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  • Response of head and neck e... Response of head and neck epithelial cells to a DNA damage‐differentiation checkpoint involving polyploidization
    Sanz‐Gómez, Natalia; Freije, Ana; Ceballos, Laura ... Head & neck, November 2018, 2018-11-00, 20181101, Volume: 40, Issue: 11
    Journal Article
    Peer reviewed

    Background Squamous epithelia of the head and neck undergo continuous cell renewal and are continuously exposed to mutagenic hazard, the main cause of cancer. How they maintain homeostasis upon cell ...
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  • Manifestaciones laríngeas d... Manifestaciones laríngeas de la enfermedad relacionada con IgG4. Revisión sistemática
    Bedia Cadelo, Jorge; Morales Angulo, Carmelo Revista ORL (Salamanca), 04/2022, Volume: 13, Issue: 1
    Journal Article
    Peer reviewed
    Open access

    Introducción y objetivos: La enfermedad relacionada con IgG4 (ER-IgG4) es un trastorno sistémico autoinmune caracterizado por la infiltración tisular por células plasmáticas positivas para IgG4, ...
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  • Manifestaciones de cabeza y... Manifestaciones de cabeza y cuello secundarias al uso de cocaína. Revisión bibliográfica
    Corriols-Noval, Patricia; Palmero-Sánchez, Beatriz; Faelens, Gianni ... Revista ORL (Salamanca), 04/2022, Volume: 13, Issue: 1
    Journal Article
    Peer reviewed
    Open access

    Introducción y objetivo: El consumo de cocaína se ha asociado a patología a múltiples niveles, pero ésta es especialmente relevante a nivel de cabeza y cuello, por ser la vía intranasal una de sus ...
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  • Auditory neuropathy in pati... Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF)
    Rodríguez-Ballesteros, Montserrat; del Castillo, Francisco J.; Martín, Yolanda ... Human mutation, December 2003, Volume: 22, Issue: 6
    Journal Article
    Peer reviewed
    Open access

    Inherited hearing impairment affects one in 2,000 newborns. Nonsyndromic prelingual forms are inherited mainly as autosomal recessive traits, for which 16 genes are currently known. Mutations in the ...
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  • DFNA8/12 caused by TECTA mu... DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss
    Hildebrand, Michael S.; Morín, Matías; Meyer, Nicole C. ... Human mutation, July 2011, Volume: 32, Issue: 7
    Journal Article
    Peer reviewed
    Open access

    The prevalence of DFNA8/DFNA12 (DFNA8/12), a type of autosomal dominant nonsyndromic hearing loss (ADNSHL), is unknown as comprehensive population‐based genetic screening has not been conducted. We ...
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  • Toma de muestras nasofaríng... Toma de muestras nasofaríngeas para diagnóstico de COVID-19
    Morales-Angulo, Carmelo; González-Zubizarreta, Rocío; Martín-Toca, Gema ... Revista ORL (Salamanca), 12/2020, Volume: 11, Issue: 4
    Journal Article
    Peer reviewed
    Open access

    RESUMEN Introducción y objetivo: La prueba de diagnóstico directo del COVID-19 de mayor sensibilidad es la toma de muestras de nasofaringe mediante un hisopo para estudio posterior mediante RT-PCR. ...
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  • Gb3/cd77 Is a Predictive Ma... Gb3/cd77 Is a Predictive Marker and Promising Therapeutic Target for Head and Neck Cancer
    García-Hevia, Lorena; Muñoz-Guerra, Débora; Casafont, Íñigo ... Biomedicines, 03/2022, Volume: 10, Issue: 4
    Journal Article
    Peer reviewed
    Open access

    Head and neck squamous cell carcinoma is the sixth leading cancer in the world. This cancer is difficult to treat and is characterized by recurrences that are often fatal. This cancer is generally ...
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  • VEXAS syndrome and otolaryn... VEXAS syndrome and otolaryngology
    Martínez-Diaz, Lucía; Morales-Angulo, Carmelo American journal of otolaryngology, May-June 2024, 2024 May-Jun, 2024-05-00, 20240501, Volume: 45, Issue: 3
    Journal Article
    Peer reviewed
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