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MICHAEL VOTRUBA, MD
MD
Diagnostic Radiology Physician
NPI: 1972527323IndividualAccepts Medicare
Specialties, Licenses & Credentials
Diagnostic Radiology PhysicianPrimary
Radiology — Diagnostic Radiology
Code: 2085R0202X
430107645(MI)
CMS Specialties
PrimaryDIAGNOSTIC RADIOLOGY
Education
STATE UNIVERSITY OF NEW YORK AT STONY BROOK, SCHOOL OF MEDICINE
Class of 1991
Research & Publications (20)
Effects of neighborhood characteristics on the mortality of black male youth: evidence from Gautreaux, Chicago.
PMID 19155115·Soc Sci Med·2009
4-observational
Redirecting patients to improve stroke outcomes: implications of a volume-based approach in one urban market.
PMID 17122718·Med Care·2006
8-other
Secondary mtDNA defects do not cause optic nerve dysfunction in a mouse model of dominant optic atrophy.
PMID 19443720·Invest Ophthalmol Vis Sci·2009
7-preclinical
OPA1 deficiency associated with increased autophagy in retinal ganglion cells in a murine model of dominant optic atrophy.
PMID 19234344·Invest Ophthalmol Vis Sci·2009
7-preclinical
A missense mutation in the murine Opa3 gene models human Costeff syndrome.
PMID 18222992·Brain·2008
7-preclinical
Comparative study of fibrillar collagen arrangement in the corneas of primates and other mammals.
PMID 17957749·Anat Rec (Hoboken)·2007
4-observational
Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function.
PMID 17428816·Hum Mol Genet·2007
7-preclinical
Medical cost savings associated with 17 alpha-hydroxyprogesterone caproate.
PMID 17346527·Am J Obstet Gynecol·2007
6-review
Overcoming bias in estimating the volume-outcome relationship.
PMID 16430610·Health Serv Res·2006
8-other
Molecular genetic basis of primary inherited optic neuropathies.
PMID 15534598·Eye (Lond)·2004
6-review
The role of bone scan in the diagnosis of Jaffé-Lichtenstein-Uehlinger syndrome.
PMID 15318318·Nucl Med Rev Cent East Eur·2004
5-case
Developmental expression profile of the optic atrophy gene product: OPA1 is not localized exclusively in the mammalian retinal ganglion cell layer.
PMID 15161824·Invest Ophthalmol Vis Sci·2004
4-observational
Electrophysiology and ocular blood flow in a family with dominant optic nerve atrophy and a mutation in the OPA1 gene.
PMID 14566653·Ophthalmic Genet·2003
8-other
Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy.
PMID 12488262·Br J Ophthalmol·2003
8-other
A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy.
PMID 12036970·Invest Ophthalmol Vis Sci·2002
4-observational
A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene.
PMID 11810296·Hum Genet·2002
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
- 3264 N EVERGREEN DR NE
GRAND RAPIDS, MI 49525 - Phone
- (616) 363-7339
Quick Facts
- NPI
- 1972527323
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 35
- Publications
- 20
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