Persistence of Essential Fatty Acid Deficiency in Cystic Fibrosis Despite Nutritional Therapy von Aldámiz-Echevarría, Luis, Prieto, José Angel, Andrade, Fernando, Elorz, Javier, Sojo, Amaia, Lage, Sergio, Sanjurjo, Pablo, Vázquez, Carlos, Rodríguez-Soriano, Juan

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Fatty acid deficiency profile in children with food allergy managed with elimination diets von Aldámiz-Echevarría, Luis, Bilbao, Agurtzane, Andrade, Fernando, Elorz, Javier, Prieto, José Angel, Rodríguez-Soriano, Juan

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Arachidonic Acid Content in Adipose Tissue Is Associated With Insulin Resistance in Healthy Children von Aldámiz‐Echevarría, Luis, Prieto, José A, Andrade, Fernando, Elorz, Javier, Sanjurjo, Pablo, Soriano, Juan Rodríguez

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Renal tubular acidosis: The clinical entity von RODRIGUEZ SORIANO, Juan

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Long-term renal follow-up of extremely low birth weight infants von Rodríguez-Soriano, Juan, Aguirre, Mireia, Oliveros, Roberto, Vallo, Alfredo

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Methylation cycle, arginine-creatine pathway and asymmetric dimethylarginine in paediatric renal transplant von ANDRADE, Fernando, RODRIGUEZ-SORIANO, Juan, PRIETO, José Angel, AGUIRRE, Mireia, ARICETA, Gema, LAGE, Sergio, AZCONA, Isabel, PRADO, Carmen, SANJURJO, Pablo, ALDAMIZ-ECHEVARRIA, Luis

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Branchio-oto-renal syndrome von Rodríguez Soriano, Juan

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Inherited Renal Tubulopathies Associated With Metabolic Alkalosis: Effects on Blood Pressure von Ariceta, Gema, Rodríguez-Soriano, Juan

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The Arginine-Creatine Pathway is Disturbed in Children and Adolescents With Renal Transplants von Andrade, Fernando, Rodríguez-Soriano, Juan, Prieto, José Angel, Elorz, Javier, Aguirre, Mireia, Ariceta, Gema, Martin, Sergio, Sanjurjo, Pablo, Aldámiz-Echevarría, Luis

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An analysis of renal tubular acidosis by the Stewart method von Corey, Howard E, Vallo, Alfredo, Rodríguez-Soriano, Juan

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Bone mineral density and bone turnover in patients with Bartter syndrome von Rodríguez-Soriano, Juan, Vallo, Alfredo, Aguirre, Mireia

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A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain von Rodríguez-Soriano, Juan, Vallo, Alfredo, Pérez de Nanclares, Gustavo, Bilbao, José Ramón, Castaño, Luis

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Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption von SIMON, D. B, YIN LU, MCCREDIE, D, MILFORD, D, SANJAD, S, LIFTON, R. P, CHOATE, K. A, VELAZQUEZ, H, AL-SABBAN, E, PRAGA, M, CASARI, G, BETTINELLI, A, COLUSSI, G, RODRIGUEZ-SORIANO, J

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Essential fatty acid deficiency profile in patients with nephrotic-range proteinuria von Aldámiz-Echevarría, Luis, Vallo, Alfredo, Aguirre, Mireia, Sanjurjo, Pablo, Gonzalez-Lamuño, Domingo, Elorz, Javier, Prieto, José Angel, Andrade, Fernando, Rodríguez-Soriano, Juan

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Fatty acid composition of skeletal muscle and adipose tissue in Spanish infants and children von Sanjurjo, Pablo, AldámizEchevarría, Luis, Prado, Carmen, Azcona, Isabel, Elorz, Javier, Prieto, José A., Ruiz, José I., Rodríguez-Soriano, Juan

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Abnormalities in plasma fatty acid composition in human immunodeficiency virus-infected children treated with protease inhibitors von ALDAMIZ-ECHEVARRIA, Luis, POCHEVILLE, Itziar, SANJURJO, Pablo, ELORZ, Javier, PRIETO, Jose Angel, RODRIGUEZ-SORIANO, Juan

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Mutations in the chloride channel gene, CLCNKB , cause Bartter's syndrome type III von Stone, Rosário, Bakkaloglu, Aysin, John, Eunice, Nayir, Ahmet, Trachtman, Howard, Alpay, Harika, Mansfield, Traci A, Simon, David B, Mendonca, Erica, Schurman, Scott, Sanjad, Sami A, Griswold, William, Nelson-Williams, Carol, Morales, Jose M, Brem, Andrew, Taylor, C. Mark, Lifton, Richard P, Richard, George A, Bindra, Ranjit S, Pilz, Daniela, Rodriguez-Soriano, Juan

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Abnormalities in plasma fatty acid composition in human immunodeficiency virus-infected children treated with protease inhibitors von Aldámiz-Echevarría, Luis, Pocheville, Itziar, Sanjurjo, Pablo, Elorz, Javier, Angel Prieto, Jose, Rodríguez-Soriano, Juan

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Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I von Lifton, Richard P, Geller, David S, Rodriguez-Soriano, Juan, Boado, Alfredo V, Schifter, Søren, Bayer, Milan, Chang, Sue S

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Branchio-oto-renal syndrome : identification of a novel mutation in the EYA1 gene von RODRIGUEZ-SORIANO, Juan, VALLO, Alfredo, BILBAO, José Ramon, CASTANO, Luis

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