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OLIVIA ROSS, DO
DO
Internal Medicine Physician
NPI: 1881485886Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
PG225321(OR)
Research & Publications (20)
Genetics of ischemic stroke: inheritance of a sporadic disorder.
PMID 19080749·Curr Neurol Neurosci Rep·2009
6-review
Genetic variation of Omi/HtrA2 and Parkinson's disease.
PMID 18790661·Parkinsonism Relat Disord·2008
8-other
Lack of evidence for association of Parkin promoter polymorphism (PRKN-258) with increased risk of Parkinson's disease.
PMID 17400506·Parkinsonism Relat Disord·2007
8-other
Hypothetical soluble KIR2DS4 natural killer cell receptor molecule does not associate with successful ageing in the Irish.
PMID 15130674·Exp Gerontol·2004
8-other
HLA haplotypes and TNF polymorphism do not associate with longevity in the Irish.
PMID 12714268·Mech Ageing Dev·2003
8-other
mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the Irish.
PMID 12670626·Exp Gerontol·2003
8-other
Increased frequency of the 2437T allele of the heat shock protein 70-Hom gene in an aged Irish population.
PMID 12742533·Exp Gerontol·2003
8-other
Study of age-association with cytokine gene polymorphisms in an aged Irish population.
PMID 12633940·Mech Ageing Dev·2003
4-observational
A novel polymorphic triplet repeat in intron five of the alpha-synuclein gene: no evidence of expansion or allelic association with idiopathic Parkinson's disease in the Irish.
PMID 12352614·Neuroreport·2002
8-other
The sick euthyroid syndrome in paediatric cardiac surgery patients.
PMID 11534559·Intensive Care Med·2001
6-review
Mitochondrial DNA polymorphism: its role in longevity of the Irish population.
PMID 11404057·Exp Gerontol·2001
8-other
Characterization of DCTN1 genetic variability in neurodegeneration.
PMID 19506225·Neurology·2009
8-other
GRN 3'UTR+78 C>T is not associated with risk for Parkinson's disease.
PMID 19473366·Eur J Neurol·2009
8-other
Reported mutations in GIGYF2 are not a common cause of Parkinson's disease.
PMID 19133664·Mov Disord·2009
8-other
A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunction.
PMID 19632874·Parkinsonism Relat Disord·2009
8-other
DRD3 Ser9Gly and HS1BP3 Ala265Gly are not associated with Parkinson disease.
PMID 19524641·Neurosci Lett·2009
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
- 3600 NW SAMARITAN DR
CORVALLIS, OR 97330 - Phone
- (541) 768-4906
Quick Facts
- NPI
- 1881485886
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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