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L V Anderson

Showing results (11-20 of 45) with videos related to

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Neurology|March 14, 2001
Normal calpain expression in genetically confirmed limb-girdle muscular dystrophy type 2AB Talim, A Ognibene, E Mattioli, et al.
Neuromuscular Disorders : NMD|April 12, 2001
The phenotype of calpainopathy: diagnosis based on a multidisciplinary approachC Pollitt, L V Anderson, R Pogue, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutationsI Mahjneh, G Marconi, K Bushby, et al.
Neuromuscular Disorders : NMD|June 6, 2000
Calpain3 expression during human cardiogenesisF Fougerousse, L V Anderson, A L Delezoide, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrieversN J Olby, N J Sharp, L V Anderson, et al.
Developmental Medicine and Child Neurology|March 1, 1995
Deletion status and intellectual impairment in Duchenne muscular dystrophyK M Bushby, R Appleton, L V Anderson, et al.
Muscle & Nerve|June 8, 2000
Partial alpha-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D familyM Vainzof, E S Moreira, M Canovas, et al.
Molecular and Cellular Neurosciences|May 30, 1998
Utrophin mRNA expression in muscle is not restricted to the neuromuscular junctionR Vater, C Young, L V Anderson, et al.
The Journal of Biological Chemistry|March 13, 1999
Characterization of the transmembrane molecular architecture of the dystroglycan complex in schwann cellsF Saito, T Masaki, K Kamakura, et al.
American Journal of Medical Genetics|April 15, 2000
Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammationE M McNally, C T Ly, H Rosenmann, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Neurology|March 14, 2001
Normal calpain expression in genetically confirmed limb-girdle muscular dystrophy type 2AB Talim, A Ognibene, E Mattioli, et al.
Neuromuscular Disorders : NMD|April 12, 2001
The phenotype of calpainopathy: diagnosis based on a multidisciplinary approachC Pollitt, L V Anderson, R Pogue, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutationsI Mahjneh, G Marconi, K Bushby, et al.
Neuromuscular Disorders : NMD|June 6, 2000
Calpain3 expression during human cardiogenesisF Fougerousse, L V Anderson, A L Delezoide, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrieversN J Olby, N J Sharp, L V Anderson, et al.
Developmental Medicine and Child Neurology|March 1, 1995
Deletion status and intellectual impairment in Duchenne muscular dystrophyK M Bushby, R Appleton, L V Anderson, et al.
Muscle & Nerve|June 8, 2000
Partial alpha-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D familyM Vainzof, E S Moreira, M Canovas, et al.
Molecular and Cellular Neurosciences|May 30, 1998
Utrophin mRNA expression in muscle is not restricted to the neuromuscular junctionR Vater, C Young, L V Anderson, et al.
The Journal of Biological Chemistry|March 13, 1999
Characterization of the transmembrane molecular architecture of the dystroglycan complex in schwann cellsF Saito, T Masaki, K Kamakura, et al.
American Journal of Medical Genetics|April 15, 2000
Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammationE M McNally, C T Ly, H Rosenmann, et al.
Pageof 5