Persones / Equip Humà

MªAngels García Cazorla

Buscador de publicacions

Publicacions

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

    Secondary abnormalities of neurotransmitters in infants with neurological disorders

    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY . 49(10): 740-744. Nº de cites: 35

    [doi:10.1111/j.1469-8749.2007.00740.x]

  • Serrano M, Ormazabal-Herrero A, Pérez-Dueñas B, Artuch-Iriberri R, Coroleu W, Krauel Vidal X, Campistol-Plana J and Garcia-Cazorla A.

    Perinatal asphyxia may cause reduction in csf dopamine metabolite concentrations

    Neurology . 69(3): 311-313. Nº de cites: 5

    [doi:10.1212/01.wnl.0000265855.13026.dd]

  • Sempere-Pérez A, Campistol-Plana J, Garcia-Cazorla A, Guillen-Quesada A and Pérez-Muñoz N.

    Multiple familial cerebral cavernomatosis

    REVISTA DE NEUROLOGIA . 44(11): 657-660. Nº de cites: 9

    [doi:10.33588/rn.4411.2006334]

  • Cardesa-Salzmann TM, Mora J, Garcia-Cazorla A, Cruz-Martínez O, Munoz-Almagro C and Campistol-Plana J.

    Epstein-Barr virus related opsoclonus-myoclonus-ataxia does not rule out the presence of occult neuroblastic tumors

    PEDIATRIC BLOOD & CANCER . 47(7): 964-967. Nº de cites: 17

    [doi:10.1002/pbc.20573]

  • Garcia-Cazorla A, Pérez-Dueñas B, Pineda M, Artuch-Iriberri R, Vilaseca MA and Campistol-Plana J.

    [Orientation of mental retardation from neurometabolic diseases].

    REVISTA DE NEUROLOGIA . 43 Suppl 1: 187-92. Nº de cites: 3

  • Gömez L, Garcia-Cazorla A, Gutiérrez A, Artuch-Iriberri R, Varea V, Martín J, Pinillos S and Vilaseca MA.

    Treatment of severe osteoporosis with alendronate in a patient with lysinuric protein intolerance

    JOURNAL OF INHERITED METABOLIC DISEASE . 29(5): 687-687. Nº de cites: 9

    [doi:10.1007/s10545-006-0236-9]

  • Gissen P, Tee L, Johnson CA, Genin E, Caliebe A, Chitayat D, Clericuzio C, Denecke J, Di Rocco M, Fischler B, FitzPatrick D, Garcia-Cazorla A, Guyot D, Jacquemont S, Koletzko S, Leheup B, Mandel H, Sanseverino MT, Houwen RH, McKiernan PJ, Kelly DA and Maher ER.

    Clinical and molecular genetic features of ARC syndrome

    HUMAN GENETICS . 120(3): 396-409. Nº de cites: 89

    [doi:10.1007/s00439-006-0232-z]

  • Garcia-Cazorla A, De Lonlay P, Rustin P, Chretien D, Touati G, Rabier D, Slama A and Saudubray JM.

    Mitochondrial respiratory chain deficiencies expressing the enzymatic deficiency in the hepatic tissue:: A study of 31 patients

    JOURNAL OF PEDIATRICS . 149(3): 401-405. Nº de cites: 14

    [doi:10.1016/j.jpeds.2006.05.036]

  • 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. Nº de cites: 44

    [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. Nº de cites: 6

    [doi:10.1157/13090262]