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Page 1
Epilepsy spectrum in cerebral creatine transporter deficiency.
Fons C, Sempere A, Sanmartí FX, Arias A, Póo P, Pineda M, Ribes A, Merinero B, Vilaseca MA, Salomons GS, Artuch R, Campistol J. Fons C, et al. Among authors: vilaseca ma. Epilepsia. 2009 Sep;50(9):2168-70. doi: 10.1111/j.1528-1167.2009.02142.x. Epilepsia. 2009. PMID: 19706062 Free article. No abstract available.
Neuropsychiatric manifestations in late-onset urea cycle disorder patients.
Serrano M, Martins C, Pérez-Dueñas B, Gómez-López L, Murgui E, Fons C, García-Cazorla A, Artuch R, Jara F, Arranz JA, Häberle J, Briones P, Campistol J, Pineda M, Vilaseca MA. Serrano M, et al. Among authors: vilaseca ma. J Child Neurol. 2010 Mar;25(3):352-8. doi: 10.1177/0883073809340696. Epub 2009 Aug 14. J Child Neurol. 2010. PMID: 19684305
Characterization of tremor in phenylketonuric patients.
Pérez-Dueñas B, Valls-Solé J, Fernández-Alvarez E, Conill J, Vilaseca MA, Artuch R, Campistol J. Pérez-Dueñas B, et al. Among authors: vilaseca ma. J Neurol. 2005 Nov;252(11):1328-34. doi: 10.1007/s00415-005-0860-6. Epub 2005 Jul 5. J Neurol. 2005. PMID: 15995796
Comparison between high performance liquid chromatography and capillary zone electrophoresis for the diagnosis of congenital disorders of glycosylation.
Quintana E, Montero R, Casado M, Navarro-Sastre A, Vilaseca MA, Briones P, Artuch R. Quintana E, et al. Among authors: vilaseca ma. J Chromatogr B Analyt Technol Biomed Life Sci. 2009 Aug 15;877(24):2513-8. doi: 10.1016/j.jchromb.2009.06.031. Epub 2009 Jun 30. J Chromatogr B Analyt Technol Biomed Life Sci. 2009. PMID: 19608465
A longitudinal study of antioxidant status in phenylketonuric patients.
Artuch R, Colomé C, Sierra C, Brandi N, Lambruschini N, Campistol J, Ugarte D, Vilaseca MA. Artuch R, et al. Among authors: vilaseca ma. Clin Biochem. 2004 Mar;37(3):198-203. doi: 10.1016/j.clinbiochem.2003.10.017. Clin Biochem. 2004. PMID: 14972641
172 results