Personas / Equipo Humano

Jaume Campistol Plana

Buscador de publicaciones

Publicaciones

  • 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: 58

    [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: 89

    [doi:10.1002/ana.10734]

  • Campistol-Plana J and Garcia-Cazorla A.

    West's syndrome.: Analysis, aetiological factors and therapeutic options

    REVISTA DE NEUROLOGIA . 37(4): 345-352. Nº de citas: 14

    [doi:10.33588/rn.3704.2003181]

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

    Plasma thiols and their determinants in phenylketonuria

    EUROPEAN JOURNAL OF CLINICAL NUTRITION . 57(8): 964-968. Nº de citas: 10

    [doi:10.1038/sj.ejcn.1601631]

  • Urreizti R, Balcells S, Rodés M, Vilarinho L, Baldellou A, Couce ML, Muñoz C, Campistol-Plana J, Pintó X, Vilaseca MA and Grinberg D.

    Spectrum of CBS mutations in 16 homocystinuric patients from the Iberian Peninsula: high prevalence of T191M and absence of I278T or G307S

    HUMAN MUTATION . 22(1): 103-103.

    [doi:10.1002/humu.9153]

  • Campistol-Plana J.

    Orally administered drugs in the treatment of spasticity

    REVISTA DE NEUROLOGIA . 37(1): 70-74. Nº de citas: 5

    [doi:10.33588/rn.3701.2003220]

  • Poo P, López-Casas JA, Galván-Manso M, Aquino-Fariña L, Terricabras-Carol L and Campistol-Plana J.

    Botulinum toxin type A. Indications and results

    REVISTA DE NEUROLOGIA . 37(1): 74-80. Nº de citas: 5

  • Curcoy A, Olsen RK, Ribes A, Trenchs-Sainz de la Maza V, Vilaseca MA, Campistol-Plana J, Osorio JH, Andresen BS and Gregersen N.

    Late-onset form of beta-electron transfer flavoprotein deficiency

    MOLECULAR GENETICS AND METABOLISM . 78(4): 247-249. Nº de citas: 29

    [doi:10.1016/S1096-7192(03)00024-6]