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GARY HUDSON, D.M.D., M.D.
D.M.D., M.D.
Oral & Maxillofacial Surgery (D.M.D.)
NPI: 1447214424Individual
Specialties, Licenses & Credentials
Oral & Maxillofacial Surgery (D.M.D.)Primary
Oral & Maxillofacial Surgery
Code: 204E00000X
12133(AL)
Oral and Maxillofacial Surgery (Dentist)
Dentist — Oral and Maxillofacial Surgery
Code: 1223S0112X
3677(AL)
Research & Publications (20)
Genetic variation in the methylenetetrahydrofolate reductase gene, MTHFR, does not alter the risk of visual failure in Leber's hereditary optic neuropathy.
PMID 19421414·Mol Vis·2009
8-other
Effects of acute and 14-day coenzyme Q10 supplementation on exercise performance in both trained and untrained individuals.
PMID 18318910·J Int Soc Sports Nutr·2008
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
Effects of caffeine and aspirin on light resistance training performance, perceived exertion, and pain perception.
PMID 18824931·J Strength Cond Res·2008
2-rct
Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background.
PMID 17668373·Am J Hum Genet·2007
4-observational
X-Inactivation patterns in females harboring mtDNA mutations that cause Leber hereditary optic neuropathy.
PMID 18199976·Mol Vis·2007
8-other
Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and Parkinsonism.
PMID 17420318·Arch Neurol·2007
8-other
Encouraging staff involvement in the security effort.
PMID 17849837·J Healthc Prot Manage·2006
8-other
POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions.
PMID 16682683·Neurology·2006
8-other
Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder.
PMID 16380918·Am J Hum Genet·2005
4-observational
Sensory ataxic neuropathy due to a novel C10Orf2 mutation with probable germline mosaicism.
PMID 15668446·Neurology·2005
5-case
OPA1 increases the risk of normal but not high tension glaucoma.
PMID 19581274·J Med Genet·2010
8-other
A possible anatomical and biomechanical explanation of the 10% rule used in the clinical assessment of prehensile hand movements and handed dominance.
PMID 19324572·J Electromyogr Kinesiol·2009
8-other
Effects of 28 days of resistance exercise and consuming a commercially available pre-workout supplement, NO-Shotgun(R), on body composition, muscle strength and mass, markers of satellite cell activation, and clinical safety markers in males.
PMID 19656392·J Int Soc Sports Nutr·2009
8-other
No association between common POLG1 variants and sporadic idiopathic Parkinson's disease.
PMID 19243043·Mov Disord·2009
8-other
Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children.
PMID 19251978·J Med Genet·2009
8-other
Quality of life in patients with leber hereditary optic neuropathy.
PMID 19255150·Invest Ophthalmol Vis Sci·2009
8-other
The acute effects of the thermogenic supplement Meltdown on energy expenditure, fat oxidation, and hemodynamic responses in young, healthy males.
PMID 19087290·J Int Soc Sports Nutr·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
- 1105 EAGLETREE LN SE
HUNTSVILLE, AL 35801 - Phone
- (256) 882-7873
Quick Facts
- NPI
- 1447214424
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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