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JOHN OKUN, M.D.
M.D.
Orthopaedic Surgery Physician
NPI: 1528021748Individual
Specialties, Licenses & Credentials
Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery
Code: 207X00000X
ME0044550(FL)
Research & Publications (20)
Minimization of metal debris while cutting and removing orthopedic implants.
PMID 11570452·Orthopedics·2001
5-case
Coenzyme Q(10) is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduria.
PMID 19504350·J Inherit Metab Dis·2009
8-other
Soluble p-selectin and the risk of primary graft dysfunction after lung transplantation.
PMID 19255296·Chest·2009
4-observational
Deorphanization of GPR109B as a receptor for the beta-oxidation intermediate 3-OH-octanoic acid and its role in the regulation of lipolysis.
PMID 19561068·J Biol Chem·2009
7-preclinical
Pathogenesis of CNS involvement in disorders of amino and organic acid metabolism.
PMID 18392748·J Inherit Metab Dis·2008
6-review
Impact of short- and medium-chain organic acids, acylcarnitines, and acyl-CoAs on mitochondrial energy metabolism.
PMID 18582432·Biochim Biophys Acta·2008
7-preclinical
Neurodegeneration and chronic renal failure in methylmalonic aciduria--a pathophysiological approach.
PMID 17846917·J Inherit Metab Dis·2008
6-review
Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency (Aldh5a1-/- mice).
PMID 17303287·Neurochem Int·2007
7-preclinical
Nitrous oxide promotes hyperhomocysteinemia in levodopa treated rats.
PMID 17240187·Parkinsonism Relat Disord·2007
7-preclinical
Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I).
PMID 17203377·J Inherit Metab Dis·2007
6-review
Positive association of schizophrenia to JARID2 gene.
PMID 16967465·Am J Med Genet B Neuropsychiatr Genet·2007
8-other
Abnormal sterol metabolism in holoprosencephaly: studies in cultured lymphoblasts.
PMID 17237122·J Med Genet·2007
8-other
Congenital glutamine deficiency with glutamine synthetase mutations.
PMID 16525152·N Engl J Med·2006
8-other
Intracerebral accumulation of glutaric and 3-hydroxyglutaric acids secondary to limited flux across the blood-brain barrier constitute a biochemical risk factor for neurodegeneration in glutaryl-CoA dehydrogenase deficiency.
PMID 16573641·J Neurochem·2006
4-observational
Secondary mitochondrial dysfunction in propionic aciduria: a pathogenic role for endogenous mitochondrial toxins.
PMID 16686602·Biochem J·2006
5-case
Comprehensive detection of disorders of purine and pyrimidine metabolism by HPLC with electrospray ionization tandem mass spectrometry.
PMID 16613999·Clin Chem·2006
8-other
Lysine intake and neurotoxicity in glutaric aciduria type I: towards a rationale for therapy?
PMID 16870879·Brain·2006
7-preclinical
Phenylalanine reduces synaptic density in mixed cortical cultures from mice.
PMID 16549526·Pediatr Res·2006
7-preclinical
Massive insulin secretion in response to anaerobic exercise in exercise-induced hyperinsulinism.
PMID 16308838·Horm Metab Res·2005
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
- 721 W ROBERTSON ST, SUITE 102
BRANDON, FL 33511 - Phone
- (813) 684-3707
Quick Facts
- NPI
- 1528021748
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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