Disease: Muscular dystrophy- congenital- merosin-positive
- A large series of immunohistochemically confirmed cases of congenital muscular dystrophy seen over a period of one decade
- Assessment of left ventricular systolic and diastolic functions in children with merosin-positive congenital muscular dystrophy
- Caudal block combined with propofol infusion using laryngeal mask airway in a spontaneously ventilating child with merosin-positive occidental type congenital muscular dystrophy
- Congenital muscular dystrophy and epilepsy: a prospective case series of pediatric patients
- Diagnosis of congenital muscular dystrophy and clinical significance of merosin expression
- Differential diagnosis of congenital muscular dystrophies
- Dystrophin-glycoproteins associated in congenital muscular dystrophy: immunohistochemical analysis of 59 Brazilian cases
- EMG and nerve conduction studies in children with congenital muscular dystrophy
- Localisation of merosin-positive congenital muscular dystrophy to chromosome 4p16.3
- Merosin-deficient congenital muscular dystrophy in two siblings
- Merosin-positive congenital muscular dystrophy with early orthopaedic problems in relation to Ullrich's disease
- Merosin-positive congenital muscular dystrophy, white matter abnormalities, and bilateral posterior occipital cortical dysplasia
- Merosin-positive congenital muscular dystrophy: neuroimaging findings
- Prenatal Diagnosis of Merosin-Deficient Muscular Dystrophy
- Subclinical cardiological involvement in Sicilian patients with pure congenital muscular dystrophy