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VIVIAN SHIH, MD
MD
Clinical Biochemical Genetics Physician
NPI: 1285600650Individual
Specialties, Licenses & Credentials
Clinical Biochemical Genetics PhysicianPrimary
Medical Genetics — Clinical Biochemical Genetics
Code: 207SG0202X
31003(MA)
Pediatrics Physician
Pediatrics
Code: 208000000X
31003(MA)
Research & Publications (20)
Complementary and alternative medicine (CAM) usage in Singaporean adult cancer patients.
PMID 19150956·Ann Oncol·2009
8-other
Kinetic control of negative feedback regulators of NF-kappaB/RelA determines their pathogen- and cytokine-receptor signaling specificity.
PMID 19487661·Proc Natl Acad Sci U S A·2009
7-preclinical
Clinical predictors of chemotherapy-induced nausea and vomiting in breast cancer patients receiving adjuvant doxorubicin and cyclophosphamide.
PMID 19193584·Ann Pharmacother·2009
8-other
Argininosuccinate lyase deficiency: longterm outcome of 13 patients detected by newborn screening.
PMID 19635676·Mol Genet Metab·2009
8-other
Evolving roles of oncology pharmacists in Singapore: a survey on prescribing patterns of antiemetics for chemotherapy induced nausea and vomiting (CINV) at a cancer centre.
PMID 18337437·J Oncol Pharm Pract·2008
8-other
Generation and activation of multiple dimeric transcription factors within the NF-kappaB signaling system.
PMID 18299388·Mol Cell Biol·2008
7-preclinical
Spectrum of medium-chain acyl-CoA dehydrogenase deficiency detected by newborn screening.
PMID 18450854·Pediatrics·2008
8-other
Liposomal doxorubicin-associated acute hypersensitivity despite appropriate preventive measures.
PMID 17873110·J Oncol Pharm Pract·2007
5-case
Proton magnetic resonance spectroscopy and diffusion-weighted imaging in isolated sulfite oxidase deficiency.
PMID 16970890·J Child Neurol·2006
5-case
Fetal fatty acid oxidation defects and maternal liver disease in pregnancy.
PMID 16394048·Obstet Gynecol·2006
4-observational
Fumarase deficiency caused by homozygous P131R mutation and paternal partial isodisomy of chromosome 1.
PMID 16575891·Am J Med Genet A·2006
5-case
Pericardial effusion in primary systemic carnitine deficiency.
PMID 16830263·J Inherit Metab Dis·2006
5-case
Isolated sulfite oxidase deficiency: a case report with a novel mutation and review of the literature.
PMID 16140720·Pediatrics·2005
5-case
Rehabilitation of orthopedic and rheumatologic disorders. 3. Total hip arthroplasty rehabilitation.
PMID 15761802·Arch Phys Med Rehabil·2005
8-other
Rehabilitation of orthopedic and rheumatologic disorders. 4. Rheumatoid arthritis and calcium pyrophosphate deposition disease.
PMID 15761803·Arch Phys Med Rehabil·2005
8-other
Rehabilitation of orthopedic and rheumatologic disorders. 5. Lumbar spinal stenosis.
PMID 15761804·Arch Phys Med Rehabil·2005
8-other
Risk factors for functional decline in older adults with arthritis.
PMID 15818691·Arthritis Rheum·2005
8-other
Racial differences in activities of daily living limitation onset in older adults with arthritis: a national cohort study.
PMID 16084802·Arch Phys Med Rehabil·2005
8-other
Ornithine aminotransferase deficiency: diagnostic difficulties in neonatal presentation.
PMID 16151897·J Inherit Metab Dis·2005
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 55 FRUIT ST YAW 6, PEDIATRIC MEDICINE
BOSTON, MA 02114 - Phone
- (617) 726-3884
Quick Facts
- NPI
- 1285600650
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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