Publications in reverse chronological order (*denotes senior author) Jadeja K.J., Grewal R.P.* Familial Arachnoid Cysts Associated with Oculopharyngeal Muscular Dystrophy. (Accepted for publication in the Journal of Clinical Neuroscience, 2002). Grewal R.P., Achari M., Matsuura T., Durazo A., Tayag E., Zu L., Pulst S., Ashizawa T. Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10 (SCA10). (Accepted for publication in the Archives of Neurology, 2002). Zumo L., Grewal R.P.* Castleman's disease-associated neuropathy: no evidence of human herpesvirus type 8 infection. Journal of the Neurological Sciences, 195(1):47-50, 2002. Dhaliwal G.K., Grewal R.P.* Mitochondrial DNA deletion mutation levels are elevated in ALS brains. NeuroReport, 11(11):2507-9, 2000. Matsuura T., Yamagata T., Burgess D., Rasmussen A., Grewal R.P.*, Watase K., Khajavi M., McCall A., Davis C.F., Zu L., Achari M., Pulst S.M., Alonso E., Noebels J.L., Nelson D.L., Zoghbi H.Y., Ashizawa T. Large Expansion of ATTCT Pentanucleotide Repeat in Spinocerebellar Ataxia Type 10. Nature Genetics, 26(2):191-194, 2000. Zu L., Figueroa K.P., Grewal R.*, Pulst S. Mapping of New Autosomal Dominant Spinocerebellar ataxia (SCA10) to chromosome 22. American Journal Human Genetics 64(2):594-599, 1999. Grewal R.P. Neurodegeneration in Xeroderma Pigmentosum: A Study of Trinucleotide Repeat Mutation Analysis. Journal of the Neurological Sciences 163:183-186, 1999. Grewal R.P., Morgan T.M., Finch C.E. C1qb and Clusterin mRNA Increase in Association with Neurodegeneration in Sporadic ALS. Neuroscience Letters 13;271(1):65-67, 1999. Grewal R.P., Cancel G., Leeflang E.P., Durr A., McPeek Mary-Sara, Draghinas D., Yao X., Stevanin G., Alnot Marie-Odile, Brice A., Arnheim N. French Machado-Joseph Disease patients do not exhibit gametic segregation distortion: A Sperm Typing Analysis. Human Molecular Genetics, 8(9):1779-1784, 1999. Grewal R.P., Karkera J.P., Grewal R.K., Detera-Wadleigh S.D. Mutation Analysis of Oculopharyngeal Muscular Dystrophy (OPMD) in Hispanic American Families. Archives of Neurology;56:1378-1381, 1999. Urschel J.D., Grewal R.P.* Thymectomy and Myasthenia Gravis. The Postgraduate Medical Journal 74: 139-144, 1998. Grewal R.P., Cantor R., Turner G., Grewal R.K., Detera-Wadleigh S.D. Genetic Mapping and Haplotype Analysis of Oculopharyngeal Muscular Dystrophy. NeuroReport 9(6): 961-965, 1998. Grewal R.P., Tayag E., Figueroa K.P., Zu L., Durazo A., Nunez C., Pulst S.M. Clinical and Genetic Analysis of a Distinct Autosomal Dominant Spinocerebellar Ataxia. Neurology 51:1423-1426, 1998. Grewal R.P., Leeflang E., Zhang L., Arnheim N.A. The Mutation Properties of Spinal and Bulbar Muscular Atrophy Alleles. Neurogenetics 1:249-252, 1998. Yoshikawa T., Sanders A.R., Overhauser J., Garnes J.A., Grewal R.*, Detera-Wadleigh S.D. Isolation of Chromosome 18-Specific Brain Transcripts as Positional Candidates for Bipolar Disorder. American Journal of Medical Genetics 74: 140-149, 1997. Grewal R.P., Yoshida T., Finch C.E., Morgan T.E.M. Scavenger Receptor mRNAs in Rat Brain Microglia are Induced by Kainic Acid Lesioning and by Cytokines. NeuroReport 8(5): 1077-1081, 1997. Grewal R.P. Brainstem Glioma Presenting with Hyperthermia, Parkinsonism and Obstructive Hydrocephalus. European Journal of Neurology 4(4): 431-432, 1997. Grewal R.P., Yu K.T., Barton N.W., Parker R.I., DiBisceglie A.M. Liver Biopsies in Patients with Lysosomal Storage Disease: Experience with Effective Sedation. Indian Journal of Pediatrics 64: 887-891, 1997. Grewal R.P. Visual Agnosia. Neuropsychiatry, Neuropsychology, and Behavioral Neurology 10(1):64-65, 1997. Trojaborg W., Grewal R.*, Weimer L., Sheriff P. Value of Latency Measurements to the Small Palm Muscles Compared to other Conduction Parameters in the Carpal Tunnel Syndrome. Muscle and Nerve 19:243-245, 1996. Grewal R.P. Awareness of Time in Dementia of the Alzheimer Type. Psychological Reports 76:717-718, 1995. Hameed S.M., Grewal R.P.*, Urschel J.D. Somatization Tendencies in Surgically Treated Neurogenic Thoracic Outlet Syndrome Patients. Vascular Surgery 29(3):185-188, 1995. Urschel J.D., Grewal R.P.* Somatoform Disorders in Nonspecific Thoracic Outlet Syndrome Patients. Acta Neurologica Scandinavica 92(4):349, 1995. Urschel J.D., Grewal R.P.