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S A Robb

Showing results (21-30 of 39) with videos related to

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Neuromuscular Disorders : NMD|May 1, 1994
Infantile axonal neuropathy in two siblingsR M Quinlivan, S A Robb, S M Hall, et al.
Neuromuscular Disorders : NMD|August 1, 1996
Cardiac function, metabolism and perfusion in Duchenne and Becker muscular dystrophyR M Quinlivan, P Lewis, P Marsden, et al.
Human Immunology|September 1, 1985
Increased frequency of IgG heavy chain marker Glm(2) and of HLA-B8 in Lambert-Eaton myasthenic syndrome with and without associated lung carcinomaN Willcox, A G Demaine, J Newsom-Davis, et al.
Neuromuscular Disorders : NMD|January 23, 2009
Interfamilial phenotypic heterogeneity in SMARD1S Joseph, S A Robb, S Mohammed, et al.
Developmental Medicine and Child Neurology|April 1, 1990
Myelination patterns on magnetic resonance of children with developmental delayM G Harbord, J P Finn, M A Hall-Craggs, et al.
Neuromuscular Disorders : NMD|November 19, 2013
Outcome of children with acetylcholine receptor (AChR) antibody positive juvenile myasthenia gravis following thymectomyH S Heng, M Lim, M Absoud, et al.
QJM : Monthly Journal of the Association of Physicians|September 2, 2005
Analysis of an adult Duchenne muscular dystrophy populationA E Parker, S A Robb, J Chambers, et al.
Annals of Neurology|April 1, 1995
A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European familiesT T Warner, L D Williams, R W Walker, et al.
American Journal of Medical Genetics|September 15, 1992
Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndromeJ Clayton-Smith, T Webb, S A Robb, et al.
Human Immunology|May 1, 1988
C4 complement allotypes in juvenile dermatomyositisS A Robb, A H Fielder, C E Saunders, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Neuromuscular Disorders : NMD|May 1, 1994
Infantile axonal neuropathy in two siblingsR M Quinlivan, S A Robb, S M Hall, et al.
Neuromuscular Disorders : NMD|August 1, 1996
Cardiac function, metabolism and perfusion in Duchenne and Becker muscular dystrophyR M Quinlivan, P Lewis, P Marsden, et al.
Human Immunology|September 1, 1985
Increased frequency of IgG heavy chain marker Glm(2) and of HLA-B8 in Lambert-Eaton myasthenic syndrome with and without associated lung carcinomaN Willcox, A G Demaine, J Newsom-Davis, et al.
Neuromuscular Disorders : NMD|January 23, 2009
Interfamilial phenotypic heterogeneity in SMARD1S Joseph, S A Robb, S Mohammed, et al.
Developmental Medicine and Child Neurology|April 1, 1990
Myelination patterns on magnetic resonance of children with developmental delayM G Harbord, J P Finn, M A Hall-Craggs, et al.
Neuromuscular Disorders : NMD|November 19, 2013
Outcome of children with acetylcholine receptor (AChR) antibody positive juvenile myasthenia gravis following thymectomyH S Heng, M Lim, M Absoud, et al.
QJM : Monthly Journal of the Association of Physicians|September 2, 2005
Analysis of an adult Duchenne muscular dystrophy populationA E Parker, S A Robb, J Chambers, et al.
Annals of Neurology|April 1, 1995
A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European familiesT T Warner, L D Williams, R W Walker, et al.
American Journal of Medical Genetics|September 15, 1992
Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndromeJ Clayton-Smith, T Webb, S A Robb, et al.
Human Immunology|May 1, 1988
C4 complement allotypes in juvenile dermatomyositisS A Robb, A H Fielder, C E Saunders, et al.
Pageof 4