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SAHAR ZUBERI, M.D.
M.D.
Family Medicine Physician
NPI: 1407291750IndividualAccepts Medicare
Specialties, Licenses & Credentials
Education
OTHER
Class of 2012
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
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Contact & Hours
- Address
- 1704 W BELL RD
PHOENIX, AZ 85023 - Phone
- (602) 837-5929
Quick Facts
- NPI
- 1407291750
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 14
- Publications
- 20
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