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I Mahjneh

Showing results (11-20 of 18) with videos related to

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Acta Neurologica Scandinavica|July 10, 2004
Muscle magnetic resonance imaging shows distinct diagnostic patterns in Welander and tibial muscular dystrophyI Mahjneh, A E Lamminen, B Udd, et al.
Human Genetics|May 12, 2005
Localisation of merosin-positive congenital muscular dystrophy to chromosome 4p16.3G S Sellick, C Longman, M Brockington, et al.
Neuromuscular Disorders : NMD|December 1, 1996
The phenotype of chromosome 2p-linked limb-girdle muscular dystrophyI Mahjneh, M R Passos-Bueno, M Zatz, et al.
Neuropediatrics|May 1, 1999
Merosin-positive congenital muscular dystrophy: a large inbred familyI Mahjneh, K Bushby, L Anderson, et al.
Neuromuscular Disorders : NMD|December 1, 1996
The molecular biology of LGMD2B--towards the identification of the LGMD gene on chromosome 2p13K Bushby, R Bashir, S Keers, et al.
Human Molecular Genetics|April 10, 1999
Dysferlin is a plasma membrane protein and is expressed early in human developmentL V Anderson, K Davison, J A Moss, et al.
Nature Genetics|September 10, 1998
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2BR Bashir, S Britton, T Strachan, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)L V Anderson, R M Harrison, R Pogue, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Acta Neurologica Scandinavica|July 10, 2004
Muscle magnetic resonance imaging shows distinct diagnostic patterns in Welander and tibial muscular dystrophyI Mahjneh, A E Lamminen, B Udd, et al.
Human Genetics|May 12, 2005
Localisation of merosin-positive congenital muscular dystrophy to chromosome 4p16.3G S Sellick, C Longman, M Brockington, et al.
Neuromuscular Disorders : NMD|December 1, 1996
The phenotype of chromosome 2p-linked limb-girdle muscular dystrophyI Mahjneh, M R Passos-Bueno, M Zatz, et al.
Neuropediatrics|May 1, 1999
Merosin-positive congenital muscular dystrophy: a large inbred familyI Mahjneh, K Bushby, L Anderson, et al.
Neuromuscular Disorders : NMD|December 1, 1996
The molecular biology of LGMD2B--towards the identification of the LGMD gene on chromosome 2p13K Bushby, R Bashir, S Keers, et al.
Human Molecular Genetics|April 10, 1999
Dysferlin is a plasma membrane protein and is expressed early in human developmentL V Anderson, K Davison, J A Moss, et al.
Nature Genetics|September 10, 1998
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2BR Bashir, S Britton, T Strachan, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)L V Anderson, R M Harrison, R Pogue, et al.
Pageof 2