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FATIMA IMTIAZ, D.O.

D.O.

Internal Medicine Physician

NPI: 1992112932Individual

Specialties, Licenses & Credentials

Internal Medicine PhysicianPrimary

Internal Medicine

Code: 207R00000X

U1924(TX)
Hospitalist Physician

Hospitalist

Code: 208M00000X

20A15390(CA)

Research & Publications (16)

Reliable prenatal diagnosis of Canavan disease by measuring N-acetylaspartate in amniotic fluid using liquid chromatography tandem mass spectrometry.
PMID 19235826·Prenat Diagn·2009
4-observational
Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease.
PMID 18978679·Genet Med·2008
8-other
Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk culture.
PMID 18179885·Am J Hum Genet·2008
7-preclinical
Genetic study of Saudi diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes.
PMID 17922473·Diabetes Metab Res Rev·2008
8-other
The T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of lactase persistence in an urban Saudi population.
PMID 17911653·J Med Genet·2007
8-other
The peroxisome proliferator-activated receptor-gamma2 P12A polymorphism and type 2 diabetes in an Arab population.
PMID 16373923·Diabetes Care·2006
8-other
Mutations underlying 3-hydroxy-3-methylglutaryl CoA lyase deficiency in the Saudi population.
PMID 17173698·BMC Med Genet·2006
8-other
LCGreen I-based real-time PCR assays for detecting common ASL and HMGCL variants.
PMID 16798975·Clin Chem·2006
8-other
Identification of a common novel mutation in Saudi patients with argininosuccinic aciduria.
PMID 16435180·J Inherit Metab Dis·2005
5-case
Monitoring of HBe antigen and alanine aminotransferase levels in hepatitis B virus DNA positive patients.
PMID 15730837·J Coll Physicians Surg Pak·2005
8-other
An apamin- and scyllatoxin-insensitive isoform of the human SK3 channel.
PMID 14978258·Mol Pharmacol·2004
8-other
Successful treatment of carbohydrate deficient glycoprotein syndrome type 1b with oral mannose.
PMID 11567948·Arch Dis Child·2001
5-case
Antioxidants enhance the susceptibility of colon carcinoma cells to 5-fluorouracil by augmenting the induction of the bax protein.
PMID 11166918·Cancer Lett·2001
8-other
Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia).
PMID 11058895·Hum Mutat·2000
8-other
Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG-Ib).
PMID 10980531·Hum Mutat·2000
6-review
Genotypes and phenotypes of patients in the UK with carbohydrate-deficient glycoprotein syndrome type 1.
PMID 10801058·J Inherit Metab Dis·2000
3-trial

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
655 MONTGOMERY ST STE 810
SAN FRANCISCO, CA 94111

Location

Practice Location

655 MONTGOMERY ST STE 810, SAN FRANCISCO, CA
(720) 734-6485

Quick Facts

NPI
1992112932
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
2
Locations
1
Publications
16

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