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Luis Varona

Showing results (81-90 of 84) with videos related to

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European Journal of Neurology|December 9, 2022
Characterizing SOD1 mutations in Spain. The impact of genotype, age, and sex in the natural history of the diseaseJuan F Vázquez-Costa, Daniel Borrego-Hernández, Carmen Paradas, et al.
Acta Neuropathologica|October 20, 2022
Loss of function variants in DNAJB4 cause a myopathy with early respiratory failureConrad C Weihl, Ana Töpf, Rocio Bengoechea, et al.
Human Mutation|September 1, 2012
Analysis of the C9orf72 gene in patients with amyotrophic lateral sclerosis in Spain and different populations worldwideAlberto García-Redondo, Oriol Dols-Icardo, Ricard Rojas-García, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 17, 2022
Clinical trials in pediatric ALS: a TRICALS feasibility studyTessa Kliest, Ruben P A Van Eijk, Ammar Al-Chalabi, et al.
Pageof 9

Showing results (81-90 of 84) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 84 results.
European Journal of Neurology|December 9, 2022
Characterizing SOD1 mutations in Spain. The impact of genotype, age, and sex in the natural history of the diseaseJuan F Vázquez-Costa, Daniel Borrego-Hernández, Carmen Paradas, et al.
Acta Neuropathologica|October 20, 2022
Loss of function variants in DNAJB4 cause a myopathy with early respiratory failureConrad C Weihl, Ana Töpf, Rocio Bengoechea, et al.
Human Mutation|September 1, 2012
Analysis of the C9orf72 gene in patients with amyotrophic lateral sclerosis in Spain and different populations worldwideAlberto García-Redondo, Oriol Dols-Icardo, Ricard Rojas-García, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 17, 2022
Clinical trials in pediatric ALS: a TRICALS feasibility studyTessa Kliest, Ruben P A Van Eijk, Ammar Al-Chalabi, et al.
Pageof 9