Professor, Pediatric Neurology, Baylor College of Medicine
Neurology
Dr. Daniel G. Glaze, MD
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Daniel Glaze practices Neurology. He went to medical school at Baylor College of Medicine. Daniel G. Glaze is also a published MD. He has 100 publication published. The most recent publication is: Rett syndrome: characterization of seizures versus non-seizures.
Publications
- Improving Treatment Trial Outcomes for Rett Syndrome: The Development of Rett-specific Anchors for the Clinical Global Impression Scale.
- The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders.
- Treatment of cardiac arrhythmias in Rett Syndrome with sodium channel blocking antiepileptic drugs.
- Age of Diagnosis in Rett Syndrome: Patterns of Recognition Among Diagnosticians and Risk Factors for Late Diagnosis.
- Pubertal Development in Rett Syndrome Deviates From Typical Females.
- Polysomnographic sleep characteristics of generally-anxious and healthy children assessed in the home environment.
- Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome.
- Brief Report: MECP2 Mutations in People Without Rett Syndrome.
- Associations of cytokines, sleep patterns, and neurocognitive function in youth with HIV infection.
- Pathogenesis of lethal cardiac arrhythmias in mecp2 mutant mice: implication for therapy in rett syndrome.
- A therapeutic trial of pro-methylation dietary supplements in Angelman syndrome.
- Abnormal circadian rhythm of melatonin in Smith-Magenis syndrome patients with RAI1 point mutations.
- Vitamin D Deficiency is Prevalent in Females with Rett Syndrome.
- Angelman syndrome: Mutations influence features in early childhood.
- Rett syndrome diagnostic criteria: lessons from the Natural History Study.
- Double-blind therapeutic trial in Angelman syndrome using betaine and folic acid.
- Profiling scoliosis in Rett syndrome.
- Longevity in Rett syndrome: analysis of the North American Database.
- Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities.
- Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome.
- Gastrostomy placement improves height and weight gain in girls with Rett syndrome.
- A study of the treatment of Rett syndrome with folate and betaine.
- Bone mineral content and bone mineral density are lower in older than in younger females with Rett syndrome.
- Sleepiness and sleep disordered breathing in Prader-Willi syndrome: relationship to genotype, growth hormone therapy, and body composition.
- Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males.
- Fractional calcium absorption is increased in girls with Rett syndrome.
- Evidence based sleep medicine--is pediatric sleep medicine ready?
- Quality of life and sleep study findings after adenotonsillectomy in children with obstructive sleep apnea.
- Childhood Insomnia: why Chris can't sleep.
- Rett syndrome: of girls and mice--lessons for regression in autism.
- Neurophysiology of Rett syndrome.
- Hand and foot growth failure in Rett syndrome.
- Epilepsy and chromosomal rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)].
- Spinal fluid 5-methyltetrahydrofolate levels are normal in Rett syndrome.
- Potential pharmacokinetic basis for zolpidem dosing in children with sleep difficulties.
- Rett syndrome: North American database.
- Radiation dose to children from x-ray and radioisotope examinations.
- Photofluorographic measurement of the roentgen area product.
- Rett syndrome: revised diagnostic criteria and nomenclature.
- Clinical severity and quality of life in children and adolescents with Rett syndrome.
- Epilepsy and the natural history of Rett syndrome.
- Roentgen area product and exposure measurements during chest radiography and nephrotomography.
- Elevated myelin basic protein levels in the cerebrospinal fluid of children with acute lymphoblastic leukemia.
- Hypoxemia associated with feeding in the preterm infant and full-term neonate.
- Sleep in Gilles de la Tourette's syndrome: disorder of arousal.
- Effect of tetrabenazine on tics and sleep of Gilles de la Tourette's syndrome.
- Tics and vocalizations in children treated with carbamazepine.
- What have we learned about sudden infant death?
- A preliminary prospective neurophysiological study of coma in children.
