Výsledky vyhledávání - Udo Vester

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  1. 1
    Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes

    Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes Autor Rainer Büscher, Anja Büscher, Stefanie Weber, Julia Mohr, Bianca Hegen, Udo Vester, Peter F. Hoyer

    Vydáno 2013
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  2. 2
    Complement Inhibitor Eculizumab in Atypical Hemolytic Uremic Syndrome

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

    Vydáno 2009
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  3. 3
    Eculizumab for Atypical Hemolytic–Uremic Syndrome

    Eculizumab for Atypical Hemolytic–Uremic Syndrome Autor Jens Nürnberger, Thomas Philipp, Oliver Witzke, Anabelle Opazo Saez, Udo Vester, Hideo A. Baba, Andreas Kribben, Lothar Bernd Zimmerhackl, Andreas Janecke, Mato Nagel, Michael Kirschfink

    Vydáno 2009
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  4. 4
    Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)

    Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD) Autor Carsten Bergmann, Jan Senderek, Ellen Windelen, Fabian Küpper, Iris Middeldorf, Frank Schneider, Christian Dornia, Sabine Rudnik–Schöneborn, Martin Konrad, Claus Peter Schmitt, Tomáš Seeman, Thomas J. Neuhaus, Udo Vester, Jutta Kirfel, Reinhard Büttner, Klaus Zerres

    Vydáno 2005
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  5. 5
    Complement Factor H–Related Protein 1 Deficiency and Factor H Antibodies in Pediatric Patients with Atypical Hemolytic Uremic Syndrome

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

    Vydáno 2012
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  6. 6
    HNF1B nephropathy has a slow-progressive phenotype in childhood—with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry

    HNF1B nephropathy has a slow-progressive phenotype in childhood—with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry Autor Christine Okorn, Anne Goertz, Udo Vester, Bodo B. Beck, Carsten Bergmann, Sandra Habbig, Jens König, Martin Konrad, Dominik Müller, Jun Oh, Nadina Ortiz‐Brüchle, Ludwig Patzer, Raphael Schild, Tomáš Seeman, Hagen Staude, Julia Thumfart, Burkhard Tönshoff, Ulrike Walden, Lutz T. Weber, Marcin Zaniew, H. Zappel, Peter F. Hoyer, Stefanie Weber

    Vydáno 2019
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  7. 7
    Intermediate Follow-up of Pediatric Patients With Hemolytic Uremic Syndrome During the 2011 Outbreak Caused by E. coli O104:H4

    Intermediate Follow-up of Pediatric Patients With Hemolytic Uremic Syndrome During the 2011 Outbreak Caused by E. coli O104:H4 Autor Sebastian Loos, Wiebke Aulbert, Bernd Höppe, Thurid Ahlenstiel-Grunow, Birgitta Kranz, Charlotte Wahl, Hagen Staude, Alexander Humberg, Kerstin Benz, Martín Krause, Martin Pöhl, Max C. Liebau, Raphael Schild, Johanna Lemke, Ortraud Beringer, Dominik N. Müller, Christoph Härtel, Marianne Wigger, Udo Vester, Martin Konrad, Dieter Haffner, Lars Pape, Jun Oh, Markus J. Kemper

    Vydáno 2017
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  8. 8
    German evidence‐ and consensus‐based guideline on the management of penile urethritis

    German evidence‐ and consensus‐based guideline on the management of penile urethritis Autor Ricardo Niklas Werner, Isabell Vader, Susan Abunijela, Markus Bickel, Anika Biel, Christoph Boesecke, Lisa Branke, Viviane Bremer, Norbert H. Brockmeyer, Susanne Buder, Stefan Eßer, Ruben Heuer, Frank‐Michael Köhn, Andrea Mais, Alexander Nast, Antonia Pennitz, Anja Potthoff, H Rasokat, Michael Sabranski, Sven Schellberg, Axel J. Schmidt, Sebastian Schmidt, Laila Schneidewind, Sören Schubert, Caroline Schulte, Christoph D. Spinner, Petra Spornraft‐Ragaller, Cord Sunderkötter, Udo Vester, Christoph Zeyen, Klaus Jansen

    Vydáno 2025
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  9. 9
    Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease

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

    Vydáno 2017
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  10. 10
    Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies

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

    Vydáno 2013
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  11. 11
    Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly

    Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly Autor Daniela A. Braun, Jia Rao, Géraldine Mollet, David Schapiro, Marie-Claire Daugeron, Weizhen Tan, Olivier Gribouval, Olivia Boyer, Patrick Revy, Tilman Jobst‐Schwan, Johanna Magdalena Schmidt, Jennifer A. Lawson, Denny Schanze, Shazia Ashraf, Jeremy F.P. Ullmann, Charlotte A. Hoogstraten, Nathalie Boddaert, Bruno Collinet, Gaëlle Martin, Dominique Liger, Svjetlana Lovric, Mónica Furlano, Ida Chiara Guerrera, Oraly Sanchez-Ferras, Jennifer Hu, Anne‐Claire Boschat, Sylvia Sanquer, Björn Menten, Sarah Vergult, Nina De Rocker, Merlin Airik, Tobias Hermle, Shirlee Shril, Eugen Widmeier, Heon Yung Gee, Won‐Il Choi, Carolin E. Sadowski, Werner L. Pabst, Jillian K. Warejko, Ankana Daga, Tamara Basta, Verena Matejas, Karin Scharmann, Sandra D. Kienast, Babak Behnam, Brendan Beeson, Amber Begtrup, M. Bruce, Gaik-Siew Ch’ng, Shuan‐Pei Lin, Jui-Hsing Chang, Chao‐Huei Chen, Megan T. Cho, Patrick M. Gaffney, Patrick Gipson, Chyong-Hsin Hsu, Jameela A. Kari, Yu-Yuan Ke, Cathy Kiraly‐Borri, Wai-ming Lai, Emmanuelle Lemyre, Rebecca O. Littlejohn, Amira Masri, Mastaneh Moghtaderi, Kazuyuki Nakamura, Fatih Özaltın, Marleen Praet, Chitra Prasad, Agnieszka Prytula-Ebels, Elizabeth Roeder, Patrick Rump, Rhonda E. Schnur, Takashi Shiihara, Manish D. Sinha, Neveen A. Soliman, Kenza Soulami, David A. Sweetser, Wen‐Hui Tsai, Jeng-Daw Tsai, Rezan Topaloĝlu, Udo Vester, David H. Viskochil, Nithiwat Vatanavicharn, Jessica L. Waxler, Klaas J. Wierenga, Matthias T. F. Wolf, Sik-Nin Wong, Sebastian A. Leidel, Gessica Truglio, Peter C. Dedon, Annapurna Poduri, Shrikant Mane, Richard P. Lifton, Maxime Bouchard, Pekka Kannus, David Chitayat, Daniella Magen, Bert Callewaert, Herman van Tilbeurgh, Martin Zenker

    Vydáno 2017
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