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GORDON HUDSON, MSW LPC PHD
MSW LPC PHD
Counselor
NPI: 1912081761Individual
Specialties, Licenses & Credentials
Marriage & Family Therapist
Marriage & Family Therapist
Code: 106H00000X
001236-042307(TX)
CounselorPrimary
Counselor
Code: 101Y00000X
8296(TX)
Research & Publications (20)
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
OPA1 increases the risk of normal but not high tension glaucoma.
PMID 19581274·J Med Genet·2010
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
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
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
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
No association between common POLG1 variants and sporadic idiopathic Parkinson's disease.
PMID 19243043·Mov Disord·2009
8-other
Leber hereditary optic neuropathy presenting in a 75-year-old man.
PMID 18562849·J Neuroophthalmol·2008
5-case
Effects of caffeine and aspirin on light resistance training performance, perceived exertion, and pain perception.
PMID 18824931·J Strength Cond Res·2008
2-rct
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
Novel mutations in the TK2 gene associated with fatal mitochondrial DNA depletion myopathy.
PMID 18508266·Neuromuscul Disord·2008
5-case
Impact of artificial recharge on dissolved noble gases in groundwater in California.
PMID 18351066·Environ Sci Technol·2008
8-other
Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase gamma (POLG1).
PMID 18208989·Arch Dis Child·2008
5-case
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
POLG1 mutations manifesting as autosomal recessive axonal Charcot-Marie-Tooth disease.
PMID 18195151·Arch Neurol·2008
5-case
Does mitochondrial DNA predispose to neuromyelitis optica (Devic's disease)?
PMID 17967805·Brain·2008
6-review
X-Inactivation patterns in females harboring mtDNA mutations that cause Leber hereditary optic neuropathy.
PMID 18199976·Mol Vis·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
- 325 E SONTERRA BLVD, SUITE 230
SAN ANTONIO, TX 78258 - Phone
- (210) 545-6860
Quick Facts
- NPI
- 1912081761
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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