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CHRISTOPHER TOMAINO, M.D.
M.D.
Gastroenterology Physician
NPI: 1558594960IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
270874(NY)
Gastroenterology PhysicianPrimary
Internal Medicine — Gastroenterology
Code: 207RG0100X
270874(NY)
Education
OTHER
Class of 2009
Research & Publications (17)
AbetaPP A713T mutation in late onset Alzheimer's disease with cerebrovascular lesions.
PMID 19363265·J Alzheimers Dis·2009
8-other
Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia.
PMID 18314228·Neurobiol Aging·2009
8-other
Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism.
PMID 18350357·J Neurol·2008
5-case
Heterogeneity within a large kindred with frontotemporal dementia: a novel progranulin mutation.
PMID 17620546·Neurology·2007
8-other
Presenilin 2 Ser130Leu mutation in a case of late-onset "sporadic" Alzheimer's disease.
PMID 17345043·J Neurol·2007
8-other
The effects of APOE and tau gene variability on risk of frontotemporal dementia.
PMID 15904995·Neurobiol Aging·2006
8-other
Circulating levels of soluble receptor for advanced glycation end products in Alzheimer disease and vascular dementia.
PMID 16286548·Arch Neurol·2005
4-observational
Relation of apolipoprotein(a) size to alzheimer's disease and vascular dementia.
PMID 15211075·Dement Geriatr Cogn Disord·2004
4-observational
A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene.
PMID 15365148·Neurology·2004
8-other
Apolipoprotein(a) null phenotype is related to a delayed age at onset of Alzheimer's disease.
PMID 15036610·Neurosci Lett·2004
8-other
Association between small apolipoprotein(a) isoforms and frontotemporal dementia in humans.
PMID 14665416·Neurosci Lett·2003
4-observational
Absence of association between Alzheimer disease and the regulatory region polymorphism of the PS2 gene in an Italian population.
PMID 12770698·Neurosci Lett·2003
8-other
Familial essential tremor is not associated with SCA-12 mutation in southern Italy.
PMID 12210890·Mov Disord·2002
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 153 N OCEAN AVE
PATCHOGUE, NY 11772 - Phone
- (631) 714-4444
Quick Facts
- NPI
- 1558594960
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 17
- Publications
- 17
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