Hasil Pencarian - Álvaro Madrid

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  1. 1
    Charcoal Hemoperfusion for Methotrexate Toxicity: A Safe and Effective Life-Rescue Alternative When Glucarpidase Is Not Available

    Charcoal Hemoperfusion for Methotrexate Toxicity: A Safe and Effective Life-Rescue Alternative When Glucarpidase Is Not Available oleh Alejandra Rosales, Alvaro Madrid, Marina Muñoz, Jose Luis Dapena, Jose Luis Dapena, Gema Ariceta

    Diterbitkan 2021-08-01
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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
    Complement Genetic Variants and FH Desialylation in S. pneumoniae-Haemolytic Uraemic Syndrome

    Complement Genetic Variants and FH Desialylation in S. pneumoniae-Haemolytic Uraemic Syndrome oleh Irene Gómez Delgado, Fernando Corvillo, Fernando Corvillo, Pilar Nozal, Pilar Nozal, Emilia Arjona, Emilia Arjona, Álvaro Madrid, Marta Melgosa, Juan Bravo, Ágnes Szilágyi, Dorottya Csuka, Nóra Veszeli, Zoltán Prohászka, Pilar Sánchez-Corral, Pilar Sánchez-Corral

    Diterbitkan 2021-03-01
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  4. 4
    Identification of a Locus on the X Chromosome Linked to Familial Membranous Nephropathy

    Identification of a Locus on the X Chromosome Linked to Familial Membranous Nephropathy oleh Mallory L. Downie, Sanjana Gupta, Mehmet C. Tekman, Chris Cheshire, Steven Arora, Christoph Licht, Lisa A. Robinson, Marina Munoz, Alvaro Madrid Aris, Ibrahim Al Attrach, Paul E. Brenchley, Daniel P. Gale, Horia Stanescu, Detlef Bockenhauer, Robert Kleta

    Diterbitkan 2021-06-01
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  5. 5
    Correction: Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis.

    Correction: Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis. oleh Félix Claverie-Martín, Víctor García-Nieto, Cesar Loris, Gema Ariceta, Inmaculada Nadal, Laura Espinosa, Ángeles Fernández-Maseda, Montserrat Antón-Gamero, África Avila, Álvaro Madrid, Hilaria González-Acosta, Elizabeth Córdoba-Lanus, Fernando Santos, Marta Gil-Calvo, Mar Espino, Elena García-Martinez, Ana Sanchez, Rafael Muley

    Diterbitkan 2013-01-01
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  6. 6
    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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  7. 7
    Claudin-19 mutations and clinical phenotype in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

    Claudin-19 mutations and clinical phenotype in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis. oleh Félix Claverie-Martín, Víctor García-Nieto, Cesar Loris, Gema Ariceta, Inmaculada Nadal, Laura Espinosa, Ángeles Fernández-Maseda, Montserrat Antón-Gamero, Africa Avila, Álvaro Madrid, Hilaria González-Acosta, Elizabeth Córdoba-Lanus, Fernando Santos, Marta Gil-Calvo, Mar Espino, Elena García-Martinez, Ana Sanchez, Rafael Muley, RenalTube Group

    Diterbitkan 2013-01-01
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