CLINICAL, IMMUNOCHEMICAL AND GENETIC STUDIES IN CONGENITAL MUSCULAR DYSTROPHY

Scientific Publications

• 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