Hakutulokset - Martin Pöhl

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  1. 1
    Henoch–Schönlein purpura nephritis

    Henoch–Schönlein purpura nephritis Tekijä Martin Pöhl

    Julkaistu 2014
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  2. 2
    Toward an etiological classification of developmental disorders of the kidney and upper urinary tract

    Toward an etiological classification of developmental disorders of the kidney and upper urinary tract Tekijä Martin Pöhl, Vibha Bhatnagar, Stanley A. Mendoza, Sanjay K. Nigám

    Julkaistu 2002
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  3. 3
    Involvement of Laminin Binding Integrins and Laminin-5 in Branching Morphogenesis of the Ureteric Bud during Kidney Development

    Involvement of Laminin Binding Integrins and Laminin-5 in Branching Morphogenesis of the Ureteric Bud during Kidney Development Tekijä Roy Zent, Kevin T. Bush, Martin Pöhl, Vito Quaranta, Naohiko Koshikawa, Zemin Wang, Jordan A. Kreidberg, Hiroyuki Sakurai, Robert O. Stuart, Sanjay K. Nigám

    Julkaistu 2001
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  4. 4
    Prospective, Randomized Trial on Late Steroid Withdrawal in Pediatric Renal Transplant Recipients Under Cyclosporine Microemulsion and Mycophenolate Mofetil

    Prospective, Randomized Trial on Late Steroid Withdrawal in Pediatric Renal Transplant Recipients Under Cyclosporine Microemulsion and Mycophenolate Mofetil Tekijä Britta Höcker, Lutz T. Weber, Reinhard Feneberg, Jens Drube, Ulrike John, Henry Fehrenbach, Martin Pöhl, Miriam Zimmering, Stefan Fründ, Günter Klaus, Elke Wühl, Burkhard Tönshoff

    Julkaistu 2009
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  5. 5
    Thrombospondin-1 inhibits alternative complement pathway activation in antineutrophil cytoplasmic antibody-associated vasculitis

    Thrombospondin-1 inhibits alternative complement pathway activation in antineutrophil cytoplasmic antibody-associated vasculitis Tekijä Swagata Konwar, Sophie Schroda, Manuel Rogg, Jessika Kleindienst, Eva L. Decker, Martin Pöhl, Barbara Zieger, Jens Panse, Hong Wang, Robert Grosse, Christoph Schell, Sílvia Vidal, Xiaobo Liu, Christian Gorzelanny, Todor Tschongov, Karsten Häffner

    Julkaistu 2025
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  6. 6
    Moss-Produced, Glycosylation-Optimized Human Factor H for Therapeutic Application in Complement Disorders

    Moss-Produced, Glycosylation-Optimized Human Factor H for Therapeutic Application in Complement Disorders Tekijä Stefan Michelfelder, Juliana Parsons, Lennard L. Bohlender, Sebastian N. W. Hoernstein, Holger Niederkrüger, Andreas Büsch, Nicola Krieghoff, Jonas P. Koch, Benjamin Fode, Andreas Schaaf, Thomas Frischmuth, Martin Pöhl, Peter F. Zipfel, Ralf Reski, Eva L. Decker, Karsten Häffner

    Julkaistu 2016
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  7. 7
    Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies

    Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies Tekijä Bodo B. Beck, Anne Baasner, Anja Buescher, Sandra Habbig, Nadine Reintjes, Markus J. Kemper, Przemysław Sikora, Christoph J. Mache, Martin Pöhl, Mirjam Stahl, Burkhard Toenshoff, Lars Pape, Henry Fehrenbach, Dorrit E. Jacob, Bernd Grohe, Matthias T. F. Wolf, Gudrun Nürnberg, Gökhan Yigit, Eduardo Salido, Bernd Höppe

    Julkaistu 2012
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  8. 8
    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 Tekijä 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

    Julkaistu 2017
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  9. 9
    Epidemiology of and Risk Factors for BK Polyomavirus Replication and Nephropathy in Pediatric Renal Transplant Recipients: An International CERTAIN Registry Study

    Epidemiology of and Risk Factors for BK Polyomavirus Replication and Nephropathy in Pediatric Renal Transplant Recipients: An International CERTAIN Registry Study Tekijä Britta Höcker, Lukas Schneble, Luisa Murer, Andrea Carraro, Lars Pape, Birgitta Kranz, Jun Oh, Matthias Zirngibl, Luca Dello Strologo, Anja Büscher, Lutz T. Weber, Atif Awan, Martin Pöhl, Martin Bald, Nikoleta Printza, Krisztina Rusai, Licia Peruzzi, Rezan Topaloĝlu, Alexander Fichtner, Kai Krupka, L. Köster, Thomas Brückner, Paul Schnitzler, Hans H. Hirsch, Burkhard Tönshoff

