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SHAHARYAR ZUBERI, MD
MD
Internal Medicine Physician
NPI: 1336715044Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
289103(MA)
Research & Publications (20)
De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin.
PMID 19589774·J Med Genet·2010
8-other
Pregabalin: preliminary experience in intractable childhood epilepsy.
PMID 19380070·Pediatr Neurol·2009
3-trial
A novel inherited mutation in the voltage sensor region of SCN1A is associated with Panayiotopoulos syndrome in siblings and generalized epilepsy with febrile seizures plus.
PMID 19339291·J Child Neurol·2009
5-case
Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
PMID 18245432·Pediatrics·2008
8-other
Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutation.
PMID 18251839·Epilepsia·2008
4-observational
Psychosocial and intellectual functioning in childhood narcolepsy.
PMID 18608355·Dev Neurorehabil·2008
8-other
Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
PMID 17846997·Am J Hum Genet·2007
8-other
Genetics of epilepsy: epilepsy research foundation workshop report.
PMID 17525034·Epileptic Disord·2007
8-other
Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures.
PMID 17675531·J Med Genet·2007
8-other
Memory consolidation and accelerated forgetting in children with idiopathic generalized epilepsy.
PMID 17715001·Epilepsy Behav·2007
8-other
Alteration of the in vivo nicotinic receptor density in ADNFLE patients: a PET study.
PMID 16815873·Brain·2006
8-other
Paediatric neurology training - a developing country perspective.
PMID 16827969·J Coll Physicians Surg Pak·2006
8-other
Developmental outcome in benign myoclonic epilepsy in infancy and reflex myoclonic epilepsy in infancy: a literature review and six new cases.
PMID 16904290·Epilepsy Res·2006
5-case
De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study.
PMID 16713920·Lancet Neurol·2006
4-observational
Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease.
PMID 16751771·Nat Genet·2006
7-preclinical
Mental distress in mothers of child psychiatric patients.
PMID 16787620·J Coll Physicians Surg Pak·2006
4-observational
Anoxic-epileptic seizures: observational study of epileptic seizures induced by syncopes.
PMID 16159903·Arch Dis Child·2005
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 550 1ST AVE
NEW YORK, NY 10016 - Phone
- (212) 263-7300
Quick Facts
- NPI
- 1336715044
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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