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JOSEPH OLDENBURG, M.D.
M.D.
Ophthalmology Physician
NPI: 1881682193IndividualAccepts Medicare
Specialties, Licenses & Credentials
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
G49343(CA)
CMS Specialties
PrimaryOPHTHALMOLOGY
Education
EMORY UNIVERSITY SCHOOL OF MEDICINE
Class of 1980
Research & Publications (20)
[Long-term toxicity after therapy for testicular cancer with special focus on sexual disorders].
PMID 19234684·Urologe A·2009
6-review
Genetic variants associated with cisplatin-induced ototoxicity.
PMID 18855538·Pharmacogenomics·2008
6-review
Association between long-term neuro-toxicities in testicular cancer survivors and polymorphisms in glutathione-s-transferase-P1 and -M1, a retrospective cross sectional study.
PMID 18162130·J Transl Med·2007
8-other
Differences in tropism and pH dependence for glycoproteins from the Clade B1 arenaviruses: implications for receptor usage and pathogenicity.
PMID 17397892·Virology·2007
4-observational
Cisplatin-induced long-term hearing impairment is associated with specific glutathione s-transferase genotypes in testicular cancer survivors.
PMID 17228018·J Clin Oncol·2007
4-observational
Late relapses of germ cell malignancies: incidence, management, and prognosis.
PMID 17158535·J Clin Oncol·2006
6-review
Postchemotherapy retroperitoneal surgery remains necessary in patients with nonseminomatous testicular cancer and minimal residual tumor masses.
PMID 12947067·J Clin Oncol·2003
8-other
The relevance of the bleeding severity in the treatment of acquired haemophilia - an update of a single-centre experience with 67 patients.
PMID 19040429·Haemophilia·2010
8-other
Exploration of platinum-induced neuropathy should be based on both objective and subjective examinations.
PMID 19484592·Acta Oncol·2009
8-other
Molecular mechanisms underlying hemophilia A phenotype in seven females.
PMID 19302446·J Thromb Haemost·2009
8-other
A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylation.
PMID 19246518·Hum Mol Genet·2009
8-other
The problem of novel FVIII missense mutations for haemophilia A genetic counseling.
PMID 19404520·Hamostaseologie·2009
8-other
VKORC1 deficiency in mice causes early postnatal lethality due to severe bleeding.
PMID 19492146·Thromb Haemost·2009
7-preclinical
Factor 5 mutation profile in German patients with homozygous and heterozygous factor V deficiency.
PMID 19486170·Haemophilia·2009
8-other
An exosite-specific ssDNA aptamer inhibits the anticoagulant functions of activated protein C and enhances inhibition by protein C inhibitor.
PMID 19389630·Chem Biol·2009
8-other
[Relevance of a single dose of 270 microg/kg recombinant factor VIIa for the treatment of patients with haemophilia and inhibitors - Recommendations from the GTH experts].
PMID 19404511·Hamostaseologie·2009
8-other
Identification of a novel factor X deletion in combination with a missense mutation in the F10 gene - Genotype-phenotype correlation in a girl with severe factor X deficiency.
PMID 19404516·Hamostaseologie·2009
5-case
Novel findings in two patients with late-diagnosed afibrinogenaemia: intraosseous haemorrhage and fingertip necrosis.
PMID 19473412·Haemophilia·2009
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3855 BROAD STREET, SUITE B
SAN LUIS OBISPO, CA 93401 - Phone
- (805) 545-7881
Quick Facts
- NPI
- 1881682193
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 46
- Publications
- 20
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