Results 101 to 110 of about 31,110 (115)

Camptocormia as presenting sign in myofibrillar myopathy

Neuromuscular Disorders, 2012
Bjarne Udd, Dimitri Renard, Giovanni Castelnovo   +2 more
exaly  

BAG3 myofibrillar myopathy presenting with cardiomyopathy

Neuromuscular Disorders, 2015
Chamindra Laverty, Gunter Scharer, Michael Collins   +2 more
exaly  

A family with adult-onset myofibrillar myopathy with BAG3 mutation (P470S) presenting with axonal polyneuropathy

Neuromuscular Disorders, 2020
Tomoko Komagamine, Norito Kokubun, Ichizo Nishino   +2 more
exaly  

Severe congenital actin related myopathy with myofibrillar myopathy features

Neuromuscular Disorders, 2015
Duygu Selcen
exaly  

A novel dominant D109A mutation in a family with myofibrillar myopathy affects αB-crystallin structure

BBA Clinical, 2017
Maria J Redowicz, Cezary Zekanowski, Jakub Piotr Fichna   +2 more
exaly  

Inheritance patterns and phenotypic features of myofibrillar myopathy associated with a BAG3 mutation

Neuromuscular Disorders, 2010
Volker Straub, Enrico Bertini, Hanns Lochmüller   +2 more
exaly  

Major myofibrillar changes in early onset myopathy due to de novo heterozygous missense mutation in lamin A/C gene

Neuromuscular Disorders, 2005
Enrico Bertini, Stefania Petrini, Adele D'Amico   +2 more
exaly  

Myofibrillar myopathy due to dominant LMNA mutations: A report of 2 cases

Muscle and Nerve, 2018
Teerin Liewluck, Margherita Milone
exaly  

Myofibrillar myopathy with desmin accumulation in a young Australian Shepherd dog

Neuromuscular Disorders, 2004
Shinichi Takayama
exaly  

Proteasomal expression, induction of immunoproteasome subunits, and local MHC class I presentation in myofibrillar myopathy and inclusion body myositis.

Journal of Neuropathology and Experimental Neurology, 2004
Montse Olive, Isidro Ferrer, José G Castaño   +2 more
exaly