LM, Butler MG, Dykens EM, Gold JA, Kimonis V, Bacino CA, Tan WH, Kothare SV, Peters SU, Percy AK, Glaze DG, Veatch OJ, Malow BA, Lee HS, Knight A, Barrish JO, Neul JL, Lane JB, Skinner SA, Kaufmann WE, Miller JL, Driscoll DJ, Bird LM, Butler MG, Dykens EM, Gold JA, Kimonis V, Bacino CA, Tan WH, Kothare SV, Peters SU, Percy AK, Glaze DG. Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental Syndromes. Pediatr Neurol. 2021 10; 123:30-37. PMID: 34388423; PMCID: PMC8429141.
      Citations: 1     Fields:    Translation:Humans
    12. Ahmad SF, Buckley AW, Glaze DG, Ahmad SF, Buckley AW, Glaze DG. Neurology of Sleep. Neurol Clin. 2021 08; 39(3):867-882. PMID: 34215391.
      Citations: 1     Fields:    Translation:Humans
    13. Thapa S, Venkatachalam A, Khan N, Naqvi M, Balderas M, Runge JK, Haag A, Hoch KM, Glaze DG, Luna RA, Motil KJ, Thapa S, Venkatachalam A, Khan N, Naqvi M, Balderas M, Runge JK, Haag A, Hoch KM, Glaze DG, Luna RA, Motil KJ. Assessment of the gut bacterial microbiome and metabolome of girls and women with Rett Syndrome. PLoS One. 2021; 16(5):e0251231. PMID: 33956889; PMCID: PMC8101921.
      Citations: 2     Fields:    Translation:Humans
    14. Motil KJ, Khan N, Coon JL, Barrish JO, Suter B, Pehlivan D, Schultz RJ, Glaze DG, Motil KJ, Khan N, Coon JL, Barrish JO, Suter B, Pehlivan D, Schultz RJ, Glaze DG. Gastrointestinal Health Questionnaire for Rett Syndrome: Tool Development. J Pediatr Gastroenterol Nutr. 2021 03 01; 72(3):354-360. PMID: 32969958.
      Citations: 1     Fields:    Translation:Humans
    15. Peters SU, Fu C, Marsh ED, Benke TA, Suter B, Skinner SA, Lieberman DN, Standridge S, Jones M, Beisang A, Feyma T, Heydeman P, Ryther R, Glaze DG, Percy AK, Neul JL, Peters SU, Fu C, Marsh ED, Benke TA, Suter B, Skinner SA, Lieberman DN, Standridge S, Jones M, Beisang A, Feyma T, Heydeman P, Ryther R, Glaze DG, Percy AK, Neul JL. Phenotypic features in MECP2 duplication syndrome: Effects of age. Am J Med Genet A. 2021 02; 185(2):362-369. PMID: 33170557; PMCID: PMC8000774.
      Citations: 3     Fields:    Translation:Humans
    16. Raspa M, Bann CM, Gwaltney A, Benke TA, Fu C, Glaze DG, Haas R, Heydemann P, Jones M, Kaufmann WE, Lieberman D, Marsh E, Peters S, Ryther R, Standridge S, Skinner SA, Percy AK, Neul JL, Raspa M, Bann CM, Gwaltney A, Benke TA, Fu C, Glaze DG, Haas R, Heydemann P, Jones M, Kaufmann WE, Lieberman D, Marsh E, Peters S, Ryther R, Standridge S, Skinner SA, Percy AK, Neul JL. A Psychometric Evaluation of the Motor-Behavioral Assessment Scale for Use as an Outcome Measure in Rett Syndrome Clinical Trials. Am J Intellect Dev Disabil. 2020 11 01; 125(6):493-509. PMID: 33211820; PMCID: PMC7778880.
      Citations: 4     Fields:    Translation:Humans
    17. Fu C, Armstrong D, Marsh E, Lieberman D, Motil K, Witt R, Standridge S, Lane J, Dinkel T, Jones M, Hale K, Suter B, Glaze D, Neul J, Percy A, Benke T, Fu C, Armstrong D, Marsh E, Lieberman D, Motil K, Witt R, Standridge S, Lane J, Dinkel T, Jones M, Hale K, Suter B, Glaze D, Neul J, Percy A, Benke T. Multisystem comorbidities in classic Rett syndrome: a scoping review. BMJ Paediatr Open. 2020; 4(1):e000731. PMID: 33024833; PMCID: PMC7509967.
      Citations: 6     Fields:    
    18. Young DR, Suter B, Levine JT, Glaze DG, Layne CS, Young DR, Suter B, Levine JT, Glaze DG, Layne CS. Characteristic behaviors associated with gait of individuals with Rett syndrome. Disabil Rehabil. 2022 04; 44(8):1508-1515. PMID: 32931336.
      Citations:    Fields:    Translation:Humans
    19. Fu C, Armstrong D, Marsh E, Lieberman D, Motil K, Witt R, Standridge S, Nues P, Lane J, Dinkel T, Coenraads M, von Hehn J, Jones M, Hale K, Suter B, Glaze D, Neul J, Percy A, Benke T, Fu C, Armstrong D, Marsh E, Lieberman D, Motil K, Witt R, Standridge S, Nues P, Lane J, Dinkel T, Coenraads M, von Hehn J, Jones M, Hale K, Suter B, Glaze D, Neul J, Percy A, Benke T. Consensus guidelines on managing Rett syndrome across the lifespan. BMJ Paediatr Open. 2020; 4(1):e000717. PMID: 32984552; PMCID: PMC7488790.
      Citations: 4     Fields:    
    20. Musso MF, Lindsey HM, Wilde EA, Hunter JV, Glaze DG, Goodrich-Hunsaker NJ, Wu TC, Black G, Biekman B, Zhang W, Zhu H, Anand GS, Friedman EM, Musso MF, Lindsey HM, Wilde EA, Hunter JV, Glaze DG, Goodrich-Hunsaker NJ, Wu TC, Black G, Biekman B, Zhang W, Zhu H, Anand GS, Friedman EM. Volumetric brain magnetic resonance imaging analysis in children with obstructive sleep apnea. Int J Pediatr Otorhinolaryngol. 2020 Nov; 138:110369. PMID: 32927352.
      Citations: 2     Fields:    Translation:Humans
    21. Neul JL, Skinner SA, Annese F, Lane J, Heydemann P, Jones M, Kaufmann WE, Glaze DG, Percy AK, Neul JL, Skinner SA, Annese F, Lane J, Heydemann P, Jones M, Kaufmann WE, Glaze DG, Percy AK. Metabolic Signatures Differentiate Rett Syndrome From Unaffected Siblings. Front Integr Neurosci. 2020; 14:7. PMID: 32161522; PMCID: PMC7052375.
      Citations: 10     
    22. Layne CS, Young DR, Lee BC, Glaze DG, Schwabe A, Suter B, Layne CS, Young DR, Lee BC, Glaze DG, Schwabe A, Suter B. Kinematics associated with treadmill walking in Rett syndrome. Disabil Rehabil. 2021 06; 43(11):1585-1593. PMID: 31613656.
      Citations:    Fields:    Translation:Humans
    23. Kaplan K, McCool C, Lupski JR, Glaze D, Potocki L, Kaplan K, McCool C, Lupski JR, Glaze D, Potocki L. Objective measures of sleep disturbances in children with Potocki-Lupski syndrome. Am J Med Genet A. 2019 10; 179(10):1982-1986. PMID: 31342617; PMCID: PMC6953247.
      Citations:    Fields:    Translation:Humans
    24. Motil KJ, Lane JB, Barrish JO, Annese F, Geerts S, McNair L, Skinner SA, Neul JL, Glaze DG, Percy AK, Motil KJ, Lane JB, Barrish JO, Annese F, Geerts S, McNair L, Skinner SA, Neul JL, Glaze DG, Percy AK. Biliary Tract Disease in Girls and Young Women With Rett Syndrome. J Pediatr Gastroenterol Nutr. 2019 06; 68(6):799-805. PMID: 30664568; PMCID: PMC6534452.
      Citations: 5     Fields:    Translation:Humans
    25. Stallworth JL, Dy ME, Buchanan CB, Chen CF, Scott AE, Glaze DG, Lane JB, Lieberman DN, Oberman LM, Skinner SA, Tierney AE, Cutter GR, Percy AK, Neul JL, Kaufmann WE, Stallworth JL, Dy ME, Buchanan CB, Chen CF, Scott AE, Glaze DG, Lane JB, Lieberman DN, Oberman LM, Skinner SA, Tierney AE, Cutter GR, Percy AK, Neul JL, Kaufmann WE. Hand stereotypies: Lessons from the Rett Syndrome Natural History Study. Neurology. 2019 05 28; 92(22):e2594-e2603. PMID: 31053667; PMCID: PMC6556084.
