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ZAYD AHMED, MD
MD
Internal Medicine Physician
NPI: 1700633906Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
125.083304(IL)
Research & Publications (20)
Management of diabetes in patients with chronic kidney disease.
PMID 19491540·Postgrad Med·2009
6-review
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.
PMID 18505454·Clin Genet·2009
8-other
Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome.
PMID 18719945·Hum Genet·2008
8-other
Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degeneration.
PMID 19057657·Mol Vis·2008
7-preclinical
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
PMID 18953341·Nat Genet·2008
7-preclinical
Clinical and neuropathologic features of progressive supranuclear palsy with severe pallido-nigro-luysial degeneration and axonal dystrophy.
PMID 18158316·Brain·2008
8-other
Combined effects of acrobatic exercise and magnetic stimulation on the functional recovery after spinal cord lesions.
PMID 18986227·J Neurotrauma·2008
7-preclinical
Actin-binding proteins coronin-1a and IBA-1 are effective microglial markers for immunohistochemistry.
PMID 17341475·J Histochem Cytochem·2007
4-observational
Progranulin in frontotemporal lobar degeneration and neuroinflammation.
PMID 17291356·J Neuroinflammation·2007
6-review
The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15.
PMID 16807332·J Neurosci·2006
7-preclinical
Structure determination of ursene-type triterpenes by NMR techniques.
PMID 16607673·Magn Reson Chem·2006
8-other
Advances in diabetic management: implications for anesthesia.
PMID 15728048·Anesth Analg·2005
6-review
Diagnostic value of C- reactive protein and haematological parameters in neonatal sepsis.
PMID 15808093·J Coll Physicians Surg Pak·2005
4-observational
Stabilisation of cables of fibronectin with micromolar concentrations of copper: in vitro cell substrate properties.
PMID 14609669·Biomaterials·2004
4-observational
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
Lung cancer in transplant recipients: a single-institution experience.
PMID 15302702·Arch Surg·2004
8-other
Paraoxonase-1 reduces monocyte chemotaxis and adhesion to endothelial cells due to oxidation of palmitoyl, linoleoyl glycerophosphorylcholine.
PMID 12504832·Cardiovasc Res·2003
8-other
Mutations of MYO6 are associated with recessive deafness, DFNB37.
PMID 12687499·Am J Hum Genet·2003
8-other
Pseudounitary symmetry and the Gaussian pseudounitary ensemble of random matrices.
PMID 12786422·Phys Rev E Stat Nonlin Soft Matter Phys·2003
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
- 1620 W HARRISON ST
CHICAGO, IL 60612 - Phone
- (312) 942-5000
Quick Facts
- NPI
- 1700633906
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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