New insights into the pathogenesis of renal tubular acidosis: from functional to molecular studies von RODRIGUEZ-SORIANO, Juan

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Equilibrium studies and modeling on the removal of 56Mn(II) by alumina and kaolinite von Badillo-Almaraz, V. E., López-Reyes, C., Soriano-Rodríguez, J. M.

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Bartter and related syndromes : the puzzle is almost solved von RODRIGUEZ-SORIANO, J

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Effect of docosahexaenoic acid administration on plasma lipid profile and metabolic parameters of children with methylmalonic acidaemia von Aldámiz‐Echevarría, L., Sanjurjo, P., Elorz, J., Prieto, J. A., Pérez, C., Andrade, F., Rodríguez‐Soriano, J.

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Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss von Stover, E H, Borthwick, K J, Bavalia, C, Eady, N, Fritz, D M, Rungroj, N, Giersch, A B S, Morton, C C, Axon, P R, Akil, I, Al-Sabban, E A, Baguley, D M, Bianca, S, Bakkaloglu, A, Bircan, Z, Chauveau, D, Clermont, M-J, Guala, A, Hulton, S A, Kroes, H, Li Volti, G, Mir, S, Mocan, H, Nayir, A, Ozen, S, Rodriguez Soriano, J, Sanjad, S A, Tasic, V, Taylor, C M, Topaloglu, R, Smith, A N, Karet, F E

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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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Hypercalcemia in neonatal distal renal tubular acidosis von Rodríguez-Soriano, J, García-Fuentes, M, Vallo, A, Alvárez-Granda, J L

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Sorption of aqueous palladium onto synthetic hydroxyapatite von Soriano-Rodríguez, J. M., Badillo-Almaraz, V. E., Alliot, C., Monroy-Guzmán, F., Vitorge, P.

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Equilibrium studies and modeling on the removal of .sup.56Mn by alumina and kaolinite von Badillo-Almaraz, V. E, López-Reyes, C, Soriano-Rodríguez, J. M

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Pathophysiology of the renal acidification defect present in the syndrome of familial hypomagnesaemia-hypercalciuria von RODRIGUEZ-SORIANO, J, VALLO, A

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Polyunsaturated fatty acid status in patients with phenylketonuria von Sanjurjo, P., Perteagudo, L., Soriano, J. Rodríguez, Vilaseca, A., Campistol, J.

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Familial hypercalcemia and hypercalciuria : no mutations in the Ca2+-sensing receptor gene von RODRIGUEZ-SORIANO, Juan, VALLO, Alfredo, QUINTELA, Maria Jesus, PEREZ DE NANCLARES, Guiomar, BILBAO, José Ramon, CASTANO, Luis

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Mutations in the Tight-Junction Gene Claudin 19 ( CLDN19) Are Associated with Renal Magnesium Wasting, Renal Failure, and Severe Ocular Involvement von Konrad, Martin, Schaller, André, Seelow, Dominik, Pandey, Amit V., Waldegger, Siegfried, Lesslauer, Annegret, Vitzthum, Helga, Suzuki, Yoshiro, Luk, John M., Becker, Christian, Schlingmann, Karl P., Schmid, Marcel, Rodriguez-Soriano, Juan, Ariceta, Gema, Cano, Francisco, Enriquez, Ricardo, Jüppner, Harald, Bakkaloglu, Sevcan A., Hediger, Matthias A., Gallati, Sabina, Neuhauss, Stephan C.F., Nürnberg, Peter, Weber, Stefanie

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Why does renal tubular acidosis cause hypercalciuria? von Rodríguez-Soriano, J

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Bartter's Syndrome Comes of Age 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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Management of neonatal citrullinemia von Sanjurjo, P., Rodríguez-Soriano, J.

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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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Renal tubular handling of potassium in children with insulin-dependent diabetes mellitus von RODRIGUEZ-SORIANO, J, VALLO, A, ARICETA, G, MARTUL, P, DE LA RICA, I

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Multiple-marker screen positive results in Noonan syndrome von Aranguren, G, García-Miñaur, S, Loridan, L, Uribarren, A, Martín Vargas, L, Rodríguez-Soriano, J

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