Luca Colantoni

Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number ofKpnI repeats at the 4q35 locus and clinical phenotype

Enzo Ricci, Giuliana Galluzzi, Giancarlo Deidda et al. · Annals of Neurology · 1999 · 301 citations

Life Sciences, Genetics, Molecular Genetics +12

Parallel protein and transcript profiles of FSHD patient muscles correlate to the D4Z4 arrangement and reveal a common impairment of slow to fast fibre differentiation and a general deregulation of MyoD‐dependent genes

Barbara Celegato, Daniele Capitanio, Mario Pescatori et al. · PROTEOMICS · 2006 · 127 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Sequence Homology between 4qter and 10qter Loci Facilitates the Instability of Subtelomeric KpnI Repeat Units Implicated in Facioscapulohumeral Muscular Dystrophy

S. Cacurri, N. Piazzo, Giancarlo Deidda et al. · The American Journal of Human Genetics · 1998 · 58 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

P2‐037: Alzheimer'S disease (ad) and mild cognitive impairment (mci) patients are characterized by increased bdnf serum levels

Francesco Angelucci, Gianfranco Spalletta, Fulvia Di Iulio et al. · Alzheimer s & Dementia · 2009 · 42 citations

Medicine, Neurology, Neuroscience +17

The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure

Mônica Lanzoni Rossi, Enzo Ricci, Luca Colantoni et al. · BMC Medical Genetics · 2007 · 28 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11