Personas / Equipo Humano

Jaume Campistol Plana

Buscador de publicaciones

Publicaciones

  • Garcia-Puig M, Fons-Estupina MC, Rives-Solà S, Berrueco-Moreno R, Cruz-Martínez O and Campistol-Plana J.

    Neurotoxicity due to methotrexate in paediatric patients. Description of the clinical symptoms and neuroimaging findings

    REVISTA DE NEUROLOGIA . 54(12): 712-718. Nº de citas: 9

    [doi:10.33588/rn.5412.2012005]

  • Campistol-Plana J, Galvez H, Garcia-Cazorla A, Málaga I, Iriondo-Sanz M and Cusi V.

    Neurological dysfunction induced by bilirrubin

    NEUROLOGIA . 27(4): 202-211. Nº de citas: 14

    [doi:10.1016/j.nrl.2010.03.013]

  • Jimenez E, Ormazabal-Herrero A, Serrano M, Ortez-Gonzalez CI, Artuch-Iriberri R, Garcia-Cazorla A and Campistol-Plana J.

    Amino acids in cerebrospinal fluid and plasma: its usefulness in the study of neuropaediatric diseases

    REVISTA DE NEUROLOGIA . 54(7): 394-398. Nº de citas: 4

    [doi:10.33588/rn.5407.2011454]

  • Campistol-Plana J, González MJ, Gutiérrez AP and Vilaseca MA.

    Treatment and control of patients with phenylketonuria: results from the Collaborative Group of Spanish Follow-up Units

    MEDICINA CLINICA . 138(5): 185-191. Nº de citas: 8

    [doi:10.1016/j.medcli.2011.03.037]

  • Fons-Estupina C, Rizzu P, Garcia-Cazorla A, Martorell-Sampol L, Ormazabal-Herrero A, Artuch-Iriberri R, Campistol-Plana J and Fernández-Alvarez E.

    TITF-1 gene mutation in a case of sporadic non-progressive chorea. Response to levodopa treatment

    BRAIN & DEVELOPMENT . 34(3): 255-257. Nº de citas: 18

    [doi:10.1016/j.braindev.2011.04.007]

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

    Alternating hemiplegia of childhood: Metabolic studies in the largest European series of patients

    EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY . 16(1): 10-14. Nº de citas: 26

    [doi:10.1016/j.ejpn.2011.08.006]

  • Roche-Martinez A, Armstrong-Moron J, Gerotina E, Fons-Estupina C, Campistol-Plana J and Pineda M.

    CDKL5 in different atypical Rett syndrome variants: description of the first eight patients from Spain

    Journal of Pediatric Epilepsy . 1(1): 27-35.

    [doi:10.3233/PEP-2012-005]

  • Villar C, Campistol-Plana J, Fons-Estupina C, Armstrong-Moron J, Mas A, Ormazabal-Herrero A and Artuch-Iriberri R.

    Glycine and L-arginine treatment causes hyperhomocysteinemia in cerebral creatine transporter deficiency patients.

    JIMD Reports . 4: 13-16. Nº de citas: 4

    [doi:10.1007/8904_2011_41]

  • Rubí S, Setoain X, Donaire A, Bargalló N, Sanmartí F, Carreño M, Rumià J, Calvo A, Aparicio J, Campistol-Plana J and Pons F.

    Validation of FDG-PET/MRI coregistration in nonlesional refractory childhood epilepsy

    Epilepsia . 52(12): 2216-2224. Nº de citas: 51

    [doi:10.1111/j.1528-1167.2011.03295.x]

  • Navarro-Sastre A, Tort F, Stehling O, Uzarska MA, Arranz JA, Del Toro M, Labayru MT, Landa J, Font A, Garcia-Villoria J, Merinero B, Ugarte M, Gutierrez-Solana LG, Campistol-Plana J, Garcia-Cazorla A, Vaquerizo J, Riudor E, Briones P, Elpeleg O, Ribes A and Lill R.

    A Fatal Mitochondrial Disease Is Associated with Defective NFU1 Function in the Maturation of a Subset of Mitochondrial Fe-S Proteins

    AMERICAN JOURNAL OF HUMAN GENETICS . 89(5): 656-667. Nº de citas: 247

    [doi:10.1016/j.ajhg.2011.10.005]