Search Results - Tristán, Enriqueta

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  1. 1
    Randomised, open-label, non-inferiority clinical trial on the efficacy and safety of a 7-day vs 14-day course of antibiotic treatment for uncomplicated enterococcal bacteraemia: the INTENSE trial protocol

    Randomised, open-label, non-inferiority clinical trial on the efficacy and safety of a 7-day vs 14-day course of antibiotic treatment for uncomplicated enterococcal bacteraemia: th... by Maldonado, Natalia, Rosso-Fernández, Clara M, Portillo-Calderón, Inés, Borreguero Borreguero, Irene, Tristán-Clavijo, Enriqueta, Palacios-Baena, Zaira R, Salamanca, Elena, Fernández-Cuenca, Felipe, De-Cueto, Marina, Stolz-Larrieu, Emilio, Rodriguez-Baño, Jesús, López-Cortés, Luis Eduardo

    Published in BMJ open
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  2. 2
    A Neuroligin-1 mutation associated with Alzheimer’s disease produces memory and age-dependent impairments in hippocampal plasticity

    A Neuroligin-1 mutation associated with Alzheimer’s disease produces memory and age-dependent impairments in hippocampal plasticity by Arias-Aragón, Francisco, Tristán-Clavijo, Enriqueta, Martínez-Gallego, Irene, Robles-Lanuza, Estefanía, Coatl-Cuaya, Heriberto, Martín-Cuevas, Celia, Sánchez-Hidalgo, Ana C., Rodríguez-Moreno, Antonio, Martinez-Mir, Amalia, Scholl, Francisco G.

    Published in iScience
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  3. 3
    Dominant-negative mutation p.Arg324Thr in KCNA1 impairs Kv1.1 channel function in episodic ataxia

    Dominant-negative mutation p.Arg324Thr in KCNA1 impairs Kv1.1 channel function in episodic ataxia by Tristán-Clavijo, Enriqueta, Scholl, Francisco G., Macaya, Alfons, Iglesias, Gemma, Rojas, Ana M., Lucas, Miguel, Castellano, Antonio, Martinez-Mir, Amalia

    Published in Movement disorders
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  4. 4
    The H syndrome: Two novel mutations affecting the same amino acid residue of hENT3

    The H syndrome: Two novel mutations affecting the same amino acid residue of hENT3 by Molho-Pessach, Vered, Suarez, José, Perrin, Christophe, Chiaverini, Christine, Doviner, Victoria, Tristan-Clavijo, Enriqueta, Colmenero, Isabel, Giuliano, Fabienne, Torrelo, Antonio, Zlotogorski, Abraham

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  5. 5
    A truncating mutation in Alzheimer's disease inactivates neuroligin-1 synaptic function

    A truncating mutation in Alzheimer's disease inactivates neuroligin-1 synaptic function by Tristán-Clavijo, Enriqueta, Camacho-Garcia, Rafael J, Robles-Lanuza, Estefanía, Ruiz, Agustín, van der Zee, Julie, Van Broeckhoven, Christine, Hernandez, Isabel, Martinez-Mir, Amalia, Scholl, Francisco G

    Published in Neurobiology of aging
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  6. 6
    The H syndrome: two novel mutations affecting the same amino acid residue of hENT3

    The H syndrome: two novel mutations affecting the same amino acid residue of hENT3 by Molho-Pessach, Vered, Suarez, José, Perrin, Christophe, Chiaverini, Christine, Doviner, Victoria, Tristan-Clavijo, Enriqueta, Colmenero, Isabel, Giuliano, Fabienne, Torrelo, Antonio, Zlotogorski, Abraham

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