      Citations: 3     Fields:    Translation:HumansCTClinical Trials
    26. Stowe RC, Glaze DG, Stowe RC, Glaze DG. Electroencephalographic Patterns During Routine Polysomnography in Childhood and Association With Future Epilepsy Diagnosis. J Clin Sleep Med. 2019 04 15; 15(4):553-562. PMID: 30952213; PMCID: PMC6457519.
      Citations: 1     Fields:    Translation:Humans
    27. Glaze DG, Neul JL, Kaufmann WE, Berry-Kravis E, Condon S, Stoms G, Oosterholt S, Della Pasqua O, Glass L, Jones NE, Percy AK, Glaze DG, Neul JL, Kaufmann WE, Berry-Kravis E, Condon S, Stoms G, Oosterholt S, Della Pasqua O, Glass L, Jones NE, Percy AK, Rett 002 Study Group. Double-blind, randomized, placebo-controlled study of trofinetide in pediatric Rett syndrome. Neurology. 2019 04 16; 92(16):e1912-e1925. PMID: 30918097; PMCID: PMC6550498.
      Citations: 21     Fields:    Translation:HumansCTClinical Trials
    28. Peters SU, Fu C, Suter B, Marsh E, Benke TA, Skinner SA, Lieberman DN, Standridge S, Jones M, Beisang A, Feyma T, Heydeman P, Ryther R, Kaufmann WE, Glaze DG, Neul JL, Percy AK, Peters SU, Fu C, Suter B, Marsh E, Benke TA, Skinner SA, Lieberman DN, Standridge S, Jones M, Beisang A, Feyma T, Heydeman P, Ryther R, Kaufmann WE, Glaze DG, Neul JL, Percy AK. Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome. Clin Genet. 2019 05; 95(5):575-581. PMID: 30788845; PMCID: PMC6465105.
      Citations: 10     Fields:    Translation:HumansCells
    29. Marafi D, Suter B, Schultz R, Glaze D, Pavlik VN, Goldman AM, Marafi D, Suter B, Schultz R, Glaze D, Pavlik VN, Goldman AM. Spectrum and time course of epilepsy and the associated cognitive decline in MECP2 duplication syndrome. Neurology. 2019 01 08; 92(2):e108-e114. PMID: 30552298; PMCID: PMC6340341.
      Citations: 10     Fields:    Translation:Humans
    30. Neul JL, Benke TA, Marsh ED, Skinner SA, Merritt J, Lieberman DN, Standridge S, Feyma T, Heydemann P, Peters S, Ryther R, Jones M, Suter B, Kaufmann WE, Glaze DG, Percy AK, Neul JL, Benke TA, Marsh ED, Skinner SA, Merritt J, Lieberman DN, Standridge S, Feyma T, Heydemann P, Peters S, Ryther R, Jones M, Suter B, Kaufmann WE, Glaze DG, Percy AK. The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2. Am J Med Genet B Neuropsychiatr Genet. 2019 01; 180(1):55-67. PMID: 30536762; PMCID: PMC6488031.
      Citations: 12     Fields:    Translation:Humans
    31. Buchanan CB, Stallworth JL, Scott AE, Glaze DG, Lane JB, Skinner SA, Tierney AE, Percy AK, Neul JL, Kaufmann WE, Buchanan CB, Stallworth JL, Scott AE, Glaze DG, Lane JB, Skinner SA, Tierney AE, Percy AK, Neul JL, Kaufmann WE. Behavioral profiles in Rett syndrome: Data from the natural history study. Brain Dev. 2019 Feb; 41(2):123-134. PMID: 30217666; PMCID: PMC6392009.
      Citations: 10     Fields:    Translation:Humans
    32. Zaghlula M, Glaze DG, Enns GM, Potocki L, Schwabe AL, Suter B, Zaghlula M, Glaze DG, Enns GM, Potocki L, Schwabe AL, Suter B. Current clinical evidence does not support a link between TBL1XR1 and Rett syndrome: Description of one patient with Rett features and a novel mutation in TBL1XR1, and a review of TBL1XR1 phenotypes. Am J Med Genet A. 2018 07; 176(7):1683-1687. PMID: 29777588.
      Citations: 7     Fields:    Translation:Humans
    33. Tarquinio DC, Hou W, Neul JL, Berkmen GK, Drummond J, Aronoff E, Harris J, Lane JB, Kaufmann WE, Motil KJ, Glaze DG, Skinner SA, Percy AK, Tarquinio DC, Hou W, Neul JL, Berkmen GK, Drummond J, Aronoff E, Harris J, Lane JB, Kaufmann WE, Motil KJ, Glaze DG, Skinner SA, Percy AK. The course of awake breathing disturbances across the lifespan in Rett syndrome. Brain Dev. 2018 Aug; 40(7):515-529. PMID: 29657083; PMCID: PMC6026556.
      Citations: 20     Fields:    Translation:Humans
    34. Layne CS, Lee BC, Young DR, Glaze DG, Schwabe A, Suter B, Layne CS, Lee BC, Young DR, Glaze DG, Schwabe A, Suter B. Temporal Gait Measures Associated With Overground and Treadmill Walking in Rett Syndrome. J Child Neurol. 2018 Jan 01; 883073818780471. PMID: 29926771.
      Citations: 1     Fields:    
    35. Glaze DG, Neul JL, Percy A, Feyma T, Beisang A, Yaroshinsky A, Stoms G, Zuchero D, Horrigan J, Glass L, Jones NE, Glaze DG, Neul JL, Percy A, Feyma T, Beisang A, Yaroshinsky A, Stoms G, Zuchero D, Horrigan J, Glass L, Jones NE. A Double-Blind, Randomized, Placebo-Controlled Clinical Study of Trofinetide in the Treatment of Rett Syndrome. Pediatr Neurol. 2017 Nov; 76:37-46. PMID: 28964591.
      Citations: 21     Fields:    Translation:HumansCTClinical Trials
    36. Lane JB, Salter AR, Jones NE, Cutter G, Horrigan J, Skinner SA, Kaufmann WE, Glaze DG, Neul JL, Percy AK, Lane JB, Salter AR, Jones NE, Cutter G, Horrigan J, Skinner SA, Kaufmann WE, Glaze DG, Neul JL, Percy AK. Assessment of Caregiver Inventory for Rett Syndrome. J Autism Dev Disord. 2017 Apr; 47(4):1102-1112. PMID: 28132121; PMCID: PMC5357458.
      Citations: 5     Fields:    Translation:Humans
    37. Killian JT, Lane JB, Lee HS, Skinner SA, Kaufmann WE, Glaze DG, Neul JL, Percy AK, Killian JT, Lane JB, Lee HS, Skinner SA, Kaufmann WE, Glaze DG, Neul JL, Percy AK. Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors. Pediatr Neurol. 2017 05; 70:20-25. PMID: 28347601; PMCID: PMC5461984.
      Citations: 14     Fields:    Translation:Humans
    38. Tarquinio DC, Hou W, Berg A, Kaufmann WE, Lane JB, Skinner SA, Motil KJ, Neul JL, Percy AK, Glaze DG, Tarquinio DC, Hou W, Berg A, Kaufmann WE, Lane JB, Skinner SA, Motil KJ, Neul JL, Percy AK, Glaze DG. Longitudinal course of epilepsy in Rett syndrome and related disorders. Brain. 2017 02; 140(2):306-318. PMID: 28007990; PMCID: PMC5278305.
      Citations: 35     Fields:    Translation:Humans
    39. Ward CS, Huang TW, Herrera JA, Samaco RC, Pitcher MR, Herron A, Skinner SA, Kaufmann WE, Glaze DG, Percy AK, Neul JL, Ward CS, Huang TW, Herrera JA, Samaco RC, Pitcher MR, Herron A, Skinner SA, Kaufmann WE, Glaze DG, Percy AK, Neul JL. Loss of MeCP2 Causes Urological Dysfunction and Contributes to Death by Kidney Failure in Mouse Models of Rett Syndrome. PLoS One. 2016; 11(11):e0165550. PMID: 27828991; PMCID: PMC5102405.
      Citations: 7     Fields:    Translation:HumansAnimals
    40. Scheimann AO, Miller J, Glaze DG, Scheimann AO, Miller J, Glaze DG. Laparoscopic sleeve gastrectomy in children and adolescents with Prader-Willi syndrome: a matched control study. Surg Obes Relat Dis. 2017 02; 13(2):366. PMID: 27692916.
