Nutritional Assessment and Support in Children with Chronic Kidney Disease: The Benefits of Working with a Registered Dietitian von Suárez-González, Marta, Ordoñez-Álvarez, Flor Ángel, Gil-Peña, Helena, Carnicero-Ramos, Sara, Hernández-Peláez, Lucía, García-Fernández, Sonia, Santos-Rodríguez, Fernando

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Quistes del rafe medio: una entidad poco habitual von Hernández Peláez, Lucía, Pontón Martino, Belén, Alonso Losada, Daniel, Ordoñez Álvarez, Flor Ángel

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Rituximab treatment in pediatric patients with steroid-dependent nephrotic syndrome: a tertiary hospital von Guzmán Morais, Beatriz, Ordóñez Álvarez, Flor Ángel, Santos Rodríguez, Fernando, Martín Ramos, Silvia, Fernández Novo, Gema

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Rituximab treatment in pediatric patients with steroid-dependent nephrotic syndrome: A tertiary hospital von Guzmán Morais, Beatriz, Ordóñez Álvarez, Flor Ángel, Santos Rodríguez, Fernando, Martín Ramos, Silvia, Fernández Novo, Gema

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Fallo renal neonatal por shock hipovolémico von González, Juan Orviz, Álvarez Izquierdo, María Luisa, Fernando Santos Rodríguez, Flor Ángel Ordoñez Álvarez, Blázquez Gómez, Cristina Julia

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Tratamiento con rituximab en pacientes pediátricos con síndrome nefrótico córtico-dependiente. Experiencia en un hospital terciario von Guzmán Morais, Beatriz, Ordóñez Álvarez, Flor Ángel, Santos Rodríguez, Fernando, Martín Ramos, Silvia, Fernández Novo, Gema

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The clinical complexity of PKHD1 gene: from neonatal lethality to casual diagnosis in late pediatric stages von Rubio-Granda, Ana, Gil-Peña, Helena, Rodríguez-Márquez, Carlos, Solís-Sánchez, Gonzalo, Ordóñez-Álvarez, Flor Angel

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Rituximab treatment in pediatric patients with steroid-dependent nephrotic syndrome: A tertiary hospital von Beatriz Guzmán Morais, Flor Ángel Ordóñez Álvarez, Fernando Santos Rodríguez, Silvia Martín Ramos, Gema Fernández Novo

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Uropathogen pattern and antimicrobial susceptibility in positive urinary cultures isolates from paediatric patients von Moya-Dionisio, V, Díaz-Zabala, M, Ibáñez-Fernández, A, Suárez-Leiva, P, Martínez-Suárez, V, Ordóñez-Álvarez, F A, Santos-Rodríguez, F

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Unexpected phenotypes in Alport syndrome: the need for genetic testing von Blázquez Gómez, Cristina J, Díaz Anadón, Lucas R, Pérez Pérez, Alicia, Ángel Ordóñez Álvarez, Flor, Santos Rodríguez, Fernando

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Clinical and genetic characteristics of Dent's disease type 1 in Europe von Burballa, Carla, Cantero-Recasens, Gerard, Prikhodina, Larisa, Lugani, Francesca, Schlingmann, Karlpeter, Ananin, Petr V, Besouw, Martine, Bockenhauer, Detlef, Madariaga, Leire, Bertholet-Thomas, Aurelia, Taroni, Francesca, Parolin, Mattia, Conlon, Peter, Emma, Francesco, Del Prete, Dorella, Chauveau, Dominique, Koster-Kamphuis, Linda, Fila, Marc, Pasini, Andrea, Castro, Isabel, Colussi, Giacomo, Gil, Marta, Mohidin, Barian, Wlodkowski, Tanja, Schaefer, Franz, Ariceta, Gema

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

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

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

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Novel mutations associated with nephrogenic diabetes insipidus. A clinical-genetic study von García Castaño, Alejandro, Pérez de Nanclares, Gustavo, Madariaga, Leire, Aguirre, Mireia, Chocron, Sara, Madrid, Alvaro, Lafita Tejedor, Francisco Javier, Gil Campos, Mercedes, Sánchez del Pozo, Jaime, Ruiz Cano, Rafael, Espino, Mar, Gomez Vida, Jose Maria, Santos, Fernando, García Nieto, Victor Manuel, Loza, Reyner, Rodríguez, Luis Miguel, Hidalgo Barquero, Emilia, Printza, Nikoleta, Camacho, Juan Antonio, Castaño, Luis, Ariceta, Gema

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RenalTube: a network tool for clinical and genetic diagnosis of primary tubulopathies von Mejía, Natalia, Santos, Fernando, Claverie-Martín, Félix, García-Nieto, Víctor, Ariceta, Gema, Castaño, Luis

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Dent’s disease: Identification of seven new pathogenic mutations in the CLCN5 gene von Ramos-Trujillo, Elena, Claverie-Martin, Felix, Garcia-Nieto, Victor, Ariceta, Gema, Vara, Julia, Gonzalez-Acosta, Hilaria, Garcia-Ramirez, Marta, Fons, Jaime, Cordoba-Lanus, Elizabeth, Gonzalez-Paredes, Javier, Valenciano, Blanca, Ramos, Leticia, Muley, Rafael, Caggiani, Marina, Alvarez-Estrada, Pilar, Madrid, Alvaro

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