Back to Search
ZAKI AHMED, MD
MD
General Practice Physician
NPI: 1295436616Individual
Specialties, Licenses & Credentials
General Practice PhysicianPrimary
General Practice
Code: 208D00000X
0101283376(VA)
Military Health Care Provider
Military Health Care Provider
Code: 171000000X
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.
PMID 18505454·Clin Genet·2009
8-other
Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degeneration.
PMID 19057657·Mol Vis·2008
7-preclinical
Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome.
PMID 18719945·Hum Genet·2008
8-other
Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan.
PMID 15447792·BMC Med Genet·2004
8-other
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23.
PMID 14570705·Hum Mol Genet·2003
7-preclinical
Mutations of MYO6 are associated with recessive deafness, DFNB37.
PMID 12687499·Am J Hum Genet·2003
8-other
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.
PMID 12107438·Hum Genet·2002
4-observational
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
PMID 11398101·Am J Hum Genet·2001
7-preclinical
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3.
PMID 19603065·Eur J Hum Genet·2010
8-other
Evaluation of pollution load of Lahore Canal by quantification of various pollutants through physicochemical characterisation.
PMID 19618286·Environ Monit Assess·2010
8-other
Overcoming the barriers experienced in conducting a medication trial in adults with aggressive challenging behaviour and intellectual disabilities.
PMID 19627427·J Intellect Disabil Res·2010
4-observational
Zoonotic potential of highly pathogenic avian H7N3 influenza viruses from Pakistan.
PMID 19535120·Virology·2009
7-preclinical
DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.
PMID 19650862·Clin Genet·2009
8-other
Epidermal growth factor receptor inhibitors promote CNS axon growth through off-target effects on glia.
PMID 19632327·Neurobiol Dis·2009
7-preclinical
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
PMID 19576567·Am J Hum Genet·2009
7-preclinical
The influence of pulsed magnetic fields (PMFs) on nonsynaptic potentials recorded from the central and peripheral nervous systems in vitro.
PMID 19551768·Bioelectromagnetics·2009
7-preclinical
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.
PMID 19646679·Am J Hum Genet·2009
8-other
Dependence of the AmII'p proline Raman band on peptide conformation.
PMID 19627094·J Phys Chem B·2009
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
- 8901 ROCKVILLE PIKE
BETHESDA, MD 20889 - Phone
- (301) 295-0537
Quick Facts
- NPI
- 1295436616
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile