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GARY MELLICK, D.O.
D.O.
Neurology Physician
NPI: 1780641506Individual
Specialties, Licenses & Credentials
Sleep Medicine (Psychiatry & Neurology) Physician
Psychiatry & Neurology — Sleep Medicine
Code: 2084S0012X
DO1117(AL)
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
02006613A(IN)DO1117(AL)
Specialist
Specialist
Code: 174400000X
055142(GA)34004503(OH)
Clinical Neurophysiology Physician
Psychiatry & Neurology — Clinical Neurophysiology
Code: 2084N0600X
DO1117(AL)
Pain Medicine (Psychiatry & Neurology) Physician
Psychiatry & Neurology — Pain Medicine
Code: 2084P2900X
DO1117(AL)
Research & Publications (20)
Screening PARK genes for mutations in early-onset Parkinson's disease patients from Queensland, Australia.
PMID 18486522·Parkinsonism Relat Disord·2009
8-other
TNF gene polymorphism and quantitative traits related to cardiovascular disease: getting to the heart of the matter.
PMID 17377521·Eur J Hum Genet·2007
8-other
CYP450, genetics and Parkinson's disease: gene x environment interactions hold the key.
PMID 17017524·J Neural Transm Suppl·2006
7-preclinical
Clinical presentation, quantitative sensory testing, and therapy of 2 patients with fourth thoracic syndrome.
PMID 16762670·J Manipulative Physiol Ther·2006
5-case
Australian data and meta-analysis lend support for alpha-synuclein (NACP-Rep1) as a risk factor for Parkinson's disease.
PMID 15670652·Neurosci Lett·2005
1-meta
A novel screen for nuclear mitochondrial gene associations with Parkinson's disease.
PMID 14767722·J Neural Transm (Vienna)·2004
4-observational
The parkin gene S/N167 polymorphism in Australian Parkinson's disease patients and controls.
PMID 11248588·Parkinsonism Relat Disord·2001
8-other
The ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism does not confer protection against idiopathic Parkinson's disease.
PMID 11027850·Neurosci Lett·2000
8-other
The monoamine oxidase B gene GT repeat polymorphism and Parkinson's disease in a Chinese population.
PMID 10701898·J Neurol·2000
8-other
Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: large-scale collaborative study.
PMID 19475631·Am J Med Genet B Neuropsychiatr Genet·2010
1-meta
Prevalence of smell loss in Parkinson's disease--a multicenter study.
PMID 19138875·Parkinsonism Relat Disord·2009
4-observational
Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?
PMID 19224617·Mov Disord·2009
8-other
Serotonin and dopamine transporter genes do not influence depression in Parkinson's disease.
PMID 18973248·Mov Disord·2009
8-other
Mitochondrial DNA haplogroups J and K are not protective for Parkinson's disease in the Australian community.
PMID 19086081·Mov Disord·2009
8-other
Haplotype analysis of the PARK 11 gene, GIGYF2, in sporadic Parkinson's disease.
PMID 19117363·Mov Disord·2009
8-other
Association study of the NEDD9 gene with the risk of developing Alzheimer's and Parkinson's disease.
PMID 18579580·Hum Mol Genet·2008
8-other
Utility of a patient survey in identifying fluctuations in early stage Parkinson's disease.
PMID 18824360·J Clin Neurosci·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
Via practice · 2 locations total
- Address
- 309 Medical Center Dr SW
Fort Payne, AL 35968 - Phone
- (256) 845-0345
Quick Facts
- NPI
- 1780641506
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 7
- Locations
- 2
- Publications
- 20
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