Personas / Equipo Humano

Jaume Campistol Plana

Buscador de publicaciones

Publicaciones

  • Gutiérrez-Mata AP, López-Casas J, Ortez-González CI, Sempere-Pérez A, Casartelli MJ and Campistol-Plana J.

    Clinical characteristics and progress of patients with migrainous headaches monitored in the headache unit in a paediatric referral hospital

    REVISTA DE NEUROLOGIA . 46(6): 331-336. Nº de citas: 7

    [doi:10.33588/rn.4606.2007461]

  • Duarte S, Sanmarti F, Gonzalez V, Pérez-Dueñas B, Ormazabal-Herrero A, Artuch-Iriberri R, Campistol-Plana J and Garcia-Cazorla A.

    Cerebrospinal fluid pterins and neurotransmitters in early severe epileptic encephalopathies

    BRAIN & DEVELOPMENT . 30(2): 106-111. Nº de citas: 18

    [doi:10.1016/j.braindev.2007.06.009]

  • Donati F, Gobbi G, Campistol-Plana J, Rapatz G, Daehler M, Sturm Y and Aldenkamp AP.

    The cognitive effects of oxcarbazepine versus carbamazepine or valproate in newly diagnosed children with partial seizures

    SEIZURE-EUROPEAN JOURNAL OF EPILEPSY . 16(8): 670-679. Nº de citas: 47

    [doi:10.1016/j.seizure.2007.05.006]

  • Ribasés M, Serrano M, Fernández-Alvarez E, Pahisa S, Ormazabal-Herrero A, Garcia-Cazorla A, Pérez-Dueñas B, Campistol-Plana J, Artuch-Iriberri R and Cormand B.

    A homozygous tyrosine hydroxylase gene promoter mutation in a patient with dopa-responsive encephalopathy:: Clinical, biochemical and genetic analysis

    MOLECULAR GENETICS AND METABOLISM . 92(3): 274-277. Nº de citas: 28

    [doi:10.1016/j.ymgme.2007.07.004]

  • Arias A, Corbella M, Fons-Estupina C, Sempere A, García-Villoria J, Ormazabal-Herrero A, Poo P, Pineda M, Vilaseca MA, Campistol-Plana J, Briones P, Pàmpols T, Salomons GS, Ribes A and Artuch-Iriberri R.

    Creatine transporter deficiency:: Prevalence among patients with mental retardation and pitfalls in metabolite screening

    CLINICAL BIOCHEMISTRY . 40(16-17): 1328-1331. Nº de citas: 52

    [doi:10.1016/j.clinbiochem.2007.07.010]

  • Serrano M, Lizarraga I, Reiss J, Dias AP, Pérez-Dueñas B, Vilaseca MA, Artuch-Iriberri R, Campistol-Plana J and Garcia-Cazorla A.

    Cranial ultrasound and chronological changes in molybdenum cofactor deficiency

    PEDIATRIC RADIOLOGY . 37(10): 1043-1046. Nº de citas: 11

    [doi:10.1007/s00247-007-0558-2]

  • Garcia-Cazorla A, Serrano M, Pérez-Dueñas B, González V, Ormazabal-Herrero A, Pineda M, Fernández-Alvarez E, Campistol-Plana J and Artuch-Iriberri R.

    Secondary abnormalities of neurotransmitters in infants with neurological disorders

    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY . 49(10): 740-744. Nº de citas: 35

    [doi:10.1111/j.1469-8749.2007.00740.x]

  • 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. Nº de citas: 5

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

  • Madruga-Garrido M, Garcia-Villoria J, Ruiz-Del Portal L, Delgado-Pecellin C, Garcia-Valdecasas MS, Blanco-Martinez B, Perez-Perez M, Ribes A, Campistol-Plana J and Rufo-Campos M.

    Glutaric aciduria type I with a low-excretion biochemical phenotype associated to a new mutation

    REVISTA DE NEUROLOGIA . 45(2): 127-128. Nº de citas: 2

    [doi:10.33588/rn.4502.2006325]

  • Sempere-Pérez A, Campistol-Plana J, Garcia-Cazorla A, Guillen-Quesada A and Pérez-Muñoz N.

    Multiple familial cerebral cavernomatosis

    REVISTA DE NEUROLOGIA . 44(11): 657-660. Nº de citas: 9

    [doi:10.33588/rn.4411.2006334]