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FIZZA ZULFIQAR, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1881338481Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (14)
Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.
PMID 18854872·Eur J Hum Genet·2009
8-other
Synthesis of carbocyclic 2-substituted adenine nucleoside and related analogs.
PMID 18788045·Nucleosides Nucleotides Nucleic Acids·2008
7-preclinical
Cannabinoid ester constituents from high-potency Cannabis sativa.
PMID 18303850·J Nat Prod·2008
7-preclinical
Synthesis of 2-modified aristeromycins and their analogs as potent inhibitors against Plasmodium falciparum S-adenosyl-L-homocysteine hydrolase.
PMID 18295495·Bioorg Med Chem·2008
7-preclinical
Isolation and characterization of new Cannabis constituents from a high potency variety.
PMID 18283614·Planta Med·2008
7-preclinical
Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
PMID 18181211·Hum Mutat·2008
7-preclinical
Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene.
PMID 17605048·Hum Genet·2007
8-other
Mutations in the gene encoding the alpha-subunit of rod phosphodiesterase in consanguineous Pakistani families.
PMID 17110911·Mol Vis·2006
8-other
A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene.
PMID 16319817·Mol Vis·2005
8-other
Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4.
PMID 16189710·Hum Genet·2005
8-other
Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.
PMID 15980210·Invest Ophthalmol Vis Sci·2005
8-other
Mutations in betaB3-crystallin associated with autosomal recessive cataract in two Pakistani families.
PMID 15914629·Invest Ophthalmol Vis Sci·2005
8-other
Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation.
PMID 15570217·Mol Vis·2004
8-other
Synthesis of carbocyclic nucleosides as potential antiviral agents.
PMID 12836263·Nucleic Acids Res Suppl·2001
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
- 500 HARVARD ST SE
MINNEAPOLIS, MN 55455 - Phone
- (612) 273-3000
Quick Facts
- NPI
- 1881338481
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 14
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