      Citations: 5     Fields:    Translation:Humans
    41. Sajan SA, Jhangiani SN, Muzny DM, Gibbs RA, Lupski JR, Glaze DG, Kaufmann WE, Skinner SA, Annese F, Friez MJ, Lane J, Percy AK, Neul JL, Sajan SA, Jhangiani SN, Muzny DM, Gibbs RA, Lupski JR, Glaze DG, Kaufmann WE, Skinner SA, Annese F, Friez MJ, Lane J, Percy AK, Neul JL. Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2. Genet Med. 2017 01; 19(1):13-19. PMID: 27171548; PMCID: PMC5107176.
      Citations: 34     Fields:    Translation:HumansCells
    42. Killian JT, Lane JB, Lee HS, Pelham JH, Skinner SA, Kaufmann WE, Glaze DG, Neul JL, Percy AK, Killian JT, Lane JB, Lee HS, Pelham JH, Skinner SA, Kaufmann WE, Glaze DG, Neul JL, Percy AK. Caretaker Quality of Life in Rett Syndrome: Disorder Features and Psychological Predictors. Pediatr Neurol. 2016 05; 58:67-74. PMID: 26995066; PMCID: PMC4899118.
      Citations: 11     Fields:    Translation:Humans
    43. Tarquinio DC, Hou W, Neul JL, Kaufmann WE, Glaze DG, Motil KJ, Skinner SA, Lee HS, Percy AK, Tarquinio DC, Hou W, Neul JL, Kaufmann WE, Glaze DG, Motil KJ, Skinner SA, Lee HS, Percy AK. The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders. Pediatr Neurol. 2015 Nov; 53(5):402-11. PMID: 26278631; PMCID: PMC4609589.
      Citations: 31     Fields:    Translation:Humans
    44. Neul JL, Glaze DG, Percy AK, Feyma T, Beisang A, Dinh T, Suter B, Anagnostou E, Snape M, Horrigan J, Jones NE, Neul JL, Glaze DG, Percy AK, Feyma T, Beisang A, Dinh T, Suter B, Anagnostou E, Snape M, Horrigan J, Jones NE. Improving Treatment Trial Outcomes for Rett Syndrome: The Development of Rett-specific Anchors for the Clinical Global Impression Scale. J Child Neurol. 2015 Nov; 30(13):1743-8. PMID: 25895911; PMCID: PMC4610825.
      Citations: 19     Fields:    Translation:HumansCTClinical Trials
    45. Herrera JA, Ward CS, Pitcher MR, Percy AK, Skinner S, Kaufmann WE, Glaze DG, Wehrens XH, Neul JL, Herrera JA, Ward CS, Pitcher MR, Percy AK, Skinner S, Kaufmann WE, Glaze DG, Wehrens XH, Neul JL. Treatment of cardiac arrhythmias in a mouse model of Rett syndrome with Na+-channel-blocking antiepileptic drugs. Dis Model Mech. 2015 Apr; 8(4):363-71. PMID: 25713300; PMCID: PMC4381335.
      Citations: 8     Fields:    Translation:Animals
    46. Tarquinio DC, Hou W, Neul JL, Lane JB, Barnes KV, O'Leary HM, Bruck NM, Kaufmann WE, Motil KJ, Glaze DG, Skinner SA, Annese F, Baggett L, Barrish JO, Geerts SP, Percy AK, Tarquinio DC, Hou W, Neul JL, Lane JB, Barnes KV, O'Leary HM, Bruck NM, Kaufmann WE, Motil KJ, Glaze DG, Skinner SA, Annese F, Baggett L, Barrish JO, Geerts SP, Percy AK. Age of diagnosis in Rett syndrome: patterns of recognition among diagnosticians and risk factors for late diagnosis. Pediatr Neurol. 2015 Jun; 52(6):585-91.e2. PMID: 25801175; PMCID: PMC4442062.
      Citations: 18     Fields:    Translation:Humans
    47. Motil KJ, Barrish JO, Neul JL, Glaze DG, Motil KJ, Barrish JO, Neul JL, Glaze DG. Low bone mineral mass is associated with decreased bone formation and diet in girls with Rett syndrome. J Pediatr Gastroenterol Nutr. 2014 Sep; 59(3):386-92. PMID: 25144778; PMCID: PMC4144049.
      Citations: 4     Fields:    Translation:Humans
    48. Killian JT, Lane JB, Cutter GR, Skinner SA, Kaufmann WE, Tarquinio DC, Glaze DG, Motil KJ, Neul JL, Percy AK, Killian JT, Lane JB, Cutter GR, Skinner SA, Kaufmann WE, Tarquinio DC, Glaze DG, Motil KJ, Neul JL, Percy AK. Pubertal development in Rett syndrome deviates from typical females. Pediatr Neurol. 2014 Dec; 51(6):769-75. PMID: 25283752; PMCID: PMC4254166.
      Citations: 11     Fields:    Translation:HumansCTClinical Trials
    49. Neul JL, Lane JB, Lee HS, Geerts S, Barrish JO, Annese F, Baggett LM, Barnes K, Skinner SA, Motil KJ, Glaze DG, Kaufmann WE, Percy AK, Neul JL, Lane JB, Lee HS, Geerts S, Barrish JO, Annese F, Baggett LM, Barnes K, Skinner SA, Motil KJ, Glaze DG, Kaufmann WE, Percy AK. Developmental delay in Rett syndrome: data from the natural history study. J Neurodev Disord. 2014; 6(1):20. PMID: 25071871; PMCID: PMC4112822.
      Citations: 58     Fields:    
    50. Patriquin MA, Mellman TA, Glaze DG, Alfano CA, Patriquin MA, Mellman TA, Glaze DG, Alfano CA. Polysomnographic sleep characteristics of generally-anxious and healthy children assessed in the home environment. J Affect Disord. 2014 Jun; 161:79-83. PMID: 24751311; PMCID: PMC4405028.
      Citations: 10     Fields:    Translation:Humans
    51. Suter B, Treadwell-Deering D, Zoghbi HY, Glaze DG, Neul JL, Suter B, Treadwell-Deering D, Zoghbi HY, Glaze DG, Neul JL. Brief report: MECP2 mutations in people without Rett syndrome. J Autism Dev Disord. 2014 Mar; 44(3):703-11. PMID: 23921973; PMCID: PMC3880396.
      Citations: 12     Fields:    Translation:Humans
    52. Cuddapah VA, Pillai RB, Shekar KV, Lane JB, Motil KJ, Skinner SA, Tarquinio DC, Glaze DG, McGwin G, Kaufmann WE, Percy AK, Neul JL, Olsen ML, Cuddapah VA, Pillai RB, Shekar KV, Lane JB, Motil KJ, Skinner SA, Tarquinio DC, Glaze DG, McGwin G, Kaufmann WE, Percy AK, Neul JL, Olsen ML. Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome. J Med Genet. 2014 Mar; 51(3):152-8. PMID: 24399845; PMCID: PMC4403764.
      Citations: 113     Fields:    Translation:Humans
    53. Chapleau CA, Lane J, Kirwin SM, Schanen C, Vinette KM, Stubbolo D, MacLeod P, Glaze DG, Motil KJ, Neul JL, Skinner SA, Kaufmann WE, Percy AK, Chapleau CA, Lane J, Kirwin SM, Schanen C, Vinette KM, Stubbolo D, MacLeod P, Glaze DG, Motil KJ, Neul JL, Skinner SA, Kaufmann WE, Percy AK. Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome. Am J Med Genet A. 2013 Jul; 161A(7):1638-46. PMID: 23696494; PMCID: PMC3689857.
      Citations: 1     Fields:    Translation:Humans
    54. Malow BA, Byars K, Johnson K, Weiss S, Bernal P, Goldman SE, Panzer R, Coury DL, Glaze DG, Malow BA, Byars K, Johnson K, Weiss S, Bernal P, Goldman SE, Panzer R, Coury DL, Glaze DG, Sleep Committee of the Autism Treatment Network. A practice pathway for the identification, evaluation, and management of insomnia in children and adolescents with autism spectrum disorders. Pediatrics. 2012 Nov; 130 Suppl 2:S106-24. PMID: 23118242.
      Citations: 54     Fields:    Translation:Humans
    55. Tarquinio DC, Motil KJ, Hou W, Lee HS, Glaze DG, Skinner SA, Neul JL, Annese F, McNair L, Barrish JO, Geerts SP, Lane JB, Percy AK, Tarquinio DC, Motil KJ, Hou W, Lee HS, Glaze DG, Skinner SA, Neul JL, Annese F, McNair L, Barrish JO, Geerts SP, Lane JB, Percy AK. Growth failure and outcome in Rett syndrome: specific growth references. Neurology. 2012 Oct 16; 79(16):1653-61. PMID: 23035069; PMCID: PMC3468773.
