D. Glaze

W. Kaufmann, S. Skinner, E. Marsh, 2018, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Gastrointestinal and Nutritional Problems Occur Frequently Throughout Life in Girls and Women With Rett Syndrome

Hye-Seung Lee, S. Skinner, K. Motil, 2012, Journal of pediatric gastroenterology and nutrition.

Surgical treatment for infantile spasms?

J. Frost, P. Kellaway, R. Hrachovy, 1991, Annals of neurology.

Prospective study of outcome of infants with infantile spasms treated during controlled studies of ACTH and prednisone.

J. Frost, P. Kellaway, R. Hrachovy, 1988, The Journal of pediatrics.

Microarray-based comparative genomic hybridization testing in deletion-bearing Angelman Syndrome patients: Genotype-phenotype correlations.

C. Bacino, T. Sahoo, S. Peters, 2005 .

Effect of tetrabenazine on tics and sleep of Gilles de la Tourette's syndrome

J. Frost, D. Glaze, J. Jankovic, 1984, Neurology.

A Psychometric Evaluation of the Motor-Behavioral Assessment Scale for Use as an Outcome Measure in Rett Syndrome Clinical Trials.

W. Kaufmann, S. Skinner, E. Marsh, 2020, American journal on intellectual and developmental disabilities.

A Double-Blind, Randomized, Placebo-Controlled Clinical Study of Trofinetide in the Treatment of Rett Syndrome.

A. Yaroshinsky, D. Glaze, A. Percy, 2017, Pediatric neurology.

Brief Report: MECP2 Mutations in People Without Rett Syndrome

H. Zoghbi, D. Glaze, B. Suter, 2014, Journal of autism and developmental disorders.

MECP2 Mutations in People without Rett Syndrome

H. Zoghbi, D. Glaze, B. Suter, 2014 .

Laparoscopic sleeve gastrectomy in children and adolescents with Prader-Willi syndrome: a matched control study.

D. Glaze, Jennifer L Miller, A. Scheimann, 2017, Surgery for obesity and related diseases : official journal of the American Society for Bariatric Surgery.

Pathogenesis of Lethal Cardiac Arrhythmias in Mecp2 Mutant Mice: Implication for Therapy in Rett Syndrome

S. Skinner, X. Wehrens, D. Glaze, 2011, Science Translational Medicine.

Consensus guidelines on managing Rett syndrome across the lifespan

E. Marsh, Cary Fu, T. Benke, 2020, BMJ paediatrics open.

Metabolic Signatures Differentiate Rett Syndrome From Unaffected Siblings

W. Kaufmann, S. Skinner, D. Glaze, 2020, Frontiers in Integrative Neuroscience.

Multisystem comorbidities in classic Rett syndrome: a scoping review

E. Marsh, Cary Fu, T. Benke, 2020, BMJ paediatrics open.

The course of awake breathing disturbances across the lifespan in Rett syndrome

W. Kaufmann, S. Skinner, Jennifer Harris, 2018, Brain and Development.

Loss of MeCP2 Causes Urological Dysfunction and Contributes to Death by Kidney Failure in Mouse Models of Rett Syndrome

Rodney C. Samaco, W. Kaufmann, S. Skinner, 2016, PloS one.

Neurophysiology of Rett Syndrome

D. Glaze, 2005, Mental retardation and developmental disabilities research reviews.

Spike Morphology in Childhood Focal Epilepsy: Relationship to Syndromic Classification

J. Frost, R. Hrachovy, D. Glaze, 1992, Epilepsia.

Population-based registries using multidisciplinary reporters: a method for the study of pediatric neurologic disorders.

D. D. del Junco, D. Glaze, A. Percy, 1995, Journal of clinical epidemiology.

Double-blind, randomized, placebo-controlled study of trofinetide in pediatric Rett syndrome

W. Kaufmann, O. Della Pasqua, E. Berry-Kravis, 2019, Neurology.

A de novo X;3 translocation in Rett syndrome.

