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MICHAEL DARAS, M.D.

M.D.

Neurology Physician

NPI: 1972604700IndividualAccepts Medicare

Specialties, Licenses & Credentials

Neurology PhysicianPrimary

Psychiatry & Neurology — Neurology

Code: 2084N0400X

126459(NY)

CMS Specialties

PrimaryNEUROLOGY

Education

OTHER

Class of 1969

Research & Publications (20)

Total hip arthroplasty in young patients with osteoarthritis.
PMID 19377644·Am J Orthop (Belle Mead NJ)·2009
6-review
Characterization of a novel TYMP splice site mutation associated with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
PMID 19056268·Neuromuscul Disord·2009
5-case
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383597·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383596·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383595·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383594·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383593·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383591·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383590·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383589·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383588·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383587·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18380023·Hum Genet·2007
8-other
Mitochondrial encephalomyopathy due to a novel mutation in the tRNAGlu of mitochondrial DNA.
PMID 17715279·J Child Neurol·2007
5-case
Horse madness (hippomania) and hippophobia.
PMID 16482685·Hist Psychiatry·2005
7-preclinical
Novel checkpoint response to genotoxic stress mediated by nucleolin-replication protein a complex formation.
PMID 15743838·Mol Cell Biol·2005
8-other
Thyrotropin-releasing hormone administration does not affect seizure threshold during electroconvulsive therapy.
PMID 12972982·J ECT·2003
3-trial
Placebos, placebo effect, and the response to the healing situation: the evolution of a concept.
PMID 11879377·Epilepsia·2001
8-other
Seizures in the critically ill: the role of imipenem.
PMID 11879372·Epilepsia·2001
8-other
Lack of correlation of functional scintigraphy with (99m)technetium-methoxyisobutylisonitrile with histological necrosis following induction chemotherapy or measures of P-glycoprotein expression in high-grade osteosarcoma.
PMID 11595696·Clin Cancer Res·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
710 W 168TH STREET
NEW YORK, NY 10032

Location

Practice Location

710 W 168TH STREET, NEW YORK, NY
(212) 305-6876

Quick Facts

NPI
1972604700
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
57
Publications
20

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