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BRUCE WERMUTH, M.D
M.D
Psychiatry Physician
NPI: 1629104617IndividualAccepts Medicare
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
G25581(CA)
Child & Adolescent Psychiatry Physician
Psychiatry & Neurology — Child & Adolescent Psychiatry
Code: 2084P0804X
G25581(CA)
CMS Specialties
PrimaryPSYCHIATRY
Education
STANFORD UNIVERSITY SCHOOL OF MEDICINE
Class of 1972
Research & Publications (20)
Favourable long-term outcome after immediate treatment of neonatal hyperammonemia due to N-acetylglutamate synthase deficiency.
PMID 19533169·Eur J Pediatr·2010
5-case
Reliability of M protein quantification: comparison of two peak integration methods on Capillarys 2.
PMID 18601614·Clin Chem Lab Med·2008
4-observational
Analysis of mRNA transcripts improves the success rate of molecular genetic testing in OTC deficiency.
PMID 18440262·Mol Genet Metab·2008
5-case
Mutational spectrum and linkage disequilibrium patterns at the ornithine transcarbamylase gene (OTC).
PMID 17044854·Ann Hum Genet·2006
8-other
A puzzling case of high serum creatinine in a healthy woman.
PMID 16364991·Nephrol Dial Transplant·2006
5-case
Differences in catalytic activity between rat testicular and ovarian carbonyl reductases are due to two amino acids.
PMID 16359670·FEBS Lett·2006
4-observational
Identification of novel mutations of the human N-acetylglutamate synthase gene and their functional investigation by expression studies.
PMID 15878741·Biochim Biophys Acta·2005
8-other
Misleading diagnosis of partial N-acetylglutamate synthase deficiency based on enzyme measurement corrected by mutation analysis.
PMID 15858972·Acta Paediatr·2005
5-case
Severe, neonatal-onset OTC deficiency in twin sisters with a de novo balanced reciprocal translocation t(X;5)(p21.1;q11).
PMID 15578616·Am J Med Genet A·2005
5-case
Mutation analysis in patients with N-acetylglutamate synthase deficiency.
PMID 12754705·Hum Mutat·2003
8-other
Gene structure of human carbamylphosphate synthetase 1 and novel mutations in patients with neonatal onset.
PMID 12655559·Hum Mutat·2003
8-other
Long-term calcineurin inhibition and magnesium balance after renal transplantation.
PMID 12595968·Transpl Int·2003
8-other
Multiorgan donation from a donor with unrecognized ornithine transcarbamylase deficiency.
PMID 11499911·Transpl Int·2001
5-case
Genetic analysis of carbamoylphosphate synthetase I and ornithine transcarbamylase deficiency using fibroblasts.
PMID 11388595·Eur J Pediatr·2001
8-other
Coenzyme specificity of human monomeric carbonyl reductase: contribution of Lys-15, Ala-37 and Arg-38.
PMID 11306102·Chem Biol Interact·2001
8-other
Late-onset ornithine transcarbamylase deficiency in two families with different mutations in the same codon.
PMID 11260212·Clin Genet·2001
8-other
Antioxidant and thyroid hormone status in selenium-deficient phenylketonuric and hyperphenylalaninemic patients.
PMID 11010940·Am J Clin Nutr·2000
8-other
Mutation of threonine-241 to proline eliminates autocatalytic modification of human carbonyl reductase.
PMID 10926830·Biochem J·2000
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
- 2542 S BASCOM AVE, STE 110
CAMPBELL, CA 95008 - Phone
- (408) 559-3403
Quick Facts
- NPI
- 1629104617
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 54
- Publications
- 20
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