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Page 1
Severe encephalopathy associated to pyruvate dehydrogenase mutations and unbalanced coenzyme Q10 content.
Asencio C, Rodríguez-Hernandez MA, Briones P, Montoya J, Cortés A, Emperador S, Gavilán A, Ruiz-Pesini E, Yubero D, Montero R, Pineda M, O'Callaghan MM, Alcázar-Fabra M, Salviati L, Artuch R, Navas P. Asencio C, et al. Among authors: artuch r. Eur J Hum Genet. 2016 Mar;24(3):367-72. doi: 10.1038/ejhg.2015.112. Epub 2015 May 27. Eur J Hum Genet. 2016. PMID: 26014431 Free PMC article.
Tocopherol in inborn errors of intermediary metabolism.
Moyano D, Vilaseca MA, Pineda M, Campistol J, Vernet A, Póo P, Artuch R, Sierra C. Moyano D, et al. Among authors: artuch r. Clin Chim Acta. 1997 Jul 25;263(2):147-55. doi: 10.1016/s0009-8981(97)00061-2. Clin Chim Acta. 1997. PMID: 9246419
Evaluation of hyperhomocysteinaemia in children with stroke.
Cardo E, Vilaseca MA, Campistol J, Artuch R, Colomé C, Pineda M. Cardo E, et al. Among authors: artuch r. Eur J Paediatr Neurol. 1999;3(3):113-7. doi: 10.1016/s1090-3798(99)90098-3. Eur J Paediatr Neurol. 1999. PMID: 10461566
[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: artuch r. Rev Neurol. 2000 Jun 16-30;30(12):1117-21. Rev Neurol. 2000. PMID: 10935234 Spanish.
3-phosphoglycerate dehydrogenase deficiency in a patient with West syndrome.
Pineda M, Vilaseca MA, Artuch R, Santos S, García González MM, Aracil A, Van Schaftingen E, Jaeken J. Pineda M, et al. Among authors: artuch r. Dev Med Child Neurol. 2000 Sep;42(9):629-33. doi: 10.1017/s0012162200001171. Dev Med Child Neurol. 2000. PMID: 11034457 Free article.
334 results