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PHILIP SPADAFORA, DO
DO
Internal Medicine Physician
NPI: 1255386959IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
1878871(NY)
Education
NEW YORK COLLEGE OF OSTEO MEDICINE OF NEW YORK INSTITUTE OF TECHNOLOGY
Class of 1989
Research & Publications (20)
Iconic sign comprehension in older adults: the role of cognitive impairment and text enhancement.
PMID 19158042·Can J Aging·2008
4-observational
A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.
PMID 18204809·J Neurol·2008
5-case
Gene dosage influences the age at onset of SCA2 in a family from southern Italy.
PMID 17850638·Clin Genet·2007
8-other
The role of VLA4 polymorphisms in multiple sclerosis: an association study.
PMID 17609118·J Neuroimmunol·2007
8-other
LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease.
PMID 17470139·Clin Genet·2007
8-other
Fas antigen and sporadic Alzheimer's disease in Southern Italy: evaluation of two polymorphisms in the TNFRSF6 gene.
PMID 17406980·Neurochem Res·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
Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study.
PMID 15824260·Arch Neurol·2005
3-trial
FRAXE intermediate alleles are associated with Parkinson's disease.
PMID 15342126·Neurosci Lett·2004
8-other
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms.
PMID 15023809·Arch Neurol·2004
4-observational
A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit.
PMID 15009235·Epilepsia·2004
5-case
Association of tau gene polymorphism with Parkinson's disease.
PMID 14600827·Neurol Sci·2003
4-observational
NACP-REP1 polymorphism is not involved in Parkinson's disease: a case-control study in a population sample from southern Italy.
PMID 14583385·Neurosci Lett·2003
8-other
Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus.
PMID 12919402·Epilepsia·2003
8-other
No evidence of association between the alpha-2 macroglobulin gene and Parkinson's disease in a case-control sample.
PMID 12123860·Neurosci Lett·2002
8-other
Association of the 5-HT6 receptor gene polymorphism C267T with Parkinson's disease.
PMID 11889255·Neurology·2002
8-other
The parkin gene is not a major susceptibility locus for typical late-onset Parkinson's disease.
PMID 11487208·Neurol Sci·2001
8-other
The parkin gene is not involved in late-onset Parkinson's disease.
PMID 11468333·Neurology·2001
8-other
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1.
PMID 11094099·Neurology·2000
8-other
Beneficial effects of viscous dietary fiber from Konjac-mannan in subjects with the insulin resistance syndrome: results of a controlled metabolic trial.
PMID 10857960·Diabetes Care·2000
3-trial
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 901 STEWART AVE, STE 275
GARDEN CITY, NY 11530 - Phone
- (516) 877-1518
Quick Facts
- NPI
- 1255386959
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 37
- Publications
- 20
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