D. Ledbetter, H. Zoghbi, D. Glaze, 1990, American journal of medical genetics.

Neurophysiology of Rett syndrome.

D. Glaze, 2005, Journal of child neurology.

Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors.

Hye-Seung Lee, W. Kaufmann, S. Skinner, 2017, Pediatric neurology.

Longevity in Rett syndrome: analysis of the North American Database.

S. Skinner, R. Kirby, D. Glaze, 2010, The Journal of pediatrics.

Rett Syndrome: North American Database

S. Skinner, D. Glaze, A. Percy, 2007, Journal of child neurology.

Exploring the characteristics and most bothersome symptoms in MECP2 duplication syndrome to pave the path toward developing parent‐oriented outcome measures

D. Pehlivan, L. Mignon, D. Glaze, 2022, Molecular genetics & genomic medicine.

Treatment of cardiac arrhythmias in a mouse model of Rett syndrome with Na+-channel-blocking antiepileptic drugs

W. Kaufmann, S. Skinner, X. Wehrens, 2015, Disease Models & Mechanisms.

Anxiety-like behavior and anxiolytic treatment in the Rett syndrome natural history study

W. Kaufmann, S. Skinner, E. Marsh, 2022, Journal of neurodevelopmental disorders.

Elevated myelin basic protein levels in the cerebrospinal fluid of children with acute lymphoblastic leukemia.

D. Glaze, D. Mahoney, D. Fernbach, 1984, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Vitamin D Deficiency Is Prevalent in Girls and Women With Rett Syndrome

S. Skinner, K. Motil, D. Glaze, 2011, Journal of pediatric gastroenterology and nutrition.

A Retrospective Study of Spontaneous Remission and Long‐Term Outcome in Patients with Infantile Spasms

J. Frost, R. Hrachovy, D. Glaze, 1991, Epilepsia.

Toward a Practical Definition of Pediatric Insomnia

J. Owens, C. Rosen, D. Glaze, 2002 .

Visual Evoked Potentials in the Newborn: Awake and Asleep

J. Frost, D. Glaze, Adrian DeGuire, 1983 .

Fractional Calcium Absorption Is Increased in Girls with Rett Syndrome

S. Abrams, K. Motil, K. Ellis, 2006, Journal of pediatric gastroenterology and nutrition.

A therapeutic trial of pro‐methylation dietary supplements in Angelman syndrome

A. Beaudet, S. Waisbren, S. Skinner, 2011, American journal of medical genetics. Part A.

Electroencephalographic Patterns During Routine Polysomnography in Childhood and Association With Future Epilepsy Diagnosis.

D. Glaze, R. Stowe, 2019, Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine.

Rett syndrome diagnostic criteria: Lessons from the Natural History Study

Hye-Seung Lee, S. Skinner, O. Khwaja, 2010, Annals of neurology.

Trisomy 17p10‐p12 due to mosaic supernumerary marker chromosome: Delineation of molecular breakpoints and clinical phenotype, and comparison to other proximal 17p segmental duplications

P. Stankiewicz, J. Lupski, R. Lewis, 2005, American journal of medical genetics. Part A.

Trisomy 17 p 10p 12 Due to Mosaic Supernumerary Marker Chromosome : Delineation of Molecular Breakpoints and Clinical Phenotype , and Comparison to Other Proximal 17 p Segmental Duplications

P. Stankiewicz, J. Lupski, R. Lewis, 2005 .

Chapter 24 – Sleep in Neurologic Disorders

S. Sheldon, D. Glaze, 2005 .

Abnormal circadian rhythm of melatonin in Smith–Magenis syndrome patients with RAI1 point mutations

J. Lupski, R. Reiter, Philip M Boone, 2011, American journal of medical genetics. Part A.

The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders.

Hye-Seung Lee, W. Kaufmann, S. Skinner, 2015, Pediatric neurology.

