Persones / Equip Humà

Jaume Campistol Plana

Buscador de publicacions

Publicacions

  • Fons-Estupina C, Campistol-Plana J, Narbona J, Velázquez R, Eiris J and García Peñas JJ.

    Alternating hemiplegia of childhood in Spanish population. Study of a series of 17 patients

    MEDICINA CLINICA . 130(15): 577-579. Nº de cites: 4

    [doi:10.1157/13119979]

  • González-Rabelino, G, Campistol-Plana J, Navarro, R, Capdevila-Cirera A and Solá, T.

    Moyamoya en la población infantil: análisis de una serie occidental y revisión de la bibliografía.

    REVISTA DE NEUROLOGIA . 46(7): 385-391.

  • Campistol-Plana J and García, MA.

    Epilepsias refractarias a fármacos antiepilépticos con respuesta a otros fármacos

    NEUROLOGIA . 4(3): 35-40.

  • 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 cites: 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 cites: 19

    [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 cites: 48

    [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 cites: 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 cites: 53

    [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 cites: 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 cites: 37

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