* Congenital Cervical Bands in Thoracic Outlet Syndrome. The American Journal of Surgery 170:524, 1995. Grewal R.P. Stroke in Fabry's Disease. Journal of Neurology 241: 153-156, 1994. Detera-Wadleigh S.D., Hsieh W.T., Berrittini W., Goldin L., Rollins D.Y., Muniec D., Grewal R.P.*, Guroff J.J., Turner G., Coffman D., Barrick J., Mills K., Murray J., Donohue S.J., Klein D.C., Saunders J., Nurnberger J.I. and Gershon E. Genetic Linkage Mapping for a Susceptibility Locus to Bipolar Illness: Chromosomes 2,3,4,7,9,10p,11p,22 and Xpter. American Journal of Medical Genetics 54:206-218, 1994. Grewal R.P. Self-Recognition in Dementia of the Alzheimer Type. Perceptual and Motor Skills 79:1009-1010, 1994. Urschel J.D., Hameed S.M., Grewal R.P.* Neurogenic Thoracic Outlet Syndrome. The Postgraduate Medical Journal 70:785-789, 1994. Grewal R.P., Urschel J.D. Why Women Want Children: A Study During Phases of Parenthood. Journal of Social Psychology, 134(4): 453-455, 1994. Grewal R.P. Psychiatric Manifestations in Fabry's Disease. International Journal of Psychiatry in Medicine 23;3: 307-312, 1993. Patterson M.C., DiBisceglie A.M., Higgins J.J., Abel R.B., Shiffman R., Parker C., Argoff C., Grewal R.P.*, Yu K., Pentchev P.G., Brady R.O., Barton N.W. The effect of cholesterol-lowering agents on hepatic and plasma cholesterol in Niemann-Pick disease, Type C. Neurology 43: 61-64, 1993. Grewal R.P. An Atypical Case of Meningococcaemia. Journal of Infection 27;3: 344-345, 1993. Sobey A., Grewal R.P.*, Hutchison K.J., Urschel J.D. Investigation of Nonspecific Neurogenic Thoracic Outlet Syndrome. Journal of Cardiovascular Surgery 34;4: 343-345, 1993. Grewal R.P. Apathetic Hyperthyroidism in an Adolescent. Journal of Psychiatry and Neuroscience 18;5: 273, 1993. Grewal R.P. Death Awareness and Brain Disease. Omega 26(3):175-179, 1992-93. Grewal R.P., McLatchy S. Cerebrovascular Manifestations in a Female Carrier of Fabry's disease. Acta Neurologica Belgica 92: 36-40, 1992. Parker R.I., Grewal R.P.*, McKeown L.P., Barton N.W. The Effect of Platelet Count on the DDAVP-Induced Shortening of the Bleeding Time in Thrombocytopenic Gaucher's Patients. The American Journal of Pediatric Hematology/Oncology 14(1): 39-43, 1992. Grewal R.P., Martinez M.M., Hoehe M., Bonner T.I., Gershon E., Detera-Wadleigh S. Genetic linkage mapping of the m4 human muscarinic receptor. Genomics 13: 239-240, 1992. Grewal R.P., Barton N.W. Fabry's Disease Presenting with Stroke. Clinical Neurology and Neurosurgery 94: 177-179, 1992. Grewal R.P. Neurons and DNA repair: Neurologic involvement in Xeroderma Pigmentosa. Medical Hypothesis 34: 171-173, 1991. Barton N.W., Brady R.O., Dambrosia J.M., DiBisceglie A.M., Doppelt S.H., Hill S.C., Mankin H.J., Murray G.J., Parker R.I., Argoff C.E., Grewal R.P.*, Yu K.T. and Collaborators. Replacement Therapy for Inherited Enzyme Deficiency: Effectiveness of Macrophage-Targeted Glucocerebrosidase in Gaucher Disease. New England Journal of Medicine 324: 1464-70, 1991. Grewal R.P., Miller B.L. Cocaine induced hypertensive encephalopathy. Acta Neurologica 13(3): 279-281, 1991. Grewal R.P., Petronas N., Barton N.W. Late onset globoid cell leukodystrophy. Journal of Neurology, Neurosurgery and Psychiatry 54;11: 1011-1012, 1991. Barton N.W., Brady R.O., Murray G.J., Argoff C.E., Grewal R.P.*, Yu K.T., Dambrosia J.M., DiBisceglie A.M., Hill S.C., Parker R.I., Doppelt S.H., Mankin H.J. Enzyme replacement therapy for Gaucher Disease. New England Journal of Medicine 325;25:1811, 1991. Grewal R.P., Doppelt S.H., Katz D., Thompson M.A., Barton N.W. Neurological Complications of Non-Neuronopathic Gaucher's Disease. Archives of Neurology 48;12: 1271-1272, 1991. Grewal R.P., Goldberg M.A. Stroke in Protein C Deficiency. The American Journal of Medicine 89: 538-539, 1990. Grewal R.P. Trigeminal sensory neuropathy and migraine: loss of headache with retention of aura. The Italian Journal of Neurological Science 11: 509, 1990. Grewal R.P., Miller B.L., Mena I., Boone K., Garrett K., Mody C., Chiang F., Hill E. Associative Visual Agnosia Secondary to an Arteriovenous Malformation. Behavioural Neurology 2: 135-142, 1989. Grewal R.P., Mody C., McIntyre H., Daly J. Mixed apnea as a Long-Term Complication of Lateral Medullary Syndrome. Bulletin of Clinical Neurosciences 53: 148-152, 1988.