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  • Serrano M, Ormazabal-Herrero A, Pérez-Dueñas B, Artuch-Iriberri R, Coroleu W, Krauel Vidal X, Campistol-Plana J and Garcia-Cazorla A.

    Perinatal asphyxia may cause reduction in csf dopamine metabolite concentrations

    Neurology . 69(3): 311-313. Number of citations: 5

    [doi:10.1212/01.wnl.0000265855.13026.dd]

  • López-Laso E, Camino R, Mateos ME, Pérez-Navero JL, Ochoa JJ, Lao-Villadóniga JI, Ormazabal-Herrero A and Artuch-Iriberri R.

    Dopa-responsive infantile hypokinetic rigid syndrome due to dominant guanosine triphosphate cyclohydrolase 1 deficiency

    JOURNAL OF THE NEUROLOGICAL SCIENCES . 256(1-2): 90-93. Number of citations: 13

    [doi:10.1016/j.jns.2007.02.007]

  • Campistol-Plana J, Arias-Dimas A, Poo P, Pineda M, Hoffman M, Vilaseca MA, Artuch-Iriberri R and Ribes A.

    Cerebral creatine transporter deficiency:: An infradiagnosed neurometabolic disease

    REVISTA DE NEUROLOGIA . 44(6): 343-347. Number of citations: 8

    [doi:10.33588/rn.4406.2006389]

  • García-Vicente S, Yraola F, Marti L, González-Muñoz E, García-Barrado MJ, Cantó C, Abella A, Bour S, Artuch-Iriberri R, Sierra-March C, Brandi-Tarrau N, Carpéné C, Moratinos J, Camps M, Palacín M, Testar X, Gumà A, Albericio F, Royo M, Mian A and Zorzano A.

    Oral insulin-mimetic compounds that act independently of insulin

    Diabetes . 56(2): 486-493. Number of citations: 61

    [doi:10.2337/db06-0269]

  • Vilaseca MA, Artuch-Iriberri R, Bauzá, FR, Pineda M, García, A and Campistol-Plana J.

    Diagnóstico diferencial de la hiperhomocisteinemia en pediatría

    Química Clínica . 26(4): 191-195.

  • Montero-Sanchez R, Pineda M, Aracil A, Vilaseca MA, Briones P, Sánchez-Alcázar JA, Navas P and Artuch-Iriberri R.

    Clinical, biochemical and molecular aspects of cerebellar ataxia and Coenzyme Q10 deficiency

    Cerebellum . 6(2): 118-122. Number of citations: 46

    [doi:10.1080/14734220601021700]

  • Garcia-Cazorla A, Pérez-Dueñas B, Pineda M, Artuch-Iriberri R, Vilaseca MA and Campistol-Plana J.

    [Orientation of mental retardation from neurometabolic diseases].

    REVISTA DE NEUROLOGIA . 43 Suppl 1: 187-92. Number of citations: 3

  • Gömez L, Garcia-Cazorla A, Gutiérrez A, Artuch-Iriberri R, Varea V, Martín J, Pinillos S and Vilaseca MA.

    Treatment of severe osteoporosis with alendronate in a patient with lysinuric protein intolerance

    JOURNAL OF INHERITED METABOLIC DISEASE . 29(5): 687-687. Number of citations: 9

    [doi:10.1007/s10545-006-0236-9]

  • Arias A, Ormazabal-Herrero A, Moreno J, González B, Vilaseca MA, García-Villoria J, Pàmpols T, Briones P, Artuch-Iriberri R and Ribes A.

    Methods for the diagnosis of creatine deficiency syndromes:: A comparative study

    JOURNAL OF NEUROSCIENCE METHODS . 156(1-2): 305-309. Number of citations: 31

    [doi:10.1016/j.jneumeth.2006.03.005]

  • López-Laso E, Ormazabal-Herrero A, Camino R, Gascón FJ, Ochoa JJ, Mateos ME, Muñoz MJ, Pérez-Navero JL, Lao JI, Vilaseca MA and Artuch-Iriberri R.

    Oral phenylalanine loading test for the diagnosis of dominant guanosine triphosphate cyclohydrolase 1 deficiency

    CLINICAL BIOCHEMISTRY . 39(9): 893-897. Number of citations: 7

    [doi:10.1016/j.clinbiochem.2006.03.002]