      Citations: 43     Fields:    Translation:Humans
    56. Motil KJ, Caeg E, Barrish JO, Geerts S, Lane JB, Percy AK, Annese F, McNair L, Skinner SA, Lee HS, Neul JL, Glaze DG, Motil KJ, Caeg E, Barrish JO, Geerts S, Lane JB, Percy AK, Annese F, McNair L, Skinner SA, Lee HS, Neul JL, Glaze DG. Gastrointestinal and nutritional problems occur frequently throughout life in girls and women with Rett syndrome. J Pediatr Gastroenterol Nutr. 2012 Sep; 55(3):292-8. PMID: 22331013; PMCID: PMC3393805.
      Citations: 61     Fields:    Translation:Humans
    57. Foster SB, Lu M, Glaze DG, Reuben JM, Harris LL, Cohen EN, Lee BN, Zhao E, Paul ME, Schwarzwald H, McMullen-Jackson C, Clark C, Armstrong FD, Brouwers PY, Miller TL, Colin AA, Scott GB, Shahzeidi S, Willen EJ, Asthana D, Lipshultz SE, Thompson BW, Shearer WT, Foster SB, Lu M, Glaze DG, Reuben JM, Harris LL, Cohen EN, Lee BN, Zhao E, Paul ME, Schwarzwald H, McMullen-Jackson C, Clark C, Armstrong FD, Brouwers PY, Miller TL, Colin AA, Scott GB, Shahzeidi S, Willen EJ, Asthana D, Lipshultz SE, Thompson BW, Shearer WT. Associations of cytokines, sleep patterns, and neurocognitive function in youth with HIV infection. Clin Immunol. 2012 Jul; 144(1):13-23. PMID: 22659030; PMCID: PMC3377781.
      Citations: 17     Fields:    Translation:HumansCells
    58. Motil KJ, Barrish JO, Lane J, Geerts SP, Annese F, McNair L, Percy AK, Skinner SA, Neul JL, Glaze DG, Motil KJ, Barrish JO, Lane J, Geerts SP, Annese F, McNair L, Percy AK, Skinner SA, Neul JL, Glaze DG. Vitamin D deficiency is prevalent in girls and women with Rett syndrome. J Pediatr Gastroenterol Nutr. 2011 Nov; 53(5):569-74. PMID: 21637127; PMCID: PMC3638258.
      Citations: 18     Fields:    Translation:Humans
    59. Lane JB, Lee HS, Smith LW, Cheng P, Percy AK, Glaze DG, Neul JL, Motil KJ, Barrish JO, Skinner SA, Annese F, McNair L, Graham J, Khwaja O, Barnes K, Krischer JP, Lane JB, Lee HS, Smith LW, Cheng P, Percy AK, Glaze DG, Neul JL, Motil KJ, Barrish JO, Skinner SA, Annese F, McNair L, Graham J, Khwaja O, Barnes K, Krischer JP. Clinical severity and quality of life in children and adolescents with Rett syndrome. Neurology. 2011 Nov 15; 77(20):1812-8. PMID: 22013176; PMCID: PMC3233210.
      Citations: 29     Fields:    Translation:Humans
    60. Bird LM, Tan WH, Bacino CA, Peters SU, Skinner SA, Anselm I, Barbieri-Welge R, Bauer-Carlin A, Gentile JK, Glaze DG, Horowitz LT, Mohan KN, Nespeca MP, Sahoo T, Sarco D, Waisbren SE, Beaudet AL, Bird LM, Tan WH, Bacino CA, Peters SU, Skinner SA, Anselm I, Barbieri-Welge R, Bauer-Carlin A, Gentile JK, Glaze DG, Horowitz LT, Mohan KN, Nespeca MP, Sahoo T, Sarco D, Waisbren SE, Beaudet AL. A therapeutic trial of pro-methylation dietary supplements in Angelman syndrome. Am J Med Genet A. 2011 Dec; 155A(12):2956-63. PMID: 22002941; PMCID: PMC3222728.
      Citations: 18     Fields:    Translation:HumansCellsCTClinical Trials
    61. Tan WH, Bacino CA, Skinner SA, Anselm I, Barbieri-Welge R, Bauer-Carlin A, Beaudet AL, Bichell TJ, Gentile JK, Glaze DG, Horowitz LT, Kothare SV, Lee HS, Nespeca MP, Peters SU, Sahoo T, Sarco D, Waisbren SE, Bird LM, Tan WH, Bacino CA, Skinner SA, Anselm I, Barbieri-Welge R, Bauer-Carlin A, Beaudet AL, Bichell TJ, Gentile JK, Glaze DG, Horowitz LT, Kothare SV, Lee HS, Nespeca MP, Peters SU, Sahoo T, Sarco D, Waisbren SE, Bird LM. Angelman syndrome: Mutations influence features in early childhood. Am J Med Genet A. 2011 Jan; 155A(1):81-90. PMID: 21204213; PMCID: PMC3563320.
      Citations: 43     Fields:    Translation:HumansCells
    62. Percy AK, Neul JL, Glaze DG, Motil KJ, Skinner SA, Khwaja O, Lee HS, Lane JB, Barrish JO, Annese F, McNair L, Graham J, Barnes K, Percy AK, Neul JL, Glaze DG, Motil KJ, Skinner SA, Khwaja O, Lee HS, Lane JB, Barrish JO, Annese F, McNair L, Graham J, Barnes K. Rett syndrome diagnostic criteria: lessons from the Natural History Study. Ann Neurol. 2010 Dec; 68(6):951-5. PMID: 21104896; PMCID: PMC3021984.
      Citations: 56     Fields:    Translation:Humans
    63. Neul JL, Kaufmann WE, Glaze DG, Christodoulou J, Clarke AJ, Bahi-Buisson N, Leonard H, Bailey ME, Schanen NC, Zappella M, Renieri A, Huppke P, Percy AK, Neul JL, Kaufmann WE, Glaze DG, Christodoulou J, Clarke AJ, Bahi-Buisson N, Leonard H, Bailey ME, Schanen NC, Zappella M, Renieri A, Huppke P, Percy AK, RettSearch Consortium. Rett syndrome: revised diagnostic criteria and nomenclature. Ann Neurol. 2010 Dec; 68(6):944-50. PMID: 21154482; PMCID: PMC3058521.
      Citations: 423     Fields:    Translation:HumansAnimals
    64. Peters SU, Bird LM, Kimonis V, Glaze DG, Shinawi LM, Bichell TJ, Barbieri-Welge R, Nespeca M, Anselm I, Waisbren S, Sanborn E, Sun Q, O'Brien WE, Beaudet AL, Bacino CA, Peters SU, Bird LM, Kimonis V, Glaze DG, Shinawi LM, Bichell TJ, Barbieri-Welge R, Nespeca M, Anselm I, Waisbren S, Sanborn E, Sun Q, O'Brien WE, Beaudet AL, Bacino CA. Double-blind therapeutic trial in Angelman syndrome using betaine and folic acid. Am J Med Genet A. 2010 Aug; 152A(8):1994-2001. PMID: 20635355; PMCID: PMC3172130.
      Citations: 19     Fields:    Translation:HumansCells
    65. Percy AK, Lee HS, Neul JL, Lane JB, Skinner SA, Geerts SP, Annese F, Graham J, McNair L, Motil KJ, Barrish JO, Glaze DG, Percy AK, Lee HS, Neul JL, Lane JB, Skinner SA, Geerts SP, Annese F, Graham J, McNair L, Motil KJ, Barrish JO, Glaze DG. Profiling scoliosis in Rett syndrome. Pediatr Res. 2010 Apr; 67(4):435-9. PMID: 20032810; PMCID: PMC2852102.
      Citations: 25     Fields:    Translation:Humans
    66. Glaze DG, Percy AK, Skinner S, Motil KJ, Neul JL, Barrish JO, Lane JB, Geerts SP, Annese F, Graham J, McNair L, Lee HS, Glaze DG, Percy AK, Skinner S, Motil KJ, Neul JL, Barrish JO, Lane JB, Geerts SP, Annese F, Graham J, McNair L, Lee HS. Epilepsy and the natural history of Rett syndrome. Neurology. 2010 Mar 16; 74(11):909-12. PMID: 20231667; PMCID: PMC2836870.
      Citations: 69     Fields:    Translation:Humans
    67. Kirby RS, Lane JB, Childers J, Skinner SA, Annese F, Barrish JO, Glaze DG, Macleod P, Percy AK, Kirby RS, Lane JB, Childers J, Skinner SA, Annese F, Barrish JO, Glaze DG, Macleod P, Percy AK. Longevity in Rett syndrome: analysis of the North American Database. J Pediatr. 2010 Jan; 156(1):135-138.e1. PMID: 19772971; PMCID: PMC2794941.
