Comparison between siblings and twins supports a role for modifier genes in ADPKD von Persu, Alexandre, Duyme, Michel, Pirson, Yves, Lens, Xosé M., Messiaen, Thierry, Breuning, Martijn H., Chauveau, Dominique, Levy, Micheline, Grünfeld, Jean-Pierre, Devuyst, Olivier

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A Novel Pattern of Mutation in Uromodulin Disorders: Autosomal Dominant Medullary Cystic Kidney Disease Type 2, Familial Juvenile Hyperuricemic Nephropathy, and Autosomal Dominant... von Lens, Xosé M., Banet, Julio F., Outeda, Patricia, Barrio-Lucía, Vicente

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A novel mutation, outside of the candidate region for diagnosis, in the inverted formin 2 gene can cause focal segmental glomerulosclerosis von Sanchez-Ares, Maria, Garcia-Vidal, Marina, Antucho, Espinosa-Estevez, Julio, Pardo, Eduardo, Vazquez-Martul, Lens, Xose M., Garcia-Gonzalez, Miguel A.

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Genomic organization and mutation screening of the human ortholog of Pkdr1 associated with polycystic kidney disease in the rat von Kaisaki, Pamela J, Bergmann, Carsten, Brown, Joanna H, Outeda, Patricia, Lens, Xosé M, Peters, Dorien J.M, Gretz, Norbert, Gauguier, Dominique, Bihoreau, Marie-Thérèse

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Homozygosity for uromodulin disorders: FJHN and MCKD-type 2 von Rezende-Lima, Wânia, Parreira, Kleber S., García-González, Miguel, Riveira, Eva, Banet, Julio F., Lens, Xosé M.

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A comparative study of three kidney biomarker tests in autosomal-dominant polycystic kidney disease von Casal, J. Antonio, Hermida, Jesús, Lens, Xosé M., Tutor, J. Carlos

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Evaluating the clinical utility of a molecular genetic test for polycystic kidney disease von Garcia-Gonzalez, Miguel A., Jones, Jeffrey G., Allen, Susan K., Palatucci, Christopher M., Batish, Sat D., Seltzer, William K., Lan, Zheng, Allen, Erica, Qian, Feng, Lens, Xose M., Pei, York, Germino, Gregory G., Watnick, Terry J.

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Enos polymorphism and renal disease progression in autosomal dominant polycystic kidney disease von Devuyst, Olivier, Persu, Alexandre, Stoenoiu, Maria S, Pirson, Yves, Lens, Xosé M, Chauveau, Dominique

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Aberrant splicing in the PKD2 gene as a cause of polycystic kidney disease von REYNOLDS, D. M, HAYASHI, T, FOSSDAL, R, COTO, E, GUANQINGWU, BREUNING, M. H, GERMINO, G. G, PETERS, D. J. M, SOMLO, S, YIQIANG CAI, VELDHUISEN, B, WATNICK, T. J, LENS, X. M, MOCHIZUKI, T, QIAN, F, MAEDA, Y, LI LI

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Genomic organization and mutation screening of the human ortholog of Pkdrl associated with polycystic kidney disease in the rat von KAISAKI, Pamela J, BERGMANN, Carsten, BROWN, Joanna H, OUTEDA, Patricia, LENS, Xosé M, PETERS, Dorien J. M, GRETZ, Norbert, GAUGUIER, Dominique, BIHOREAU, Marie-Thérèse

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Long-term anti-proteinuric effect of Losartan in renal transplant recipients treated for hypertension von Calviño, Jesús, Lens, Xose M., Romero, Rafael, Sánchez-Guisande, Domingo

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An Unusual Pattern of Mutation in the Duplicated Portion of PKD1 Is Revealed by Use of a Novel Strategy for Mutation Detection von Watnick, Terry J., Piontek, Klaus B., Cordal, Teresa M., Weber, Horst, Gandolph, Michael A., Qian, Feng, Lens, Xose M., Neumann, Hartmut P. H., Germino, Gregory G.

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GENETIC DISORDERS - DEVELOPMENT: Comparison between siblings and twins supports a role for modifier genes in ADPKD von Persu, Alexandre, Duyme, Michel, Pirson, Yves, Lens, Xose M, Messiaen, Thierry, Breuning, Martijn H, Chauveau, Dominique, Levy, Micheline, Gruenfeld, Jean-Pierre, Devuyst, Olivier

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Novel stop and frameshifting mutations in the autosomal dominant polycystic kidney disease 2 (PKD2) gene von VIRIBAY, M, HAYASHI, T, SAN MILLAN, J. L, TELLERIA, D, MOCHIZUKI, T, REYNOLDS, D. M, ALONSO, R, LENS, X. M, MORENO, F, HARRIS, P. C, SOMLO, S

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An Integrated Genetic and Physical Map of the Autosomal Recessive Polycystic Kidney Disease Region von Lens, Xose M., Onuchic, Luiz F., Wu, Guanqing, Hayashi, Tomohito, Daoust, Martin, Mochizuki, Toshio, Santarina, Lorenzo B., Stockwin, John M., Mücher, Gabi, Becker, Jutta, Sweeny, William E., Avner, Ellis D., Guay-Woodford, Lisa, Zerres, Klaus, Somlo, Stefan, Germino, Gregory G.

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Renal artery rupture secondary to pretransplantation Candida contamination of the graft in two different recipients von Calviño, Jesus, Romero, Rafael, Pintos, Elena, Novoa, Daniel, Mardaras, Javier, Arcocha, Victor, Lens, Xose M., Sanchez-Guisande, Domingo

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Voluntary Ingestion of Cortinarius Mushrooms Leading to Chronic Interstitial Nephritis von Calviño, Jesus, Romero, Rafael, Pintos, Elena, Novoa, Daniel, Güimil, Dolores, Cordal, Teresa, Mardaras, Javier, Arcocha, Victor, Lens, XoseM, Sanchez-Guisande, Domingo

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Cyclooxygenase-2 in normal, hyperplastic and neoplastic follicular cells of the human thyroid gland von GARCIA-GONZALEZ, Miguel, ABDULKADER, Ihab, VAZQUEZ BOQUETE, Angel, LENS NEO, Xosé Manuel, FORTEZA, Jeronimo, CAMESELLE-TEIJEIRO, José

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Mutations in the COL4A4 and COL4A3 genes cause familial benign hematuria von BADENAS, Cèlia, PRAGA, Manuel, DAVILA, Sonia, MILA, Montse, ANTIGNAC, Corinne, DARNELL, Alejandro, TORRA, Roser, TAZON, Barbara, HEIDET, Laurence, ARRONDEL, Christelle, ARMENGOL, Anna, ANDRES, Amado, MORALES, Enrique, CAMACHO, Juan Antonio, LENS, Xose

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Autosomal recessive Alport’s syndrome and benign familial hematuria are collagen type IV diseases von Vega, Bárbara Tazón, Badenas, Cèlia, Ars, Elisabet, Lens, Xose, Milà, Montse, Darnell, Alejandro, Torra, Roser

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