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VERONICA DAVID, MD
MD
Internal Medicine Physician
NPI: 1427014877Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
A53613(CA)
Research & Publications (20)
Matrix extracellular phosphoglycoprotein (MEPE) is a new bone renal hormone and vascularization modulator.
PMID 19520780·Endocrinology·2009
7-preclinical
Cryptococcal granulomatous interstitial nephritis and dissemination in a patient with untreated lupus nephritis.
PMID 19525518·Nephrol Dial Transplant·2009
5-case
Mechanical loading down-regulates peroxisome proliferator-activated receptor gamma in bone marrow stromal cells and favors osteoblastogenesis at the expense of adipogenesis.
PMID 17317771·Endocrinology·2007
7-preclinical
A homozygous single-base deletion in MLPH causes the dilute coat color phenotype in the domestic cat.
PMID 16860533·Genomics·2006
7-preclinical
Two-week longitudinal survey of bone architecture alteration in the hindlimb-unloaded rat model of bone loss: sex differences.
PMID 16467486·Am J Physiol Endocrinol Metab·2006
7-preclinical
Anxiogenic-like effects limit rewarding effects of cocaine in balb/cbyj mice.
PMID 11166520·Neuropsychopharmacology·2001
7-preclinical
Determination of cycloserine in human plasma by high-performance liquid chromatography with fluorescence detection, using derivatization with p-benzoquinone.
PMID 11585129·J Chromatogr B Biomed Sci Appl·2001
8-other
Enhanced chemiluminescent determination of chloramphenicol and related nitro compounds by 'on-line' photochemical reaction.
PMID 10984928·Analyst·2000
8-other
Anatomical and pharmacological specificity of the rewarding effect elicited by microinjections of morphine into the nucleus accumbens of mice.
PMID 10867973·Psychopharmacology (Berl)·2000
7-preclinical
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
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
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
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
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
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
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
Host cell entry by apicomplexa parasites requires actin polymerization in the host cell.
PMID 19286135·Cell Host Microbe·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
An autosomal genetic linkage map of the domestic cat, Felis silvestris catus.
PMID 19059333·Genomics·2009
7-preclinical
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 600 COFFEE RD
MODESTO, CA 95355 - Phone
- (209) 521-6097
Quick Facts
- NPI
- 1427014877
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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