      Citations: 27     Fields:    Translation:Humans
    68. Samaco RC, Mandel-Brehm C, Chao HT, Ward CS, Fyffe-Maricich SL, Ren J, Hyland K, Thaller C, Maricich SM, Humphreys P, Greer JJ, Percy A, Glaze DG, Zoghbi HY, Neul JL, Samaco RC, Mandel-Brehm C, Chao HT, Ward CS, Fyffe-Maricich SL, Ren J, Hyland K, Thaller C, Maricich SM, Humphreys P, Greer JJ, Percy A, Glaze DG, Zoghbi HY, Neul JL. Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities. Proc Natl Acad Sci U S A. 2009 Dec 22; 106(51):21966-71. PMID: 20007372; PMCID: PMC2799790.
      Citations: 121     Fields:    Translation:AnimalsCells
    69. Ramocki MB, Peters SU, Tavyev YJ, Zhang F, Carvalho CM, Schaaf CP, Richman R, Fang P, Glaze DG, Lupski JR, Zoghbi HY, Ramocki MB, Peters SU, Tavyev YJ, Zhang F, Carvalho CM, Schaaf CP, Richman R, Fang P, Glaze DG, Lupski JR, Zoghbi HY. Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome. Ann Neurol. 2009 Dec; 66(6):771-82. PMID: 20035514; PMCID: PMC2801873.
      Citations: 140     Fields:    Translation:HumansCells
    70. Motil KJ, Morrissey M, Caeg E, Barrish JO, Glaze DG, Motil KJ, Morrissey M, Caeg E, Barrish JO, Glaze DG. Gastrostomy placement improves height and weight gain in girls with Rett syndrome. J Pediatr Gastroenterol Nutr. 2009 Aug; 49(2):237-42. PMID: 19525868.
      Citations: 12     Fields:    Translation:Humans
    71. Glaze DG, Percy AK, Motil KJ, Lane JB, Isaacs JS, Schultz RJ, Barrish JO, Neul JL, O'Brien WE, Smith EO, Glaze DG, Percy AK, Motil KJ, Lane JB, Isaacs JS, Schultz RJ, Barrish JO, Neul JL, O'Brien WE, Smith EO. A study of the treatment of Rett syndrome with folate and betaine. J Child Neurol. 2009 May; 24(5):551-6. PMID: 19225139; PMCID: PMC2760386.
      Citations: 15     Fields:    Translation:Humans
    72. Motil KJ, Ellis KJ, Barrish JO, Caeg E, Glaze DG, Motil KJ, Ellis KJ, Barrish JO, Caeg E, Glaze DG. Bone mineral content and bone mineral density are lower in older than in younger females with Rett syndrome. Pediatr Res. 2008 Oct; 64(4):435-9. PMID: 18535484; PMCID: PMC2663405.
      Citations: 20     Fields:    Translation:Humans
    73. Hopkins B, Glaze D, Hopkins B, Glaze D. Disorders of arousal in children. Pediatr Ann. 2008 Jul; 37(7):481-7. PMID: 18710138.
      Citations:    Fields:    Translation:Humans
    74. Huckeba W, Chapieski L, Hiscock M, Glaze D, Huckeba W, Chapieski L, Hiscock M, Glaze D. Arithmetic performance in children with Tourette syndrome: relative contribution of cognitive and attentional factors. J Clin Exp Neuropsychol. 2008 May; 30(4):410-20. PMID: 18938679.
      Citations: 5     Fields:    Translation:Humans
    75. Williams K, Scheimann A, Sutton V, Hayslett E, Glaze DG, Williams K, Scheimann A, Sutton V, Hayslett E, Glaze DG. Sleepiness and sleep disordered breathing in Prader-Willi syndrome: relationship to genotype, growth hormone therapy, and body composition. J Clin Sleep Med. 2008 Apr 15; 4(2):111-8. PMID: 18468308; PMCID: PMC2335405.
      Citations: 24     Fields:    Translation:Humans
    76. Neul JL, Fang P, Barrish J, Lane J, Caeg EB, Smith EO, Zoghbi H, Percy A, Glaze DG, Neul JL, Fang P, Barrish J, Lane J, Caeg EB, Smith EO, Zoghbi H, Percy A, Glaze DG. Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome. Neurology. 2008 Apr 15; 70(16):1313-21. PMID: 18337588; PMCID: PMC2677974.
      Citations: 187     Fields:    Translation:Humans
    77. Percy AK, Lane JB, Childers J, Skinner S, Annese F, Barrish J, Caeg E, Glaze DG, MacLeod P, Percy AK, Lane JB, Childers J, Skinner S, Annese F, Barrish J, Caeg E, Glaze DG, MacLeod P. Rett syndrome: North American database. J Child Neurol. 2007 Dec; 22(12):1338-41. PMID: 18174548.
      Citations: 32     Fields:    Translation:Humans
    78. Blumer JL, Reed MD, Steinberg F, O'Riordan MA, Rosen CL, Springer MA, Christensen M, Glaze D, Blumer JL, Reed MD, Steinberg F, O'Riordan MA, Rosen CL, Springer MA, Christensen M, Glaze D, NICHD PPRU Network. Potential pharmacokinetic basis for zolpidem dosing in children with sleep difficulties. Clin Pharmacol Ther. 2008 Apr; 83(4):551-8. PMID: 17957186.
      Citations: 4     Fields:    Translation:HumansCTClinical Trials
    79. Potocki L, Bi W, Treadwell-Deering D, Carvalho CM, Eifert A, Friedman EM, Glaze D, Krull K, Lee JA, Lewis RA, Mendoza-Londono R, Robbins-Furman P, Shaw C, Shi X, Weissenberger G, Withers M, Yatsenko SA, Zackai EH, Stankiewicz P, Lupski JR, Potocki L, Bi W, Treadwell-Deering D, Carvalho CM, Eifert A, Friedman EM, Glaze D, Krull K, Lee JA, Lewis RA, Mendoza-Londono R, Robbins-Furman P, Shaw C, Shi X, Weissenberger G, Withers M, Yatsenko SA, Zackai EH, Stankiewicz P, Lupski JR. Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype. Am J Hum Genet. 2007 Apr; 80(4):633-49. PMID: 17357070; PMCID: PMC1852712.
      Citations: 141     Fields:    Translation:HumansCells
    80. del Gaudio D, Fang P, Scaglia F, Ward PA, Craigen WJ, Glaze DG, Neul JL, Patel A, Lee JA, Irons M, Berry SA, Pursley AA, Grebe TA, Freedenberg D, Martin RA, Hsich GE, Khera JR, Friedman NR, Zoghbi HY, Eng CM, Lupski JR, Beaudet AL, Cheung SW, Roa BB, del Gaudio D, Fang P, Scaglia F, Ward PA, Craigen WJ, Glaze DG, Neul JL, Patel A, Lee JA, Irons M, Berry SA, Pursley AA, Grebe TA, Freedenberg D, Martin RA, Hsich GE, Khera JR, Friedman NR, Zoghbi HY, Eng CM, Lupski JR, Beaudet AL, Cheung SW, Roa BB. Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males. Genet Med. 2006 Dec; 8(12):784-92. PMID: 17172942.
      Citations: 121     Fields:    Translation:HumansCells
    81. Mindell JA, Emslie G, Blumer J, Genel M, Glaze D, Ivanenko A, Johnson K, Rosen C, Steinberg F, Roth T, Banas B, Mindell JA, Emslie G, Blumer J, Genel M, Glaze D, Ivanenko A, Johnson K, Rosen C, Steinberg F, Roth T, Banas B. Pharmacologic management of insomnia in children and adolescents: consensus statement. Pediatrics. 2006 Jun; 117(6):e1223-32. PMID: 16740821.
      Citations: 39     Fields:    Translation:Humans
    82. Motil KJ, Schultz RJ, Abrams S, Ellis KJ, Glaze DG, Motil KJ, Schultz RJ, Abrams S, Ellis KJ, Glaze DG. Fractional calcium absorption is increased in girls with Rett syndrome. J Pediatr Gastroenterol Nutr. 2006 Apr; 42(4):419-26. PMID: 16641581.
      Citations: 13     Fields:    Translation:Humans
    83. Goldman AM, Potocki L, Walz K, Lynch JK, Glaze DG, Lupski JR, Noebels JL, Goldman AM, Potocki L, Walz K, Lynch JK, Glaze DG, Lupski JR, Noebels JL. Epilepsy and chromosomal rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)]. J Child Neurol. 2006 Feb; 21(2):93-8. PMID: 16566870.
      Citations: 13     Fields:    Translation:HumansCells
    84. Yatsenko SA, Treadwell-Deering D, Krull K, Lewis RA, Glaze D, Stankiewicz P, Lupski JR, Potocki L, Yatsenko SA, Treadwell-Deering D, Krull K, Lewis RA, Glaze D, Stankiewicz P, Lupski JR, Potocki L. Trisomy 17p10-p12 due to mosaic supernumerary marker chromosome: delineation of molecular breakpoints and clinical phenotype, and comparison to other proximal 17p segmental duplications. Am J Med Genet A. 2005 Oct 01; 138A(2):175-80. PMID: 16152635.
      Citations: 9     Fields:    Translation:HumansCells
    85. Sahoo T, Peters SU, Madduri NS, Glaze DG, German JR, Bird LM, Barbieri-Welge R, Bichell TJ, Beaudet AL, Bacino CA, Sahoo T, Peters SU, Madduri NS, Glaze DG, German JR, Bird LM, Barbieri-Welge R, Bichell TJ, Beaudet AL, Bacino CA. Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: genotype-phenotype correlations. J Med Genet. 2006 Jun; 43(6):512-6. PMID: 16183798; PMCID: PMC2564536.
      Citations: 35     Fields:    Translation:HumansCells
    86. Glaze DG, Glaze DG. Neurophysiology of Rett syndrome. J Child Neurol. 2005 Sep; 20(9):740-6. PMID: 16225829.
      Citations: 43     Fields:    Translation:Humans
    87. Glaze DG, Glaze DG. Evidence based sleep medicine--is pediatric sleep medicine ready? J Clin Sleep Med. 2005 Jul 15; 1(3):255-6. PMID: 17566184.
      Citations:    Fields:    Translation:Humans
    88. Neul JL, Maricich SM, Islam M, Barrish J, Smith EO, Bottiglieri T, Hyland K, Humphreys P, Percy A, Glaze D, Neul JL, Maricich SM, Islam M, Barrish J, Smith EO, Bottiglieri T, Hyland K, Humphreys P, Percy A, Glaze D. Spinal fluid 5-methyltetrahydrofolate levels are normal in Rett syndrome. Neurology. 2005 Jun 28; 64(12):2151-2. PMID: 15985595.
      Citations: 2     Fields:    Translation:Humans
    89. Stewart MG, Glaze DG, Friedman EM, Smith EO, Bautista M, Stewart MG, Glaze DG, Friedman EM, Smith EO, Bautista M. Quality of life and sleep study findings after adenotonsillectomy in children with obstructive sleep apnea. Arch Otolaryngol Head Neck Surg. 2005 Apr; 131(4):308-14. PMID: 15837898.
      Citations: 16     Fields:    Translation:Humans
    90. Amir RE, Fang P, Yu Z, Glaze DG, Percy AK, Zoghbi HY, Roa BB, Van den Veyver IB, Amir RE, Fang P, Yu Z, Glaze DG, Percy AK, Zoghbi HY, Roa BB, Van den Veyver IB. Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome. J Med Genet. 2005 Feb; 42(2):e15. PMID: 15689438; PMCID: PMC1735975.
      Citations: 18     Fields:    Translation:Humans
    91. Owens JA, Babcock D, Blumer J, Chervin R, Ferber R, Goetting M, Glaze D, Ivanenko A, Mindell J, Rappley M, Rosen C, Sheldon S, Owens JA, Babcock D, Blumer J, Chervin R, Ferber R, Goetting M, Glaze D, Ivanenko A, Mindell J, Rappley M, Rosen C, Sheldon S. The use of pharmacotherapy in the treatment of pediatric insomnia in primary care: rational approaches. A consensus meeting summary. J Clin Sleep Med. 2005 Jan 15; 1(1):49-59. PMID: 17561616.
      Citations: 24     Fields:    Translation:HumansPHPublic Health
    92. Glaze DG, Glaze DG. Childhood insomnia: why Chris can't sleep. Pediatr Clin North Am. 2004 Feb; 51(1):33-50, vi. PMID: 15008581.
      Citations: 8     Fields:    Translation:Humans
    93. Glaze DG, Glaze DG. Rett syndrome: of girls and mice--lessons for regression in autism. Ment Retard Dev Disabil Res Rev. 2004; 10(2):154-8. PMID: 15362175.
      Citations: 16     Fields:    Translation:HumansAnimalsCells
    94. Culhane-Shelburne K, Chapieski L, Hiscock M, Glaze D, Culhane-Shelburne K, Chapieski L, Hiscock M, Glaze D. Executive functions in children with frontal and temporal lobe epilepsy. J Int Neuropsychol Soc. 2002 Jul; 8(5):623-32. PMID: 12164672.
      Citations: 14     Fields:    Translation:HumansCTClinical Trials
    95. Glaze DG, Glaze DG. Neurophysiology of Rett syndrome. Ment Retard Dev Disabil Res Rev. 2002; 8(2):66-71. PMID: 12112729.
      Citations: 9     Fields:    Translation:Humans
    96. Deguchi K, Reyes C, Chakraborty S, Antalffy B, Glaze D, Armstrong D, Deguchi K, Reyes C, Chakraborty S, Antalffy B, Glaze D, Armstrong D. Substance P immunoreactivity in the enteric nervous system in Rett syndrome. Brain Dev. 2001 Dec; 23 Suppl 1:S127-32. PMID: 11738858.
      Citations: 3     Fields:    Translation:HumansCells
    97. Potocki L, Glaze D, Tan DX, Park SS, Kashork CD, Shaffer LG, Reiter RJ, Lupski JR, Potocki L, Glaze D, Tan DX, Park SS, Kashork CD, Shaffer LG, Reiter RJ, Lupski JR. Circadian rhythm abnormalities of melatonin in Smith-Magenis syndrome. J Med Genet. 2000 Jun; 37(6):428-33. PMID: 10851253; PMCID: PMC1734604.
      Citations: 52     Fields:    Translation:HumansCells
    98. Amir RE, Van den Veyver IB, Schultz R, Malicki DM, Tran CQ, Dahle EJ, Philippi A, Timar L, Percy AK, Motil KJ, Lichtarge O, Smith EO, Glaze DG, Zoghbi HY, Amir RE, Van den Veyver IB, Schultz R, Malicki DM, Tran CQ, Dahle EJ, Philippi A, Timar L, Percy AK, Motil KJ, Lichtarge O, Smith EO, Glaze DG, Zoghbi HY. Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes. Ann Neurol. 2000 May; 47(5):670-9. PMID: 10805343.
      Citations: 80     Fields:    Translation:HumansCells
    99. Deguchi K, Antalffy BA, Twohill LJ, Chakraborty S, Glaze DG, Armstrong DD, Deguchi K, Antalffy BA, Twohill LJ, Chakraborty S, Glaze DG, Armstrong DD. Substance P immunoreactivity in Rett syndrome. Pediatr Neurol. 2000 Apr; 22(4):259-66. PMID: 10788742.
      Citations: 16     Fields:    Translation:HumansCells
    100. Motil KJ, Schultz RJ, Browning K, Trautwein L, Glaze DG, Motil KJ, Schultz RJ, Browning K, Trautwein L, Glaze DG. Oropharyngeal dysfunction and gastroesophageal dysmotility are present in girls and women with Rett syndrome. J Pediatr Gastroenterol Nutr. 1999 Jul; 29(1):31-7. PMID: 10400100.
      Citations: 20     Fields:    Translation:Humans
    101. Armstrong DD, Dunn JK, Schultz RJ, Herbert DA, Glaze DG, Motil KJ, Armstrong DD, Dunn JK, Schultz RJ, Herbert DA, Glaze DG, Motil KJ. Organ growth in Rett syndrome: a postmortem examination analysis. Pediatr Neurol. 1999 Feb; 20(2):125-9. PMID: 10082341.
      Citations: 10     Fields:    Translation:Humans
    102. Motil KJ, Schultz RJ, Wong WW, Glaze DG, Motil KJ, Schultz RJ, Wong WW, Glaze DG. Increased energy expenditure associated with repetitive involuntary movement does not contribute to growth failure in girls with Rett syndrome. J Pediatr. 1998 Feb; 132(2):228-33. PMID: 9506632.
      Citations: 6     Fields:    Translation:Humans
    103. Schultz R, Glaze D, Motil K, Hebert D, Percy A, Schultz R, Glaze D, Motil K, Hebert D, Percy A. Hand and foot growth failure in Rett syndrome. J Child Neurol. 1998 Feb; 13(2):71-4. PMID: 9512306.
      Citations: 6     Fields:    Translation:Humans
    104. Glaze DG, Schultz RJ, Frost JD, Glaze DG, Schultz RJ, Frost JD. Rett syndrome: characterization of seizures versus non-seizures. Electroencephalogr Clin Neurophysiol. 1998 Jan; 106(1):79-83. PMID: 9680167.
