Funder
Ministero della Salute
Fondazione Malattie Miotoniche
Associazione Italiana per la Ricerca sul Cancro
Fondazione Cariplo
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference34 articles.
1. The myotonic dystrophies: molecular, clinical, and therapeutic challenges;Udd;Lancet Neurol,2012
2. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member;Brook;Cell,1992
3. Report of the first outcome measures in myotonic dystrophy type 1 (OMMYD-1) international workshop: Clearwater, Florida, November 30, 2011;Gagnon;Neuromuscul Disord,2013
4. Distinct neuromuscular phenotypes in myotonic dystrophy types 1 and 2: a whole body highfield MRI study;Kornblum;J Neurol,2006
5. Quantitative assessment of skeletal muscle degeneration in patients with myotonic dystrophy type 1 using MRI;Hiba;J Magn Reson Imaging,2012
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