Persones / Equip Humà

Jaume Campistol Plana

Buscador de publicacions

Publicacions

  • De Grandis E, Serrano M, Pérez-Dueñas B, Ormazabal-Herrero A, Montero-Sanchez R, Veneselli E, Pineda M, González V, Sanmartí F, Fons-Estupina C, Sans A, Cormand B, Puelles L, Alonso A, Campistol-Plana J, Artuch-Iriberri R and Garcia-Cazorla A.

    Cerebrospinal fluid alterations of the serotonin product, 5-hydroxyindolacetic acid, in neurological disorders

    JOURNAL OF INHERITED METABOLIC DISEASE . 33(6): 803-809. Nº de cites: 33

    [doi:10.1007/s10545-010-9200-9]

  • Russi ME, González V and Campistol-Plana J.

    Cerebral venous thromboses in the paediatric age: clinical presentation, risk factors, diagnosis and treatment

    REVISTA DE NEUROLOGIA . 51(11): 661-668. Nº de cites: 3

    [doi:10.33588/rn.5111.2010355]

  • Panagiotakaki E, Gobbi G, Neville B, Ebinger F, Campistol-Plana J, Nevsímalová S, Laan L, Casaer P, Spiel G, Giannotta M, Fons-Estupina C, Ninan M, Sange G, Schyns T, Vavassori R, Poncelin D and Arzimanoglou A.

    Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults

    BRAIN . 133(12): 3598-3610. Nº de cites: 127

    [doi:10.1093/brain/awq295]

  • Tondo M, Lambruschini N, Gomez-Lopez L, Gutierrez A, Moreno J, Garcia-Cazorla A, Pérez-Dueñas B, Pineda M, Campistol-Plana J, Vilaseca MA and Artuch-Iriberri R.

    The monitoring of trace elements in blood samples from patients with inborn errors of metabolism

    JOURNAL OF INHERITED METABOLIC DISEASE . 33: 43-49. Nº de cites: 3

    [doi:10.1007/s10545-009-9015-8]

  • Serrano M, Vilaseca MA and Campistol-Plana J.

    Inborn errors of metabolism and sports

    Apunts Sports Medicine . 45(167): 185-189.

  • Herranz JL, Casas-Fernández C, Campistol-Plana J, Campos-Castelló J, Rufo-Campos M, Torres-Falcón A and de Rosendo J.

    Lennox-Gastaut syndrome in Spain: a descriptive retrospective epidemiological study

    REVISTA DE NEUROLOGIA . 50(12): 711-717. Nº de cites: 9

    [doi:10.33588/rn.5012.2010294]

  • Iqbal F, Item CB, Vilaseca MA, Jalan A, Mühl A, Couce ML, Duat A, Delgado MP, Bosch J, Puche A, Campistol-Plana J, Pineda M and Bodamer OA.

    The identification of novel mutations in the biotinidase gene using denaturing high pressure liquid chromatography (dHPLC)

    MOLECULAR GENETICS AND METABOLISM . 100(1): 42-45. Nº de cites: 17

    [doi:10.1016/j.ymgme.2009.12.016]

  • López-Sala A, Palacio-Navarro A, Donaire A, García G, Colomé-Roura R, Boix Lluch C, Sans A, Campistol-Plana J and Sanmartí FX.

    Variables predictoras de retraso mental en una unidad de monitorización videoelectroencefalográfica pediátrica. Evaluación neuropsicológica.

    REVISTA DE NEUROLOGIA . 50 Suppl 3(s3): 59-67. Nº de cites: 1

  • Serrano M, Martins C, Pérez-Dueñas B, Gomez-Lopez L, Murgui E, Fons-Estupina C, Garcia-Cazorla A, Artuch-Iriberri R, Jara F, Arranz JA, Häberle J, Briones P, Campistol-Plana J, Pineda M and Vilaseca MA.

    Neuropsychiatric Manifestations in Late-Onset Urea Cycle Disorder Patients

    JOURNAL OF CHILD NEUROLOGY . 25(3): 352-358. Nº de cites: 38

    [doi:10.1177/0883073809340696]

  • Fons-Estupina C, Arias A, Sempere A, Poo P, Pineda M, Mas A, López-Sala A, Garcia-Villoria J, Vilaseca MA, Ozaez L, Lluch M, Artuch-Iriberri R, Campistol-Plana J and Ribes A.

    Response to creatine analogs in fibroblasts and patients with creatine transporter deficiency

    MOLECULAR GENETICS AND METABOLISM . 99(3): 296-299. Nº de cites: 23

    [doi:10.1016/j.ymgme.2009.10.186]