Results 241 to 250 of about 48,457 (271)

Anti-HMGCR myopathy overlaps with dermatomyositis-like rash: a distinct subtype of idiopathic inflammatory myopathy

Journal of Neurology, 2021
Ying Hou, K. Shao, Yaping Yan, T. Dai, Wei Li, Yuying Zhao, Duoling Li, Jian-Qiang Lu, G. Norman, Chuanzhu Yan   +9 more
semanticscholar   +1 more source

Study of the correlation between the noncanonical pathway of pyroptosis and idiopathic inflammatory myopathy.

International Immunopharmacology, 2021
Miao Ma, K. Chai, Rui Deng
semanticscholar   +1 more source

The significance of myositis autoantibodies in idiopathic inflammatory myopathy concomitant with interstitial lung disease

Neurological Sciences, 2020
Hung-Ling Huang, Wen-Chih Lin, Po-Yu Lin, M. Weng, Yuan-Ting Sun   +4 more
semanticscholar   +1 more source

Immune-mediated necrotizing myopathy: clinical features and pathogenesis

Nature Reviews Rheumatology, 2020
Yves Allenbach, Olivier Benveniste, Werner Stenzel   +2 more
exaly  

Idiopathic inflammatory myopathy.

Medicina clínica (Ed. impresa)
A. Selva-O’Callaghan, E. Trallero-Araguás, A. Gil-Vila   +2 more
semanticscholar   +1 more source

Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease

Nature Genetics, 2019
Hiroyuki Ishiura, Jun Yoshimura, Yuta Suzuki   +2 more
exaly  

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

Nature Genetics, 2004
Margaret J Kovach, Michael P Whyte, Virginia E Kimonis   +2 more
exaly  

Mutations in dynamin 2 cause dominant centronuclear myopathy

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

Mortality in idiopathic inflammatory myopathy: results from a Swedish nationwide population-based cohort study

Annals of the Rheumatic Diseases, 2017
Gerd Cecilie Dobloug, J. Svensson, I. Lundberg, M. Holmqvist   +3 more
semanticscholar   +1 more source

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