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  • Campistol-Plana J, Poo P, Fernández-Alvarez E and Carratalá F.

    Parasagittal cerebral injury: Magnetic resonance findings

    JOURNAL OF CHILD NEUROLOGY . 14(10): 683-685. Nº de citas: 9

    [doi:10.1177/088307389901401011]

  • Climent C, García-Pérez MA, Sanjurjo P, Ruiz-Sanz JI, Vilaseca MA, Pineda M, Campistol-Plana J and Rubio V.

    Identification of a cytogenetic deletion and of four novel mutations (Q69X, I172F, G188V, G197R) affecting the gene for ornithine transcarbamylase (OTC) in Spanish patients with OTC deficiency

    HUMAN MUTATION . 14(4): 352-353.

    [doi:10.1002/(SICI)1098-1004(199910)14:4<352::AID-HUMU15>3.0.CO;2-D]

  • Jordán-García I, Cambra-Lasaosa FJ, Alcover E, Colomer J, Campistol-Plana J, Caritg Bosch J and Palomeque A.

    Acquired polyneuropathy of the pediatric critical patient

    REVISTA DE NEUROLOGIA . 29(5): 432-435. Nº de citas: 2

    [doi:10.33588/rn.2905.99259]

  • May Llanas ME, Alcover Bloch E, Cambra-Lasaosa FJ, Campistol-Plana J and Palomeque A.

    Hemorragia cerebral no traumtica en la infancia: etiologa, manifestaciones clnicas y manejo.

    ANALES DE PEDIATRIA . 51(3): 257-261.

  • Campistol-Plana J, Fernández A and Ortega J.

    Status epilepticus in children experience with intravenous valproate. Update of treatment guidelines

    REVISTA DE NEUROLOGIA . 29(4): 359-365. Nº de citas: 26

    [doi:10.33588/rn.2904.99092]

  • Guitet M, Campistol-Plana J and Medina M.

    Menkes disease: Experience in copper salts therapy

    REVISTA DE NEUROLOGIA . 29(2): 127-130. Nº de citas: 6

    [doi:10.33588/rn.2902.99288]

  • Artuch-Iriberri R, Colomé C, Vilaseca MA, Pineda M and Campistol-Plana J.

    Ubiquinone:: Metabolism and functions.: Ubiquinone deficiency and its implication in mitochondrial encephalomyopathies.: Treatment with ubiquinone

    REVISTA DE NEUROLOGIA . 29(1): 59-63. Nº de citas: 6

    [doi:10.33588/rn.2901.99204]

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

    Biochemical phenotype and its relationship with genotype in hyperphenylalaninemia heterozygotes

    MOLECULAR GENETICS AND METABOLISM . 67(2): 156-161. Nº de citas: 13

    [doi:10.1006/mgme.1999.2862]

  • Cardo E, Campistol-Plana J, Caritg J, Ruiz S, Vilaseca MA, Kirkham F and Blom HJ.

    Fatal haemorrhagic infarct in an infant with homocystinuria

    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY . 41(2): 132-135. Nº de citas: 19

    [doi:10.1017/S0012162299000250]

  • Campistol-Plana J.

    Reaching a diagnosis in congenital metabolic disorders using neuroimaging

    REVISTA DE NEUROLOGIA . 28(1): 16-23. Nº de citas: 11

    [doi:10.33588/rn.2801.98342]