Persones / Equip Humà

Mercedes Serrano Gimaré

Buscador de publicacions

Publicacions

  • Ribasés M, Serrano M, Fernández-Alvarez E, Pahisa S, Ormazabal-Herrero A, Garcia-Cazorla A, Pérez-Dueñas B, Campistol-Plana J, Artuch-Iriberri R and Cormand B.

    A homozygous tyrosine hydroxylase gene promoter mutation in a patient with dopa-responsive encephalopathy:: Clinical, biochemical and genetic analysis

    MOLECULAR GENETICS AND METABOLISM . 92(3): 274-277. Nº de cites: 28

    [doi:10.1016/j.ymgme.2007.07.004]

  • Serrano M, Lizarraga I, Reiss J, Dias AP, Pérez-Dueñas B, Vilaseca MA, Artuch-Iriberri R, Campistol-Plana J and Garcia-Cazorla A.

    Cranial ultrasound and chronological changes in molybdenum cofactor deficiency

    PEDIATRIC RADIOLOGY . 37(10): 1043-1046. Nº de cites: 11

    [doi:10.1007/s00247-007-0558-2]

  • 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: 37

    [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]

  • Serrano M, García-Alix A, López JC, Pérez J and Quero J.

    Retained central venous lines in the newborn: report of one case and systematic review of the literature.

    Neonatal Network : Nn . 26(2): 105-10. Nº de cites: 14

    [doi:10.1891/0730-0832.26.2.105]

  • Sebastiani G, Costa Orvay JA, Serrano M and Iriondo-Sanz M.

    [Scrotal edema: a rare complication of percutaneous central venous atheters].

    ANALES DE PEDIATRIA . 65(4): 377-80. Nº de cites: 3

    [doi:10.1157/13092493]

  • Trujillano L, Valenzuela I, Costa-Roger M, Cuscó I, Fernandez-Alvarez P, Cueto-González A, Lasa-Aranzasti A, Masotto B, Abulí A, Codina-Solà M, Del Campo M, Ruiz Moreno JA, Pardo Domínguez C, Palma Milla C, Pérez de la Fuente R, Quesada-Espinosa JF, Núñez-Enamorado N, Gener B, Ballesta-Martínez MJ, Brea-Fernández AJ, Fernández-Prieto M, Trujillo-Quintero JP, Ruiz A, Santos-Simarro F, Rosello M, Orellana C, Martinez F, Martinez-Monseny T, Casas-Alba D, Serrano M, Palomares-Bralo M, Rikeros-Orozco E, Gómez-Cano MÁ, Tirado-Requero P, Pié Juste J, Ramos FJ, García-Arumí E and Tizzano EF.

    Comprehensive Clinical and Genetic Characterization of a Spanish Cohort of 22 Patients With Bainbridge-Ropers Syndrome.

    CLINICAL GENETICS . : .

    [doi:10.1111/cge.14701]