Personas / Equipo Humano

Rafael Artuch Iriberri

Buscador de publicaciones

Publicaciones

  • Ormazabal-Herrero A, Garcia-Cazorla A, Fernández Y, Fernández-Alvarez E, Campistol-Plana J and Artuch-Iriberri R.

    HPLC with electrochemical and fluorescence detection procedures for the diagnosis of inborn errors of biogenic amines and pterins

    JOURNAL OF NEUROSCIENCE METHODS . 142(1): 153-158. Nº de citas: 100

    [doi:10.1016/j.jneumeth.2004.08.007]

  • Pancho C, Garcia-Cazorla A, Varea V, Artuch-Iriberri R, Ferrer I, Vilaseca MA, Briones P and Campistol-Plana J.

    Congenital disorder of glycosylation type la revealed by hypertransaminasemia and failure to thrive in a young boy with normal neurodevelopment

    JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION . 40(2): 230-232. Nº de citas: 12

    [doi:10.1097/00005176-200502000-00030]

  • Pintó X, Vilaseca MA, Balcells S, Artuch-Iriberri R, Corbella E, Meco JF, Vila R, Pujol R and Grinberg-Vaisman DR.

    A folate-rich diet is as effective as folic acid from supplements in decreasing plasma homocysteine concentrations.

    INTERNATIONAL JOURNAL OF MEDICAL SCIENCES . 2(2): 58-63. Nº de citas: 21

    [doi:10.7150/ijms.2.58]

  • Montero-Sanchez R, Artuch-Iriberri R, Briones P, Nascimento-Osorio A, Garcia-Cazorla A, Vilaseca MA, Sánchez-Alcázar JA, Navas P, Montoya J and Pineda M.

    Muscle coenzyme Q10 concentrations in patients with probable and definite diagnosis of respiratory chain disorders

    Biofactors . 25(1-4): 109-115. Nº de citas: 38

    [doi:10.1002/biof.5520250112]

  • Pérez-Dueñas B, Vilaseca MA, Mas A, Lambruschini N, Artuch-Iriberri R, Gomez-Lopez L, Pineda J, Gutiérrez A, Mila M and Campistol-Plana J.

    Tetrahydrobiopterin responsiveness in patients with phenylketonuria

    CLINICAL BIOCHEMISTRY . 37(12): 1083-1090. Nº de citas: 43

    [doi:10.1016/j.clinbiochem.2004.09.005]

  • Ormazabal-Herrero A, Artuch-Iriberri R, Vilaseca MA, Garcia-Cazorla A and Campistol-Plana J.

    Pathogenetic mechanisms in phenylketonuria:: Disorders affecting the metabolism of neurotransmitters and the antioxidant system

    REVISTA DE NEUROLOGIA . 39(10): 956-961. Nº de citas: 7

    [doi:10.33588/rn.3910.2004221]

  • Noguera-Julián A, Fortuny-Guasch C, Munoz-Almagro C, Sanchez E, Vilaseca MA, Artuch-Iriberri R, Pou Fernández J and Jimenez R.

    Hyperlactatemia in human immunodeficiency virus-uninfected infants who are exposed to antiretrovirals

    Pediatrics . 114(5): 598-603. Nº de citas: 73

    [doi:10.1542/peds.2004-0955]

  • Pineda M, Solano A, Artuch-Iriberri R, Andreu AL, Playan A, Vilaseca MA, Colomer J, Briones P, Casademont J and Montoya J.

    Peripheral neuropathy with ataxia in childhood as a result of the G8363A mutation in mitochondrial DNA

    PEDIATRIC RESEARCH . 56(1): 55-59. Nº de citas: 9

    [doi:10.1203/01.PDR.0000130475.20571.98]

  • Pineda M, Playán-Ariso A, Alcaine-Villarroya MJ, Vernet AM, Serra-Castanera A, Solano A, Vilaseca MA, Artuch-Iriberri R, López-Pérez M, Briones-Godino MP, Andreu A and Montoya J.

    Familiar chronic progressive external ophthalmoplegia of mitochondrial origin

    REVISTA DE NEUROLOGIA . 38(11): 1023-1027. Nº de citas: 8

    [doi:10.33588/rn.3811.2004019]

  • Vilaseca MA, Artuch-Iriberri R and Briones, P.

    Congenital disorders of glycosylation: state of the art and Spanish experience

    MEDICINA CLINICA . 122(18): 707-716. Nº de citas: 4