Results 231 to 240 of about 3,092 (251)

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

Neuromuscular Disorders, 1995
J Philpot
exaly  

Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse

Neuromuscular Disorders, 1997
Y Sunada, Teruo Shimizu
exaly  

Deficiency of Merosin (Laminin M or α2) in Congenital Muscular Dystrophy Associated with Cerebral White Matter Alterations

Neuropediatrics, 1995
Mariz Vainzof, Suely K N Marie, Maria Rita Passos-Bueno   +2 more
exaly  

Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin status

Neuromuscular Disorders, 1999
Eugenio Mercuri, J Philpot, Serena J Counsell   +2 more
exaly  

Merosin (Laminin-2)

2009
openaire   +1 more source

Mild clinical phenotype in a 12-year-old boy with partial merosin deficiency and central and peripheral nervous system abnormalities

Neuromuscular Disorders, 1996
Marina Mora, Isabella Moroni, Graziella Uziel   +2 more
exaly  

Basement membrane abnormality in merosin-negative congenital muscular dystrophy

Acta Neuropathologica, 1996
Osamu Kobayashi, Yuzo Tanabe
exaly  

Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging

Neuromuscular Disorders, 1999
J Philpot, F Cowan, Francesco Muntoni
exaly  

Merosin-deficient congenital muscular dystrophy: neuropathology case reports

Journal of Cellular and Molecular Medicine, 2000
Emilia Manole
exaly  

A Homozygous <i>LAMA2</i> Mutation of c.818G>A Caused Partial Merosin Deficiency in a Japanese Patient

Internal Medicine, 2018
Akatsuki Kubota, Hiroyuki Ishiura, Jun Mitsui   +2 more
exaly