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Identification and characterization of the novel point mutation m.3634A>G in the mitochondrial MT-ND1 gene associated with LHON syndrome.
Carreño-Gago L, Gamez J, Cámara Y, Alvarez de la Campa E, Aller-Alvarez JS, Moncho D, Salvado M, Galan A, de la Cruz X, Pinós T, García-Arumí E. Carreño-Gago L, et al. Among authors: aller alvarez js. Biochim Biophys Acta Mol Basis Dis. 2017 Jan;1863(1):182-187. doi: 10.1016/j.bbadis.2016.09.002. Epub 2016 Sep 7. Biochim Biophys Acta Mol Basis Dis. 2017. PMID: 27613247 Free article.
Myoclonic epilepsy in Down syndrome and Alzheimer disease.
Aller-Alvarez JS, Menéndez-González M, Ribacoba-Montero R, Salvado M, Vega V, Suárez-Moro R, Sueiras M, Toledo M, Salas-Puig J, Álvarez-Sabin J. Aller-Alvarez JS, et al. Neurologia. 2017 Mar;32(2):69-73. doi: 10.1016/j.nrl.2014.12.008. Epub 2015 Feb 7. Neurologia. 2017. PMID: 25661268 Free article. English, Spanish.
[Numb chin syndrome. A case report].
Aller-Alvarez JS, Palasi A, Olivera P, Salamero O, Barios M, Castellvi J, Siurana S, Rovira A, Alvarez-Sabin J. Aller-Alvarez JS, et al. Rev Neurol. 2015 Sep 16;61(6):286-7. Rev Neurol. 2015. PMID: 26350780 Free article. Spanish. No abstract available.