Tubulopathy meets Sherlock Holmes: biochemical fingerprinting of disorders of altered kidney tubular salt handling von Bockenhauer, Detlef, Kleta, Robert

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Salt-Losing Tubulopathies in Children: What's New, What's Controversial? von Kleta, Robert, Bockenhauer, Detlef

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HNF1B-associated clinical phenotypes: the kidney and beyond von Bockenhauer, Detlef, Jaureguiberry, Graciana

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Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia von Haffner, Dieter, Emma, Francesco, Eastwood, Deborah M., Duplan, Martin Biosse, Bacchetta, Justine, Schnabel, Dirk, Wicart, Philippe, Bockenhauer, Detlef, Santos, Fernando, Levtchenko, Elena, Harvengt, Pol, Kirchhoff, Martha, Di Rocco, Federico, Chaussain, Catherine, Brandi, Maria Louisa, Savendahl, Lars, Briot, Karine, Kamenicky, Peter, Rejnmark, Lars, Linglart, Agnès

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Mitochondrial DNA mutations in renal disease: an overview von Govers, Larissa P., Toka, Hakan R., Hariri, Ali, Walsh, Stephen B., Bockenhauer, Detlef

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Nomenclature for kidney function and disease: report of a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference von Levey, Andrew S., Eckardt, Kai-Uwe, Dorman, Nijsje M., Christiansen, Stacy L., Hoorn, Ewout J., Ingelfinger, Julie R., Inker, Lesley A., Levin, Adeera, Mehrotra, Rajnish, Palevsky, Paul M., Perazella, Mark A., Tong, Allison, Allison, Susan J., Bockenhauer, Detlef, Briggs, Josephine P., Bromberg, Jonathan S., Davenport, Andrew, Feldman, Harold I., Fouque, Denis, Gansevoort, Ron T., Gill, John S., Greene, Eddie L., Hemmelgarn, Brenda R., Kretzler, Matthias, Lambie, Mark, Lane, Pascale H., Laycock, Joseph, Leventhal, Shari E., Mittelman, Michael, Morrissey, Patricia, Ostermann, Marlies, Rees, Lesley, Ronco, Pierre, Schaefer, Franz, St. Clair Russell, Jennifer, Vinck, Caroline, Walsh, Stephen B., Weiner, Daniel E., Cheung, Michael, Jadoul, Michel, Winkelmayer, Wolfgang C.

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International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people von Gimpel, Charlotte, Bergmann, Carsten, Bockenhauer, Detlef, Breysem, Luc, Cadnapaphornchai, Melissa A., Cetiner, Metin, Dudley, Jan, Emma, Francesco, Konrad, Martin, Harris, Tess, Harris, Peter C., König, Jens, Liebau, Max C., Marlais, Matko, Mekahli, Djalila, Metcalfe, Alison M., Oh, Jun, Perrone, Ronald D., Sinha, Manish D., Titieni, Andrea, Torra, Roser, Weber, Stefanie, Winyard, Paul J. D., Schaefer, Franz

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Genetic Forms of Nephrogenic Diabetes Insipidus: Vasopressin Receptor Defect (X-linked) and Aquaporin Defect (Autosomal Recessive and Dominant) von Bichet, Daniel G., MD, Bockenhauer, Detlef, MD, PhD

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Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference von Blanchard, Anne, Bockenhauer, Detlef, Bolignano, Davide, Calò, Lorenzo A., Cosyns, Etienne, Devuyst, Olivier, Ellison, David H., Karet Frankl, Fiona E., Knoers, Nine V.A.M., Konrad, Martin, Lin, Shih-Hua, Vargas-Poussou, Rosa

