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MOHAMMAD SARFARAZI, M.D.
M.D.
Interventional Cardiology Physician
NPI: 1326103227IndividualAccepts Medicare
Specialties, Licenses & Credentials
Interventional Cardiology PhysicianPrimary
Internal Medicine — Interventional Cardiology
Code: 207RI0011X
D0048042(MD)
CMS Specialties
PrimaryCARDIOVASCULAR DISEASE (CARDIOLOGY)
Education
UNIVERSITY OF MARYLAND SCHOOL OF MEDICINE
Class of 1992
Research & Publications (20)
Evaluation of LOXL1 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma.
PMID 18385788·Mol Vis·2008
8-other
The use of microarray technology in deciphering the cause of genetic eye diseases: LOXL1 and exfoliation syndrome.
PMID 18282488·Am J Ophthalmol·2008
8-other
Primary non-syndromic lymphoedema (Meige disease) is not caused by mutations in FOXC2.
PMID 18197197·Eur J Hum Genet·2008
8-other
Characterization of the biochemical and structural phenotypes of four CYP1B1 mutations observed in individuals with primary congenital glaucoma.
PMID 18622259·Pharmacogenet Genomics·2008
8-other
Genetic screening of leber congenital amaurosis in a large consanguineous Iranian family.
PMID 18161624·Ophthalmic Genet·2007
8-other
CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.
PMID 17591938·J Mol Diagn·2007
4-observational
Cyp1b1 protein in the mouse eye during development: an immunohistochemical study.
PMID 17325023·Drug Metab Dispos·2007
7-preclinical
A new locus (GLC1H) for adult-onset primary open-angle glaucoma maps to the 2p15-p16 region.
PMID 17210857·Arch Ophthalmol·2007
8-other
Embryonic expression of the optineurin (glaucoma) gene in different stages of mouse development.
PMID 17893645·Mol Vis·2007
7-preclinical
The role of the WDR36 gene on chromosome 5q22.1 in a large family with primary open-angle glaucoma mapped to this region.
PMID 16966629·Arch Ophthalmol·2006
8-other
Physiological significance and expression of P450s in the developing eye.
PMID 16684663·Drug Metab Rev·2006
6-review
Genotype and phenotype correlations in congenital glaucoma.
PMID 17471339·Trans Am Ophthalmol Soc·2006
8-other
Genotype and phenotype correlations in congenital glaucoma: CYP1B1 mutations, goniodysgenesis, and clinical characteristics.
PMID 17157584·Am J Ophthalmol·2006
8-other
Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1.
PMID 15677485·Hum Mol Genet·2005
7-preclinical
Clinical features and course of patients with glaucoma with the E50K mutation in the optineurin gene.
PMID 16043855·Invest Ophthalmol Vis Sci·2005
8-other
Analysis of rare variants and common haplotypes in the optineurin gene in Swedish glaucoma cases.
PMID 16020311·Ophthalmic Genet·2005
4-observational
Molecular cloning and expression profiling of optineurin in the rhesus monkey.
PMID 15980228·Invest Ophthalmol Vis Sci·2005
4-observational
Lymphoedema-distichiasis and FOXC2: unreported mutations, de novo mutation estimate, families without coding mutations.
PMID 15906099·Hum Genet·2005
8-other
Expression patterns of mouse and human CYP orthologs (families 1-4) during development and in different adult tissues.
PMID 15752708·Arch Biochem Biophys·2005
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 7525 GREENWAY CENTER DR STE 309
GREENBELT, MD 20770 - Phone
- (301) 345-4465
Quick Facts
- NPI
- 1326103227
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 2
- Years in Practice
- 34
- Publications
- 20
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