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ERIC STONE, MD
MD
Gastroenterology Physician
NPI: 1669511689IndividualAccepts Medicare
Specialties, Licenses & Credentials
Gastroenterology PhysicianPrimary
Internal Medicine — Gastroenterology
Code: 207RG0100X
35780(MT)
CMS Specialties
PrimaryGASTROENTEROLOGY
Education
INDIANA UNIVERSITY SCHOOL OF MEDICINE
Class of 2001
Research & Publications (20)
Localization of complement 1 inhibitor (C1INH/SERPING1) in human eyes with age-related macular degeneration.
PMID 19607829·Exp Eye Res·2009
8-other
A transcriptional network associated with natural variation in Drosophila aggressive behavior.
PMID 19607677·Genome Biol·2009
7-preclinical
Phenotypic variability due to a novel Glu292Lys variation in exon 8 of the BEST1 gene causing best macular dystrophy.
PMID 19597114·Arch Ophthalmol·2009
8-other
The genetics of quantitative traits: challenges and prospects.
PMID 19584810·Nat Rev Genet·2009
6-review
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy.
PMID 19578027·Invest Ophthalmol Vis Sci·2009
8-other
The natural history of stargardt disease with specific sequence mutation in the ABCA4 gene.
PMID 19578016·Invest Ophthalmol Vis Sci·2009
8-other
A comparison of summertime secondary organic aerosol source contributions at contrasting urban locations.
PMID 19544838·Environ Sci Technol·2009
4-observational
Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganization.
PMID 19503738·Mol Vis·2009
8-other
Chromatic pupil responses: preferential activation of the melanopsin-mediated versus outer photoreceptor-mediated pupil light reflex.
PMID 19501408·Ophthalmology·2009
5-case
Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataract.
PMID 19461930·Mol Vis·2009
8-other
Modulated modularity clustering as an exploratory tool for functional genomic inference.
PMID 19424432·PLoS Genet·2009
4-observational
Progress toward effective treatments for human photoreceptor degenerations.
PMID 19414246·Curr Opin Genet Dev·2009
6-review
CRB1 gene mutations are associated with keratoconus in patients with leber congenital amaurosis.
PMID 19407021·Invest Ophthalmol Vis Sci·2009
8-other
Peripapillary retinal nerve fiber layer thinning in patients with autosomal recessive cone-rod dystrophy.
PMID 19406377·Am J Ophthalmol·2009
8-other
Seed treatment with 2,4-diacetylphloroglucinol-producing pseudomonads improves crop health in low-pH soils by altering patterns of nutrient uptake.
PMID 19351246·Phytopathology·2009
8-other
Glycosyltransferase function in core 2-type protein O glycosylation.
PMID 19349303·Mol Cell Biol·2009
7-preclinical
Alcohol sensitivity in Drosophila: translational potential of systems genetics.
PMID 19652175·Genetics·2009
7-preclinical
Marked behavioral activation from inhibitory stimulation of locus coeruleus alpha1-adrenoceptors by a full agonist.
PMID 19632210·Brain Res·2009
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1930 W BROADWAY ST STE A
MISSOULA, MT 59808 - Phone
- (406) 541-6844
Quick Facts
- NPI
- 1669511689
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 25
- Publications
- 20
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