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The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis von Xie, Jingyuan, Liu, Lili, Mladkova, Nikol, Li, Yifu, Hu, Xiaofan, Yu, Xialian, Xu, Jing, Caliskan, Yasar, Sidore, Carlo, Rosen, Raphael J., Bodria, Monica, Zanoni, Francesca, Zhang, Jun Y., Krithivasan, Priya, Mehl, Karla, Marasa, Maddalena, Khan, Atlas, Ozay, Fatih, Bomback, Andrew S., Appel, Gerald B., Sanna-Cherchi, Simone, Sampson, Matthew G., Mariani, Laura H., Perkowska-Ptasinska, Agnieszka, Durlik, Magdalena, Mucha, Krzysztof, Moszczuk, Barbara, Foroncewicz, Bartosz, Pączek, Leszek, Habura, Ireneusz, Ars, Elisabet, Ballarin, Jose, Mani, Laila-Yasmin, Vogt, Bruno, Ozturk, Savas, Yildiz, Abdülmecit, Seyahi, Nurhan, Arikan, Hakki, Koc, Mehmet, Basturk, Taner, Karahan, Gonca, Akgul, Sebahat Usta, Sever, Mehmet Sukru, Santoro, Domenico, Londrino, Francesco, Gesualdo, Loreto, Reiterova, Jana, Izzi, Claudia, Savoldi, Silvana, Spotti, Donatella, Marcantoni, Carmelita, Messa, Piergiorgio, Roccatello, Dario, Granata, Simona, Zaza, Gianluigi, Pisani, Isabella, Allegri, Landino, Sprangers, Ben, Park, Jin-Ho, Cho, BeLong, Kim, Yon Su, Kim, Dong Ki, Suzuki, Hitoshi, Amoroso, Antonio, Pani, Antonello, Hamilton, Patrick, Harris, Shelly, Gupta, Sanjana, Cheshire, Chris, Issler, Naomi, Pepper, Ruth J., Connolly, John, Powis, Stephen, Bockenhauer, Detlef, Stanescu, Horia C., Ashman, Neil, Loos, Ruth J. F., Kenny, Eimear E., Wuttke, Matthias, Eckardt, Kai-Uwe, Köttgen, Anna, Hofstra, Julia M., Coenen, Marieke J. H., Kiemeney, Lambertus A., Kretzler, Matthias, Beck, Lawrence H., Debiec, Hanna, Ronco, Pierre, Wetzels, Jack F. M., Zoledziewska, Magdalena, Cucca, Francesco, Ionita-Laza, Iuliana, Lee, Hajeong, Hoxha, Elion, Stahl, Rolf A. K., Zhao, Ming-hui, Gharavi, Ali G., Kleta, Robert, Chen, Nan, Kiryluk, Krzysztof

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Novel insights in the genetics of steroid-sensitive nephrotic syndrome in childhood von Dufek-Kamperis, Stephanie, Kleta, Robert, Bockenhauer, Detlef, Gale, Daniel, Downie, Mallory L.

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Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubul... von Konrad, Martin, Nijenhuis, Tom, Ariceta, Gema, Bertholet-Thomas, Aurelia, Calo, Lorenzo A., Capasso, Giovambattista, Emma, Francesco, Schlingmann, Karl P., Singh, Mandeep, Trepiccione, Francesco, Walsh, Stephen B., Whitton, Kirsty, Vargas-Poussou, Rosa, Bockenhauer, Detlef

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A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome von Sadowski, Carolin E, Lovric, Svjetlana, Ashraf, Shazia, Pabst, Werner L, Gee, Heon Yung, Kohl, Stefan, Engelmann, Susanne, Vega-Warner, Virginia, Fang, Humphrey, Halbritter, Jan, Somers, Michael J, Tan, Weizhen, Shril, Shirlee, Fessi, Inès, Lifton, Richard P, Bockenhauer, Detlef, El-Desoky, Sherif, Kari, Jameela A, Zenker, Martin, Kemper, Markus J, Mueller, Dominik, Fathy, Hanan M, Soliman, Neveen A, Hildebrandt, Friedhelm

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Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working Group von Boyer, Olivia, Schaefer, Franz, Haffner, Dieter, Bockenhauer, Detlef, Hölttä, Tuula, Bérody, Sandra, Webb, Hazel, Heselden, Marie, Lipska-Zie˛tkiewicz, Beata S., Ozaltin, Fatih, Levtchenko, Elena, Vivarelli, Marina