    Julkaistu 2018
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  10. 10
    Results of a multicenter, randomized trial examining a new transition model for post-kidney transplant adolescents

    Results of a multicenter, randomized trial examining a new transition model for post-kidney transplant adolescents Tekijä Martin Kreuzer, Jenny Prüfe, Marie‐Luise Dierks, Silvia Müther, Dirk Bethe, Anja Büscher, Krisztina Heindl-Rusai, Sabine Hollenbach, Bernd Höppe, Ulrike John-Kroegel, Nele Kanzelmeyer, Günter Klaus, Birgitta Kranz, Jun Oh, Martin Pöhl, Susanne Rieger, Bettina Ruckenbrodt, Katja Sauerstein, Hagen Staude, Christina Taylan, Julia Thumfart, Marcus Weitz, Rieke Ringlstetter, Anika Großhennig, Lars Pape

    Julkaistu 2025
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  11. 11
    A Multi-layered Quantitative In Vivo Expression Atlas of the Podocyte Unravels Kidney Disease Candidate Genes

    A Multi-layered Quantitative In Vivo Expression Atlas of the Podocyte Unravels Kidney Disease Candidate Genes Tekijä Markus M. Rinschen, Markus Gödel, Florian Grahammer, Stefan Zschiedrich, Martin Helmstädter, Oliver Kretz, Mostafa Zarei, Daniela A. Braun, S Dittrich, Caroline Pahmeyer, Patricia Schröder, Carolin Teetzen, Heon Yung Gee, Ghaleb H. Daouk, Martin Pöhl, Elisa Kuhn, Bernhard Schermer, Victoria Küttner, Melanie Boerries, Hauke Busch, Mario Schiffer, Carsten Bergmann, Marcus Krüger, Friedhelm Hildebrandt, Jörn Dengjel, Thomas Benzing, Tobias B. Huber

    Julkaistu 2018
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  12. 12
    Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosis

    Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosis Tekijä Tilman Jobst‐Schwan, Verena Klämbt, Maureen Tarsio, John F. Heneghan, Amar J. Majmundar, Shirlee Shril, Florian Buerger, Isabel Ottlewski, Boris E. Shmukler, Rezan Topaloĝlu, Seema Hashmi, Farkhanda Hafeez, Francesco Emma, Marcella Greco, Guido F. Laube, Hanan Fathy, Martin Pöhl, Jutta Gellermann, Danko Milošević, Michelle A. Baum, Shrikant Mane, Richard P. Lifton, Patricia M. Kane, Seth L. Alper, Friedhelm Hildebrandt

    Julkaistu 2019
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  13. 13
    Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome

    Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome Tekijä Daniela A. Braun, Carolin E. Sadowski, Stefan Kohl, Svjetlana Lovric, Susanne Adina Astrinidis, Werner L. Pabst, Heon Yung Gee, Shazia Ashraf, Jennifer A. Lawson, Shirlee Shril, Merlin Airik, Weizhen Tan, David Schapiro, Jia Rao, Won‐Il Choi, Tobias Hermle, Markus J. Kemper, Martin Pöhl, Fatih Özaltın, Martin Konrad, Radovan Bogdanović, Rainer Büscher, U. Helmchen, Erkin Serdaroğlu, Richard P. Lifton, Wolfram Antonin, Friedhelm Hildebrandt

    Julkaistu 2016
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  14. 14
    Transitional Care and Adherence of Adolescents and Young Adults After Kidney Transplantation in Germany and Austria

    Transitional Care and Adherence of Adolescents and Young Adults After Kidney Transplantation in Germany and Austria Tekijä Martin Kreuzer, Jenny Prüfe, Martina Oldhafer, Dirk Bethe, Marie‐Luise Dierks, Silvia Müther, Julia Thumfart, Bernd Höppe, Anja Büscher, Wolfgang Rascher, Matthias Hansen, Martin Pöhl, Markus J. Kemper, Jens Drube, Susanne Rieger, Ulrike John, Christina Taylan, Katalin Dittrich, Sabine Hollenbach, Günter Klaus, Henry Fehrenbach, Birgitta Kranz, Carmen Montoya, Bärbel Lange-Sperandio, Bettina Ruckenbrodt, Heiko Billing, Hagen Staude, Krisztina Heindl-Rusai, R. Brunkhorst, Lars Pape

    Julkaistu 2015
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  15. 15
    Clinical and Molecular Characterization of Patients with Heterozygous Mutations in Wilms Tumor Suppressor Gene 1

