Nephrotic Syndrome in the First Year of Life: Two Thirds of Cases Are Caused by Mutations in 4 Genes (NPHS1, NPHS2, WT1, and LAMB2) von Hinkes, Bernward G, Mucha, Bettina, Vlangos, Christopher N, Gbadegesin, Rasheed, Liu, Jinhong, Hasselbacher, Katrin, Hangan, Daniela, Ozaltin, Fatih, Zenker, Martin, Hildebrandt, Friedhelm, members of Arbeitsgemeinschaft fur Paediatrische Nephrologie Study Group

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A novel TRPC6 mutation that causes childhood FSGS von Heeringa, Saskia F, Möller, Clemens C, Du, Jianyang, Yue, Lixia, Hinkes, Bernward, Chernin, Gil, Vlangos, Christopher N, Hoyer, Peter F, Reiser, Jochen, Hildebrandt, Friedhelm

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Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS) von Gbadegesin, Rasheed, Hinkes, Bernward G., Hoskins, Bethan E., Vlangos, Christopher N., Heeringa, Saskia F., Liu, Jinhong, Loirat, Chantal, Ozaltin, Fatih, Hashmi, Seema, Ulmer, Francis, Cleper, Roxanna, Ettenger, Robert, Antignac, Corinne, Wiggins, Roger C., Zenker, Martin, Hildebrandt, Friedhelm

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NPHS3: new clues for understanding idiopathic nephrotic syndrome von Hinkes, Bernward G.

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Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome von Chernin, Gil, Heeringa, Saskia F., Gbadegesin, Rasheed, Liu, Jinhong, Hinkes, Bernward G., Vlangos, Christopher N., Vega-Warner, Virginia, Hildebrandt, Friedhelm

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A systematic approach to mapping recessive disease genes in individuals from outbred populations von Hildebrandt, Friedhelm, Heeringa, Saskia F, Rüschendorf, Franz, Attanasio, Massimo, Nürnberg, Gudrun, Becker, Christian, Seelow, Dominik, Huebner, Norbert, Chernin, Gil, Vlangos, Christopher N, Zhou, Weibin, O'Toole, John F, Hoskins, Bethan E, Wolf, Matthias T F, Hinkes, Bernward G, Chaib, Hassan, Ashraf, Shazia, Schoeb, Dominik S, Ovunc, Bugsu, Allen, Susan J, Vega-Warner, Virginia, Wise, Eric, Harville, Heather M, Lyons, Robert H, Washburn, Joseph, Macdonald, James, Nürnberg, Peter, Otto, Edgar A

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Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome von Gbadegesin, Rasheed, Hinkes, Bernward, Vlangos, Christopher, Mucha, Bettina, Liu, Jinhong, Hopcian, Jeff, Hildebrandt, Friedhelm

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A complex microdeletion 17q12 phenotype in a patient with recurrent de novo membranous nephropathy von Hinkes, Bernward, Hilgers, Karl F, Bolz, Hanno J, Goppelt-Struebe, Margarete, Amann, Kerstin, Nagl, Sandra, Bergmann, Carsten, Rascher, Wolfgang, Eckardt, Kai-Uwe, Jacobi, Johannes

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Childhood pineoblastoma: experiences from the prospective multicenter trials HIT-SKK87, HIT-SKK92 and HIT91 von Hinkes, Bernward G, von Hoff, Katja, Deinlein, Frank, Warmuth-Metz, Monika, Soerensen, Niels, Timmermann, Beate, Mittler, Uwe, Urban, Christian, Bode, Udo, Pietsch, Torsten, Schlegel, Paul G, Kortmann, Rolf D, Kuehl, Joachim, Rutkowski, Stefan

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COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness von Heeringa, Saskia F, Chernin, Gil, Chaki, Moumita, Zhou, Weibin, Sloan, Alexis J, Ji, Ziming, Xie, Letian X, Salviati, Leonardo, Hurd, Toby W, Vega-Warner, Virginia, Killen, Paul D, Raphael, Yehoash, Ashraf, Shazia, Ovunc, Bugsu, Schoeb, Dominik S, McLaughlin, Heather M, Airik, Rannar, Vlangos, Christopher N, Gbadegesin, Rasheed, Hinkes, Bernward, Saisawat, Pawaree, Trevisson, Eva, Doimo, Mara, Casarin, Alberto, Pertegato, Vanessa, Giorgi, Gianpietro, Prokisch, Holger, Rötig, Agnès, Nürnberg, Gudrun, Becker, Christian, Wang, Su, Ozaltin, Fatih, Topaloglu, Rezan, Bakkaloglu, Aysin, Bakkaloglu, Sevcan A, Müller, Dominik, Beissert, Antje, Mir, Sevgi, Berdeli, Afig, Varpizen, Seza, Zenker, Martin, Matejas, Verena, Santos-Ocaña, Carlos, Navas, Placido, Kusakabe, Takehiro, Kispert, Andreas, Akman, Sema, Soliman, Neveen A, Krick, Stefanie, Mundel, Peter, Reiser, Jochen, Nürnberg, Peter, Clarke, Catherine F, Wiggins, Roger C, Faul, Christian, Hildebrandt, Friedhelm

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Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectruma von Matejas, Verena, Hinkes, Bernward, Alkandari, Faisal, Al-Gazali, Lihadh, Annexstad, Ellen, Aytac, Mehmet B, Barrow, Margaret, Bláhová, Květa, Bockenhauer, Detlef, Cheong, Hae Il, Maruniak-Chudek, Iwona, Cochat, Pierre, Dötsch, Jörg, Gajjar, Priya, Hennekam, Raoul C, Janssen, Françoise, Kagan, Mikhail, Kariminejad, Ariana, Kemper, Markus J, Koenig, Jens, Kogan, Jillene, Kroes, Hester Y, Kuwertz-Bröking, Eberhard, Lewanda, Amy F, Medeira, Ana, Muscheites, Jutta, Niaudet, Patrick, Pierson, Michel, Saggar, Anand, Seaver, Laurie, Suri, Mohnish, Tsygin, Alexey, Wühl, Elke, Zurowska, Aleksandra, Uebe, Steffen, Hildebrandt, Friedhelm, Antignac, Corinne, Zenker, Martin