Behavioral profiles in Rett syndrome: Data from the natural history study

W. Kaufmann, S. Skinner, D. Glaze, 2019, Brain and Development.

Profiling Scoliosis in Rett Syndrome

Hye-Seung Lee, S. Skinner, K. Motil, 2010, Pediatric Research.

Biliary Tract Disease in Girls and Young Women With Rett Syndrome

S. Skinner, K. Motil, D. Glaze, 2019, Journal of pediatric gastroenterology and nutrition.

Hand stereotypies

W. Kaufmann, L. Oberman, G. Cutter, 2019, Neurology.

Age of diagnosis in Rett syndrome: patterns of recognition among diagnosticians and risk factors for late diagnosis.

Heather M. O'Leary, W. Kaufmann, S. Skinner, 2015, Pediatric neurology.

Title Developmental delay in Rett syndrome : Data from the natural history study

Hye-Seung Lee, W. Kaufmann, S. Skinner, 2014 .

Improving Treatment Trial Outcomes for Rett Syndrome

E. Anagnostou, D. Glaze, B. Suter, 2015, Journal of child neurology.

Improving Treatment Trial Outcomes for Rett Syndrome: The Development of Rett-specific Anchors for the Clinical Global Impression Scale

E. Anagnostou, D. Glaze, B. Suter, 2015 .

Clinical severity and quality of life in children and adolescents with Rett syndrome

J. Krischer, Hye-Seung Lee, S. Skinner, 2011, Neurology.

Coupling of focal electrical seizure discharges with infantile spasms: incidence during long-term monitoring in newly diagnosed patients.

J. Frost, R. Hrachovy, D. Glaze, 1994, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.

High-dose, long-duration versus low-dose, short-duration corticotropin therapy for infantile spasms.

J. Frost, R. Hrachovy, D. Glaze, 1994, The Journal of pediatrics.

Assessment of Caregiver Inventory for Rett Syndrome

W. Kaufmann, S. Skinner, J. Horrigan, 2017, Journal of Autism and Developmental Disorders.

Epilepsy and the natural history of Rett syndrome

S. Skinner, K. Motil, D. Glaze, 2010, Neurology.

Pharmacotherapy for pediatric sleep disturbances: Current patterns of use and target populations for controlled clinical trials

J. Owens, M. Scher, C. Rosen, 2002 .

Diagnosis and management of sleep disorders in Prader-Willi syndrome.

P. Zee, D. Glaze, M. Picone, 2022, Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine.

Brief Report: MECP2 Mutations in People Without Rett Syndrome

H. Zoghbi, D. Glaze, B. Suter, 2013, Journal of Autism and Developmental Disorders.

A Study of the Treatment of Rett Syndrome With Folate and Betaine

W. O'Brien, K. Motil, D. Glaze, 2009, Journal of child neurology.

Hypoxemia associated with feeding in the preterm infant and full-term neonate.

J. Frost, C. Rosen, D. Glaze, 1984, American journal of diseases of children.

Pharmacologic Management of Insomnia in Children and Adolescents: Consensus Statement

T. Roth, M. Genel, C. Rosen, 2006, Pediatrics.

Sleep Modulation of Interictal Spike Configuration in Untreated Children with Partial Seizures

J D Frost, J. Frost, R. Hrachovy, 1991, Epilepsia.

Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males

Ankita Patel, J. Lupski, S. Cheung, 2006, Genetics in Medicine.

Enrichment of mutations in chromatin regulators in people with Rett Syndrome lacking mutations in MECP2

J. Lupski, R. Gibbs, D. Muzny, 2016, Genetics in Medicine.

Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

H. Zoghbi, O. Lichtarge, A. Philippi, 2000, Annals of neurology.

Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: genotype-phenotype correlations

A. Beaudet, L. Bird, C. Bacino, 2005, Journal of Medical Genetics.

Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype.

Lorraine Potocki, Pawel Stankiewicz, Weimin Bi, 2007, American journal of human genetics.

Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome

J. Lupski, H. Zoghbi, C. Schaaf, 2009, Annals of neurology.

Assessment of the gut bacterial microbiome and metabolome of girls and women with Rett Syndrome

Anthony M. Haag, S. Thapa, R. A. Luna, 2021, PloS one.

Angelman syndrome: Mutations influence features in early childhood

A. Beaudet, S. Waisbren, Hye-Seung Lee, 2011, American journal of medical genetics. Part A.

Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)

C McCluggage, F Greenberg, J. Lupski, 1996, American journal of medical genetics.

Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A

D. Ledbetter, J. Lupski, P. Patel, 1992, Nature Genetics.

Sleep Organization and Energy Expenditure of Breast-Fed and Formula-Fed Infants

J. Frost, N. Butte, J. K. Moon, 1992, Pediatric Research.

Rett's Syndrome: Correlation of Electroencephalographic Characteristics With Clinical Staging

J. Frost, H. Zoghbi, D. Glaze, 1987 .

The pattern of growth failure in Rett syndrome.

D. D. del Junco, K. Motil, D. Glaze, 1993, American journal of diseases of children.

Polysomnographic sleep characteristics of generally-anxious and healthy children assessed in the home environment.

C. Alfano, T. Mellman, M. Patriquin, 2014, Journal of affective disorders.

Objective measures of sleep disturbances in children with Potocki–Lupski syndrome

J. Lupski, L. Potocki, D. Glaze, 2019, American journal of medical genetics. Part A.

Topical Review: Epilepsy and Chromosomal Rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)]

J. Lupski, A. Goldman, J. Noebels, 2006, Journal of child neurology.

(del(17)(p11.2p11.2)) Topical Review: Epilepsy and Chromosomal Rearrangements in Smith-Magenis Syndrome

J. Lupski, A. Goldman, L. Potocki, 2013 .

Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome

W. Kaufmann, S. Skinner, K. Motil, 2014, Journal of Medical Genetics.

Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome

H. Zoghbi, R. Amir, D. Glaze, 2005, Journal of Medical Genetics.

Potential Pharmacokinetic Basis for Zolpidem Dosing in Children With Sleep Difficulties

D. Glaze, M. Christensen, M. Reed, 2008, Clinical pharmacology and therapeutics.

Childhood insomnia: why Chris can't sleep.

D. Glaze, 2004, Pediatric clinics of North America.

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

G. Enns, L. Potocki, M. Zaghlula, 2018, American journal of medical genetics. Part A.

Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities

Rodney C. Samaco, C. Thaller, H. Zoghbi, 2009, Proceedings of the National Academy of Sciences.

Substance P immunoreactivity in the enteric nervous system in Rett syndrome

D. Glaze, D. Armstrong, B. Antalffy, 2001, Brain and Development.

Quality of life and sleep study findings after adenotonsillectomy in children with obstructive sleep apnea.

Michael Stewart, M. Stewart, E. Friedman, 2005, Archives of otolaryngology--head & neck surgery.

Rett syndrome: of girls and mice--lessons for regression in autism.

D. Glaze, Daniel G Glaze, 2004, Mental retardation and developmental disabilities research reviews.

Tics and vocalizations in children treated with carbamazepine.

J. Neglia, D. Glaze, T. Zion, 1984, Pediatrics.

Double‐blind therapeutic trial in Angelman syndrome using betaine and folic acid

A. Beaudet, S. Waisbren, L. Bird, 2010, American journal of medical genetics. Part A.

Computed tomography in infantile spasms: effects of hormonal therapy.

J. Frost, R. Bryan, R. Hrachovy, 1986, Pediatric neurology.

Home monitor follow-up of persistent apnea and bradycardia in preterm infants.

J. Frost, C. Rosen, D. Glaze, 1986, A M A Journal of Diseases of Children.

Spinal fluid 5-methyltetrahydrofolate levels are normal in Rett syndrome

T. Bottiglieri, S. Maricich, D. Glaze, 2005, Neurology.

Increased energy expenditure associated with repetitive involuntary movement does not contribute to growth failure in girls with Rett syndrome.

