French National Protocol for diagnosis and care of facioscapulohumeral muscular dystrophy (FSHD)-Reference-Cited by-同舟云学术

French National Protocol for diagnosis and care of facioscapulohumeral muscular dystrophy (FSHD)

Published:2024-07-02 Issue:9 Volume:271 Page:5778-5803
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Attarian Shahram^ORCID,Beloribi-Djefaflia Sadia,Bernard Rafaelle,Nguyen Karine,Cances Claude,Gavazza Carole,Echaniz-Laguna Andoni,Espil Caroline,Evangelista Teresinha,Feasson Léonard,Audic Frédérique,Zagorda Berenice,Milhe De Bovis Virginie,Stojkovic Tanya,Sole Guilhem,Salort-Campana Emmanuelle,Sacconi Sabrina

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s00415-024-12538-3.pdf

Reference185 articles.

1. Guien C, Blandin G, Lahaut P et al (2018) The French National Registry of patients with facioscapulohumeral muscular dystrophy. Orphanet J Rare Dis 13:218. https://doi.org/10.1186/s13023-018-0960-x

2. Padberg GW, Frants RR, Brouwer OF et al (1995) Facioscapulohumeral muscular dystrophy in the Dutch population. Muscle Nerve Suppl 18(S13):S81–S84

3. Mostacciuolo M, Pastorello E, Vazza G et al (2009) Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample. Clin Genet 75:550–555. https://doi.org/10.1111/j.1399-0004.2009.01158.x

4. Deenen JCW, Arnts H, van der Maarel SM et al (2014) Population-based incidence and prevalence of facioscapulohumeral dystrophy. Neurology 83:1056–1059. https://doi.org/10.1212/WNL.0000000000000797

5. Lutz KL, Holte L, Kliethermes SA et al (2013) Clinical and genetic features of hearing loss in facioscapulohumeral muscular dystrophy. Neurology 81:1374–1377. https://doi.org/10.1212/WNL.0b013e3182a84140

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