Hasil Pencarian - Gustavo Pérez de Nanclares

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  1. 1
    Identification of a novel large CASR deletion in a patient with familial hypocalciuric hypercalcemia

    Identification of a novel large CASR deletion in a patient with familial hypocalciuric hypercalcemia oleh Alejandro García-Castaño, Leire Madariaga, Sharona Azriel, Gustavo Pérez de Nanclares, Idoia Martínez de LaPiscina, Rosa Martínez, Inés Urrutia, Aníbal Aguayo, Sonia Gaztambide, Luis Castaño

    Diterbitkan 2018-12-01
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  2. 2
    Genetics of type III Bartter syndrome in Spain, proposed diagnostic algorithm.

    Genetics of type III Bartter syndrome in Spain, proposed diagnostic algorithm. oleh Alejandro García Castaño, Gustavo Pérez de Nanclares, Leire Madariaga, Mireia Aguirre, Alvaro Madrid, Inmaculada Nadal, Mercedes Navarro, Elena Lucas, Julia Fijo, Mar Espino, Zilac Espitaletta, Luis Castaño, Gema Ariceta, RenalTube Group

    Diterbitkan 2013-01-01
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  3. 3
    Genetic profile of a large Spanish cohort with hypercalcemia

    Genetic profile of a large Spanish cohort with hypercalcemia oleh Alejandro García-Castaño, Leire Madariaga, Sara Gómez-Conde, Pedro González, Gema Grau, Itxaso Rica, Gustavo Pérez de Nanclares, Ana Belén De la Hoz, Aníbal Aguayo, Rosa Martínez, Inés Urrutia, Sonia Gaztambide, Calcium Phosphorus Metabolism Molecular Biology Group, Luis Castaño

    Diterbitkan 2024-03-01
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  4. 4
    Novel variant in the CNNM2 gene associated with dominant hypomagnesemia.

    Novel variant in the CNNM2 gene associated with dominant hypomagnesemia. oleh Alejandro García-Castaño, Leire Madariaga, Montserrat Antón-Gamero, Natalia Mejia, Jenny Ponce, Sara Gómez-Conde, Gustavo Pérez de Nanclares, Ana Belén De la Hoz, Rosa Martínez, Laura Saso, Idoia Martínez de LaPiscina, Inés Urrutia, Olaia Velasco, Aníbal Aguayo, Luis Castaño, Sonia Gaztambide

    Diterbitkan 2020-01-01
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  5. 5
    Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome.

    Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome. oleh Alejandro García Castaño, Gustavo Pérez de Nanclares, Leire Madariaga, Mireia Aguirre, Álvaro Madrid, Sara Chocrón, Inmaculada Nadal, Mercedes Navarro, Elena Lucas, Julia Fijo, Mar Espino, Zilac Espitaletta, Víctor García Nieto, David Barajas de Frutos, Reyner Loza, Guillem Pintos, Luis Castaño, RenalTube Group, Gema Ariceta

    Diterbitkan 2017-01-01
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  6. 6
    Novel variant in the CNNM2 gene associated with dominant hypomagnesemia

    Novel variant in the CNNM2 gene associated with dominant hypomagnesemia oleh Alejandro García-Castaño, Leire Madariaga, Montserrat Antón-Gamero, Natalia Mejia, Jenny Ponce, Sara Gómez-Conde, Gustavo Pérez de Nanclares, Ana Belén De la Hoz, Rosa Martínez, Laura Saso, Idoia Martínez de LaPiscina, Inés Urrutia, Olaia Velasco, Aníbal Aguayo, Luis Castaño, Sonia Gaztambide, Obul Reddy Bandapalli

    Diterbitkan 2020-01-01
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  7. 7
    Five patients with disorders of calcium metabolism presented with GCM2 gene variants

    Five patients with disorders of calcium metabolism presented with GCM2 gene variants oleh Alejandro García-Castaño, Leire Madariaga, Sara Gómez-Conde, Carmen Lourdes Rey Cordo, María López-Iglesias, Yolanda Garcia-Fernández, Alicia Martín, Pedro González, Ignacio Goicolea, Gustavo Pérez de Nanclares, Ana Belén De la Hoz, Aníbal Aguayo, Idoia Martínez de LaPiscina, Rosa Martínez, Laura Saso, Inés Urrutia, Olaia Velasco, Luis Castaño, Sonia Gaztambide

    Diterbitkan 2021-02-01
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