Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials-Reference-Cited by-同舟云学术

Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials

Published:2021-12-06 Issue:3 Volume:29 Page:843-854
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Euro J of Neurology

Author:

Garibaldi Matteo¹^ORCID,Nicoletti Tommaso²³^ORCID,Bucci Elisabetta¹,Fionda Laura¹^ORCID,Leonardi Luca¹,Morino Stefania¹,Tufano Laura¹,Alfieri Girolamo¹,Lauletta Antonio¹,Merlonghi Gioia¹,Perna Alessia²³,Rossi Salvatore²³,Ricci Enzo²³,Alonso Perez Jorge⁴,Tartaglione Tommaso⁵,Petrucci Antonio⁶,Pennisi Elena Maria⁷,Salvetti Marco¹⁸,Cutter Gary⁹,Díaz‐Manera Jordi⁴¹⁰¹¹^ORCID,Silvestri Gabriella²³^ORCID,Antonini Giovanni¹

Affiliation:

1. Neuromuscular and Rare Disease Centre Department of Neuroscience Mental Health and Sensory Organs (NESMOS) Sapienza University of RomeSant'Andrea Hospital Rome Italy

2. UOC Neurologia Fondazione Policlinico Universitario ‘A. Gemelli’ IRCCS Rome Italy

3. Department of Neurosciences Facoltà di Medicina e Chirurgia Università Cattolica del Sacro Cuore Rome Italy

4. Neuromuscular Disorders Unit, Neurology Department, Universitat Autònoma de Barcelona, Hospital de la Santa Creu I Sant Pau Barcelona Spain

5. Department of Radiology Istituto Dermopatico dell'ImmacolataIRCCS Rome Italy

6. Neurology Unit San Camillo‐Forlanini Hospital Rome Italy

7. Neurology Unit San Filippo Neri Hospital Rome Italy

8. IRCCS Istituto Neurologico Mediterraneo (INM) Neuromed Pozzilli Italy

9. Department of Biostatistics University of Alabama at Birmingham Birmingham Alabama USA

10. John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute Newcastle UniversityNewcastle Hospitals NHS Foundation Trust Newcastle upon Tyne UK

11. Centro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER) Barcelona Spain

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ene.15174

Reference53 articles.

1. The myotonic dystrophies: diagnosis and management

2. Anatomy of a founder effect: myotonic dystrophy in Northeastern Quebec

3. Recruitment of human muscleblind proteins to (CUG)n expansions associated with myotonic dystrophy

4. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member

5. A 34-year longitudinal study on long-term cardiac outcomes in DM1 patients with normal ECG at baseline at an Italian clinical centre

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