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R W Orrell

Showing results (31-40 of 52) with videos related to

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Neurology|November 26, 2003
Compound heterozygous PANK2 mutations confirm HARP and Hallervorden-Spatz syndromes are allelicH Houlden, S Lincoln, M Farrer, et al.
Muscle & Nerve|December 8, 1998
Spontaneous abdominal hematoma in dermatomyositisR W Orrell, H M Johnston, C Gibson, et al.
European Journal of Neurology|November 29, 2013
A novel mutation of SOD-1 (Gly 108 Val) in familial amyotrophic lateral sclerosisR W Orrell, J J Habgood, D I Shepherd, et al.
Annals of Neurology|June 1, 1996
Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosisR W Orrell, J Habgood, P Rudge, et al.
Neuromuscular Disorders : NMD|November 27, 2004
A case of severe congenital chronic inflammatory demyelinating polyneuropathy with complete spontaneous remissionA Majumdar, L Hartley, A Y Manzur, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|January 29, 2005
Effects of resistance training on myosin function studied by the in vitro motility assay in young and older menM Canepari, R Rossi, M A Pellegrino, et al.
Neurology|June 17, 1999
Definitive molecular diagnosis of facioscapulohumeral dystrophyR W Orrell, R Tawil, J Forrester, et al.
Annals of Neurology|July 1, 1995
Oculomotor function in amyotrophic lateral sclerosis: evidence for frontal impairmentS Shaunak, R W Orrell, E O'Sullivan, et al.
Journal of the Neurological Sciences|December 14, 1999
Clinical characteristics of SOD1 gene mutations in UK families with ALSR W Orrell, J J Habgood, A Malaspina, et al.
Clinical Neurology and Neurosurgery|May 1, 1995
Myopathy in acquired partial lipodystrophyR W Orrell, R C Peatfield, C E Collins, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Neurology|November 26, 2003
Compound heterozygous PANK2 mutations confirm HARP and Hallervorden-Spatz syndromes are allelicH Houlden, S Lincoln, M Farrer, et al.
Muscle & Nerve|December 8, 1998
Spontaneous abdominal hematoma in dermatomyositisR W Orrell, H M Johnston, C Gibson, et al.
European Journal of Neurology|November 29, 2013
A novel mutation of SOD-1 (Gly 108 Val) in familial amyotrophic lateral sclerosisR W Orrell, J J Habgood, D I Shepherd, et al.
Annals of Neurology|June 1, 1996
Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosisR W Orrell, J Habgood, P Rudge, et al.
Neuromuscular Disorders : NMD|November 27, 2004
A case of severe congenital chronic inflammatory demyelinating polyneuropathy with complete spontaneous remissionA Majumdar, L Hartley, A Y Manzur, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|January 29, 2005
Effects of resistance training on myosin function studied by the in vitro motility assay in young and older menM Canepari, R Rossi, M A Pellegrino, et al.
Neurology|June 17, 1999
Definitive molecular diagnosis of facioscapulohumeral dystrophyR W Orrell, R Tawil, J Forrester, et al.
Annals of Neurology|July 1, 1995
Oculomotor function in amyotrophic lateral sclerosis: evidence for frontal impairmentS Shaunak, R W Orrell, E O'Sullivan, et al.
Journal of the Neurological Sciences|December 14, 1999
Clinical characteristics of SOD1 gene mutations in UK families with ALSR W Orrell, J J Habgood, A Malaspina, et al.
Clinical Neurology and Neurosurgery|May 1, 1995
Myopathy in acquired partial lipodystrophyR W Orrell, R C Peatfield, C E Collins, et al.
Pageof 6