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Page 1
Coenzyme Q₁₀ deficiency in mitochondrial DNA depletion syndromes.
Montero R, Grazina M, López-Gallardo E, Montoya J, Briones P, Navarro-Sastre A, Land JM, Hargreaves IP, Artuch R; Coenzyme Q₁₀ Deficiency Study Group. Montero R, et al. Among authors: montoya j. Mitochondrion. 2013 Jul;13(4):337-41. doi: 10.1016/j.mito.2013.04.001. Epub 2013 Apr 11. Mitochondrion. 2013. PMID: 23583954
[Aspects of neuropathy in mitochondrial diseases].
Colomer J, Iturriaga C, Bestué M, Artuch R, Briones P, Montoya J, Vilaseca MA, Pineda M. Colomer J, et al. Among authors: montoya j. Rev Neurol. 2000 Jun 16-30;30(12):1117-21. Rev Neurol. 2000. PMID: 10935234 Spanish.
[Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA].
Coelho-Miranda L, Playan A, Artuch R, Vilaseca MA, Colomer J, Briones P, Coll-Cantí J, Conill J, Sans A, López de Munain A, Solano A, Alcaine MJ, Montoya J, Pineda M. Coelho-Miranda L, et al. Among authors: montoya j. Rev Neurol. 2000 Nov 1-15;31(9):804-11. Rev Neurol. 2000. PMID: 11127079 Spanish.
[Familiar chronic progressive external ophthalmoplegia of mitochondrial origin].
Pineda M, Playán-Ariso A, Alcaine-Villarroya MJ, Vernet AM, Serra-Castanera A, Solano A, Vilaseca MA, Artuch R, López-Pérez M, Briones-Godino MP, Andreu A, Montoya J. Pineda M, et al. Among authors: montoya j. Rev Neurol. 2004 Jun 1-15;38(11):1023-7. Rev Neurol. 2004. PMID: 15202078 Free article. Spanish.
966 results