Personas / Equipo Humano

Jaume Campistol Plana

Buscador de publicaciones

Publicaciones

  • Colomé C, Artuch-Iriberri R, Lambruschini N, Cambra-Lasaosa FJ, Campistol-Plana J and Vilaseca MA.

    Is there a relationship between plasma phenylalanine and cholesterol in phenylketonuric patients under dietary treatment?

    CLINICAL BIOCHEMISTRY . 34(5): 373-376. Nº de citas: 21

    [doi:10.1016/S0009-9120(01)00249-1]

  • Gudiño M, Campistol-Plana J, Poo P and Iriondo-Sanz M.

    Cerebellar hemorrhage in full-term newborn babies

    REVISTA DE NEUROLOGIA . 32(7): 624-627.

    [doi:10.33588/rn.3207.2000450]

  • García-Koerner MC, Campistol-Plana J, Agut-Quijano T, Alcorta I, Caritg Bosch J, Estella J and Mateo M.

    Neurological form of onset in haemophagocytic lymphohistiocytosis

    REVISTA DE NEUROLOGIA . 32(4): 333-335.

  • Mallolas J, Vilaseca MA, Pavia C, Lambruschini N, Cambra-Lasaosa FJ, Campistol-Plana J, Gómez D, Carrió A, Estivill X and Milà M.

    Large de novo deletion in chromosome 12 affecting the PAH, IGF1, ASCL1, and TRA1 genes

    JOURNAL OF MOLECULAR MEDICINE-JMM . 78(12): 721-724. Nº de citas: 4

    [doi:10.1007/s001090000160]

  • Artuch-Iriberri R, Colomé C, Vilaseca MA, Sierra-March C, Cambra-Lasaosa FJ, Lambruschini N and Campistol-Plana J.

    Plasma phenylalanine is associated with decreased serum ubiquinone-10 concentrations in phenylketonuria

    JOURNAL OF INHERITED METABOLIC DISEASE . 24(3): 359-366. Nº de citas: 25

    [doi:10.1023/A:1010500502275]

  • Mallolas J, Vilaseca MA, Campistol-Plana J, Lambruschini N, Cambra-Lasaosa FJ, Fusté ME and Milà M.

    Clinical, biochemical, neurological and molecular studies of 11 patients with novel mutations of the PAH gene

    REVISTA DE NEUROLOGIA . 31(10): 907-910. Nº de citas: 7

    [doi:10.33588/rn.3110.2000350]

  • Campistol-Plana J.

    Neonatal neurological advances

    REVISTA DE NEUROLOGIA . 31(7): 601-604. Nº de citas: 2

    [doi:10.33588/rn.3107.2000328]

  • Campistol-Plana J.

    Seizures and epileptic syndromes in the newborn. Forms of presentation, protocol for investigation and treatment

    REVISTA DE NEUROLOGIA . 31(7): 624-631. Nº de citas: 7

    [doi:10.33588/rn.3107.2000320]

  • Busquets C, Merinero B, Christensen E, Gelpí JL, Campistol-Plana J, Pineda M, Fernández-Alvarez E, Prats JM, Sans A, Arteaga R, Martí M, Campos J, Martínez-Pardo M, Martínez-Bermejo A, Ruiz-Falcó ML, Vaquerizo J, Orozco M, Ugarte M, Coll MJ and Ribes A.

    Glutaryl-CoA dehydrogenase deficiency in Spain: Evidence of two groups of patients, genetically, and biochemically distinct

    PEDIATRIC RESEARCH . 48(3): 315-322. Nº de citas: 108

    [doi:10.1203/00006450-200009000-00009]

  • Campistol-Plana J.

    Epileptic syndromes in the first year of life and congenital errors of metabolism

    REVISTA DE NEUROLOGIA . 30: 60-74. Nº de citas: 14