Results 221 to 230 of about 35,591 (238)

Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patients

Brain and Development, 2015
Kazuhiro Kobayashi, Jiangxi Xiao, Tatsushi Toda   +2 more
exaly  

Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal

Neuromuscular Disorders, 1995
Caroline A Sewry
exaly  

Congenital muscular dystrophy: molecular and cellular aspects

Cellular and Molecular Life Sciences, 2005
Cecilia Jimenez-Mallebrera
exaly  

Congenital muscular dystrophy

Brain and Development, 1983
R. Korinthenberg, D. Palm
openaire   +1 more source

Fukuyama‐type congenital muscular dystrophy (FCMD) and α‐dystroglycanopathy

Congenital Anomalies (discontinued), 2003
Tatsushi Toda, Kazuhiro Kobayashi, Yoshitaka Nagai   +2 more
exaly  

Congenital progressive muscular dystrophy of the fukuyama type — clinical, genetic and pathological considerations —

Brain and Development, 1981
exaly  

A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complex

Neuromuscular Disorders, 2007
Peter Pytel, Elizabeth M McNally
exaly  

Congenital Muscular Dystrophy and Rigid Spine Syndrome

Neuropediatrics, 1983
exaly  

Congenital Muscular Dystrophy

2016
openaire   +2 more sources

Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy

Lancet, The, 1996
exaly