W. Wong, K. Motil, D. Glaze, 1998, The Journal of pediatrics.

Temporal Gait Measures Associated With Overground and Treadmill Walking in Rett Syndrome

C. Layne, Beom-Chan Lee, David R Young, 2018, Journal of child neurology.

Assessing the Burden on Caregivers of MECP2 Duplication Syndrome.

D. Pehlivan, L. Mignon, D. Glaze, 2022, Pediatric neurology.

Altered Energy Balance May Account for Growth Failure in Rett Syndrome

K. Motil, D. Glaze, A. Percy, 1994, Journal of child neurology.

contractility in C57BL/6J mice Chronic intermittent hypoxia increases left ventricular

Stephen H. Smith, S. Shroff, W. Kaufmann, 2015 .

Gastrointestinal Health Questionnaire (GHQ) for Rett Syndrome: Tool Development.

D. Pehlivan, K. Motil, D. Glaze, 2020, Journal of pediatric gastroenterology and nutrition.

Low Bone Mineral Mass Is Associated With Decreased Bone Formation and Diet in Girls With Rett Syndrome

K. Motil, D. Glaze, J. Barrish, 2014, Journal of pediatric gastroenterology and nutrition.

Rett syndrome: Controlled study of an oral opiate antagonist, naltrexone

J. Frost, J. Jankovic, H. Zoghbi, 1994, Annals of neurology.

Treatment of Infantile Spasms with Methysergide and α‐Methylparatyrosine

J. Frost, R. Hrachovy, D. Glaze, 1989 .

Sleepiness and sleep disordered breathing in Prader-Willi syndrome: relationship to genotype, growth hormone therapy, and body composition.

Korwyn L Williams, D. Glaze, A. Scheimann, 2008, Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine.

The Use of Pharmacotherapy in the Treatment of Pediatric Insomnia in Primary Care : Rational Approaches . A Consensus Meeting Summary REVIEW ARTICLES

R. Chervin, M. Goetting, J. Owens, 2005 .

Treatment of infantile spasms with methysergide and alpha-methylparatyrosine.

J. Frost, R. Hrachovy, D. Glaze, 1989, Epilepsia.

Characteristic behaviors associated with gait of individuals with Rett syndrome

C. Layne, David R Young, D. Glaze, 2020, Disability and rehabilitation.

Developmental delay in Rett syndrome: data from the natural history study

Hye-Seung Lee, W. Kaufmann, S. Skinner, 2014, Journal of Neurodevelopmental Disorders.

Spectrum and time course of epilepsy and the associated cognitive decline in MECP2 duplication syndrome

A. Goldman, Dana Marafi, V. Pavlik, 2018, Neurology.

A Practice Pathway for the Identification, Evaluation, and Management of Insomnia in Children and Adolescents With Autism Spectrum Disorders

S. Weiss, B. Malow, D. Coury, 2012, Pediatrics.

Design and outcome measures of LAVENDER, a phase 3 study of trofinetide for Rett syndrome.

S. Peters, E. Berry-Kravis, T. Benke, 2022, Contemporary clinical trials.

Clinical application of home sleep apnea testing in children: a prospective pilot study.

C. Minard, D. Glaze, D. Guffey, 2021, Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine.

Sleep in Gilles de la Tourette's syndrome

J. Frost, D. Glaze, J. Jankovic, 1983, Neurology.

Infantile Spasms Following Near‐Drowning: A Report of Two Cases

J. Frost, S. Gospe, D. Glaze, 1987, Epilepsia.

Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental Syndromes.

D. J. Driscoll, Hye-Seung Lee, W. Kaufmann, 2021, Pediatric neurology.

Establishing the content validity of the Epworth Sleepiness Scale for Children and Adolescents in Prader-Willi Syndrome.

