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ELLIOTT SHERR, M.D.
M.D.
Neurology with Special Qualifications in Child Neurology Physician
NPI: 1508893207Individual
Specialties, Licenses & Credentials
Neurology Physician
Psychiatry & Neurology — Neurology
Code: 2084N0400X
G84339(CA)
Neurology with Special Qualifications in Child Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology with Special Qualifications in Child Neurology
Code: 2084N0402X
G84339(CA)
Research & Publications (20)
Genomic microarray analysis identifies candidate loci in patients with corpus callosum anomalies.
PMID 16275846·Neurology·2005
5-case
The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypes.
PMID 14631200·Curr Opin Pediatr·2003
6-review
Diffusion abnormalities and reduced volume of the ventral cingulum bundle in agenesis of the corpus callosum: a 3T imaging study.
PMID 19246528·AJNR Am J Neuroradiol·2009
8-other
Variability of homotopic and heterotopic callosal connectivity in partial agenesis of the corpus callosum: a 3T diffusion tensor imaging and Q-ball tractography study.
PMID 19001538·AJNR Am J Neuroradiol·2009
8-other
Agenesis of the corpus callosum: an MR imaging analysis of associated abnormalities in the fetus.
PMID 18988682·AJNR Am J Neuroradiol·2009
8-other
The importance of metabolic testing in the evaluation of intellectual disability.
PMID 18756505·Ann Neurol·2008
8-other
Agenesis of the corpus callosum in California 1983-2003: a population-based study.
PMID 18642362·Am J Med Genet A·2008
8-other
Dilated perivascular spaces: an informative radiologic finding in Sanfilippo syndrome type A.
PMID 18410855·Pediatr Neurol·2008
5-case
Hematopoietic stem cell transplantation for the treatment of childhood cerebral X-linked adrenoleukodystrophy.
PMID 18212787·Nat Clin Pract Neurol·2008
8-other
ARHGEF9 disruption in a female patient is associated with X linked mental retardation and sensory hyperarousal.
PMID 17893116·J Med Genet·2008
5-case
Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum.
PMID 17668379·Am J Hum Genet·2007
5-case
Agenesis of the corpus callosum, optic coloboma, intractable seizures, craniofacial and skeletal dysmorphisms: an autosomal recessive disorder similar to Temtamy syndrome.
PMID 17632789·Am J Med Genet A·2007
5-case
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders.
PMID 17564967·Am J Hum Genet·2007
8-other
NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects.
PMID 17530927·PLoS Genet·2007
7-preclinical
Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity.
PMID 17375041·Nat Rev Neurosci·2007
6-review
Anomalies of the corpus callosum: an MR analysis of the phenotypic spectrum of associated malformations.
PMID 17056927·AJR Am J Roentgenol·2006
8-other
Mutation analysis of the FRAS1 gene demonstrates new mutations in a propositus with Fraser syndrome.
PMID 16894541·Am J Med Genet A·2006
5-case
The effects of pulse dye laser double-pass treatment intervals on depth of vessel coagulation.
PMID 16444693·Lasers Surg Med·2006
8-other
Activity and phylogenetic diversity of bacterial cells with high and low nucleic acid content and electron transport system activity in an upwelling ecosystem.
PMID 16332746·Appl Environ Microbiol·2005
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 400 PARNASSUS AVE FL 8
SAN FRANCISCO, CA 94143 - Phone
- (415) 353-7596
Quick Facts
- NPI
- 1508893207
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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