Search Results - "Sarasa, J.L"

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    Cavernoma raquídeo epidural en reloj de arena. Presentación de un caso y revisión de la literatura by Iglesias, S, Ayerbe, J, Sousa, P, Torres, C, Ruiz-Barnés, P, Sarasa, J.L

    Published in Neurocirugía (Asturias, Spain) (2008)
    “…Resumen Los cavernomas raquídeos epidurales son malformaciones vasculares muy poco frecuentes que, excepcionalmente, pueden adquirir una morfología en “reloj…”
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    Journal Article
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    Aberrant methylation of multiple genes in neuroblastic tumours: relationship with MYCN amplification and allelic status at 1p by Gonzalez-Gomez, P, Bello, M.J, Lomas, J, Arjona, D, Alonso, M.E, Amiñoso, C, Lopez-Marin, I, Anselmo, N.P, Sarasa, J.L, Gutierrez, M, Casartelli, C, Rey, J.A

    Published in European journal of cancer (1990) (01-07-2003)
    “…Aberrant hypermethylation occurs in tumour cell CpG islands and is an important pathway for the repression of gene transcription in cancers. We investigated…”
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    Verruciform xanthoma of the penis with acantholytic cells by Requena, L, Sarasa, J L, Martin, L, Pique, E, Farina, M C, Olivares, M, Escalonilla, P

    Published in Clinical and experimental dermatology (01-11-1995)
    “…Verucciform xanthoma is an unusual lesion characterized by verrucous epithelial proliferation accompanied by a prominent replacement of the dermal papillae…”
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    hRAD54 Gene and 1p High-Resolution Deletion-Mapping Analyses in Oligodendrogliomas by Bello, M.J, de Campos, J.M, Vaquero, J, Ruiz-Barnés, P, Kusak, M.E, Sarasa, J.L, Rey, J.A

    Published in Cancer genetics and cytogenetics (15-01-2000)
    “…The hRAD54 protein belongs to a superfamily of DNA helicases, and mutations in genes with DNA helicase function have been found to be responsible for…”
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    Cytogenetic clones in a recurrent neurofibroma by Rey, J A, Bello, M J, de Campos, J M, Benítez, J, Sarasa, J L, Boixados, J R, Sánchez Cascos, A

    Published in Cancer genetics and cytogenetics (01-05-1987)
    “…Chromosome studies were performed on a plexiform neurofibroma arising in a probable von Recklinghausen's disease patient, who also showed a de novo…”
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