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A large multicenter study of pediatric myotonic dystrophy type 1 for evidence-based management.
Neurology. 2019 Feb 19;92(8):e852-e865. doi: 10.1212/WNL.0000000000006948. Epub 2019 Jan 18.
Neurology. 2019.
PMID: 30659139
Implementation of Motor Function Measure score percentile curves - Predicting motor function loss in Duchenne muscular dystrophy.
Hafner P, Schmidt S, Schädelin S, Rippert P, Hamroun D, Fabien S, Henzi B, Putananickal N, Rubino-Nacht D, Vuillerot C, Fischer D; MFM registry Study Group.
Hafner P, et al.
Eur J Paediatr Neurol. 2022 Jan;36:78-83. doi: 10.1016/j.ejpn.2021.11.004. Epub 2021 Dec 14.
Eur J Paediatr Neurol. 2022.
PMID: 34929615
Free article.
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The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care.
De Antonio M, Dogan C, Daidj F, Eymard B, Puymirat J, Mathieu J, Gagnon C, Katsahian S; Filnemus Myotonic Dystrophy Study Group; Hamroun D, Bassez G.
De Antonio M, et al.
Orphanet J Rare Dis. 2019 Jun 3;14(1):122. doi: 10.1186/s13023-019-1088-3.
Orphanet J Rare Dis. 2019.
PMID: 31159885
Free PMC article.
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Motor function measure: validation of a short form for young children with neuromuscular diseases.
de Lattre C, Payan C, Vuillerot C, Rippert P, de Castro D, Bérard C, Poirot I; MFM-20 Study Group.
de Lattre C, et al.
Arch Phys Med Rehabil. 2013 Nov;94(11):2218-26. doi: 10.1016/j.apmr.2013.04.001. Epub 2013 Apr 18.
Arch Phys Med Rehabil. 2013.
PMID: 23602884
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