Showing 1 - 7 results of 7 for search 'Alejandro Garcia-Castaño', query time: 0.04s Refine Results
  1. 1
    Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis

    Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis by Alejandro García‐Castaño, Ana Perdomo‐Ramirez, Mònica Vall‐Palomar, Elena Ramos‐Trujillo, Leire Madariaga, Gema Ariceta, Felix Claverie‐Martin

    Published 2020-11-01
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  2. 2
    Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3

    Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3 by Alejandro García-Castaño, Sara Gómez-Conde, Leire Gondra, María Herrero, Mireia Aguirre, Ana-Belén de la Hoz, Luis Castaño, Renaltube group, Leire Madariaga

    Published 2023-08-01
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  3. 3
    Genetic profile of a large Spanish cohort with hypercalcemia

    Genetic profile of a large Spanish cohort with hypercalcemia by 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

    Published 2024-03-01
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  4. 4
    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. by 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

    Published 2017-01-01
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  5. 5
    Novel variant in the CNNM2 gene associated with dominant hypomagnesemia

    Novel variant in the CNNM2 gene associated with dominant hypomagnesemia by 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

    Published 2020-01-01
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  6. 6
    Five patients with disorders of calcium metabolism presented with GCM2 gene variants

    Five patients with disorders of calcium metabolism presented with GCM2 gene variants by 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

    Published 2021-02-01
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  7. 7
    Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?

    Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role? by Idoia Martínez de LaPiscina, Laura C. Hernández-Ramírez, Nancy Portillo, Nancy Portillo, Ana L. Gómez-Gila, Inés Urrutia, Rosa Martínez-Salazar, Alejandro García-Castaño, Aníbal Aguayo, Itxaso Rica, Itxaso Rica, Sonia Gaztambide, Sonia Gaztambide, Fabio R. Faucz, Margaret F. Keil, Maya B. Lodish, Maya B. Lodish, Martha Quezado, Nathan Pankratz, Prashant Chittiboina, John Lane, Denise M. Kay, James L. Mills, Luis Castaño, Constantine A. Stratakis

    Published 2020-07-01
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