Cinzia Bragato

Identification of new ANG gene mutations in a large cohort of Italian patients with amyotrophic lateral sclerosis

Cinzia Gellera, Claudia Colombrita, Nicola Ticozzi et al. · Neurogenetics · 2007 · 112 citations

Amyotrophic Lateral Sclerosis, Mendelian Disorder, Neurological Disorder +8

Exosomes and exosomal miRNAs from muscle-derived fibroblasts promote skeletal muscle fibrosis

Simona Zanotti, Sara Gibertini, Flavia Blàsevich et al. · Matrix Biology · 2018 · 86 citations

Exosomal Mirnas, Fibrosis, Developmental Biology +9

Centronuclear myopathy related to dynamin 2 mutations: Clinical, morphological, muscle imaging and genetic features of an Italian cohort

Michela Catteruccia, Fabiana Fattori, Valentina Codemo et al. · Neuromuscular Disorders · 2013 · 62 citations · Full text

Mitochondrial Myopathy, Mendelian Disorder, Medicine +8

Centronuclear myopathies: genotype–phenotype correlation and frequency of defined genetic forms in an Italian cohort

Fabiana Fattori, Lorenzo Maggi, Claudio Bruno et al. · Journal of Neurology · 2015 · 60 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

Novel PTRF mutation in a child with mild myopathy and very mild congenital lipodystrophy

Anna Ardissone, Cinzia Bragato, Lorella Caffi et al. · BMC Medical Genetics · 2013 · 49 citations · Full text