People / Staff

Rafael Artuch Iriberri

Search publications

Publications

  • Artuch-Iriberri R, Colome, C, Playan, A, Alcaine, MJ, Briones, P, Montoya, J, Vilaseca MA and Pineda M.

    Oxygen consumption measurement in lymphocytes for the diagnosis of pediatric patients with oxidative phosphorylation diseases

    CLINICAL BIOCHEMISTRY . 33(6): 481-485. Number of citations: 11

    [doi:10.1016/S0009-9120(00)00137-5]

  • Colomer J, Iturriaga, C, Bestue, M, Artuch-Iriberri R, Briones, P, Montoya, J, Vilaseca MA and Pineda M.

    Characterization of the neuropathy in mitochondrial disorders

    REVISTA DE NEUROLOGIA . 30(12): 1117-1121. Number of citations: 9

    [doi:10.33588/rn.3012.2000079]

  • Campistol-Plana J, Chávez B, Vilaseca MA and Artuch-Iriberri R.

    Antiepileptic drugs and carnitine

    REVISTA DE NEUROLOGIA . 30: 105-109. Number of citations: 12

  • Cardo E, Monrós E, Colomé C, Artuch-Iriberri R, Campistol-Plana J, Pineda M and Vilaseca MA.

    Children with stroke:: Polymorphism of the MTHFR gene, mild hyperhomocysteinemia, and vitamin status

    JOURNAL OF CHILD NEUROLOGY . 15(5): 295-298. Number of citations: 63

    [doi:10.1177/088307380001500505]

  • Pavia, C, Artuch-Iriberri R, Ferrer, I, Colome, C, Valls, C and Vilaseca MA.

    Total homocysteine in patients with type 1 diabetes

    Diabetes Care . 23(1): 84-87. Number of citations: 54

    [doi:10.2337/diacare.23.1.84]

  • Cardo E, Pineda M, Vilaseca MA, Artuch-Iriberri R and Campistol-Plana J.

    Risk factors in cerebrovascular disease in childhood

    REVISTA DE NEUROLOGIA . 30(1): 21-27. Number of citations: 11

    [doi:10.33588/rn.3001.99459]

  • Cardo, E, Pineda M, Artuch-Iriberri R, Vilaseca MA and Campistol-Plana J.

    Propuesta de protocolo de estudio de las enfermedades cerebrovasculares de la infancia

    ANALES DE PEDIATRIA . 52(5): 435-442.

  • Pampols, T, Arranz, JA, Baiget, M, Borja, F, Briones, P, Casals, T, Chabas, A, Monrós E, Vilardell, LL and Artuch-Iriberri R.

    Errors congènits del metabolisme (ECM)

    Pediatría Catalana . 60: 561-570.

  • Quintillá-Martínez JM, Campistol-Plana J, Boleda Vall-Llobera, MD, Vilaseca MA, Artuch-Iriberri R, Palomeque A, Briones, P and Ribes Rubió, A.

    Síndrome de Reye-like como manifestacion inicial de enfermedad mitocondrial

    ANALES DE PEDIATRIA . 52(5): 479-482.

  • Vilaseca MA, Monrós E, Artuch-Iriberri R, Colomé C, Farré C, Valls C, Cardo E and Pineda M.

    Anti-epileptic drug treatment in children: hyperhomocysteinaemia, B-vitamins and the 677C-->T mutation of the methylenetetrahydrofolate reductase gene.

    EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY . 4(6): 269-77. Number of citations: 55

    [doi:10.1053/ejpn.2000.0379]