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PAUL TARANTINO, M.D.
M.D.
Specialist
NPI: 1366475089IndividualAccepts Medicare
Specialties, Licenses & Credentials
SpecialistPrimary
Specialist
Code: 174400000X
D43467(MD)
Education
BALTIMORE UNIVERSITY SCHOOL OF MEDICINE
Class of 1987
Research & Publications (20)
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism.
PMID 18722801·Parkinsonism Relat Disord·2009
8-other
The shortness of Pygmies is associated with severe under-expression of the growth hormone receptor.
PMID 19541519·Mol Genet Metab·2009
8-other
The DRD2 TaqIA polymorphism associated with changed midbrain volumes in healthy individuals.
PMID 19476502·Genes Brain Behav·2009
8-other
The value, qualification, and regulatory use of surrogate end points in drug development.
PMID 19474783·Clin Pharmacol Ther·2009
6-review
Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia.
PMID 18976783·J Neurol Sci·2009
8-other
Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease.
PMID 17975812·Mov Disord·2008
4-observational
Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease.
PMID 17918232·Am J Med Genet B Neuropsychiatr Genet·2008
8-other
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy.
PMID 18074383·Mov Disord·2008
8-other
Identification of the novel D297fsX318 PINK1 mutation and phenotype variation in a family with early-onset Parkinson's disease.
PMID 18329316·Parkinsonism Relat Disord·2008
5-case
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease.
PMID 18350653·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease.
PMID 18350652·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease.
PMID 18350651·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease.
PMID 18350649·Hum Genet·2007
8-other
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy.
PMID 17324557·Epilepsy Res·2007
8-other
LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease.
PMID 17470139·Clin Genet·2007
8-other
Gene dosage influences the age at onset of SCA2 in a family from southern Italy.
PMID 17850638·Clin Genet·2007
8-other
SIL1 and SARA2 mutations in Marinesco-Sjögren and chylomicron retention diseases.
PMID 17309654·Clin Genet·2007
8-other
Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.
PMID 16149094·Mov Disord·2006
8-other
Hybrid antibacterials. DNA polymerase-topoisomerase inhibitors.
PMID 16480282·J Med Chem·2006
7-preclinical
Biological effects of 6 mT static magnetic fields: a comparative study in different cell types.
PMID 16724329·Bioelectromagnetics·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
- 806 LANDMARK DR, STE 114
GLEN BURNIE, MD 21061 - Phone
- (410) 590-9260
Quick Facts
- NPI
- 1366475089
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 39
- Publications
- 20
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