Epilepsy in LAMA2 ‐related muscular dystrophy: An electro‐clinico‐radiological characterization-Reference-Cited by-同舟云学术

Epilepsy in LAMA2 ‐related muscular dystrophy: An electro‐clinico‐radiological characterization

Published:2020-04-08 Issue:5 Volume:61 Page:971-983
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Natera‐de Benito Daniel¹^ORCID,Muchart Jordi²,Itzep Debora¹,Ortez Carlos¹,González‐Quereda Lidia³,Gallano Pía³,Ramirez Alia⁴,Aparicio Javier⁴,Domínguez‐Carral Jana⁴,Carrera‐García Laura¹^ORCID,Expósito‐Escudero Jessica¹,Pardo Cardozo Nathalia¹,Cuadras Daniel⁵,Codina Anna⁶,Jou Cristina⁶,Jimenez‐Mallebrera Cecilia¹,Palau Francesc⁷⁸⁹¹⁰,Colomer Jaume¹,Arzimanoglou Alexis⁴¹¹,Nascimento Andrés¹,San Antonio‐Arce Victoria⁴

Affiliation:

1. Neuromuscular Unit Neuropaediatrics Department Institut de Recerca Hospital Sant Joan de Déu and CIBERER U703 Barcelona Spain

2. Department of Radiology Hospital Sant Joan de Déu Barcelona Spain

3. Department of Genetics Hospital de la Santa Creu i Sant Pau and CIBERER U705 Barcelona Spain

4. Unit of Epilepsy, Sleep and Neurophysiology Neuropaediatrics Department Hospital Sant Joan de Déu Barcelona Spain

5. Statistics Department Fundació Sant Joan de Déu Barcelona Spain

6. Department of Pathology Hospital Sant Joan de Déu Barcelona Spain

7. Department of Genetic and Molecular Medicine Hospital Sant Joan de Déu Barcelona Spain

8. Laboratory of Neurogenetics and Molecular Medicine Institut de Recerca Sant Joan de Déu Barcelona Spain

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

10. Institute of Medicine and Dermatology Hospital Clínic and Division of Pediatrics University of Barcelona School of Medicine and Health Sciences Barcelona Spain

11. Epileptology, Sleep Disorders and Functional Pediatric Neurology Member of ERN‐EpiCARE; HFME Hospices Civils de Lyon Bron France

Funder

Fundación Mutua Madrileña

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/epi.16493

Reference36 articles.

1. Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for α2 chain of laminin)

2. The ever-expanding spectrum of congenital muscular dystrophies