Results 331 to 340 of about 183,642 (350)

Mutations in dynamin 2 cause dominant centronuclear myopathy

Nature Genetics, 2005
Marc Bitoun, Jocelyn Laporte, Hanns Lochmüller   +2 more
exaly  

Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy

Nature Genetics, 2007
Anne-Sophie Nicot, Anne Toussaint, Erik Iwarsson   +2 more
exaly  

Critical illness polyneuropathy and myopathy: a major cause of muscle weakness and paralysis

Lancet Neurology, The, 2011
Nicola Latronico
exaly  

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

Nature Genetics, 2001
Hagit Hochner, Tsviya Olender, Mark Barash   +2 more
exaly  

Steroid myopathy

Journal of Allergy and Clinical Immunology, 1985
openaire   +2 more sources

Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy

Nature Genetics, 2005
Jan Senderek, Nicole I Wolf, Kathryn N North   +2 more
exaly  

A Comprehensive Overview on Myositis-Specific Antibodies: New and Old Biomarkers in Idiopathic Inflammatory Myopathy

Clinical Reviews in Allergy and Immunology, 2015
Minoru Satoh, Angela Ceribelli, S John Calise   +2 more
exaly  

Myotubular myopathy

Journal of the Neurological Sciences, 1969
B, Badurska, A, Fidziańska, Z, Kamieniecka, J, Prot, H, Strugalska   +4 more
openaire   +2 more sources

Autoantibodies against 3-hydroxy-3-methylglutaryl-coenzyme A reductase in patients with statin-associated autoimmune myopathy

Arthritis and Rheumatism, 2011
Tae Chung, Lisa Christopher-Stine
exaly  

Emetine myopathy

Neurology, 1970
D D, Duane, A G, Engel
openaire   +3 more sources