Novel myosin heavy chain immunohistochemical double staining developed for the routine diagnostic separation of I, IIA and IIX fibers
Olayinka Raheem(Tampere University Hospital), Bjarne Udd(Folkhälsans Forskningscentrum), Sanna Huovinen(Vaasa Central Hospital), Tiina Suominen(Tampere University), Hannu Haapasalo(Tampere University Hospital)
Cited by 31
Related Papers
The myotonic dystrophies: molecular, clinical, and therapeutic challenges
|The Lancet Neurology|2012|487
Tibial Muscular Dystrophy Is a Titinopathy Caused by Mutations in TTN, the Gene Encoding the Giant Skeletal-Muscle Protein Titin
|The American Journal of Human Genetics|2002|484
Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy
|Nature Medicine|2011|333
Distinct muscle imaging patterns in myofibrillar myopathies
|Neurology|2008|261
The gene disrupted in Marinesco-Sjögren syndrome encodes SIL1, an HSPA5 cochaperone
|Nature Genetics|2005|241