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GIACINTO GRIECO, M.D.

M.D.

Neurology Physician

NPI: 1659402030IndividualAccepts Medicare

Specialties, Licenses & Credentials

Brain Injury Medicine (Psychiatry & Neurology) Physician

Psychiatry & Neurology — Brain Injury Medicine

Code: 2084P0301X

134960(NY)
Hospitalist Physician

Hospitalist

Code: 208M00000X

134960(NY)
Neurology PhysicianPrimary

Psychiatry & Neurology — Neurology

Code: 2084N0400X

134960(NY)

CMS Specialties

PrimaryNEUROLOGY

Education

MEDICAL COLLEGE OF WISCONSIN

Class of 1977

Research & Publications (20)

Drug consumption in medication overuse headache is influenced by brain-derived neurotrophic factor Val66Met polymorphism.
PMID 19517061·J Headache Pain·2009
8-other
The interplay of two single nucleotide polymorphisms in the CACNA1A gene may contribute to migraine susceptibility.
PMID 19429006·Neurosci Lett·2009
8-other
Mitochondrial DNA haplogroups influence the therapeutic response to riboflavin in migraineurs.
PMID 19414726·Neurology·2009
3-trial
An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing loss.
PMID 19031088·Neurogenetics·2009
8-other
Interferometer for ground-based observations of emitted spectral radiance from the troposphere: evaluation and retrieval performance.
PMID 18641761·Appl Opt·2008
8-other
The wolframin His611Arg polymorphism influences medication overuse headache.
PMID 17719176·Neurosci Lett·2007
8-other
Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop.
PMID 17292920·J Neurol Sci·2007
5-case
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study.
PMID 16636238·Neurology·2006
8-other
Dipyridamole plus aspirin: the best regimen for stroke prevention after noncardioembolic focal cerebral ischemia.
PMID 16567930·Cerebrovasc Dis·2006
8-other
A novel ATP1A2 mutation in a family with FHM type II.
PMID 16472340·Cephalalgia·2006
4-observational
Familial basilar migraine associated with a new mutation in the ATP1A2 gene.
PMID 16344534·Neurology·2005
8-other
Skeletal muscle wasting in tumor-bearing rats is associated with MyoD down-regulation.
PMID 15870883·Int J Oncol·2005
7-preclinical
Editorial comment--an approach to the estimation of the risk of TTP during clopidogrel therapy.
PMID 14757895·Stroke·2004
8-other
Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum.
PMID 14745065·Neurology·2004
5-case
Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type.
PMID 14718707·Neurology·2004
5-case
Potential value of triple antiplatelet therapy for secondary stroke prevention.
PMID 14512584·Stroke·2003
1-meta
Six novel mutations of the RUNX2 gene in Italian patients with cleidocranial dysplasia.
PMID 12815605·Hum Mutat·2003
8-other
Multicentre Italian family-based association study on tyrosine hydroxylase, catechol-O-methyl transferase and Wolfram syndrome 1 polymorphisms in mood disorders.
PMID 12782971·Psychiatr Genet·2003
8-other
Increased muscle proteasome activity correlates with disease severity in gastric cancer patients.
PMID 12616123·Ann Surg·2003
8-other
Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene.
PMID 12565915·Neuromuscul Disord·2003
5-case

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
462 FIRST AVE - SEVENTH FLOOR, NYU LANGONE HEALTH
NEW YORK, NY 11016

Location

Practice Location

462 FIRST AVE - SEVENTH FLOOR, NEW YORK, NY
(646) 501-6823

Quick Facts

NPI
1659402030
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
3
Locations
1
Years in Practice
49
Publications
20

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