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Research
Area of Specialty: Neuromuscular Neurology, Neurogenetics
Professional Appointments: Attending Physician, New Jersey Neuroscience Institute at JFK Medical Center, Edison, New Jersey.
Academic Appointments: Associate Professor of Neuroscience, Seton Hall University's School of Graduate Medical Education, South Orange, New Jersey.
Graduate Medical Education: Fellowship in Electromyography, the Neurological Institute of New York, Department of Neurology, Columbia University, New York, New York, 1993-1994; Visiting Staff Associate, Developmental and Metabolic Neurology Branch, NINDS and Clinical Neurogenetics Branch, NIMH, National Institutes of Health, Bethesday, Maryland, 1990-1991; Visiting Staff Associate, Developmental and Metabolic Neurology Branch, NINDS, National Institutes of Health, Bethesda, Maryland, 1989-1990; Chief Resident, Department of Neurology, Harbor-UCLA Medical Center, UCLA School of Medicine, Torrance, California, 1988-1989; Residency in Neurology, Harbor-UCLA Medical Center, UCLA School of Medicine, Torrance, California, 1986-1988; Alberta Heritage Foundation Scholar in Department Biochemistry, Faculty of Medicine, University of Alberta, Edmonton, Canada, 1985-1986; Resident in Internal Medicine, Department of Medicine, University of Alberta, Edmonton, Canada, 1984-1985; Rotating internship at Memorial University of Newfoundland, Newfoundland, Canada, 1982-1983.
Medical School: Faculty of Medicine, University of Alberta, Edmonton, Alberta, Canada.
Certification: Diplomate of the American Board of Psychiatry and Neurology; National Board of Medical Examiners; and Licentiate of Medical Council of Canada.
Representatiave Publications:
Quinzii CM, Vu TH, Min KC, Tanji K, Barral S, Grewal RP, Kattah A, Camaņo P, Otaegui D, Kunimatsu T, Blake DM, Wilhelmsen KC, Rowland LP, Hays AP, Bonilla E, Hirano M. X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1. Am J Hum Genet. 2008 Jan;82(1):208-13.
Peddareddygari LR, Dutra AV, Levenstien MA, Sen S, Grewal RP. An analysis of Methylenetetrahydrofolate reductase and Glutathione S-transferase omega-1 genes as modifiers of the cerebral response to ischemia. BMC Neurol. 2009 Jul 22;9(1):37
Reddy, P.L and Grewal, R.P. Effect of Methyltetrahydrofolate reductase (MTHFR) C677T and Glutathione S-transferase omega-1 (GSTO-1) C419A polymorphisms on cerebral response to ischemia. The American Journal of Human Genetics, Abstracts Supplement, 2008.
Reddy, P.L. and Grewal, R.P.* The G1138A mutation rate in the fibroblast growth factor receptor 3 gene is increased in cells carrying the t (4; 14) translocation. Genetics and Molecular Research, 2009
Lysenko, L., Grewal, P., and Rosenberg, M. Rhabdomyolysis: A rare life threatening side effect of statin medication. Poster Presentation at Seton Hall University, June 2008.
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