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Raji Grewal

Research Profile

Concepts & Ideas

Disorders

Genes & Molecular Sequences

Physiology

Chemicals & Drugs

Repetitive Sequences, Nucleic Acid

Procedures

Anatomy

Chromosomes, Human, Pair 22

Living Beings

Homozygote

Co-author Network

Publications

TOP 3
Danijela Levacic; David Nochlin; Leema Reddy Peddareddygari; Leroy R Sharer; Raji P Grewal
Inclusion-body myositis associated with Alzheimer's disease.
Sushanth Bhat; Raji P Grewal; Howard W Sander; Sudhansu Chokroverty
Sleep disordered breathing and other sleep dysfunction in myotonic dystrophy type 2.
Leema Reddy Peddareddygari; Victoria Surgan; Raji P Grewal
Limb-girdle muscular dystrophy type 2A resulting from homozygous G2338C transversion mutation in the calpain-3 gene.

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All Publications

2013: Danijela Levacic; David Nochlin; Leema Reddy Peddareddygari; Leroy R Sharer; Raji P Grewal
Inclusion-body myositis associated with Alzheimer's disease.
Case reports in medicine 2013;2013():536231.
2012: Sushanth Bhat; Raji P Grewal; Howard W Sander; Sudhansu Chokroverty
Sleep disordered breathing and other sleep dysfunction in myotonic dystrophy type 2.
Sleep medicine 2012;13(9):1207-8.
2010: Leema Reddy Peddareddygari; Victoria Surgan; Raji P Grewal
Limb-girdle muscular dystrophy type 2A resulting from homozygous G2338C transversion mutation in the calpain-3 gene.
Journal of clinical neuromuscular disease 2010;12(2):62-5.
2010: Liudmila Lysenko; Raji P Grewal; Wei Ma; Leema Reddy Peddareddygari
Homozygous Machado Joseph Disease: a case report and review of literature.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2010;37(4):521-3.
2010: Souvik Sen; P Leema Reddy; Raji P Grewal; Marjorie Busby; Patricia Chang; Alan Hinderliter
Hyperhomocysteinemia is Associated with Aortic Atheroma Progression in Stroke/TIA Patients.
Frontiers in neurology 2010;1():131.
2010: Olukayode Onasanya; David Nochlin; Victor Casas; Leema Reddy Peddareddygari; Raji P Grewal
Kikuchi-fujimoto disease associated with myasthenia gravis: a case report.
Case reports in medicine 2010;2010():.
2009: P Leema Reddy; Raji P Grewal
Resolution of muscle cramps and fasciculations with treatment of sleep apnea.
Journal of clinical neuromuscular disease 2009;11(1):66-7.
2009: Leema Reddy Peddareddygari; Ana Virginia Dutra; Mark A Levenstien; Souvik Sen; Raji P Grewal
An analysis of methylenetetrahydrofolate reductase and glutathione S-transferase omega-1 genes as modifiers of the cerebral response to ischemia.
BMC neurology 2009;9():37.
2008: Archana Hinduja; Sudhanshu Chokroverty; Philip Hanna; Raji P Grewal
Dystonia with superimposed myasthenia gravis: An experiment in nature.
Movement disorders : official journal of the Movement Disorder Society 2008;23(11):1626-7.
2008: Catarina M Quinzii; Tuan H Vu; K Christopher Min; Kurenai Tanji; Sandra Barral; Raji P Grewal; Andrea Kattah; Pilir Camaño; David Otaegui; Teruhito Kunimatsu; David M Blake; Kirk Wilhelmsen; Lewis P Rowland; Arthur P Hays; Eduardo Bonilla; Michio Hirano
X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1.
American journal of human genetics 2008;82(1):208-13.
2007: P Leema Reddy; William K Seltzer; Raji P Grewal
Possible anticipation in hereditary spastic paraplegia type 4 (SPG4).
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2007;34(2):208-10.
2007: P Leema Reddy; Raji P Grewal
Friedreich's ataxia: a clinical and genetic analysis.
Clinical neurology and neurosurgery 2007;109(2):200-2.
