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Validation of Motor Outcome Measures in Myotonic Dystrophy Type 2

Introduction: Myotonic dystrophy type 2 (DM2) lacks disease-specific, validated, motor outcome measures (OMs), and patients' reported outcomes (PROs). This represents a limit for the monitoring of disease progression and treatment response. Our aim was to identify the most appropriate OMs to be...

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Detaylı Bibliyografya
Yayımlandı:Front Neurol
Asıl Yazarlar: Montagnese, Federica, Rastelli, Emanuele, Khizanishvili, Nina, Massa, Roberto, Stahl, Kristina, Schoser, Benedikt
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Frontiers Media S.A. 2020
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7186332/
https://ncbi.nlm.nih.gov/pubmed/32373059
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2020.00306
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