CLINICAL, IMMUNOCHEMICAL AND GENETIC STUDIES IN CONGENITAL MUSCULAR DYSTROPHY
- 2 Anni 1995/1997
- 51.646€ Totale Fondi
Descrizione non disponibile
Pubblicazioni Scientifiche
- CHILDS NERVOUS SYSTEM
Brain alterations in the classical form of congenital muscular dystrophy - Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle
- EUROPEAN NEUROLOGY
Congenital muscular dystrophy with partial merosin deficiency and late onset epilepsy
- HUMAN GENETICS
Genetic epidemiology of congenital muscular dystrophy in a sample from north-east Italy
- JOURNAL OF NEUROLOGY
Clinical and neuroimaging study of central nervous system in congenital myotonic dystrophy
- NEUROLOGY
A novel laminin α2 isoform in severe laminin α2 deficient congenital muscular dystrophy
- NEUROLOGY
Laminin α2 muscular dystrophy -: Genotype/phenotype studies of 22 patients
