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SARAH SHALEV, M.D.
M.D.
Neurology Physician
NPI: 1922248137Individual
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
A108288(CA)
Research & Publications (20)
A novel missense mutation in CIAS1 encoding the pyrin-like protein, cryopyrin, causes familial cold autoinflammatory syndrome in a family of Ethiopian origin.
PMID 17284928·Int Arch Allergy Immunol·2007
5-case
An association of Hutchinson-Gilford progeria and malignancy.
PMID 17618517·Am J Med Genet A·2007
5-case
A syndrome characterized by intra-uterine lower limb dislocation, gracile bones, clubfeet, and other skeletal features.
PMID 17256795·Am J Med Genet A·2007
8-other
XRF study of archaeological and metallurgical material from an ancient copper-smelting site near Ein-Yahav, Israel.
PMID 18970859·Talanta·2006
8-other
Clinical variation of Aarskog syndrome in a large family with 2189delA in the FGD1 gene.
PMID 16353258·Am J Med Genet A·2006
8-other
Evidence for blood chimerism in dizygotic spontaneous twin pregnancy discordant for Down syndrome.
PMID 16927328·Prenat Diagn·2006
5-case
A syndrome characterized by contractures and pterygia of upper body associated with umbilical hernia, short stature, and distinctive face in an Arabic family.
PMID 16158430·Am J Med Genet A·2005
8-other
Long-term follow-up of three individuals with Kabuki syndrome.
PMID 14981723·Am J Med Genet A·2004
5-case
Behavioral pattern profile: a tool for the description of behavior to be used in the genetics clinic.
PMID 15264284·Am J Med Genet A·2004
8-other
[A comprehensive program for prevention of genetic diseases among Arabs in Israel].
PMID 14631914·Harefuah·2003
8-other
Another adult with Meier-Gorlin syndrome--insights into the natural history.
PMID 14564153·Clin Dysmorphol·2003
5-case
Dynamic modification strategy of the Israeli carrier screening protocol: inclusion of the Oriental Jewish Group to the cystic fibrosis panel.
PMID 19265749·Genet Med·2009
8-other
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response.
PMID 19525956·Nat Genet·2009
8-other
Sickle cell anemia in northern Israel: screening and prevention.
PMID 19603597·Isr Med Assoc J·2009
8-other
A targeted population carrier screening program for severe and frequent genetic diseases in Israel.
PMID 19107146·Eur J Hum Genet·2009
8-other
Mutated NDUFS6 is the cause of fatal neonatal lactic acidemia in Caucasus Jews.
PMID 19259137·Eur J Hum Genet·2009
5-case
Alopecia, neurological defects, and endocrinopathy syndrome caused by decreased expression of RBM28, a nucleolar protein associated with ribosome biogenesis.
PMID 18439547·Am J Hum Genet·2008
8-other
Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9.
PMID 18678320·Am J Hum Genet·2008
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1501 TROUSDALE DR
BURLINGAME, CA 94010 - Phone
- (650) 652-8350
Quick Facts
- NPI
- 1922248137
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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