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Genetic, pathophysiological, and clinical aspects of nephrocalcinosis von Oliveira, Ben, Kleta, Robert, Bockenhauer, Detlef, Walsh, Stephen B

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Mistargeting of Peroxisomal EHHADH and Inherited Renal Fanconi's Syndrome von Klootwijk, Enriko D, Reichold, Markus, Helip-Wooley, Amanda, Tolaymat, Asad, Broeker, Carsten, Robinette, Steven L, Reinders, Joerg, Peindl, Dominika, Renner, Kathrin, Eberhart, Karin, Assmann, Nadine, Oefner, Peter J, Dettmer, Katja, Sterner, Christina, Schroeder, Josef, Zorger, Niels, Witzgall, Ralph, Reinhold, Stephan W, Stanescu, Horia C, Bockenhauer, Detlef, Jaureguiberry, Graciana, Courtneidge, Holly, Hall, Andrew M, Wijeyesekera, Anisha D, Holmes, Elaine, Nicholson, Jeremy K, O'Brien, Kevin, Bernardini, Isa, Krasnewich, Donna M, Arcos-Burgos, Mauricio, Izumi, Yuichiro, Nonoguchi, Hiroshi, Jia, Yuzhi, Reddy, Janardan K, Ilyas, Mohammad, Unwin, Robert J, Gahl, William A, Warth, Richard, Kleta, Robert

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Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities von Boyden, Lynn M., Choi, Murim, Choate, Keith A., Nelson-Williams, Carol J., Farhi, Anita, Toka, Hakan R., Tikhonova, Irina R., Bjornson, Robert, Mane, Shrikant M., Colussi, Giacomo, Lebel, Marcel, Gordon, Richard D., Semmekrot, Ben A., Poujol, Alain, Välimäki, Matti J., De Ferrari, Maria E., Sanjad, Sami A., Gutkin, Michael, Karet, Fiona E., Tucci, Joseph R., Stockigt, Jim R., Keppler-Noreuil, Kim M., Porter, Craig C., Anand, Sudhir K., Whiteford, Margo L., Davis, Ira D., Dewar, Stephanie B., Bettinelli, Alberto, Fadrowski, Jeffrey J., Belsha, Craig W., Hunley, Tracy E., Nelson, Raoul D., Trachtman, Howard, Cole, Trevor R. P., Pinsk, Maury, Bockenhauer, Detlef, Shenoy, Mohan, Vaidyanathan, Priya, Foreman, John W., Rasoulpour, Majid, Thameem, Farook, Al-Shahrouri, Hania Z., Radhakrishnan, Jai, Gharavi, Ali G., Goilav, Beatrice, Lifton, Richard P.

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Integrin α3 Mutations with Kidney, Lung, and Skin Disease von Has, Cristina, Spartà, Giuseppina, Kiritsi, Dimitra, Weibel, Lisa, Moeller, Alexander, Vega-Warner, Virginia, Waters, Aoife, He, Yinghong, Anikster, Yair, Esser, Philipp, Straub, Beate K, Hausser, Ingrid, Bockenhauer, Detlef, Dekel, Benjamin, Hildebrandt, Friedhelm, Bruckner-Tuderman, Leena, Laube, Guido F

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A case of alkaptonuria presenting with unexplained dark-stained diapers and spurious hyperoxaluria and proteinuria due to homogentisic acid interference von Vanhove, Thibault, Aertgeerts, Margo, Witters, Peter, Rymen, Daisy, Böckenhauer, Detlef, Frans, Glynis, Vermeersch, Pieter

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Cyclophosphamide and rituximab in frequently relapsing/steroid-dependent nephrotic syndrome von Webb, Hazel, Jaureguiberry, Graciana, Dufek, Stephanie, Tullus, Kjell, Bockenhauer, Detlef

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