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GARY COX, DO
DO
Emergency Medicine Physician
NPI: 1366022790IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
7633(OK)
CMS Specialties
PrimaryEMERGENCY MEDICINE
Education
OKLAHOMA STATE UNIVERSITY COLLEGE OF OSTEOPATHIC MEDICINE
Class of 2021
Research & Publications (20)
Haploinsufficiency of AFG3L2, the gene responsible for spinocerebellar ataxia type 28, causes mitochondria-mediated Purkinje cell dark degeneration.
PMID 19625515·J Neurosci·2009
7-preclinical
The deacetylase HDAC4 controls myocyte enhancing factor-2-dependent structural gene expression in response to neural activity.
PMID 18780762·FASEB J·2009
7-preclinical
20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits.
PMID 18812404·J Med Genet·2009
7-preclinical
Circulating fibrocytes are an indicator of poor prognosis in idiopathic pulmonary fibrosis.
PMID 19151190·Am J Respir Crit Care Med·2009
8-other
First reported case of Cryptococcus gattii in the Southeastern USA: implications for travel-associated acquisition of an emerging pathogen.
PMID 19516904·PLoS One·2009
5-case
Anthropometric and fitness characteristics of elite Australian female water polo players.
PMID 19620909·J Strength Cond Res·2009
8-other
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.
PMID 18805830·J Med Genet·2009
8-other
Understanding the muscular dystrophy caused by deletion of choline kinase beta in mice.
PMID 19236939·Biochim Biophys Acta·2009
7-preclinical
Biochemical and genetic evidence for a role of IGHMBP2 in the translational machinery.
PMID 19299493·Hum Mol Genet·2009
7-preclinical
Mechanical model for a collagen fibril pair in extracellular matrix.
PMID 19132359·Eur Biophys J·2009
8-other
Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis I.
PMID 19117887·Pediatrics·2009
4-observational
Genetic interaction between the m-AAA protease isoenzymes reveals novel roles in cerebellar degeneration.
PMID 19289403·Hum Mol Genet·2009
7-preclinical
A dose-optimization trial of laronidase (Aldurazyme) in patients with mucopolysaccharidosis I.
PMID 19038563·Mol Genet Metab·2009
4-observational
Upper limb dysfunction following selective neck dissection: a retrospective questionnaire study.
PMID 19260131·Head Neck·2009
8-other
Age, experience and genetic background influence treadmill walking in mice.
PMID 19027767·Physiol Behav·2009
7-preclinical
A novel hypomorphic MECP2 point mutation is associated with a neuropsychiatric phenotype.
PMID 18989701·Hum Genet·2009
5-case
The role of venous capacitance, circulating catecholamines, and heart rate in the hemodynamic response to increased temperature and hypoxia in the dogfish.
PMID 19176885·Am J Physiol Regul Integr Comp Physiol·2009
7-preclinical
Differential effects of Usp14 and Uch-L1 on the ubiquitin proteasome system and synaptic activity.
PMID 18771733·Mol Cell Neurosci·2008
7-preclinical
The varying nature of the professional educational preparation among clinical anesthesia providers who practice unsafe injection practices.
PMID 18947158·AANA J·2008
8-other
Femoral neck stress fractures in military personnel--a case series.
PMID 19090388·J R Army Med Corps·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
- 4401 S WESTERN AVE
OKLAHOMA CITY, OK 73109 - Phone
- (405) 636-7000
Quick Facts
- NPI
- 1366022790
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 5
- Publications
- 20
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