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ZAIN AHMED M.D.
M.D.
Cardiovascular Disease Physician
NPI: 1952782567IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
LP03522(RI)
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
71523(CT)
Education
CLVLND CLINIC LERNER COLLEGE OF MED OF CASE WSTN RSV UNIVERSITY
Class of 2015
Research & Publications (20)
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.
PMID 18505454·Clin Genet·2009
8-other
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
The mechanism of magnetic field-induced increase of excitability in hippocampal neurons.
PMID 18554576·Brain Res·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
Lung cancer in transplant recipients: a single-institution experience.
PMID 15302702·Arch Surg·2004
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
Benign expectoration of a surgical clip through a pneumonectomy stump.
PMID 12407389·J Thorac Cardiovasc Surg·2002
5-case
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.
PMID 12107438·Hum Genet·2002
4-observational
A solid-state NMR study of the phospholamban transmembrane domain: local structure and interactions with Ca(2+)-ATPase.
PMID 11018663·Biochim Biophys Acta·2000
7-preclinical
Low concentrations of fibrinogen increase cell migration speed on fibronectin/fibrinogen composite cables.
PMID 10842329·Cell Motil Cytoskeleton·2000
7-preclinical
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
Evaluation of pollution load of Lahore Canal by quantification of various pollutants through physicochemical characterisation.
PMID 19618286·Environ Monit Assess·2010
8-other
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3.
PMID 19603065·Eur J Hum Genet·2010
8-other
Optimisation of siRNA-mediated RhoA silencing in neuronal cultures.
PMID 19340932·Mol Cell Neurosci·2009
7-preclinical
UV resonance Raman determination of molecular mechanism of poly(N-isopropylacrylamide) volume phase transition.
PMID 19260666·J Phys Chem B·2009
8-other
A survey of cricoid pressure use among pediatric anesthesiologists.
PMID 19207915·Paediatr Anaesth·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
Via practice · 3 locations total
- Address
- 20 YORK STREET, YNHH - IM INFECTIOUS DISEASES
NEW HAVEN, CT 06510 - Phone
- (203) 688-4242
Quick Facts
- NPI
- 1952782567
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 3
- Years in Practice
- 11
- Publications
- 20
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