      Citations: 18     Fields:    Translation:Humans
    105. Greenberg F, Lewis RA, Potocki L, Glaze D, Parke J, Killian J, Murphy MA, Williamson D, Brown F, Dutton R, McCluggage C, Friedman E, Sulek M, Lupski JR, Greenberg F, Lewis RA, Potocki L, Glaze D, Parke J, Killian J, Murphy MA, Williamson D, Brown F, Dutton R, McCluggage C, Friedman E, Sulek M, Lupski JR. Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2) Am J Med Genet. 1996 Mar 29; 62(3):247-54. PMID: 8882782.
      Citations: 87     Fields:    Translation:HumansCells
    106. Kozinetz CA, Skender ML, MacNaughton NL, del Junco DJ, Almes MJ, Schultz RJ, Glaze DG, Percy AK, Kozinetz CA, Skender ML, MacNaughton NL, del Junco DJ, Almes MJ, Schultz RJ, Glaze DG, Percy AK. Population-based registries using multidisciplinary reporters: a method for the study of pediatric neurologic disorders. J Clin Epidemiol. 1995 Aug; 48(8):1069-76. PMID: 7775994.
      Citations: 2     Fields:    Translation:HumansPHPublic Health
    107. Glaze DG, Glaze DG. Commentary: the challenge of Rett syndrome. Neuropediatrics. 1995 Apr; 26(2):78-80. PMID: 7566458.
      Citations: 1     Fields:    Translation:Humans
    108. Frost JD, Hrachovy RA, Glaze DG, Rettig GM, Frost JD, Hrachovy RA, Glaze DG, Rettig GM. Alpha rhythm slowing during initiation of carbamazepine therapy: implications for future cognitive performance. J Clin Neurophysiol. 1995 Jan; 12(1):57-63. PMID: 7896910.
      Citations: 5     Fields:    Translation:Humans
    109. Hrachovy RA, Frost JD, Glaze DG, Hrachovy RA, Frost JD, Glaze DG. Coupling of focal electrical seizure discharges with infantile spasms: incidence during long-term monitoring in newly diagnosed patients. J Clin Neurophysiol. 1994 Jul; 11(4):461-4. PMID: 7962492.
      Citations:    Fields:    Translation:Humans
    110. Sekul EA, Moak JP, Schultz RJ, Glaze DG, Dunn JK, Percy AK, Sekul EA, Moak JP, Schultz RJ, Glaze DG, Dunn JK, Percy AK. Electrocardiographic findings in Rett syndrome: an explanation for sudden death? J Pediatr. 1994 Jul; 125(1):80-2. PMID: 8021793.
      Citations: 31     Fields:    Translation:Humans
    111. Motil KJ, Schultz R, Brown B, Glaze DG, Percy AK, Motil KJ, Schultz R, Brown B, Glaze DG, Percy AK. Altered energy balance may account for growth failure in Rett syndrome. J Child Neurol. 1994 Jul; 9(3):315-9. PMID: 7930413.
      Citations: 3     Fields:    Translation:Humans
    112. Hrachovy RA, Frost JD, Glaze DG, Hrachovy RA, Frost JD, Glaze DG. High-dose, long-duration versus low-dose, short-duration corticotropin therapy for infantile spasms. J Pediatr. 1994 May; 124(5 Pt 1):803-6. PMID: 8176573.
      Citations: 43     Fields:    Translation:HumansCTClinical Trials
    113. Percy AK, Glaze DG, Schultz RJ, Zoghbi HY, Williamson D, Frost JD, Jankovic JJ, del Junco D, Skender M, Waring S, Percy AK, Glaze DG, Schultz RJ, Zoghbi HY, Williamson D, Frost JD, Jankovic JJ, del Junco D, Skender M, Waring S, et al. Rett syndrome: controlled study of an oral opiate antagonist, naltrexone. Ann Neurol. 1994 Apr; 35(4):464-70. PMID: 8154874.
      Citations: 14     Fields:    Translation:HumansCTClinical Trials
    114. Schultz RJ, Glaze DG, Motil KJ, Armstrong DD, del Junco DJ, Hubbard CR, Percy AK, Schultz RJ, Glaze DG, Motil KJ, Armstrong DD, del Junco DJ, Hubbard CR, Percy AK. The pattern of growth failure in Rett syndrome. Am J Dis Child. 1993 Jun; 147(6):633-7. PMID: 8506830.
      Citations: 20     Fields:    Translation:Humans
    115. Kozinetz CA, Skender ML, MacNaughton N, Almes MJ, Schultz RJ, Percy AK, Glaze DG, Kozinetz CA, Skender ML, MacNaughton N, Almes MJ, Schultz RJ, Percy AK, Glaze DG. Epidemiology of Rett syndrome: a population-based registry. Pediatrics. 1993 Feb; 91(2):445-50. PMID: 8424025.
      Citations: 26     Fields:    Translation:HumansPHPublic Health
    116. Butte NF, Jensen CL, Moon JK, Glaze DG, Frost JD, Butte NF, Jensen CL, Moon JK, Glaze DG, Frost JD. Sleep organization and energy expenditure of breast-fed and formula-fed infants. Pediatr Res. 1992 Nov; 32(5):514-9. PMID: 1480450.
      Citations: 7     Fields:    Translation:Humans
    117. Frost JD, Hrachovy RA, Glaze DG, Frost JD, Hrachovy RA, Glaze DG. Spike morphology in childhood focal epilepsy: relationship to syndromic classification. Epilepsia. 1992 May-Jun; 33(3):531-6. PMID: 1592033.
      Citations: 1     Fields:    Translation:Humans
    118. Lupski JR, Wise CA, Kuwano A, Pentao L, Parke JT, Glaze DG, Ledbetter DH, Greenberg F, Patel PI, Lupski JR, Wise CA, Kuwano A, Pentao L, Parke JT, Glaze DG, Ledbetter DH, Greenberg F, Patel PI. Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A. Nat Genet. 1992 Apr; 1(1):29-33. PMID: 1301995.
      Citations: 63     Fields:    Translation:HumansCells
    119. Frost JD, Hrachovy RA, Glaze DG, McCully MI, Frost JD, Hrachovy RA, Glaze DG, McCully MI. Sleep modulation of interictal spike configuration in untreated children with partial seizures. Epilepsia. 1991 May-Jun; 32(3):341-6. PMID: 1904344.
      Citations: 3     Fields:    Translation:Humans
    120. Hrachovy RA, Glaze DG, Frost JD, Hrachovy RA, Glaze DG, Frost JD. A retrospective study of spontaneous remission and long-term outcome in patients with infantile spasms. Epilepsia. 1991 Mar-Apr; 32(2):212-4. PMID: 1848513.
      Citations: 14     Fields:    Translation:Humans
    121. Hrachovy RA, Frost JD, Glaze DG, Kellaway P, Hrachovy RA, Frost JD, Glaze DG, Kellaway P. Surgical treatment for infantile spasms? Ann Neurol. 1991 Jan; 29(1):110-2. PMID: 1996874.
      Citations: 2     Fields:    Translation:Humans
    122. FitzGerald PM, Jankovic J, Glaze DG, Schultz R, Percy AK, FitzGerald PM, Jankovic J, Glaze DG, Schultz R, Percy AK. Extrapyramidal involvement in Rett's syndrome. Neurology. 1990 Feb; 40(2):293-5. PMID: 2073236.
      Citations: 12     Fields:    Translation:Humans
    123. Zoghbi HY, Ledbetter DH, Schultz R, Percy AK, Glaze DG, Zoghbi HY, Ledbetter DH, Schultz R, Percy AK, Glaze DG. A de novo X;3 translocation in Rett syndrome. Am J Med Genet. 1990 Jan; 35(1):148-51. PMID: 2301468.
      Citations: 13     Fields:    Translation:HumansCells
    124. Hrachovy RA, Frost JD, Glaze DG, Rose D, Hrachovy RA, Frost JD, Glaze DG, Rose D. Treatment of infantile spasms with methysergide and alpha-methylparatyrosine. Epilepsia. 1989 Sep-Oct; 30(5):607-10. PMID: 2571497.
      Citations: 1     Fields:    Translation:HumansCTClinical Trials
    125. Zoghbi HY, Milstien S, Butler IJ, Smith EO, Kaufman S, Glaze DG, Percy AK, Zoghbi HY, Milstien S, Butler IJ, Smith EO, Kaufman S, Glaze DG, Percy AK. Cerebrospinal fluid biogenic amines and biopterin in Rett syndrome. Ann Neurol. 1989 Jan; 25(1):56-60. PMID: 2913929.
