Diagnostic interest of whole-body MRI in early- and late-onset LAMA2 muscular dystrophies: a large international cohort-Reference-Cited by-同舟云学术

Diagnostic interest of whole-body MRI in early- and late-onset LAMA2 muscular dystrophies: a large international cohort

Published:2021-09-24 Issue: Volume: Page:
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Quijano-Roy Susana,Haberlova Jana,Castiglioni Claudia,Vissing John,Munell Francina,Rivier François,Stojkovic Tanya,Malfatti Edoardo,Gómez García de la Banda Marta,Tasca Giorgio,Costa Comellas Laura,Benezit Audrey,Amthor Helge,Dabaj Ivana,Gontijo Camelo Clara,Laforêt Pascal,Rendu John,Romero Norma B.,Cavassa Eliana,Fattori Fabiana,Beroud Christophe,Zídková Jana,Leboucq Nicolas,Løkken Nicoline,Sanchez-Montañez Ángel,Ortega Ximena,Kynčl Martin,Metay Corinne,Gómez-Andrés David^ORCID,Carlier Robert Y.

Funder

European Cooperation in Science and Technology

Instituto de Salud Carlos III

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

https://link.springer.com/content/pdf/10.1007/s00415-021-10806-0.pdf

Reference41 articles.

1. Allamand V, Guicheney P (2002) Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin). Eur J Hum Genet EJHG 10(2):91–94: https://doi.org/10.1038/sj.ejhg.5200743

2. Geranmayeh F, Clement E, Feng LH et al (2010) Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations. Neuromuscul Disord NMD 20(4):241–250. https://doi.org/10.1016/j.nmd.2010.02.001