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OZLEM GOKER-ALPAN, M.D.
M.D.
Pediatrics Physician
NPI: 1427270313IndividualAccepts Medicare
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
D0051189(MD)
Education
OTHER
Class of 1990
Research & Publications (17)
The association between mutations in the lysosomal protein glucocerebrosidase and parkinsonism.
PMID 19425057·Mov Disord·2009
6-review
Optimization and validation of two miniaturized glucocerebrosidase enzyme assays for high throughput screening.
PMID 19075603·Comb Chem High Throughput Screen·2008
4-observational
The spectrum of parkinsonian manifestations associated with glucocerebrosidase mutations.
PMID 18852351·Arch Neurol·2008
8-other
Cognitive outcome in treated patients with chronic neuronopathic Gaucher disease.
PMID 18571543·J Pediatr·2008
8-other
Uniparental disomy of chromosome 1 causing concurrent Charcot-Marie-Tooth and Gaucher disease Type 3.
PMID 18347322·Neurology·2008
5-case
Treating patients with Gaucher disease and parkinsonism: misrepresentation in a title.
PMID 17350320·Parkinsonism Relat Disord·2008
8-other
Glucocerebrosidase mutations in Chinese subjects from Taiwan with sporadic Parkinson disease.
PMID 17462935·Mol Genet Metab·2007
8-other
Three classes of glucocerebrosidase inhibitors identified by quantitative high-throughput screening are chaperone leads for Gaucher disease.
PMID 17670938·Proc Natl Acad Sci U S A·2007
8-other
Glucocerebrosidase mutations are an important risk factor for Lewy body disorders.
PMID 16790605·Neurology·2006
4-observational
Glucocerebrosidase mutations are not found in association with LRRK2 G2019S in subjects with parkinsonism.
PMID 16781064·Neurosci Lett·2006
8-other
Skin abnormalities as an early predictor of neurologic outcome in Gaucher disease.
PMID 16630170·Clin Genet·2006
8-other
Divergent phenotypes in Gaucher disease implicate the role of modifiers.
PMID 15937077·J Med Genet·2005
8-other
Glucocerebrosidase mutations in subjects with parkinsonism.
PMID 14728994·Mol Genet Metab·2004
8-other
Phenotypic continuum in neuronopathic Gaucher disease: an intermediate phenotype between type 2 and type 3.
PMID 12970647·J Pediatr·2003
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 3 locations total
- Address
- 35 Convent Drive, 1A211
Bethesda, MD 20892 - Phone
- (301) 451-0900
Quick Facts
- NPI
- 1427270313
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 3
- Years in Practice
- 36
- Publications
- 17
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