Rezultati pretrage - Vester, Udo

The diagnostic value of ultrasound in cystic kidney diseases od Vester, Udo, Kranz, Birgitta, Hoyer, Peter F.

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No evidence for point mutations in the novel renal cystine transporter AGT1/SLC7A13 contributing to the etiology of cystinuria od Olschok, Kathrin, Vester, Udo, Lahme, Sven, Kurth, Ingo, Eggermann, Thomas

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Decreased systemic bioavailability of L-arginine in patients with cystic fibrosis od Grasemann, Hartmut, Schwiertz, Raphael, Grasemann, Corinna, Vester, Udo, Racké, Kurt, Ratjen, Felix

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Cyclosporine-A-induced nephrotoxicity in children with minimal-change nephrotic syndrome: long-term treatment up to 10 years od Kranz, Birgitta, Vester, Udo, Büscher, Rainer, Wingen, Anne-Margret, Hoyer, Peter F.

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Complement Inhibitor Eculizumab in Atypical Hemolytic Uremic Syndrome od Mache, Christoph J., Acham-Roschitz, Birgit, Frémeaux-Bacchi, Veronique, Kirschfink, Michael, Zipfel, Peter F., Roedl, Siegfried, Vester, Udo, Ring, Ekkehard

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Comparison of different normalization strategies for the analysis of glomerular microRNAs in IgA nephropathy od Bockmeyer, Clemens L., Säuberlich, Karen, Wittig, Juliane, Eßer, Marc, Roeder, Sebastian S., Vester, Udo, Hoyer, Peter F., Agustian, Putri A., Zeuschner, Philip, Amann, Kerstin, Daniel, Christoph, Becker, Jan U.

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Etiology of Kidney Diseases With Proteinuria in the Gambia/West Africa od Vester, Udo, Fombah, Augustin, Hölscher, Maite, Garba, Danlami, Tapgun, Mary, N‘Jai, Pamela Collier, Mendy, Philipp, Bass, Gibril, Muhammad, Abdul K., Anderson, Suzanne T., Sanneh, Abdoulie, Onyeama, Charles, Helmchen, Udo, Bojang, Khalifa, Hoyer, Peter F., Corrah, Tumani

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Complement Factor H–Related Protein 1 Deficiency and Factor H Antibodies in Pediatric Patients with Atypical Hemolytic Uremic Syndrome od Hofer, Johannes, Janecke, Andreas R., Zimmerhackl, L.B., Riedl, Magdalena, Rosales, Alejandra, Giner, Thomas, Cortina, Gerard, Haindl, Carola J., Petzelberger, Barbara, Pawlik, Miriam, Jeller, Verena, Vester, Udo, Gadner, Bettina, van Husen, Michael, Moritz, Michael L., Würzner, Reinhard, Jungraithmayr, Therese

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Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivo od Heinemann, Falko M., Jindra, Peter T., Bockmeyer, Clemens L., Zeuschner, Philip, Wittig, Juliane, Höflich, Heike, Eßer, Marc, Abbas, Mahmoud, Dieplinger, Georg, Stolle, Katharina, Vester, Udo, Hoyer, Peter F., Immenschuh, Stephan, Heinold, Andreas, Horn, Peter A., Li, Wentian, Eisenberger, Ute, Becker, Jan U.

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Author Correction: Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivo od Heinemann, Falko M., Jindra, Peter T., Bockmeyer, Clemens L., Zeuschner, Philip, Wittig, Juliane, Höflich, Heike, Eßer, Marc, Abbas, Mahmoud, Dieplinger, Georg, Stolle, Katharina, Vester, Udo, Hoyer, Peter F., Immenschuh, Stephan, Heinold, Andreas, Horn, Peter A., Li, Wentian, Eisenberger, Ute, Becker, Jan U.

