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VIVEK DAVID, M.D.
M.D.
Diagnostic Radiology Physician
NPI: 1407830268Individual
Specialties, Licenses & Credentials
Diagnostic Radiology PhysicianPrimary
Radiology — Diagnostic Radiology
Code: 2085R0202X
MD31199(DC)D0053608(MD)O101058285(VA)MD00043982(WA)
Research & Publications (20)
MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations.
PMID 19592390·J Med Genet·2010
5-case
Rhombencephalosynapsis and related anomalies: a neuropathological study of 40 fetal cases.
PMID 19057916·Acta Neuropathol·2009
8-other
Cryptococcal granulomatous interstitial nephritis and dissemination in a patient with untreated lupus nephritis.
PMID 19525518·Nephrol Dial Transplant·2009
5-case
Matrix extracellular phosphoglycoprotein (MEPE) is a new bone renal hormone and vascularization modulator.
PMID 19520780·Endocrinology·2009
7-preclinical
The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.
PMID 19603532·Hum Mutat·2009
8-other
Pancreatic enzyme replacement therapy for young cystic fibrosis patients.
PMID 18718819·J Cyst Fibros·2009
4-observational
A domestic cat X chromosome linkage map and the sex-linked orange locus: mapping of orange, multiple origins and epistasis over nonagouti.
PMID 19189955·Genetics·2009
7-preclinical
A new mutation in the hepcidin promoter impairs its BMP response and contributes to a severe phenotype in HFE related hemochromatosis.
PMID 19286879·Haematologica·2009
5-case
Validation of an LC-MS/MS assay of terpene trilactones in Ginkgo biloba extracts and pharmaceutical formulations through standard addition method.
PMID 19556092·J Pharm Biomed Anal·2009
4-observational
The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism.
PMID 19177455·Hum Mutat·2009
8-other
Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: an updated map of candidate loci.
PMID 19431187·Hum Mutat·2009
8-other
Morphological and functional evaluation of intrapericardial cyst as a cause of severe right heart failure: dual source computed tomography and magnetic resonance imaging.
PMID 19430351·J Cardiovasc Med (Hagerstown)·2009
5-case
An autosomal genetic linkage map of the domestic cat, Felis silvestris catus.
PMID 19059333·Genomics·2009
7-preclinical
Assay of free captopril in human plasma as monobromobimane derivative, using RPLC/(+)ESI/MS/MS: validation aspects and bioequivalence evaluation.
PMID 19402182·Biomed Chromatogr·2009
2-rct
Host cell entry by apicomplexa parasites requires actin polymerization in the host cell.
PMID 19286135·Cell Host Microbe·2009
7-preclinical
2q23.1 microdeletion identified by array comparative genomic hybridisation: an emerging phenotype with Angelman-like features?
PMID 18812405·J Med Genet·2009
8-other
[The educational director; assistance in running therapeutic patient education sessions. Using the example of cystic fibrosis].
PMID 19107022·Rev Mal Respir·2008
8-other
Effect of large volume injection of hydrophobic solvents on the retention of less hydrophobic pharmaceutical solutes in RP-LC.
PMID 18785144·J Sep Sci·2008
8-other
A pancreatico-pleural fistula diagnosed with magnetic resonance cholangiopancreatography.
PMID 18762699·JOP·2008
5-case
Global cardiac evaluation without heart rate control: preliminary experience with dual source CT (DSCT).
PMID 19092734·Minerva Cardioangiol·2008
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
- 3301 NEW MEXICO AVE NW, SUITE 102
WASHINGTON, DC 20016 - Phone
- (202) 966-0606
Quick Facts
- NPI
- 1407830268
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 4
- Locations
- 1
- Publications
- 20
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