Personas / Equipo Humano

Judith Silvia Armstrong Morón

Buscador de publicaciones

Publicaciones

  • Armstrong-Moron J, Bonaventura I, Rojo A, González G, Corral J, Nadal N, Volpini V and Ferrer I.

    Spinocerebellar ataxia type 2 (SCA2) with white matter involvement

    NEUROSCIENCE LETTERS . 381(3): 247-251. Nº de citas: 16

    [doi:10.1016/j.neulet.2005.02.063]

  • Corral J, Genís D, Banchs I, San Nicolás H, Armstrong-Moron J and Volpini V.

    Giant SCA8 alleles in nine children whose mother has two moderately large ones

    ANNALS OF NEUROLOGY . 57(4): 549-553. Nº de citas: 12

    [doi:10.1002/ana.20421]

  • Ballestar E, Ropero S, Alaminos M, Armstrong-Moron J, Setien F, Agrelo R, Fraga MF, Herranz M, Avila S, Pineda M, Monros E and Esteller M.

    The impact of MECP2 mutations in the expression patterns of Rett syndrome patients

    HUMAN GENETICS . 116(1-2): 91-104. Nº de citas: 71

    [doi:10.1007/s00439-004-1200-0]

  • Armstrong-Moron J, Aracil A and Pineda M.

    Síndrome de Rett, del diagnóstico clínico al diagnóstico molecular

    Neurocirugia . (1): 38-43.

  • Armstrong-Moron J, Boada M, Rey MJ, Vidal N and Ferrer I.

    Familial Alzheimer disease associated with A713T mutation in APP

    NEUROSCIENCE LETTERS . 370(2-3): 241-243. Nº de citas: 38

    [doi:10.1016/j.neulet.2004.08.026]

  • Armstrong-Moron J, Aibar E, Pineda M, Pérez MM, Gean Molins E, Carrera M, Casas C, Martínez F and Monrós E.

    Prenatal diagnosis in Rett syndrome

    FETAL DIAGNOSIS AND THERAPY . 17(4): 200-204. Nº de citas: 6

    [doi:10.1159/000059370]

  • Monrós E, Armstrong-Moron J, Aibar E, Poo P, Canós I and Pineda M.

    Rett syndrome in Spain:: mutation analysis and clinical correlations

    BRAIN & DEVELOPMENT . 23: 251-253. Nº de citas: 78

    [doi:10.1016/S0387-7604(01)00374-6]

  • Armstrong-Moron J, Pineda M and Monrós E.

    Mutation analysis of 16S rRNA in patients with Rett syndrome

    PEDIATRIC NEUROLOGY . 23(1): 85-87. Nº de citas: 6

    [doi:10.1016/S0887-8994(00)00158-2]

  • Pineda M, Armstrong-Moron J and Monrós E.

    Síndrome de Rett. Hallazgo del gen MECP2 como marcador genético

    Archivos de Pediatría . 51: 83-85.

  • Cortés-Saladelafont E, Molero M, Duarte S, Casado-Rio M, Sierra-March C, O'Callaghan-Gordo M, Sanmarti FX, Fons-Estupina C, González V, Pérez-Dueñas B, Poo P, Ramos F, García-Alix A, Armstrong-Moron J, Artuch-Iriberri R and Garcia-Cazorla A.

    Supplementation with pyridoxal phosphate may be useful in diverse neuropediatric disorders.

    EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY . : .