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DR. MARIZA DARAS M.D.
M.D.
Neurology Physician
NPI: 1811158264IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
149360(NC)
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
263783(NY)C164148(CA)0101278605(VA)
Education
COLUMBIA UNIVERSITY COLLEGE OF PHYSICIANS AND SURGEONS
Class of 2008
Research & Publications (20)
Characterization of a novel TYMP splice site mutation associated with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
PMID 19056268·Neuromuscul Disord·2009
5-case
Total hip arthroplasty in young patients with osteoarthritis.
PMID 19377644·Am J Orthop (Belle Mead NJ)·2009
6-review
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 18383590·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 18383593·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 18383595·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 18383597·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
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18380023·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 18383589·Hum Genet·2007
8-other
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
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
Placebos, placebo effect, and the response to the healing situation: the evolution of a concept.
PMID 11879377·Epilepsia·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
- 1001 E LEIGH ST
RICHMOND, VA 23298 - Phone
- (804) 828-9350
Quick Facts
- NPI
- 1811158264
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 4
- Locations
- 1
- Years in Practice
- 18
- Publications
- 20
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