Results 191 to 200 of about 14,641 (210)

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

Cell, 1995
Isabelle Richard, Mayana Zatz, Jay Arnold Tischfield   +2 more
exaly  

Clinical and Molecular Characterization of Patients With Limb-Girdle Muscular Dystrophy Type 2I

Archives of Neurology, 2005
Giovanna Cenacchi, Gabriele Siciliano, Corrado Angelini   +2 more
exaly  

Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A

Nature Medicine, 1999
Stephen Baghdiguian, Isabelle Richard, Adolfo López de Munain   +2 more
exaly  

DISTINCTION OF BECKER FROM LIMB-GIRDLE MUSCULAR DYSTROPHY BY MEANS OF DYSTROPHIN cDNA PROBES

Lancet, The, 1989
exaly  

A Gene for Autosomal Recessive Limb-Girdle Muscular Dystrophy in Manitoba Hutterites Maps to Chromosome Region 9q31-q33: Evidence for Another Limb-Girdle Muscular Dystrophy Locus

American Journal of Human Genetics, 1998
Tracey A Weiler
exaly  

Limb Girdle Muscular Dystrophies

2018
Samah K. Aburahma, Matthew P. Wicklund
openaire   +1 more source

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Nature Genetics, 1998
Isabel Illa, Corrado Angelini, Saeed Bohlega   +2 more
exaly  

Limb-Girdle Muscular Dystrophy in the United States

Journal of Neuropathology and Experimental Neurology, 2006
Daniel E Michele, Rita Barresi, Kevin P Campbell   +2 more
exaly  

Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients

Human Mutation, 2008
Francesca Magri, Maria Grazia D'Angelo, Alessandro Prelle   +2 more
exaly  

HYPERTROPHY OF EXTENSOR DIGITORUM BREVIS IN LIMB-GIRDLE MUSCULAR DYSTROPHY

Lancet, The, 1974
exaly