D. Glaze, A. Patroneva, E. Merikle, 2021, Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine.

Treatment of Infantile Spasms with Tetrabenazine

J. Frost, R. Hrachovy, D. Glaze, 1988, Epilepsia.

1148 Obstructive Sleep Apnea in the Setting of Epilepsy and Vagus Nerve Stimulation

D. Glaze, Ameeben Patel, L. Casturi, 2018 .

Serologic HLA Typing in Infantile Spasms

J. Frost, R. Hrachovy, D. Glaze, 1988, Epilepsia.

Epidemiology of Rett syndrome: a population-based registry.

D. Glaze, A. Percy, C. Kozinetz, 1993, Pediatrics.

Commentary: the challenge of Rett syndrome.

D. Glaze, 1995, Neuropediatrics.

Longitudinal course of epilepsy in Rett syndrome and related disorders

W. Kaufmann, A. Berg, S. Skinner, 2017, Brain : a journal of neurology.

Associations of cytokines, sleep patterns, and neurocognitive function in youth with HIV infection.

S. Lipshultz, J. Reuben, Bang‐Ning Lee, 2012, Clinical immunology.

Changes in epileptic spike configuration associated with attainment of seizure control

J D Frost, P Kellaway, J. Frost, 1986, Annals of neurology.

Trofinetide for the treatment of Rett syndrome: a randomized phase 3 study

E. Marsh, E. Berry-Kravis, D. Glaze, 2023, Nature Medicine.

Disorders of arousal in children.

D. Glaze, B. Hopkins, 2008, Pediatric annals.

Rate and filter dependence of the middle-latency response in infants.

J. Frost, J. Jerger, D. Glaze, 1987, Audiology : official organ of the International Society of Audiology.

Caretaker Quality of Life in Rett Syndrome: Disorder Features and Psychological Predictors

Hye-Seung Lee, W. Kaufmann, S. Skinner, 2022 .

A review of the Rett Syndrome Behaviour Questionnaire and its utilization in the assessment of symptoms associated with Rett syndrome.

E. Marsh, D. Glaze, A. Percy, 2023, Frontiers in pediatrics.

Rett syndrome: Discrimination of typical and variant forms

H. Zoghbi, D. Glaze, A. Percy, 1987, Brain and Development.

Exploring gastrointestinal health in MECP2 duplication syndrome.

D. Pehlivan, K. Motil, D. Glaze, 2023, Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society.

Assessment of Caregiver Inventory for Rett Syndrome

W. Kaufmann, G. Cutter, S. Skinner, 2017, Journal of Autism and Developmental Disorders.

The use of pharmacotherapy in the treatment of pediatric insomnia in primary care: rational approaches. A consensus meeting summary.

R. Chervin, M. Goetting, J. Owens, 2005, Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine.

Sleep Apnea and Other Sleep Abnormalities in Primary Headache Disorders

J. Frost, D. Glaze, N. Mathew, 1985 .

Organ growth in Rett syndrome: a postmortem examination analysis.

K. Motil, D. Glaze, D. Armstrong, 1999, Pediatric neurology.

Sleep and Sleep Disorders in Rett Syndrome

D. Glaze, Ameeben Patel, 2020 .

Correlation of Electroencephalographic Characteristics With Clinical Staging

J. Frost, H. Zoghbi, D. Glaze, 2016 .

Caretaker Quality of Life in Rett Syndrome: Disorder Features and Psychological Predictors.

Hye-Seung Lee, W. Kaufmann, J. Killian, 2016, Pediatric neurology.

Behavioral profiles in Rett syndrome: Data from the natural history study

W. Kaufmann, D. Glaze, A. Percy, 2019, Brain and Development.

Pathogenesis of Lethal Cardiac Arrhythmias in Mecp2 Mutant Mice: Implication for Therapy in Rett Syndrome

X. Wehrens, D. Glaze, A. Percy, 2011, Science Translational Medicine.

Anthropometric Measures Correspond with Functional Motor Outcomes in Females with Rett Syndrome.

K. Motil, D. Glaze, J. Lane, 2022, The Journal of pediatrics.

Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome

H. Zoghbi, D. Glaze, A. Percy, 2008, Neurology.