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

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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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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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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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Bartter's Syndrome Comes of Age von Rodriguez-Soriano, Juan

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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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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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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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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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Autosomal dominant pseudohypoaldosteronism type 1 : Mechanisms, evidence for neonatal lethality, and phenotypic expression in adults von GELLER, David S, JUNHUI ZHANG, HAQQ, Andrea M, COREY, Howard, JANSSENS, Sandra, CORVOL, Pierre, LIFTON, Richard P, ZENNARO, Maria-Christina, VALLO-BOADO, Alberto, RODRIGUEZ-SORIANO, Juan, FURU, Laszlo, HAWS, Robert, METZGER, Daniel, BOTELHO, Barbara, KARAVITI, Lefkothea

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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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Mutations in the gene encoding B1 subunit of H + -ATPase cause renal tubular acidosis with sensorineural deafness von Lifton, Richard P, Karet, Fiona E, Finberg, Karin E, Nelson, Raoul D, Nayir, Ahmet, Mocan, Hilal, Sanjad, Sami A, Rodriguez-Soriano, Juan, Santos, Fernando, Cremers, Cor W.R.J, Pietro, Antonio Di, Hoffbrand, Barry I, Winiarski, Jacek, Bakkaloglu, Aysin, Ozen, Seza, Dusunsel, Ruhan, Goodyer, Paul, Hulton, Sally A, Wu, Doris K, Skvorak, Anne B, Morton, Cynthia C, Cunningham, Michael J, Jha, Vivekanand

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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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Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK von SIMON, D. B, KARET, F. E, RODRIGUEZ-SORIANO, J, HAMDAN, J. H, DIPIETRO, A, TRACHTMAN, H, SANJAD, S. A, LIFTON, R. P

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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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