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BETH KAUFMAN, MD
MD
Pediatric Cardiology Physician
NPI: 1750301073IndividualAccepts Medicare
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
MD424682(PA)C55584(CA)
Pediatric Cardiology PhysicianPrimary
Pediatrics — Pediatric Cardiology
Code: 2080P0202X
MD424682(PA)C55584(CA)
CMS Specialties
PrimaryPEDIATRIC MEDICINE
Education
OTHER
Class of 1996
Research & Publications (20)
Haplotypes of the I157T CHEK2 germline mutation in ethnically diverse populations.
PMID 19609724·Fam Cancer·2009
4-observational
Lapatinib monotherapy in patients with HER2-overexpressing relapsed or refractory inflammatory breast cancer: final results and survival of the expanded HER2+ cohort in EGF103009, a phase II study.
PMID 19394894·Lancet Oncol·2009
3-trial
Haplotype of the C61G BRCA1 mutation in Polish and Jewish individuals.
PMID 19594371·Genet Test Mol Biomarkers·2009
8-other
The mitochondrial transcription factor TFAM coordinates the assembly of multiple DNA molecules into nucleoid-like structures.
PMID 17581862·Mol Biol Cell·2007
7-preclinical
The P1812A and P25T BRCA1 and the 5164del4 BRCA2 mutations: occurrence in high-risk non-Ashkenazi Jews.
PMID 17020472·Genet Test·2006
5-case
A function for the mitochondrial chaperonin Hsp60 in the structure and transmission of mitochondrial DNA nucleoids in Saccharomyces cerevisiae.
PMID 14597775·J Cell Biol·2003
8-other
Chest radiograph interpretation skills of anesthesiologists.
PMID 11748512·J Cardiothorac Vasc Anesth·2001
3-trial
Debilitating chronic pain syndromes after presumed intraneural injections.
PMID 10692629·Pain·2000
5-case
In organello formaldehyde crosslinking of proteins to mtDNA: identification of bifunctional proteins.
PMID 10869431·Proc Natl Acad Sci U S A·2000
8-other
Ethnic differences in bone geometry and strength are apparent in childhood.
PMID 19442622·Bone·2009
8-other
Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome.
PMID 19503089·Nat Genet·2009
8-other
The RNF146 and ECHDC1 genes as candidates for inherited breast and ovarian cancer in Jewish Ashkenazi women.
PMID 19517271·Fam Cancer·2009
8-other
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.
PMID 19656774·Hum Mol Genet·2009
4-observational
SULT1E1 and ID2 genes as candidates for inherited predisposition to breast and ovarian cancer in Jewish women.
PMID 18821033·Fam Cancer·2009
8-other
Hormone receptor expression is associated with a unique pattern of metastatic spread and increased survival among HER2-overexpressing breast cancer patients.
PMID 19564785·Am J Clin Oncol·2009
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
- 725 WELCH RD
PALO ALTO, CA 94304 - Phone
- (650) 497-8000
Quick Facts
- NPI
- 1750301073
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 4
- Locations
- 1
- Years in Practice
- 30
- Publications
- 20
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