2007: Raji P Grewal; Ana Virginia Dutra; Yi C Liao; Suh-Hang Hank Juo; Nikolaos I.H. Papamitsakis
The intron 4c allele of the NOS3 gene is associated with ischemic stroke in African Americans.
BMC medical genetics 2007;8():76.
2006: Subramanian Hariharan; John E Donahue; Cecial Garre; Paola Origone; Raji P Grewal
Clinicopathologic and genetic analysis of siblings with NF1 and adult-onset gliomas.
Journal of the neurological sciences 2006;247(1):105-8.
2006: Ana Virginia Dutra; Hsiu-Fen Lin; Suh-Hang Hank Juo; Melanie Boyadjis; Michael Moussouttas; P Leema Reddy; Raji P Grewal
Analysis of the endothelial nitric oxide synthase gene as a modifier of the cerebral response to ischemia.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2006;15(3):128-31.
2006: Michael Moussouttas; Abuhuziefa Abubakr; Raji P Grewal; Nikolaos I.H. Papamitsakis
Eclamptic subarachnoid haemorrhage without hypertension.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2006;13(4):474-6.
2006: Ana Virginia Dutra; Hsiu-Fen Lin; Suh-Hang Hank Juo; Harvey W Mohrenweiser; Souvik Sen; Raji P Grewal
Analysis of the XRCC1 gene as a modifier of the cerebral response in ischemic stroke.
BMC medical genetics 2006;7():78.
2004: Raji P Grewal; Shanxiang Zhang; Wei Ma; Michael Rosenberg; Ralf Krahe
Clinical and genetic analysis of a family with PROMM.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2004;11(6):603-5.
2004: Tohru Matsuura; Ping Fang; Xi Lin; Mehrdad Khajavi; Kuniko Tsuji; Astrid Rasmussen; Raji P Grewal; Madhureeta Achari; Maria E Alonso; Stef pulst; Huda Y Zoghbi; David L Nelson; Benjamin B Roa; Tetsuo Ashizawa
Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10.
American journal of human genetics 2004;74(6):1216-24.
2003: R Kakar; W Ma; Ana Virginia Dutra; W K Seltzer; Raji P Grewal
Clinical and genetic analysis of CMT1B in a Nigerian family.
Muscle & nerve 2003;27(5):628-30.
2003: K J Jadeja; Raji P Grewal
Familial arachnoid cysts associated with oculopharyngeal muscular dystrophy.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2003;10(1):125-7.
2003: Raji P Grewal
Severe amnesia following a unilateral temporal lobe stroke.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2003;10(1):102-4.
2002: W Ma; M Farrukh Nizam; Raji P Grewal
X-linked Charcot-Marie-Tooth disease caused by a novel point mutation in the connexin-32 gene.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2002;23(4):195-7.
2002: Raji P Grewal; Madhureeta Achari; Tohru Matsuura; Alberto Durazo; Emilio Tayag; Lan Zu; Stef pulst; Tetsuo Ashizawa
Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10.
Archives of neurology 2002;59(8):1285-90.
2002: L Zumo; Raji P Grewal
Castleman's disease-associated neuropathy: no evidence of human herpesvirus type 8 infection.
Journal of the neurological sciences 2002;195(1):47-50.
2000: Tohru Matsuura; T Yamagata; Daniel L Burgess; A Rasmussen; Raji P Grewal; Kei Watase; Mehrdad Khajavi; AE McCall; Caleb F Davis; Lan Zu; Madhureeta Achari; Stef pulst; E Alonso; Jeffrey L Noebels; David L Nelson; Huda Y Zoghbi; Tetsuo Ashizawa
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.
Nature genetics 2000;26(2):191-4.
1999: Lan Zu; Karla P Figueroa; Raji P Grewal; Stef pulst
Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22.
American journal of human genetics 1999;64(2):594-9.
1998: Raji P Grewal; E Tayag; Karla P Figueroa; Lan Zu; A Durazo; C Nunez; Stef pulst
Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxia.
Neurology 1998;51(5):1423-6.