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PAUL LEITNER, MD
MD
Geriatric Medicine (Internal Medicine) Physician
NPI: 1912093865Individual
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
A42193(CA)
Geriatric Medicine (Internal Medicine) PhysicianPrimary
Internal Medicine — Geriatric Medicine
Code: 207RG0300X
A42193(CA)
Research & Publications (13)
Parkin protects mitochondrial genome integrity and supports mitochondrial DNA repair.
PMID 19617636·Hum Mol Genet·2009
7-preclinical
High-throughput homogeneous mass cleave assay technology for the diagnosis of autosomal recessive Parkinson's disease.
PMID 18403612·J Mol Diagn·2008
7-preclinical
A unique case of coincidence of early onset Parkinson's disease and multiple sclerosis.
PMID 17914725·Mov Disord·2007
5-case
A novel LRRK2 mutation in an Austrian cohort of patients with Parkinson's disease.
PMID 17523199·Mov Disord·2007
8-other
Transcranial ultrasound in different monogenetic subtypes of Parkinson's disease.
PMID 17415511·J Neurol·2007
8-other
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease.
PMID 16333314·Eur J Hum Genet·2006
7-preclinical
The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations.
PMID 16443856·J Med Genet·2006
8-other
Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*.
PMID 16251215·Brain·2005
8-other
The spatial organization of lipid synthesis in the yeast Saccharomyces cerevisiae derived from large scale green fluorescent protein tagging and high resolution microscopy.
PMID 15716577·Mol Cell Proteomics·2005
8-other
PARK11 is not linked with Parkinson's disease in European families.
PMID 15523496·Eur J Hum Genet·2005
8-other
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
PMID 15541309·Neuron·2004
8-other
The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval.
PMID 14691730·Am J Hum Genet·2004
8-other
Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's disease.
PMID 12827450·Neurogenetics·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
- Address
- 8540 S SEPULVEDA BLVD, SUITE 910
LOS ANGELES, CA 90045 - Phone
- (310) 410-1944
Quick Facts
- NPI
- 1912093865
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 13
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