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KEVIN HEATH, MD
MD
Gastroenterology Physician
NPI: 1992702336Individual
Specialties, Licenses & Credentials
Gastroenterology PhysicianPrimary
Internal Medicine — Gastroenterology
Code: 207RG0100X
C6835(AR)
Research & Publications (20)
Primary acid-labile subunit deficiency due to recessive IGFALS mutations results in postnatal growth deficit associated with low circulating insulin growth factor (IGF)-I, IGF binding protein-3 levels, and hyperinsulinemia.
PMID 18303074·J Clin Endocrinol Metab·2008
8-other
The coevolutionary genetics of plant-microbe interactions. Joint annual meetings of the Society for the Study of Evolution (SSE), Society of Systematic Biologists (SSB), and American Society of Naturalists (ASN), Minneapolis, MN, USA, June 2008.
PMID 19138218·New Phytol·2008
8-other
Context dependence in the coevolution of plant and rhizobial mutualists.
PMID 17535796·Proc Biol Sci·2007
8-other
Vitamin D deficiency: implications in the rehabilitation setting.
PMID 17079965·Am J Phys Med Rehabil·2006
6-review
Antiretroviral treatment patterns and incident HIV-associated morphologic and lipid abnormalities in a population-based chort.
PMID 12138351·J Acquir Immune Defic Syndr·2002
8-other
Analysis of fluoride levels retained intraorally or ingested following routine clinical applications of topical fluoride products.
PMID 11355237·Aust Dent J·2001
8-other
Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.
PMID 11590545·Am J Hum Genet·2001
8-other
A molecular genetic service for diagnosing individuals with familial hypercholesterolaemia (FH) in the United Kingdom.
PMID 11313767·Eur J Hum Genet·2001
8-other
Low-density lipoprotein receptor gene (LDLR) world-wide website in familial hypercholesterolaemia: update, new features and mutation analysis.
PMID 11137106·Atherosclerosis·2001
8-other
Universal primer quantitative fluorescent multiplex (UPQFM) PCR: a method to detect major and minor rearrangements of the low density lipoprotein receptor gene.
PMID 10745045·J Med Genet·2000
8-other
Mesenteric fibrosis--a histologic marker of previous blunt abdominal trauma in early childhood.
PMID 19205718·Int J Legal Med·2010
5-case
CDKN1C mutations in HELLP/preeclamptic mothers of Beckwith-Wiedemann Syndrome (BWS) patients.
PMID 19386358·Placenta·2009
5-case
Polymorphic genes of major effect: consequences for variation, selection and evolution in Arabidopsis thaliana.
PMID 19416942·Genetics·2009
8-other
Discordant longitudinal clines in flowering time and phytochrome C in Arabidopsis thaliana.
PMID 18752603·Evolution·2008
4-observational
Fertility intentions of women of reproductive age living with HIV in British Columbia, Canada.
PMID 17159593·AIDS·2007
4-observational
Compound heterozygosity of SHOX-encompassing and downstream PAR1 deletions results in Langer mesomelic dysplasia (LMD).
PMID 17394206·Am J Med Genet A·2007
5-case
Serologic evidence for exposure to Rickettsia rickettsii in eastern Arizona and recent emergence of Rocky Mountain spotted fever in this region.
PMID 17187578·Vector Borne Zoonotic Dis·2006
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 455 HOGAN LN
CONWAY, AR 72034 - Phone
- (501) 513-0799
Quick Facts
- NPI
- 1992702336
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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