Back to Search
RODNEY MCFARLAND, MD
MD
Family Medicine Physician
NPI: 1609825330Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
R1A75(MO)
Research & Publications (20)
Oxidative stress, nitric oxide, and the mechanisms of cell death in Lurcher Purkinje cells.
PMID 17565706·Dev Neurobiol·2007
7-preclinical
Urine heteroplasmy is the best predictor of clinical outcome in the m.3243A>G mtDNA mutation.
PMID 19204268·Neurology·2009
8-other
Death and survival of heterozygous Lurcher Purkinje cells in vitro.
PMID 19294643·Dev Neurobiol·2009
7-preclinical
Batteries not included: diagnosis and management of mitochondrial disease.
PMID 19192037·J Intern Med·2009
6-review
Clinical reasoning: Blurred vision and dancing feet: restless legs syndrome presenting in mitochondrial disease.
PMID 19414717·Neurology·2009
5-case
Brief communication: self-suckling in Barbary macaque (Macaca sylvanus) mothers before and after the death of their infant.
PMID 19591209·Am J Phys Anthropol·2009
7-preclinical
Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children.
PMID 19251978·J Med Genet·2009
8-other
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.
PMID 18065439·Brain·2008
8-other
Further pitfalls in the diagnosis of mtDNA mutations: homoplasmic mt-tRNA mutations.
PMID 18178636·J Med Genet·2008
8-other
Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase gamma (POLG1).
PMID 18208989·Arch Dis Child·2008
5-case
Overexpression of human mitochondrial valyl tRNA synthetase can partially restore levels of cognate mt-tRNAVal carrying the pathogenic C25U mutation.
PMID 18400783·Nucleic Acids Res·2008
8-other
The m.5650G>A mitochondrial tRNAAla mutation is pathogenic and causes a phenotype of pure myopathy.
PMID 17825557·Neuromuscul Disord·2008
5-case
Pre-eclampsia and magnesium toxicity with therapeutic plasma level in a woman with m.3243A>G melas mutation.
PMID 18569490·J Obstet Gynaecol·2008
5-case
Endovascular repair of iliac artery injury complicating lumbar disc surgery.
PMID 17712578·Eur Spine J·2008
5-case
Diabetes and deafness: is it sufficient to screen for the mitochondrial 3243A>G mutation alone?
PMID 17540956·Diabetes Care·2007
8-other
Prevalence and progression of diabetes in mitochondrial disease.
PMID 17653689·Diabetologia·2007
8-other
Integer quantum Hall effect on a six-valley hydrogen-passivated silicon (111) surface.
PMID 17678178·Phys Rev Lett·2007
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
- 336 S JEFFERSON
NEOSHO, MO 64850 - Phone
- (417) 455-4200
Quick Facts
- NPI
- 1609825330
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile