People / Staff

Aida Ormazabal Herrero

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Publications

  • López-Laso E, Ormazabal-Herrero A, Camino R, Gascón FJ, Ochoa JJ, Mateos ME, Muñoz MJ, Pérez-Navero JL, Lao JI, Vilaseca MA and Artuch-Iriberri R.

    Oral phenylalanine loading test for the diagnosis of dominant guanosine triphosphate cyclohydrolase 1 deficiency

    CLINICAL BIOCHEMISTRY . 39(9): 893-897. Number of citations: 8

    [doi:10.1016/j.clinbiochem.2006.03.002]

  • Ormazabal-Herrero A, Garcia-Cazorla A, Pérez-Dueñas B, Gonzalez V, Fernández-Alvarez E, Pineda M, Campistol-Plana J and Artuch-Iriberri R.

    Determination of 5-methyltetrahydrofolate in cerebrospinal fluid of paediatric patients:: Reference values for a paediatric population

    CLINICA CHIMICA ACTA . 371(1-2): 159-162. Number of citations: 45

    [doi:10.1016/j.cca.2006.03.004]

  • Ormazabal-Herrero A, Garcia-Cazorla A, Pérez-Dueñas B, Pineda M, Ruiz A, López Laso E, García Silva M, Carilho I, Barbot C, Cormand B, Ribases M, Moller L, Fernández-Alvarez E, Campistol-Plana J and Artuch-Iriberri R.

    Usefulness of analysis of cerebrospinal fluid for the diagnosis of neurotransmitters and pterin defects and glucose and folate transport deficiencies across blood brain barrier

    MEDICINA CLINICA . 127(3): 81-85. Number of citations: 7

    [doi:10.1157/13090262]

  • Pineda M, Ormazabal-Herrero A, López-Gallardo E, Nascimento-Osorio A, Solano A, Herrero MD, Vilaseca MA, Briones P, Ibañez-Toda L, Montoya J and Artuch-Iriberri R.

    Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletion

    ANNALS OF NEUROLOGY . 59(2): 394-398. Number of citations: 92

    [doi:10.1002/ana.20746]

  • Ormazabal-Herrero A, Artuch-Iriberri R, Vilaseca MA, Aracil A and Pineda M.

    Cerebrospinal fluid concentrations of folate, biogenic amines and pterins in Rett syndrome: Treatment with folinic acid

    Neuropediatrics . 36(6): 380-385. Number of citations: 32

    [doi:10.1055/s-2005-873078]

  • Ormazabal-Herrero A, Vilaseca MA, Pérez-Dueñas B, Lambruschini N, Gomez-Lopez L, Campistol-Plana J and Artuch-Iriberri R.

    Platelet serotonin concentrations in PKU patients under dietary control and tetrahydrobiopterin treatment

    JOURNAL OF INHERITED METABOLIC DISEASE . 28(6): 863-870. Number of citations: 20

    [doi:10.1007/s10545-005-0153-3]

  • Møller LB, Romstad A, Paulsen M, Hougaard P, Ormazabal-Herrero A, Pineda M, Blau N, Güttler F and Artuch-Iriberri R.

    Pre- and postnatal diagnosis of tyrosine hydroxylase deficiency

    PRENATAL DIAGNOSIS . 25(8): 671-675. Number of citations: 12

    [doi:10.1002/pd.1193]

  • Garcia-Cazorla A, Ormazabal-Herrero A, Artuch-Iriberri R, Pérez-Dueñas B, López-Casas J, Fernández-Alvarez E and Campistol-Plana J.

    Inborn errors of neurotransmitters in neuropaediatrics

    REVISTA DE NEUROLOGIA . 41(2): 99-108. Number of citations: 5

    [doi:10.33588/rn.4102.2004377]

  • Varea V, Martín-de-Carpi J, Puig C, Alda JA, Camacho E, Ormazabal-Herrero A, Artuch-Iriberri R and Gomez-Lopez L.

    Malabsorption of carbohydrates and depression in children and adolescents

    JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION . 40(5): 561-565. Number of citations: 12

    [doi:10.1097/01.MPG.0000153005.61234.28]

  • Ormazabal-Herrero A, Garcia-Cazorla A, Fernández Y, Fernández-Alvarez E, Campistol-Plana J and Artuch-Iriberri R.

    HPLC with electrochemical and fluorescence detection procedures for the diagnosis of inborn errors of biogenic amines and pterins

    JOURNAL OF NEUROSCIENCE METHODS . 142(1): 153-158. Number of citations: 111

    [doi:10.1016/j.jneumeth.2004.08.007]