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Mutations in DZIP1L, which encodes a ciliary transition zone protein, cause autosomal recessive polycystic kidney disease od Lu, Hao, Galeano, Maria C. Rondón, Ott, Elisabeth, Kaeslin, Geraldine, Kausalya, P. Jaya, Kramer, Carina, Ortiz-Brüchle, Nadina, Hilger, Nadescha, Metzis, Vicki, Hiersche, Milan, Tay, Shang Yew, Tunningley, Robert, Vij, Shubha, Courtney, Andrew D., Whittle, Belinda, Wühl, Elke, Vester, Udo, Hartleben, Björn, Neuber, Steffen, Frank, Valeska, Little, Melissa H., Epting, Daniel, Papathanasiou, Peter, Perkins, Andrew C., Wright, Graham D., Hunziker, Walter, Gee, Heon Yung, Otto, Edgar A., Zerres, Klaus, Hildebrandt, Friedhelm, Roy, Sudipto, Wicking, Carol, Bergmann, Carsten

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Whole exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies od Gee, Heon Yung, Otto, Edgar A., Hurd, Toby W., Ashraf, Shazia, Chaki, Moumita, Cluckey, Andrew, Vega-Warner, Virginia, Saisawat, Pawaree, Diaz, Katrina A., Fang, Humphrey, Kohl, Stefan, Allen, Susan J., Airik, Rannar, Zhou, Weibin, Ramaswami, Gokul, Janssen, Sabine, Fu, Clementine, Innis, Jamie L., Weber, Stefanie, Vester, Udo, Davis, Erica E., Katsanis, Nicholas, Fathy, Hanan M., Jeck, Nikola, Klaus, Gunther, Nayir, Ahmet, Rahim, Khawla A., Attrach, Ibrahim Al, Hassoun, Ibrahim Al, Ozturk, Savas, Drozdz, Dorota, Helmchen, Udo, O’Toole, John F., Attanasio, Massimo, Nürnberg, Gudrun, Nürnberg, Peter, Washburn, Joseph, MacDonald, James, James, Jeffrey W., Levy, Shawn, Hildebrandt, Friedhelm

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Mutations in the evolutionarily highly conserved KEOPS complex genes cause nephrotic syndrome with microcephaly od Braun, Daniela A., Rao, Jia, Mollet, Geraldine, Schapiro, David, Daugeron, Marie-Claire, Tan, Weizhen, Gribouval, Olivier, Boyer, Olivia, Revy, Patrick, Jobst-Schwan, Tilman, Schmidt, Johanna Magdalena, Lawson, Jennifer A., Schanze, Denny, Ashraf, Shazia, Boddaert, Nathalie, Collinet, Bruno, Martin, Gaëlle, Liger, Dominique, Lovric, Svjetlana, Furlano, Monica, Guerrera, I. Chiara, Sanchez-Ferras, Oraly, Menten, Björn, Vergult, Sarah, De Rocker, Nina, Airik, Merlin, Hermle, Tobias, Shril, Shirlee, Widmeier, Eugen, Gee, Heon Yung, Choi, Won-Il, Sadowski, Carolin E., Pabst, Werner L., Warejko, Jillian, Daga, Ankana, LeBerre, Tamara Basta, Matejas, Verena, Behnam, Babak, Beeson, Brendan, Begtrup, Amber, Bruce, Malcolm, Ch'ng, Gaik-Siew, Lin, Shuan-Pei, Chang, Jui-Hsing, Chen, Chao-Huei, Cho, Megan T., Gipson, Patrick E., Hsu, Chyong-Hsin, Kari, Jameela A., Ke, Yu-Yuan, Kiraly-Borri, Cathy, Lai, Wai-ming, Lemyre, Emmanuelle, Littlejohn, Rebecca Okasha, Masri, Amira, Moghtaderi, Mastaneh, Nakamura, Kazuyuki, Praet, Marleen, Prasad, Chitra, Prytula, Agnieszka, Roeder, Elizabeth, Rump, Patrick, Schnur, Rhonda E., Shiihara, Takashi, Sinha, Manish, Soliman, Neveen A, Soulami, Kenza, Sweetser, David A., Tsai, Wen-Hui, Tsai, Jeng-Daw, Vester, Udo, Viskochil, David H., Vatanavicharn, Nithiwat, Waxler, Jessica L., Wolf, Matthias T.F., Wong, Sik-Nin, Poduri, Annapurna, Truglio, Gessica, Mane, Shrikant, Lifton, Richard P., Bouchard, Maxime, Kannu, Peter, Chitayat, David, Magen, Daniella, Calleweart, Bert, van Tilbeurgh, Herman, Zenker, Martin, Antignac, Corinne, Hildebrandt, Friedhelm

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