    Clinical and Molecular Characterization of Patients with Heterozygous Mutations in Wilms Tumor Suppressor Gene 1 Tekijä A. Lehnhardt, Claartje Karnatz, Thurid Ahlenstiel-Grunow, Kerstin Benz, Marcus R. Benz, Klemens Budde, Anja Büscher, Thomas Fehr, Markus Feldkötter, Norbert Graf, Britta Höcker, Therese Jungraithmayr, Günter Klaus, B Koehler, Martin Konrad, Birgitta Kranz, Carmen Montoya, Dominik N. Müller, Thomas J. Neuhaus, Jun Oh, Lars Pape, Martin Pöhl, Brigitte Royer‐Pokora, Uwe Querfeld, Reinhard Schneppenheim, Hagen Staude, Giuseppina Spartà, Kirsten Timmermann, Frauke Wilkening, Simone Wygoda, Carsten Bergmann, Markus J. Kemper

    Julkaistu 2015
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  16. 16
    ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3

    ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3 Tekijä Sylvia Hoff, Jan Halbritter, Daniel Epting, Valeska Frank, Thanh-Minh T. Nguyen, Jeroen van Reeuwijk, Christopher Boehlke, Christoph Schell, Takayuki Yasunaga, Martin Helmstädter, Miriam Mergen, Emilie Filhol, Karsten Boldt, Nicola Horn, Marius Ueffing, Edgar A. Otto, Tobias Eisenberger, Mariet W. Elting, J. A. E. van Wijk, Detlef Böckenhauer, Neil J. Sebire, Søren Rittig, Mogens Vyberg, Troels Ring, Martin Pöhl, Lars Pape, Thomas J. Neuhaus, Neveen A. Soliman, Sarah Koon, Peter C. Harris, Florian Grahammer, Tobias B. Huber, E. Wolfgang Kuehn, Albrecht Kramer-Zucker, Hanno J. Bolz, Ronald Roepman, Sophie Saunier, Gerd Walz, Friedhelm Hildebrandt, Carsten Bergmann, Soeren S. Lienkamp

    Julkaistu 2013
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  17. 17
    Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease

    Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease Tekijä Kathrin Burgmaier, Kevin Kunzmann, Gema Ariceta, Carsten Bergmann, Anja Buescher, Mathias Burgmaier, İsmail Dursun, Ali Düzova, Loai Eid, Florian Erger, Markus Feldkoetter, Matthias Galiano, Michaela Geßner, Heike Goebel, İbrahim Gökçe, Dieter Haffner, Nakysa Hooman, Bernd Höppe, Augustina Jankauskiené, Günter Klaus, Jens König, Mieczysław Litwin, Laura Massella, Djalila Mekahli, Engin Melek, Sevgı Mır, Lars Pape, Larisa Prikhodina, Bruno Ranchin, Raphael Schild, Tomáš Seeman, Lale Sever, Rukshana Shroff, Neveen A. Soliman, Stella Stabouli, Małgorzata Stańczyk, Yılmaz Tabel, Katarzyna Taranta‐Janusz, Sara Testa, Julia Thumfart, Rezan Topaloĝlu, Lutz T. Weber, Dorota Wicher, Elke Wühl, Simone Wygoda, Alev Yılmaz, Katarzyna Zachwieja, Ilona Zagożdżon, Klaus Zerres, Jörg Dötsch, Franz Schaefer, Max C. Liebau, Nadejda Ranguelov, Nathalie Godefroid, Laure Collard, Jacques Lombet, Julie Maquet, Gesa Schalk, Uwe Querfeld, Bodo B. Beck, Thomas Benzing, Reinhard Buettner, Franziska Grundmann, Christine Kurschat, Kerstin Benz, Anja Tzschoppe, Bjoern Buchholz, Rainer Buescher, Karsten Häffner, Martin Pöhl, Oliver Groß, Jenny Krügel, Johanna Stock, Ludwig Patzer, Jun Oh, Wanja M. Bernhardt, Anke Doyon, Tobias Vinke, Anja Sander, Michael Henn, Ute Derichs, Rolf Beetz, Nikola Jeck, Bärbel Lange-Sperandio, Sabine Ponsel, Franziska Kusser, Barbara Uetz, Marcus R. Benz, Silke Schmidt, C. J. Huppertz-Kessler, Birgitta Kranz, Andrea Titieni, Donald Wurm, Heinz E. Leichter, Martin Bald, Heiko Billing, Marwa M. Nabhan, Luis Enrique Lara, Fotiοs Papachristou, Francesco Emma

    Julkaistu 2018
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