DANIEL GLAZE to Adult
This is a "connection" page, showing publications DANIEL GLAZE has written about Adult.
Connection Strength
0.287
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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: 0.024
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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.
Score: 0.020
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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: 0.017
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Profiling scoliosis in Rett syndrome. Pediatr Res. 2010 Apr; 67(4):435-9.
Score: 0.015
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Epilepsy and the natural history of Rett syndrome. Neurology. 2010 Mar 16; 74(11):909-12.
Score: 0.014
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A study of the treatment of Rett syndrome with folate and betaine. J Child Neurol. 2009 May; 24(5):551-6.
Score: 0.013
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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.
Score: 0.013
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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: 0.013
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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: 0.013
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Spinal fluid 5-methyltetrahydrofolate levels are normal in Rett syndrome. Neurology. 2005 Jun 28; 64(12):2151-2.
Score: 0.010
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Assessing the Burden on Caregivers of MECP2 Duplication Syndrome. Pediatr Neurol. 2022 08; 133:1-8.
Score: 0.008
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Assessment of the gut bacterial microbiome and metabolome of girls and women with Rett Syndrome. PLoS One. 2021; 16(5):e0251231.
Score: 0.008
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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: 0.008
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Oropharyngeal dysfunction and gastroesophageal dysmotility are present in girls and women with Rett syndrome. J Pediatr Gastroenterol Nutr. 1999 Jul; 29(1):31-7.
Score: 0.007
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Hand stereotypies: Lessons from the Rett Syndrome Natural History Study. Neurology. 2019 05 28; 92(22):e2594-e2603.
Score: 0.007
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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: 0.007
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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: 0.007
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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: 0.007
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Behavioral profiles in Rett syndrome: Data from the natural history study. Brain Dev. 2019 Feb; 41(2):123-134.
Score: 0.007
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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: 0.006
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Rett syndrome: characterization of seizures versus non-seizures. Electroencephalogr Clin Neurophysiol. 1998 Jan; 106(1):79-83.
Score: 0.006
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Assessment of Caregiver Inventory for Rett Syndrome. J Autism Dev Disord. 2017 Apr; 47(4):1102-1112.
Score: 0.006
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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: 0.006
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Caretaker Quality of Life in Rett Syndrome: Disorder Features and Psychological Predictors. Pediatr Neurol. 2016 05; 58:67-74.
Score: 0.005
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The Changing Face of Survival in Rett Syndrome and?MECP2-Related Disorders. Pediatr Neurol. 2015 Nov; 53(5):402-11.
Score: 0.005
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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.
Score: 0.005
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Commentary: the challenge of Rett syndrome. Neuropediatrics. 1995 Apr; 26(2):78-80.
Score: 0.005
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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: 0.005
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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: 0.005
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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: 0.003
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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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Substance P immunoreactivity in the enteric nervous system in Rett syndrome. Brain Dev. 2001 Dec; 23 Suppl 1:S127-32.
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: 0.002
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Substance P immunoreactivity in Rett syndrome. Pediatr Neurol. 2000 Apr; 22(4):259-66.
Score: 0.002
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Organ growth in Rett syndrome: a postmortem examination analysis. Pediatr Neurol. 1999 Feb; 20(2):125-9.
Score: 0.002
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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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Electrocardiographic findings in Rett syndrome: an explanation for sudden death? J Pediatr. 1994 Jul; 125(1):80-2.
Score: 0.001
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Extrapyramidal involvement in Rett's syndrome. Neurology. 1990 Feb; 40(2):293-5.
Score: 0.001
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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: 0.001