Chief, Division of Child Neurology University of California, San Diego Rady Children's Hospital-San Diego
Child Neurology
Dr. Jeffrey L. Neul, MD
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Doctor Jeffrey L. Neul, MD practices Child Neurology. He researched medicine at University of Chicago Pritzker School of Medicine. University of Chicago Pritzker School of Medicine is ranked 10 in research and 19 in primary care medicine He has 2 awards "Circle of Angels award for dedication to research on Rett syndrome" and "Philip R. Dodge Young Investigator Award". Dr. Jeffrey L. Neul is a published physician. He published 49 publications, including: 'Spatially restricted activation of the SAX receptor by SCW modulates DPP/TKV signaling in Drosophila dorsal-ventral patterning.'
Publications
- Caretaker Quality of Life in Rett Syndrome: Disorder Features and Psychological Predictors.
- 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.
- Origin of a Non-Clarke's Column Division of the Dorsal Spinocerebellar Tract and the Role of Caudal Proprioceptive Neurons in Motor Function.
- 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.
- Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgene.
- Mutual antagonism between Sox10 and NFIA regulates diversification of glial lineages and glioma subtypes.
- Low bone mineral mass is associated with decreased bone formation and diet in girls with Rett syndrome.
- Pubertal Development in Rett Syndrome Deviates From Typical Females.
- Developmental delay in Rett syndrome: data from the natural history study.
- Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndrome.
- 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.
- Breathing challenges in Rett Syndrome: Lessons learned from humans and animal models.
- Insulinotropic treatments exacerbate metabolic syndrome in mice lacking MeCP2 function.
- The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy.
- Overexpression of Methyl-CpG Binding Protein 2 Impairs TH1 Responses.
- Preclinical research in Rett syndrome: setting the foundation for translational success.
- Growth failure and outcome in Rett syndrome: Specific growth references.
- Female Mecp2(+/-) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies.
- Atoh1 governs the migration of postmitotic neurons that shape respiratory effectiveness at birth and chemoresponsiveness in adulthood.
- The relationship of Rett syndrome and MECP2 disorders to autism.
- Pathogenesis of lethal cardiac arrhythmias in mecp2 mutant mice: implication for therapy in rett syndrome.
- MeCP2 Is Critical within HoxB1-Derived Tissues of Mice for Normal Lifespan.
- Neurodevelopmental disorders: Clinical criteria for Rett syndrome.
- Complexities of Rett Syndrome and MeCP2.
- Vitamin D Deficiency is Prevalent in Females with Rett Syndrome.
- Unfolding neurodevelopmental disorders: The mystery of developing connections.
- Rett syndrome diagnostic criteria: lessons from the Natural History Study.
- Profiling scoliosis in Rett syndrome.
- Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities.
- A study of the treatment of Rett syndrome with folate and betaine.
- Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males.
- Neurologic complications associated with influenza A in children during the 2003-2004 influenza season in Houston, Texas.
- Rett syndrome: a prototypical neurodevelopmental disorder.
- Spinal fluid 5-methyltetrahydrofolate levels are normal in Rett syndrome.
- Cerebral folate deficiency with developmental delay, autism, and response to folinic acid.
- Deletion of Mecp2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress.
- Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
- A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome.
- Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.
- Epilepsy and the natural history of Rett syndrome.
- Interested in a career as a clinician-scientist?
- Spatially restricted activation of the SAX receptor by SCW modulates DPP/TKV signaling in Drosophila dorsal-ventral patterning.
- The Xenopus dorsalizing factor noggin ventralizes Drosophila embryos by preventing DPP from activating its receptor.
- Rett syndrome: revised diagnostic criteria and nomenclature.
- Clinical severity and quality of life in children and adolescents with Rett syndrome.
Conditions Treated
- Dystonia
- Epilepsy
- Migraine
- Tremor
Doctors Specialties
- Pediatric Neurology
- Child Neurology
Accepted Insurances
Awards
- Circle of Angels award for dedication to research on Rett syndrome
- Philip R. Dodge Young Investigator Award
Education
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Baylor College of Medicine -
University of Chicago Pritzker School of Medicine
Hospital
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Rady Children's Hospital - San Diego -
Texas Children's Hospital
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