Raji Paul Grewal, M.D.
Practice | Publications
Publications:
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.
