Personas / Equipo Humano

Jaume Campistol Plana

Buscador de publicaciones

Publicaciones

  • Ormazabal-Herrero A, Artuch-Iriberri R, Vilaseca MA, Garcia-Cazorla A and Campistol-Plana J.

    Pathogenetic mechanisms in phenylketonuria:: Disorders affecting the metabolism of neurotransmitters and the antioxidant system

    REVISTA DE NEUROLOGIA . 39(10): 956-961. Nº de citas: 7

    [doi:10.33588/rn.3910.2004221]

  • Moreno-Torres, A, Martinez-Perez, I, Baquero, M, Campistol-Plana J, Capdevila, A, Arus, C and Pujol, J.

    Taurine detection by proton magnetic resonance spectroscopy in medulloblastoma: Contribution to noninvasive differential diagnosis with cerebellar astrocytoma

    Neurosurgery . 55(4): 824-829. Nº de citas: 50

    [doi:10.1227/01.NEU.0000137655.53303.C8]

  • Guerrini R, Mei D, Sisodiya S, Sicca F, Harding B, Takahashi Y, Dorn T, Yoshida A, Campistol-Plana J, Krämer G, Moro F, Dobyns WB and Parrini E.

    Germline and mosaic mutations of FLN1 in men with periventricular heterotopia

    Neurology . 63(1): 51-56. Nº de citas: 101

    [doi:10.1212/01.WNL.0000132818.84827.4D]

  • Rafia S, García-Peña JJ, López-Pisón J, Aguirre-Rodríguez J, Ramos-Lizana J, García-Pérez A, Martínez-Granero MA, Sans A, Campistol-Plana J, Peña-Segura JL and Espino-Hernández M.

    Growth charts for the Spanish population with neurofibromatosis type 1

    REVISTA DE NEUROLOGIA . 38(11): 1009-1012. Nº de citas: 1

    [doi:10.33588/rn.3811.2004007]

  • Alcover-Bloch E, Campistol-Plana J and Iriondo-Sanz M.

    Neonatal seizures, our experience

    REVISTA DE NEUROLOGIA . 38(9): 808-812. Nº de citas: 12

    [doi:10.33588/rn.3809.2003287]

  • Garcia-Cazorla A, Olivan, JA, Pancho, C, Sans, A, Boix, C and Campistol-Plana J.

    Infectious acute hemicerebellitis

    JOURNAL OF CHILD NEUROLOGY . 19(5): 390-392. Nº de citas: 20

    [doi:10.1177/088307380401900514]

  • Garcia-Cazorla A, Sans, A, Baquero, M, Garcia-Bargo, MD, Arellano, M, Poo, P, Gean, E and Campistol-Plana J.

    White matter alterations associated with chromosomal disorders

    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY . 46(3): 148-153. Nº de citas: 19

    [doi:10.1017/S0012162204000271]

  • Artuch-Iriberri R, Colomé C, Sierra-March C, Brandi-Tarrau N, Lambruschini N, Campistol-Plana J, Ugarte D and Vilaseca MA.

    A longitudinal study of antioxidant status in phenylketonuric patients

    CLINICAL BIOCHEMISTRY . 37(3): 198-203. Nº de citas: 57

    [doi:10.1016/j.clinbiochem.2003.10.017]

  • Lobato-Salinas Z, Cambra-Lasaosa FJ, Campistol-Plana J, Toll-Costa T, Pons-Odena M, Palomeque A and Martín JM.

    Factor V Leiden mutation as a cause of venous thrombosis

    REVISTA DE NEUROLOGIA . 38(2): 136-139. Nº de citas: 2

    [doi:10.33588/rn.3802.2003176]

  • Ugalde C, Triepels RH, Coenen MJ, van den Heuvel LP, Smeets R, Uusimaa J, Briones P, Campistol-Plana J, Majamaa K, Smeitink JA and Nijtmans LG.

    Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene

    ANNALS OF NEUROLOGY . 54(5): 665-669. Nº de citas: 86

    [doi:10.1002/ana.10734]