- Commentary: the challenge of Rett syndrome.
- Population-based registries using multidisciplinary reporters: a method for the study of pediatric neurologic disorders.
- Alpha rhythm slowing during initiation of carbamazepine therapy: implications for future cognitive performance.
- Altered energy balance may account for growth failure in Rett syndrome.
- Coupling of focal electrical seizure discharges with infantile spasms: incidence during long-term monitoring in newly diagnosed patients.
- Electrocardiographic findings in Rett syndrome: an explanation for sudden death?
- Rett syndrome: controlled study of an oral opiate antagonist, naltrexone.
- High-dose, long-duration versus low-dose, short-duration corticotropin therapy for infantile spasms.
- Epidemiology of Rett syndrome: a population-based registry.
- The pattern of growth failure in Rett syndrome.
- Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A.
- Sleep organization and energy expenditure of breast-fed and formula-fed infants.
- Spike morphology in childhood focal Epilepsy: relationship to syndromic classification.
- A retrospective study of spontaneous remission and long-term outcome in patients with infantile spasms.
- Sleep modulation of interictal spike configuration in untreated children with partial seizures.
- Surgical treatment for infantile spasms?
- Extrapyramidal involvement in Rett's syndrome.
- A de novo X;3 translocation in Rett syndrome.
- Reduction of biogenic amine levels in the Rett syndrome.
- Prospective study of outcome of infants with infantile spasms treated during controlled studies of ACTH and prednisone.
- Treatment of infantile spasms with methysergide and alpha-methylparatyrosine.
- Computed tomography in infantile spasms: effects of hormonal therapy.
- Cerebrospinal fluid biogenic amines and biopterin in Rett syndrome.
- Changes in epileptic spike configuration associated with attainment of seizure control.
- Serologic HLA typing in infantile spasms.
- Treatment of infantile spasms with tetrabenazine.
- Munchausen's syndrome by proxy and video surveillance.
- Rett syndrome: discrimination of typical and variant forms.
- Rett's syndrome: characterization of respiratory patterns and sleep.
- Rett's syndrome. Correlation of electroencephalographic characteristics with clinical staging.
- Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
- Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome.
- Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: genotype-phenotype correlations.
- Rett syndrome: characterization of seizures versus non-seizures.
- Organ growth in Rett syndrome: a postmortem examination analysis.
- Oropharyngeal dysfunction and gastroesophageal dysmotility are present in girls and women with Rett syndrome.
- Home monitor follow-up of persistent apnea and bradycardia in preterm infants.
- Child abuse and recurrent infant apnea.
- Infantile spasms following near-drowning: a report of two cases.
- Substance P immunoreactivity in Rett syndrome.
- Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes.
- Increased energy expenditure associated with repetitive involuntary movement does not contribute to growth failure in girls with Rett syndrome.
- Disorders of arousal in children.
- Arithmetic performance in children with Tourette syndrome: relative contribution of cognitive and attentional factors.
- Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype.
- The use of pharmacotherapy in the treatment of pediatric Insomnia in primary care: rational approaches. A consensus meeting summary.
- Pharmacologic management of Insomnia in children and adolescents: consensus statement.
- Trisomy 17p10-p12 due to mosaic supernumerary marker chromosome: delineation of molecular breakpoints and clinical phenotype, and comparison to other proximal 17p segm...
- Executive functions in children with frontal and temporal lobe Epilepsy.
- Caretaker Quality of Life in Rett Syndrome: Disorder Features and Psychological Predictors.
Schools
Baylor College Of Medicine
Baylor Affil Hosps
Procedures Preformed
- EEG (Electroencephalogram)
Conditions Treated
- Convulsions
- Epilepsy
- Headache
- Insomnia
- View All
Doctors Specialties
- Pediatric Neurology
- Neurology
Accepted Insurances
Education
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Baylor College of Medicine
Hospital
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Texas Children's Hospital
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