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Long-term outcome and clinical prognostic factors in children with medulloblastoma treated in the prospective randomised multicentre trial HIT'91 von VON HOFF, Katja, HINKES, Bernward, GOETTE, Heiko, SCHLEGEL, Paul G, PIETSCH, Torsten, KORTMANN, Rolf D, KUEHL, Joachim, RUTKOWSKI, Stefan, GERBER, Nicolas U, DEINLEIN, Frank, MITTLER, Uwe, URBAN, Christian, BENESCH, Martin, WARMUTH-METZ, Monika, SOERENSEN, Niels, ZWIENER, Isabella

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Cyclosporin A is superior to cyclophosphamide in children with steroid-resistant nephrotic syndrome—a randomized controlled multicentre trial by the Arbeitsgemeinschaft für Pädiatr... von Plank, Christian, Kalb, Veronica, Hinkes, Bernward, Hildebrandt, Friedhelm, Gefeller, Olaf, Rascher, Wolfgang

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Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible von Hildebrandt, Friedhelm, Hinkes, Bernward, Wiggins, Roger C, Gbadegesin, Rasheed, Vlangos, Christopher N, Seelow, Dominik, Nürnberg, Gudrun, Garg, Puneet, Verma, Rakesh, Chaib, Hassan, Hoskins, Bethan E, Ashraf, Shazia, Becker, Christian, Hennies, Hans Christian, Goyal, Meera, Wharram, Bryan L, Schachter, Asher D, Mudumana, Sudha, Drummond, Iain, Kerjaschki, Dontscho, Waldherr, Rüdiger, Dietrich, Alexander, Ozaltin, Fatih, Bakkaloglu, Aysin, Cleper, Roxana, Basel-Vanagaite, Lina, Pohl, Martin, Griebel, Martin, Tsygin, Alexey N, Soylu, Alper, Müller, Dominik, Sorli, Caroline S, Bunney, Tom D, Katan, Matilda, Liu, Jinhong, Attanasio, Massimo, O'Toole, John F, Hasselbacher, Katrin, Mucha, Bettina, Otto, Edgar A, Airik, Rannar, Kispert, Andreas, Kelley, Grant G, Smrcka, Alan V, Gudermann, Thomas, Holzman, Lawrence B, Nürnberg, Peter

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Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectrum von Matejas, Verena, Hinkes, Bernward, Alkandari, Faisal, Al-Gazali, Lihadh, Annexstad, Ellen, Aytac, Mehmet B., Barrow, Margaret, Bláhová, Květa, Bockenhauer, Detlef, Cheong, Hae Il, Maruniak-Chudek, Iwona, Cochat, Pierre, Dötsch, Jörg, Gajjar, Priya, Hennekam, Raoul C., Janssen, Françoise, Kagan, Mikhail, Kariminejad, Ariana, Kemper, Markus J., Koenig, Jens, Kogan, Jillene, Kroes, Hester Y., Kuwertz-Bröking, Eberhard, Lewanda, Amy F., Medeira, Ana, Muscheites, Jutta, Niaudet, Patrick, Pierson, Michel, Saggar, Anand, Seaver, Laurie, Suri, Mohnish, Tsygin, Alexey, Wühl, Elke, Zurowska, Aleksandra, Uebe, Steffen, Hildebrandt, Friedhelm, Antignac, Corinne, Zenker, Martin

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Frequency, Risk-Factors and Survival of Children With Atypical Teratoid Rhabdoid Tumors (AT/RT) of the CNS Diagnosed between 1988 and 2004, and Registered to the German HIT Databas... von von Hoff, Katja, Hinkes, Bernward, Dannenmann-Stern, Elke, von Bueren, André O., Warmuth-Metz, Monika, Soerensen, Niels, Emser, Angela, Zwiener, Isabella, Schlegel, Paul G., Kuehl, Joachim, Frühwald, Michael C., Kortmann, Rolf D., Pietsch, Torsten, Rutkowski, Stefan

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User-Centered Development of an Online Platform for Drug Dosing Recommendations in Pediatrics von Rödle, Wolfgang, Wimmer, Stefan, Zahn, Julia, Prokosch, Hans-Ulrich, Hinkes, Bernward, Neubert, Antje, Rascher, Wolfgang, Kraus, Stefan, Toddenroth, Dennis, Sedlmayr, Brita

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Specific Podocin Mutations Correlate with Age of Onset in Steroid-Resistant Nephrotic Syndrome von HINKES, Bernward, VLANGOS, Christopher, HEERINGA, Saskia, MUCHA, Bettina, GBADEGESIN, Rasheed, JINHONG LIU, HASSELBACHER, Katrin, OZALTIN, Fatih, HILDEBRANDT, Friedhelm

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Ependymoma gene expression profiles associated with histological subtype, proliferation, and patient survival von Lukashova-v Zangen, Inna, Kneitz, Susanne, Monoranu, Camelia-Maria, Rutkowski, Stefan, Hinkes, Bernward, Vince, Giles Hamilton, Huang, Bei, Roggendorf, Wolfgang

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“Strawberry wees forever?”: questions von Hinkes, Bernward, Benz, Kerstin, Köhler, Julia, Rascher, Wolfgang, Hirsch, Karin

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