Back to Search
MATTHEW PERCY, MD
MD
Family Medicine Physician
NPI: 1982993838IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
0054060(CO)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
UNIVERSITY OF COLORADO SCHOOL OF MEDICINE, DENVER
Class of 2011
Research & Publications (20)
Involvement of ApoE E4 and H63D in sporadic Alzheimer's disease in a folate-supplemented Ontario population.
PMID 18525129·J Alzheimers Dis·2008
8-other
Quality of care: or why you have to evaluate your program.
PMID 17233671·J Spec Pediatr Nurs·2007
8-other
School health. Using a developmental-relational model in the school setting.
PMID 16774533·J Spec Pediatr Nurs·2006
6-review
Characterization of an NF-kappaB-regulated, miRNA-146a-mediated down-regulation of complement factor H (CFH) in metal-sulfate-stressed human brain cells.
PMID 19540598·J Inorg Biochem·2009
8-other
Genetic origins and clinical phenotype of familial and acquired erythrocytosis and thrombocytosis.
PMID 19006225·Am J Hematol·2009
6-review
Erythrocytosis-associated HIF-2alpha mutations demonstrate a critical role for residues C-terminal to the hydroxylacceptor proline.
PMID 19208626·J Biol Chem·2009
8-other
G protein-coupled receptors disrupted in human genetic disease.
PMID 18370233·Methods Mol Biol·2008
6-review
Novel exon 12 mutations in the HIF2A gene associated with erythrocytosis.
PMID 18378852·Blood·2008
5-case
Familial erythrocytosis: molecular links to red blood cell control.
PMID 18591620·Haematologica·2008
8-other
Thrombospondins 1 and 2 are necessary for synaptic plasticity and functional recovery after stroke.
PMID 18594557·J Cereb Blood Flow Metab·2008
7-preclinical
Familial erythrocytosis arising from a gain-of-function mutation in the HIF2A gene of the oxygen sensing pathway.
PMID 18711622·Ulster Med J·2008
6-review
Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency.
PMID 18318771·Br J Haematol·2008
6-review
A gain-of-function mutation in the HIF2A gene in familial erythrocytosis.
PMID 18184961·N Engl J Med·2008
5-case
Metal sulfate-mediated induction of pathogenic genes and repression by phenyl butyl nitrone and Feralex-G.
PMID 18185117·Neuroreport·2008
8-other
Stages of smoking acquisition of young Taiwanese adolescents: self-efficacy and decisional balance.
PMID 18213639·Res Nurs Health·2008
8-other
Mutation of the von Hippel-Lindau gene alters human cardiopulmonary physiology.
PMID 18085246·Adv Exp Med Biol·2008
8-other
NADH-cytochrome b5 reductase in a Turkish family with recessive congenital methaemoglobinaemia type I.
PMID 18820099·J Clin Pathol·2008
5-case
Mutations and polymorphisms in hemoglobin genes and the risk of pulmonary hypertension and death in sickle cell disease.
PMID 17724704·Am J Hematol·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
- 195 W 14TH
RIFLE, CO 81650 - Phone
- (970) 945-2840
Quick Facts
- NPI
- 1982993838
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 15
- Publications
- 20
Are you this provider?
Claim Your Profile