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Author Picchio L |
Available item(s) by this author (6)
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Article
Picchio L, Author ; Legagneux V ; Deschamps S ; Renaud Y ; Chauveau S ; Paillard L ; Jagla K | 2018Article
Xèmes Journées Annuelles de la Société française de Myologie (SFM) (14-16 novembre 2012; Grenoble (France)) ; Picchio L ; Plantié E ; Yoan R ; Preethi P ; Krzysztof J | Société Française de Myologie SFM | 2012Myotonic dystrophy type 1 (DM1) is a multisystemic RNA-dominant disorder characterized by myotonia and muscle degeneration. In DM1 patients, the mutant dmpk transcripts containing expanded CUG repeats form nuclear foci and interfere with biogene[...]Article
IXèmes Journées Annuelles de la Société française de Myologie (SFM) (3-5 novembre 2011; Angers) ; Picchio L ; Preethi P ; Da Ponte JP ; Jagla C | 2011Introduction : Myotonic dystrophy type 1 (DM1) is a dominant neuromuscular disorder affecting 1/8000 individuals worldwide. This disease is caused by an unstable expansion of CTG trinucleotide repeats located in the 3' untranslated region of the[...]Article
IXèmes Journées Annuelles de la Société française de Myologie (SFM) (3-5 novembre 2011; Angers) ; Picchio L ; Taghli O ; Da Ponte JP ; Jagla C | 2011INTRODUCTION : Myotonic dystrophy type 1 (DM1) is a dominant neuromuscular disorder affecting 1/8000 individuals worldwide. This disease is caused by an unstable expansion of CTG trinucleotide repeats located in the 3' untranslated region of the[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Picchio L ; Taghli O ; DaPonte JP ; Jagla C | 2011Myotonic dystrophy type 1 (DM1) is a dominant neuromuscular disorder affecting 1/8000 individuals worldwide. This disease is caused by an unstable expansion of CTG trinucleotide repeats located in the 3' untranslated region of the dystrophy myot[...]