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SARA HERON, M.D.
M.D.
Child & Adolescent Psychiatry Physician
NPI: 1417103383Individual
Specialties, Licenses & Credentials
Child & Adolescent Psychiatry PhysicianPrimary
Psychiatry & Neurology — Child & Adolescent Psychiatry
Code: 2084P0804X
A112236(CA)
Research & Publications (20)
The safety of low-dose Larrea tridentata (DC) Coville (creosote bush or chaparral): a retrospective clinical study.
PMID 11327523·J Altern Complement Med·2001
5-case
De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin.
PMID 19589774·J Med Genet·2010
8-other
Promoting diversity in emergency medicine: summary recommendations from the 2008 Council of Emergency Medicine Residency Directors (CORD) Academic Assembly Diversity Workgroup.
PMID 19344454·Acad Emerg Med·2009
8-other
Motion and disparity processing informs Bayesian 3D motion estimation.
PMID 19047624·Proc Natl Acad Sci U S A·2008
8-other
Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disability.
PMID 18479385·Epilepsia·2008
8-other
Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants.
PMID 17696120·Ann Neurol·2007
8-other
Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures.
PMID 17675531·J Med Genet·2007
8-other
Generalized epilepsy with febrile seizures plus-associated sodium channel beta1 subunit mutations severely reduce beta subunit-mediated modulation of sodium channel function.
PMID 17629415·Neuroscience·2007
8-other
Method development for a quantitative analysis performed without any standard using an evaporative light-scattering detector.
PMID 17583717·J Chromatogr A·2007
4-observational
A polygenic heterogeneity model for common epilepsies with complex genetics.
PMID 17559416·Genes Brain Behav·2007
6-review
A childhood epilepsy mutation reveals a role for developmentally regulated splicing of a sodium channel.
PMID 17467289·Mol Cell Neurosci·2007
8-other
Association studies and functional validation or functional validation alone?
PMID 17433625·Epilepsy Res·2007
8-other
SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum.
PMID 17386050·Epilepsia·2007
4-observational
Racial and ethnic disparities in the emergency department: a public health perspective.
PMID 16982346·Emerg Med Clin North Am·2006
6-review
An efficient helper-virus-free method for rescue of recombinant paramyxoviruses and rhadoviruses from a cell line suitable for vaccine development.
PMID 16569439·J Virol Methods·2006
7-preclinical
Utilization of services by abused, low-income African-American women.
PMID 16390509·J Gen Intern Med·2006
8-other
Is variation in the GABA(B) receptor 1 gene associated with temporal lobe epilepsy?
PMID 15857448·Epilepsia·2005
4-observational
Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations.
PMID 14738422·Epilepsia·2004
8-other
Failure to confirm association of a polymorphism in ABCB1 with multidrug-resistant epilepsy.
PMID 15452306·Neurology·2004
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 3010 COLBY ST STE 221
BERKELEY, CA 94705 - Phone
- (510) 922-9757
Quick Facts
- NPI
- 1417103383
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 2
- Publications
- 20
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