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Raji Paul Grewal, M.D.
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 Peer Reviewed Journal Articles from 2006/2007:
1. Moussouttas M., Abubakr A., Grewal R. P., Papmitsakis, N. Eclamptic Subarachnoid Hemorrahage with Hypertension. Journal of Clinical Neuroscience 13: 474-476, 2006.
2. Grewal R. P., Landolfi J., Kumar S. Anti-Hu Associated Paraneoplastic Cerebellar Degeneration and Gastric Adenocarcinoma. Journal of Neurological Sciences 12; (1)8: 43-45, 2006.
3. Dutra A.V., Lin H.F., Juo S.H.H., Boyadis M., Moussouttas M., Reddy P.I., Grewal R. P., * Analysis of the Endothelial Nitric Oxide Synthasc Gene as a Modifier of the Cerebral Response to Ischemia. Journal of Stroke and Cerebrovascular Diseases 15; (3): 128-13, 2006.
4. Hariharan S., Donahue J., Garre C., Orgone P., Grewal R. P., * Clinicopathologic and genetic analysis of siblings with NF1 and adult onset gliomas. Journal of the Neurological Sciences 247; (1): 105-108, 2006.
5. Reddy P.L., Grewal R. P., * Hereditary spastic paraplegia 4 associated with polyneuropathy. Journal of Clinical Neuromuscular Disease 8; (2): 99-100, 2006.
6. Dutra A. V. C., Lin H.F., Juo S.II. H., Mohrenweiser II., Sen S., Grewal R. P., * Analysis of the XRCC1 gene as a modifier of the cerebral response in ischemic strok. BMC Med Geneet Nov 6; 7(1): 78 2006 [Epub ahead of print].
7. Reddy P. L., Gizzi M.S., Dutra A. V. C., Abubakr A., Grewal R. P. * Autosomal dominant benign paroxysmal positional vertigo. Journal of New Jersey Neuroscience Institute June 2:(1): 10-14, 2007.
8. Grewal R.P. Axonal Neuropathy cause by Epothilone B. Neurol India Apr-Jun; 55 (2); 178l-9, 2007.
9. Reddy P.L., Seltzer W. K., Grewal R. P., * Possible anticipation in hereditary spastic paraparesis type 4 (SPG4). Canadian Journal of Neurological Sciences 34 (2); 208-210, 2007.
10. Reddy P.L., Grewal R. P., * Friedreich's ataxia: A clinical and genetic analysis. Clinical Neurol Neurosurg Feb; 109(2): 200-2 {epub 2006 Oct 17}, 2007.
11. Mehta D., Macri E., Hanna P., Steineke T., Grewal R. P. * Cervical lipoma causing Myelopathy. Journal of the New Jersey Neuroscience Institute June 2; (1): 2, 2007.
12. Quinzii C. M., Vu T., Min T. M., Tanji K., Barral S., Grewal R. P., Kattah A., Camano P., Otaegui D., Blake D. M., Wihelmsen K. C., Rowland L., P., Hays A. P., Bonilla E., Iiirano M., X-linked dominant scapuloperoncal myopathy is due to a mutation in the gene encoding four and a half LIM protein 1 (FHL1) (Accepted for Publication in American Journal of Human Genetices, 2007).

