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GARY VITA, MD
MD
Anesthesiology Physician
NPI: 1073699864IndividualAccepts Medicare
Education
HAHNEMANN UNIVERSITY COLLEGE OF MEDICINE
Class of 1990
Research & Publications (20)
New aspects on patients affected by dysferlin deficient muscular dystrophy.
PMID 19528035·J Neurol Neurosurg Psychiatry·2010
8-other
Immune-mediated rippling muscle disease with myasthenia gravis: a report of seven patients with long-term follow-up in two.
PMID 19208478·Neuromuscul Disord·2009
5-case
Reliability of the North Star Ambulatory Assessment in a multicentric setting.
PMID 19553120·Neuromuscul Disord·2009
3-trial
Sleep disorders in children with Attention-Deficit/Hyperactivity Disorder (ADHD) recorded overnight by video-polysomnography.
PMID 19527942·Sleep Med·2009
8-other
miR-21 and 221 upregulation and miR-181b downregulation in human grade II-IV astrocytic tumors.
PMID 19159078·J Neurooncol·2009
8-other
Development of Hashimoto's thyroiditis after subacute thyroiditis: an unusual patient.
PMID 19072672·Thyroid·2009
5-case
A patient with stress-related onset and exacerbations of Graves disease.
PMID 19029994·Nat Clin Pract Endocrinol Metab·2009
5-case
Psychosocial impact of presymptomatic genetic testing for transthyretin amyloidotic polyneuropathy.
PMID 19084401·Neuromuscul Disord·2009
8-other
Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A.
PMID 18346232·J Peripher Nerv Syst·2008
4-observational
Charcot-Marie-Tooth disease type 1B: marked phenotypic variation of the Ser78Leu mutation in five Italian families.
PMID 18422810·Acta Neurol Scand·2008
8-other
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study.
PMID 18612763·Neurol Sci·2008
4-observational
Charcot-Marie-Tooth type X: unusual phenotype of a novel CX32 mutation.
PMID 18717720·Eur J Neurol·2008
5-case
Nuclear factor-kappaB activation and differential expression of survivin and Bcl-2 in human grade 2-4 astrocytomas.
PMID 18327814·Cancer·2008
8-other
Natural history of CMT1A including QoL: a 2-year prospective study.
PMID 18242090·Neuromuscul Disord·2008
4-observational
Novel SHOX gene mutation in a short boy with Becker muscular dystrophy: double trouble in two adjacent genes.
PMID 18059093·Horm Res·2008
5-case
Charcot-Marie-Tooth and pain: correlations with neurophysiological, clinical, and disability findings.
PMID 18612771·Neurol Sci·2008
4-observational
Expression of transglutaminase 2 does not differentiate focal myositis from generalized inflammatory myopathies.
PMID 18005224·Acta Neurol Scand·2008
8-other
Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiency.
PMID 17651973·Neuromuscul Disord·2007
8-other
Evidence of cardiovascular autonomic impairment in mitochondrial disorders.
PMID 17987253·J Neurol·2007
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 7505 OSLER DR
TOWSON, MD 21204 - Phone
- (410) 337-5337
Quick Facts
- NPI
- 1073699864
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 2
- Years in Practice
- 36
- Publications
- 20
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