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Acute myopathy with skin manifestations, not always idiopathic and autoimmune.
Neuromuscul Disord. 2021 Nov;31(11):1218-1219. doi: 10.1016/j.nmd.2021.10.001. Epub 2021 Oct 9.
Neuromuscul Disord. 2021.
PMID: 34728123
No abstract available.
Novel autosomal dominant TPM3 mutation causes a combined congenital fibre type disproportion-cap disease histological pattern.
Bevilacqua JA, Contreras JP, Trangulao A, Hernández Ú, Brochier G, Díaz J, Hughes R, Campero M, Romero NB.
Bevilacqua JA, et al.
Neuromuscul Disord. 2022 Aug;32(8):687-691. doi: 10.1016/j.nmd.2022.05.014. Epub 2022 May 28.
Neuromuscul Disord. 2022.
PMID: 35688744
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Idiopathic inflammatory myopathy human derived cells retain their ability to increase mitochondrial function.
Basualto-Alarcón C, Urra FA, Bozán MF, Jaña F, Trangulao A, Bevilacqua JA, Cárdenas JC.
Basualto-Alarcón C, et al.
PLoS One. 2020 Nov 20;15(11):e0242443. doi: 10.1371/journal.pone.0242443. eCollection 2020.
PLoS One. 2020.
PMID: 33216776
Free PMC article.
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Toward an objective measure of functional disability in dysferlinopathy.
Woudt L, Di Capua GA, Krahn M, Castiglioni C, Hughes R, Campero M, Trangulao A, González-Hormazábal P, Godoy-Herrera R, Lévy N, Urtizberea JA, Jara L, Bevilacqua JA.
Woudt L, et al.
Muscle Nerve. 2016 Jan;53(1):49-57. doi: 10.1002/mus.24685. Epub 2015 May 23.
Muscle Nerve. 2016.
PMID: 25900324
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Genetic Profile of Patients with Limb-Girdle Muscle Weakness in the Chilean Population.
Cerino M, González-Hormazábal P, Abaji M, Courrier S, Puppo F, Mathieu Y, Trangulao A, Earle N, Castiglioni C, Díaz J, Campero M, Hughes R, Vargas C, Cortés R, Kleinsteuber K, Acosta I, Urtizberea JA, Lévy N, Bartoli M, Krahn M, Jara L, Caviedes P, Gorokhova S, Bevilacqua JA.
Cerino M, et al.
Genes (Basel). 2022 Jun 16;13(6):1076. doi: 10.3390/genes13061076.
Genes (Basel). 2022.
PMID: 35741838
Free PMC article.
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