Persones / Equip Humà

Rafael Artuch Iriberri

Buscador de publicacions

Publicacions

  • O'Callaghan-Gordo M, Emperador S, López-Gallardo E, Jou-Munoz C, Buján N, Montero-Sanchez R, Garcia-Cazorla A, Gonzaga D, Ferrer I, Briones P, Ruiz-Pesini E, Pineda M, Artuch-Iriberri R and Montoya J.

    New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset

    Neurogenetics . 13(3): 245-250. Nº de cites: 18

    [doi:10.1007/s10048-012-0322-0]

  • Pérez-Dueñas B, Sempere A, Campistol-Plana J, Alonso-Colmenero I, Díez M, González V, Merinero B, Desviat LR and Artuch-Iriberri R.

    Novel features in the evolution of adenylosuccinate lyase deficiency

    EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY . 16(4): 343-348. Nº de cites: 15

    [doi:10.1016/j.ejpn.2011.08.008]

  • Casado-Rio M, O'Callaghan-Gordo M, Montero-Sanchez R, Pérez-Cerda C, Pérez B, Briones P, Quintana E, Muchart-Lopez J, Aracil A, Pineda M and Artuch-Iriberri R.

    Mild Clinical and Biochemical Phenotype in Two Patients with PMM2-CDG (Congenital Disorder of Glycosylation Ia)

    Cerebellum . 11(2): 557-563. Nº de cites: 23

    [doi:10.1007/s12311-011-0313-y]

  • López-Laso E, Beyer K, Opladen T, Artuch-Iriberri R and Saunders-Pullman R.

    Dyskinesias as a Limiting Factor in the Treatment of Segawa Disease

    PEDIATRIC NEUROLOGY . 46(6): 404-406. Nº de cites: 15

    [doi:10.1016/j.pediatrneurol.2012.03.003]

  • Jimenez E, Ormazabal-Herrero A, Serrano M, Ortez-Gonzalez CI, Artuch-Iriberri R, Garcia-Cazorla A and Campistol-Plana J.

    Amino acids in cerebrospinal fluid and plasma: its usefulness in the study of neuropaediatric diseases

    REVISTA DE NEUROLOGIA . 54(7): 394-398. Nº de cites: 4

    [doi:10.33588/rn.5407.2011454]

  • Salviati L, Trevisson E, Rodriguez Hernandez MA, Casarin A, Pertegato V, Doimo M, Cassina M, Agosto C, Desbats MA, Sartori G, Sacconi S, Memo L, Zuffardi O, Artuch-Iriberri R, Quinzii C, Dimauro S, Hirano M, Santos-Ocaña C and Navas P.

    Haploinsufficiency of COQ4 causes coenzyme Q10 deficiency

    JOURNAL OF MEDICAL GENETICS . 49(3): 187-191. Nº de cites: 96

    [doi:10.1136/jmedgenet-2011-100394]

  • Fons-Estupina C, Rizzu P, Garcia-Cazorla A, Martorell-Sampol L, Ormazabal-Herrero A, Artuch-Iriberri R, Campistol-Plana J and Fernández-Alvarez E.

    TITF-1 gene mutation in a case of sporadic non-progressive chorea. Response to levodopa treatment

    BRAIN & DEVELOPMENT . 34(3): 255-257. Nº de cites: 18

    [doi:10.1016/j.braindev.2011.04.007]

  • Fons-Estupina C, Campistol-Plana J, Panagiotakaki, E, Giannotta, M, Arzimanoglou A, Gobbi, G, Neville, B, Ebinger, F, Nevsímalová, S, Laan, L, Casaer, P, Spiel, G, Ninan, M, Sange, G, Artuch-Iriberri R, Schyns, T, Vavassori, R and Poncelin, D.

    Alternating hemiplegia of childhood: Metabolic studies in the largest European series of patients

    EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY . 16(1): 10-14. Nº de cites: 26

    [doi:10.1016/j.ejpn.2011.08.006]

  • Villar C, Campistol-Plana J, Fons-Estupina C, Armstrong-Moron J, Mas A, Ormazabal-Herrero A and Artuch-Iriberri R.

    Glycine and L-arginine treatment causes hyperhomocysteinemia in cerebral creatine transporter deficiency patients.

    JIMD Reports . 4: 13-16. Nº de cites: 4

    [doi:10.1007/8904_2011_41]

  • López-Laso E, Sánchez-Raya A, Moriana JA, Martínez-Gual E, Camino-León R, Mateos-González ME, Pérez-Navero JL, Ochoa-Sepúlveda JJ, Ormazabal-Herrero A, Opladen T, Klein C, Lao-Villadóniga JI, Beyer K and Artuch-Iriberri R.

    Neuropsychiatric symptoms and intelligence quotient in autosomal dominant Segawa disease

    JOURNAL OF NEUROLOGY . 258(12): 2155-2162. Nº de cites: 25

    [doi:10.1007/s00415-011-6079-9]