DANIEL GLAZE to Male
This is a "connection" page, showing publications DANIEL GLAZE has written about Male.
Connection Strength
0.281
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Clinical application of home sleep apnea testing in children: a prospective pilot study. J Clin Sleep Med. 2022 Feb 01; 18(2):533-540.
Score: 0.026
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Electroencephalographic Patterns During Routine Polysomnography in Childhood and Association With Future Epilepsy Diagnosis. J Clin Sleep Med. 2019 04 15; 15(4):553-562.
Score: 0.021
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A Double-Blind, Randomized, Placebo-Controlled Clinical Study of Trofinetide in the Treatment of Rett Syndrome. Pediatr Neurol. 2017 Nov; 76:37-46.
Score: 0.019
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Longitudinal course of epilepsy in Rett syndrome and related disorders. Brain. 2017 02; 140(2):306-318.
Score: 0.018
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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.
Score: 0.013
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Profiling scoliosis in Rett syndrome. Pediatr Res. 2010 Apr; 67(4):435-9.
Score: 0.011
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Epilepsy and the natural history of Rett syndrome. Neurology. 2010 Mar 16; 74(11):909-12.
Score: 0.011
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Arithmetic performance in children with Tourette syndrome: relative contribution of cognitive and attentional factors. J Clin Exp Neuropsychol. 2008 May; 30(4):410-20.
Score: 0.010
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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.
Score: 0.010
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Executive functions in children with frontal and temporal lobe epilepsy. J Int Neuropsychol Soc. 2002 Jul; 8(5):623-32.
Score: 0.007
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Anthropometric Measures Correspond with Functional Motor Outcomes in Females with Rett Syndrome. J Pediatr. 2022 05; 244:169-177.e3.
Score: 0.006
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Phenotypic features in MECP2 duplication syndrome: Effects of age. Am J Med Genet A. 2021 02; 185(2):362-369.
Score: 0.006
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Volumetric brain magnetic resonance imaging analysis in children with obstructive sleep apnea. Int J Pediatr Otorhinolaryngol. 2020 Nov; 138:110369.
Score: 0.006
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Objective measures of sleep disturbances in children with Potocki-Lupski syndrome. Am J Med Genet A. 2019 10; 179(10):1982-1986.
Score: 0.005
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Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome. Clin Genet. 2019 05; 95(5):575-581.
Score: 0.005
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Spectrum and time course of epilepsy and the associated cognitive decline in MECP2 duplication syndrome. Neurology. 2019 01 08; 92(2):e108-e114.
Score: 0.005
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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.
Score: 0.005
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The course of awake breathing disturbances across the lifespan in Rett syndrome. Brain Dev. 2018 Aug; 40(7):515-529.
Score: 0.005
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Assessment of Caregiver Inventory for Rett Syndrome. J Autism Dev Disord. 2017 Apr; 47(4):1102-1112.
Score: 0.005
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Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors. Pediatr Neurol. 2017 05; 70:20-25.
Score: 0.005
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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.
Score: 0.004
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Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2. Genet Med. 2017 01; 19(1):13-19.
Score: 0.004
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Caretaker Quality of Life in Rett Syndrome: Disorder Features and Psychological Predictors. Pediatr Neurol. 2016 05; 58:67-74.
Score: 0.004
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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.
Score: 0.004
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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.
Score: 0.004
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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.
Score: 0.004
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Polysomnographic sleep characteristics of generally-anxious and healthy children assessed in the home environment. J Affect Disord. 2014 Jun; 161:79-83.
Score: 0.004
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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.
Score: 0.004
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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.
Score: 0.004
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Growth failure and outcome in Rett syndrome: specific growth references. Neurology. 2012 Oct 16; 79(16):1653-61.
Score: 0.003
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Associations of cytokines, sleep patterns, and neurocognitive function in youth with HIV infection. Clin Immunol. 2012 Jul; 144(1):13-23.
Score: 0.003
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A therapeutic trial of pro-methylation dietary supplements in Angelman syndrome. Am J Med Genet A. 2011 Dec; 155A(12):2956-63.
Score: 0.003
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Rett syndrome diagnostic criteria: lessons from the Natural History Study. Ann Neurol. 2010 Dec; 68(6):951-5.
Score: 0.003
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Double-blind therapeutic trial in Angelman syndrome using betaine and folic acid. Am J Med Genet A. 2010 Aug; 152A(8):1994-2001.
Score: 0.003
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Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome. Ann Neurol. 2009 Dec; 66(6):771-82.
Score: 0.003
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Potential pharmacokinetic basis for zolpidem dosing in children with sleep difficulties. Clin Pharmacol Ther. 2008 Apr; 83(4):551-8.
Score: 0.002
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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.
Score: 0.002
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Infantile spasms following near-drowning: a report of two cases. Epilepsia. 1987 Jan-Feb; 28(1):45-8.
Score: 0.002
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Child abuse and recurrent infant apnea. J Pediatr. 1986 Dec; 109(6):1065-7.
Score: 0.002
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Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males. Genet Med. 2006 Dec; 8(12):784-92.
Score: 0.002
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Epilepsy and chromosomal rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)]. J Child Neurol. 2006 Feb; 21(2):93-8.
Score: 0.002
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Infantile spasms. Curr Probl Pediatr. 1985 Nov; 15(11):1-39.
Score: 0.002
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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.
Score: 0.002
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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.
Score: 0.002
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Sleep in Gilles de la Tourette's syndrome: disorder of arousal. Neurology. 1983 May; 33(5):586-92.
Score: 0.002
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Circadian rhythm abnormalities of melatonin in Smith-Magenis syndrome. J Med Genet. 2000 Jun; 37(6):428-33.
Score: 0.001
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Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2) Am J Med Genet. 1996 Mar 29; 62(3):247-54.
Score: 0.001
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Sleep organization and energy expenditure of breast-fed and formula-fed infants. Pediatr Res. 1992 Nov; 32(5):514-9.
Score: 0.001
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Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A. Nat Genet. 1992 Apr; 1(1):29-33.
Score: 0.001
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Home monitor follow-up of persistent apnea and bradycardia in preterm infants. Am J Dis Child. 1986 Jun; 140(6):547-50.
Score: 0.001
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Hypoxemia associated with feeding in the preterm infant and full-term neonate. Am J Dis Child. 1984 Jul; 138(7):623-8.
Score: 0.000
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Tics and vocalizations in children treated with carbamazepine. Pediatrics. 1984 Jun; 73(6):841-4.
Score: 0.000
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Effect of tetrabenazine on tics and sleep of Gilles de la Tourette's syndrome. Neurology. 1984 May; 34(5):688-92.
Score: 0.000
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A preliminary prospective neurophysiological study of coma in children. Am J Dis Child. 1984 May; 138(5):492-5.
Score: 0.000