      Citations: 24     Fields:    Translation:Humans
    126. Hrachovy RA, Frost JD, Pollack MS, Glaze DG, Hrachovy RA, Frost JD, Pollack MS, Glaze DG. Serologic HLA typing in infantile spasms. Epilepsia. 1988 Nov-Dec; 29(6):817-9. PMID: 3191897.
      Citations: 1     Fields:    Translation:Humans
    127. Hrachovy RA, Frost JD, Glaze DG, Hrachovy RA, Frost JD, Glaze DG. Treatment of infantile spasms with tetrabenazine. Epilepsia. 1988 Sep-Oct; 29(5):561-3. PMID: 3409841.
      Citations: 1     Fields:    Translation:Humans
    128. Frost JD, Glaze DG, Rosen CL, Frost JD, Glaze DG, Rosen CL. Munchausen's syndrome by proxy and video surveillance. Am J Dis Child. 1988 Sep; 142(9):917-8. PMID: 3414617.
      Citations:    Fields:    Translation:Humans
    129. Glaze DG, Hrachovy RA, Frost JD, Kellaway P, Zion TE, Glaze DG, Hrachovy RA, Frost JD, Kellaway P, Zion TE. Prospective study of outcome of infants with infantile spasms treated during controlled studies of ACTH and prednisone. J Pediatr. 1988 Mar; 112(3):389-96. PMID: 2450190.
      Citations: 11     Fields:    Translation:Humans
    130. Glaze DG, Frost JD, Zoghbi HY, Percy AK, Glaze DG, Frost JD, Zoghbi HY, Percy AK. Rett's syndrome. Correlation of electroencephalographic characteristics with clinical staging. Arch Neurol. 1987 Oct; 44(10):1053-6. PMID: 3632378.
      Citations: 12     Fields:    Translation:Humans
    131. Glaze DG, Frost JD, Zoghbi HY, Percy AK, Glaze DG, Frost JD, Zoghbi HY, Percy AK. Rett's syndrome: characterization of respiratory patterns and sleep. Ann Neurol. 1987 Apr; 21(4):377-82. PMID: 3579223.
      Citations: 24     Fields:    Translation:Humans
    132. Hrachovy RA, Frost JD, Gospe SM, Glaze DG, Hrachovy RA, Frost JD, Gospe SM, Glaze DG. Infantile spasms following near-drowning: a report of two cases. Epilepsia. 1987 Jan-Feb; 28(1):45-8. PMID: 3792289.
      Citations: 1     Fields:    Translation:Humans
    133. Percy AK, Zoghbi HY, Glaze DG, Percy AK, Zoghbi HY, Glaze DG. Rett syndrome: discrimination of typical and variant forms. Brain Dev. 1987; 9(5):458-61. PMID: 3434720.
      Citations: 3     Fields:    Translation:Humans
    134. Jerger J, Chmiel R, Glaze D, Frost JD, Jerger J, Chmiel R, Glaze D, Frost JD. Rate and filter dependence of the middle-latency response in infants. Audiology. 1987; 26(5):269-83. PMID: 3675311.
      Citations: 1     Fields:    Translation:Humans
    135. Rosen CL, Frost JD, Glaze DG, Rosen CL, Frost JD, Glaze DG. Child abuse and recurrent infant apnea. J Pediatr. 1986 Dec; 109(6):1065-7. PMID: 3783332.
      Citations: 7     Fields:    Translation:Humans
    136. Frost JD, Kellaway P, Hrachovy RA, Glaze DG, Mizrahi EM, Frost JD, Kellaway P, Hrachovy RA, Glaze DG, Mizrahi EM. Changes in epileptic spike configuration associated with attainment of seizure control. Ann Neurol. 1986 Dec; 20(6):723-6. PMID: 3101580.
      Citations: 3     Fields:    Translation:Humans
    137. Rosen CL, Glaze DG, Frost JD, Rosen CL, Glaze DG, Frost JD. Home monitor follow-up of persistent apnea and bradycardia in preterm infants. Am J Dis Child. 1986 Jun; 140(6):547-50. PMID: 3706233.
      Citations: 3     Fields:    Translation:Humans
    138. Glaze DG, Hrachovy RA, Frost JD, Zion TE, Bryan RN, Glaze DG, Hrachovy RA, Frost JD, Zion TE, Bryan RN. Computed tomography in infantile spasms: effects of hormonal therapy. Pediatr Neurol. 1986 Jan-Feb; 2(1):23-7. PMID: 2854738.
      Citations: 3     Fields:    Translation:HumansCTClinical Trials
    139. Glaze DG, Zion TE, Glaze DG, Zion TE. Infantile spasms. Curr Probl Pediatr. 1985 Nov; 15(11):1-39. PMID: 2996835.
      Citations: 1     Fields:    Translation:HumansCTClinical Trials
    140. Zoghbi HY, Percy AK, Glaze DG, Butler IJ, Riccardi VM, Zoghbi HY, Percy AK, Glaze DG, Butler IJ, Riccardi VM. Reduction of biogenic amine levels in the Rett syndrome. N Engl J Med. 1985 Oct 10; 313(15):921-4. PMID: 2412119.
      Citations: 36     Fields:    Translation:Humans
    141. Rosen CL, Glaze DG, Frost JD, Rosen CL, Glaze DG, Frost JD. Hypoxemia associated with feeding in the preterm infant and full-term neonate. Am J Dis Child. 1984 Jul; 138(7):623-8. PMID: 6428217.
      Citations: 12     Fields:    Translation:Humans
    142. Neglia JP, Glaze DG, Zion TE, Neglia JP, Glaze DG, Zion TE. Tics and vocalizations in children treated with carbamazepine. Pediatrics. 1984 Jun; 73(6):841-4. PMID: 6587312.
      Citations: 3     Fields:    Translation:Humans
    143. Jankovic J, Glaze DG, Frost JD, Jankovic J, Glaze DG, Frost JD. Effect of tetrabenazine on tics and sleep of Gilles de la Tourette's syndrome. Neurology. 1984 May; 34(5):688-92. PMID: 6584743.
      Citations: 17     Fields:    Translation:Humans
    144. Strickbine-Van Reet P, Glaze DG, Hrachovy RA, Strickbine-Van Reet P, Glaze DG, Hrachovy RA. A preliminary prospective neurophysiological study of coma in children. Am J Dis Child. 1984 May; 138(5):492-5. PMID: 6711506.
      Citations: 2     Fields:    Translation:Humans
    145. Hrachovy RA, Frost JD, Glaze DG, Hrachovy RA, Frost JD, Glaze DG. What have we learned about sudden infant death? N Engl J Med. 1984 Mar 22; 310(12):787-8. PMID: 6700660.
      Citations:    Fields:    Translation:Humans
    146. Mahoney DH, Fernbach DJ, Glaze DG, Cohen SR, Mahoney DH, Fernbach DJ, Glaze DG, Cohen SR. Elevated myelin basic protein levels in the cerebrospinal fluid of children with acute lymphoblastic leukemia. J Clin Oncol. 1984 Jan; 2(1):58-61. PMID: 6199479.
      Citations: 4     Fields:    Translation:Humans
    147. Glaze DG, Frost JD, Jankovic J, Glaze DG, Frost JD, Jankovic J. Sleep in Gilles de la Tourette's syndrome: disorder of arousal. Neurology. 1983 May; 33(5):586-92. PMID: 6573576.
      Citations: 12     Fields:    Translation:Humans
    148. Bushong SC, Glaze D, Glaze S, Singleton E, Bushong SC, Glaze D, Glaze S, Singleton E. Radiation dose to children from x-ray and radioisotope examinations. Health Phys. 1978 Nov; 35(5):720-1. PMID: 744741.
      Citations:    Fields:    Translation:Humans
    149. Bushong SC, Pogonowska MJ, Gerlock AJ, Glaze SA, Glaze DG, Bushong SC, Pogonowska MJ, Gerlock AJ, Glaze SA, Glaze DG. Roentgen area product and exposure measurements during chest radiography and nephrotomography. Acta Radiol Diagn (Stockh). 1973 Nov; 14(6):461-8. PMID: 4774992.
      Citations:    Fields:    Translation:Humans
    150. Bushong S, Kothari S, Williams CD, Prasad N, Glaze D, Bushong S, Kothari S, Williams CD, Prasad N, Glaze D. Photofluorographic measurement of the roentgen area product. Radiology. 1973 Jun; 107(3):673-4. PMID: 4702548.
      Citations:    Fields:    Translation:HumansPHPublic Health
    GLAZE's Networks
    Click the
    Explore
    buttons for more information and interactive visualizations!
    Concepts (494)
    Explore
    _
    Co-Authors (54)
    Explore
    _
    Similar People (60)
    Explore
    _
    Same Department Expand Description
    Explore
    _
    Physical Neighbors
    _