CLINICAL, IMMUNOCHEMICAL AND GENETIC STUDIES IN CONGENITAL MUSCULAR DYSTROPHY
- 2 Anni 1995/1997
- 51.646€ Totale Fondi
Descrizione non disponibile
Pubblicazioni Scientifiche
- 1998 EUROPEAN NEUROLOGY
Congenital muscular dystrophy with partial merosin deficiency and late onset epilepsy
- 1998 NEUROLOGY
Laminin alpha 2 muscular dystrophy - Genotype/phenotype studies of 22 patients
- 1996 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
- 1996 HUMAN GENETICS
Genetic epidemiology of congenital muscular dystrophy in a sample from north-east Italy
- 2000 NEUROLOGY
A novel laminin alpha 2 isoform in severe laminin alpha 2 deficient congenital muscular dystrophy
- 1999 JOURNAL OF NEUROLOGY
Clinical and neuroimaging study of central nervous system in congenital myotonic dystrophy
