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ALISON RENNER, DO
DO
Family Medicine Physician
NPI: 1366029662IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
LL83588(SC)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
CMS Specialties
PrimaryFAMILY PRACTICE
Education
EDWARD VIA COL OF OSTEO MEDICINE-CAROLINAS CAMPUS
Class of 2021
Research & Publications (20)
[Foreign knowledge being tested: European physicians fighting the Moscow plague of 1771].
PMID 17212228·Ber Wiss·2006
8-other
High-throughput functional annotation of novel gene products using document clustering.
PMID 10902156·Pac Symp Biocomput·2000
4-observational
Polo-like kinase 1 is overexpressed in acute myeloid leukemia and its inhibition preferentially targets the proliferation of leukemic cells.
PMID 19458358·Blood·2009
8-other
[Clinical manifestations of functional disturbances of the retinal pigment epithelium].
PMID 19340431·Ophthalmologe·2009
6-review
[Evolution of health-related self-help. Experience from 40 years of work in self-help].
PMID 19189149·Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz·2009
6-review
Phenotypic variability and long-term follow-up of patients with known and novel PRPH2/RDS gene mutations.
PMID 19038374·Am J Ophthalmol·2009
8-other
Progression of retinal pigment epithelial alterations during long-term follow-up in female carriers of choroideremia and report of a novel CHM mutation.
PMID 19597113·Arch Ophthalmol·2009
8-other
ERG variability in X-linked congenital retinoschisis patients with mutations in the RS1 gene and the diagnostic importance of fundus autofluorescence and OCT.
PMID 17987333·Doc Ophthalmol·2008
8-other
Heterotopic rat heart transplantation (Lewis to F344): early ICAM-1 expression after 8 hours of cold ischemia.
PMID 18765197·J Heart Lung Transplant·2008
7-preclinical
Mutation analysis identifies GUCY2D as the major gene responsible for autosomal dominant progressive cone degeneration.
PMID 18487367·Invest Ophthalmol Vis Sci·2008
4-observational
[Tamoxifen retinopathy: a case series of clinical and functional data].
PMID 18415107·Ophthalmologe·2008
8-other
Pumpless extracorporeal lung assist as supportive therapy in a patient with diffuse alveolar hemorrhage.
PMID 18373323·Int J Artif Organs·2008
5-case
ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies.
PMID 18285826·Eur J Hum Genet·2008
8-other
Liver-specific increase of UTP and UDP-sugar concentrations in rats induced by dietary vitamin B6-deficiency and its relation to complex N-glycan structures of liver membrane-proteins.
PMID 17577663·Glycoconj J·2007
7-preclinical
The corticotropin-releasing factor receptor type 2a contains an N-terminal pseudo signal peptide.
PMID 16766521·J Biol Chem·2006
7-preclinical
Up-regulation of S100A8 and S100A9 protein in bronchial epithelial cells by lipopolysaccharide.
PMID 17090475·Exp Lung Res·2006
8-other
Choroideremia: variability of clinical and electrophysiological characteristics and first report of a negative electroretinogram.
PMID 16935340·Ophthalmology·2006
8-other
Fundus autofluorescence and mfERG for early detection of retinal alterations in patients using chloroquine/hydroxychloroquine.
PMID 16877425·Invest Ophthalmol Vis Sci·2006
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 853 N CHURCH ST STE 510
SPARTANBURG, SC 29303 - Phone
- (864) 560-6193
Quick Facts
- NPI
- 1366029662
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 5
- Publications
- 20
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