Pages that link to "Q28256516"

The following pages link to Prevalence of congenital muscular dystrophy in Italy: a population study (Q28256516):

Displaying 12 items.

• Congenital muscular dystrophy: from muscle to brain (Q27023097) (← links)
• Improving Reproducibility of Phenotypic Assessments in the DyW Mouse Model of Laminin-α2 Related Congenital Muscular Dystrophy (Q33787898) (← links)
• Compound heterozygous POMT1 mutations in a Chinese family with autosomal recessive muscular dystrophy-dystroglycanopathy C1. (Q33844672) (← links)
• The evolution of the dystroglycan complex, a major mediator of muscle integrity (Q41820882) (← links)
• Cardiac manifestations of congenital LMNA-related muscular dystrophy in children: three case reports and recommendations for care. (Q46953467) (← links)
• Lamins and bone disorders: current understanding and perspectives. (Q54945496) (← links)
• Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study (Q58695079) (← links)
• The roles of dystroglycan in the nervous system: insights from animal models of muscular dystrophy (Q60300741) (← links)
• Compound heterozygous POMGNT1 mutations leading to muscular dystrophy-dystroglycanopathy type A3: a case report (Q64065905) (← links)
• A Qualitative Approach to Health Related Quality-of-Life in Congenital Muscular Dystrophy (Q88457883) (← links)
• Muscular dystrophies (Q91594164) (← links)
• Current understanding and treatment of cardiac and skeletal muscle pathology in laminin-α2 chain-deficient congenital muscular dystrophy (Q91906240) (← links)