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

    Clinical and nutritional evaluation of phenylketonuric patients on tetrahydrobiopterin monotherapy

    MOLECULAR GENETICS AND METABOLISM . 86: 54-60. Number of citations: 81

    [doi:10.1016/j.ymgme.2005.05.014]

  • Millet P, Vilaseca MA, Valls C, Pérez-Dueñas B, Artuch-Iriberri R, Gomez-Lopez L, Lambruschini N and Campistol-Plana J.

    Is deoxypyridinoline a good resorption marker to detect osteopenia in phenylketonuria?

    CLINICAL BIOCHEMISTRY . 38(12): 1127-1132. Number of citations: 26

    [doi:10.1016/j.clinbiochem.2005.09.002]

  • Pérez-Dueñas B, Valls-Solé J, Fernández-Alvarez E, Conill J, Vilaseca MA, Artuch-Iriberri R and Campistol-Plana J.

    Characterization of tremor in phenylketonuric patients

    JOURNAL OF NEUROLOGY . 252(11): 1328-1334. Number of citations: 25

    [doi:10.1007/s00415-005-0860-6]

  • Gassió-Subirachs R, Fusté E, López-Sala A, Artuch-Iriberri R, Vilaseca MA and Campistol-Plana J.

    School performance in early and continuously treated phenylketonuria

    PEDIATRIC NEUROLOGY . 33(4): 267-271. Number of citations: 55

    [doi:10.1016/j.pediatrneurol.2005.05.003]

  • Garcia-Cazorla A, Ormazabal-Herrero A, Artuch-Iriberri R, Pérez-Dueñas B, López-Casas J, Fernández-Alvarez E and Campistol-Plana J.

    Inborn errors of neurotransmitters in neuropaediatrics

    REVISTA DE NEUROLOGIA . 41(2): 99-108. Number of citations: 5

    [doi:10.33588/rn.4102.2004377]

  • Gassió-Subirachs R, Artuch-Iriberri R, Vilaseca MA, Fusté E, Boix Lluch C, Sans A and Campistol-Plana J.

    Cognitive functions in classic phenylketonuria and mild hyperphenyl-alaninaemia:: experience in a paediatric population

    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY . 47(7): 443-448. Number of citations: 78

    [doi:10.1017/S0012162205000861]

  • Gutiérrez-Aguilar G, Abenia-Usón P, Vilaseca MA and Campistol-Plana J.

    Encephalopathy with methylmalonic aciduria and homocystinuria secondary to a deficient exogenous supply of vitamin B-12

    REVISTA DE NEUROLOGIA . 40(10): 605-608. Number of citations: 6

    [doi:10.33588/rn.4010.2004472]

  • Campistol-Plana J, Malaga-Dieguez, I, Garcia-Cazorla A, Krauel-Vidal, X and Vilaseca MA.

    Inborn errors of metabolism with neurological symptomathology in the neonatal period

    REVISTA DE NEUROLOGIA . 40(6): 321-326. Number of citations: 2

    [doi:10.33588/rn.4006.2004232]

  • 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. Number of citations: 104

    [doi:10.1016/j.jneumeth.2004.08.007]

  • Galván-Manso M, Campistol-Plana J, Conill J and Sanmarti FX.

    Analysis of the characteristics of epilepsy in 37 patients with the molecular diagnosis of Angelman syndrome

    EPILEPTIC DISORDERS . 7(1): 19-25. Number of citations: 37