Bilaketaren emaitzak - Lutz T. Weber

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  1. 1
    Nephropathic Cystinosis: Symptoms, Treatment, and Perspectives of a Systemic Disease

    Nephropathic Cystinosis: Symptoms, Treatment, and Perspectives of a Systemic Disease nork Sören Bäumner, Lutz T. Weber

    Argitaratua 2018
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  2. 2
    SGLT2 inhibitors: approved for adults and cats but not for children with CKD

    SGLT2 inhibitors: approved for adults and cats but not for children with CKD nork Oliver Groß, Dieter Haffner, Franz Schaefer, Lutz T. Weber

    Argitaratua 2024
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  3. 3
    Molecular causes of congenital anomalies of the kidney and urinary tract (CAKUT)

    Molecular causes of congenital anomalies of the kidney and urinary tract (CAKUT) nork Stefan Kohl, Sandra Habbig, Lutz T. Weber, Max C. Liebau

    Argitaratua 2021
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  4. 4
    Mycophenolate Mofetil versus Cyclosporin A in Children with Frequently Relapsing Nephrotic Syndrome

    Mycophenolate Mofetil versus Cyclosporin A in Children with Frequently Relapsing Nephrotic Syndrome nork Jutta Gellermann, Lutz T. Weber, Lars Pape, Burkhard Tönshoff, Peter F. Hoyer, Uwe Querfeld

    Argitaratua 2013
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  5. 5
    The Pharmacokinetic-Pharmacodynamic Relationship for Total and Free Mycophenolic Acid in Pediatric Renal Transplant Recipients

    The Pharmacokinetic-Pharmacodynamic Relationship for Total and Free Mycophenolic Acid in Pediatric Renal Transplant Recipients nork Lutz T. Weber, Maria Shipkova, Victor W. Armstrong, Natalie Wagner, Ekkehard Schütz, Otto Mehls, Lothar Bernd Zimmerhackl, Michael Oellerich, Burkhard Tönshoff

    Argitaratua 2002
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  6. 6
    Comparison of the Emit Immunoassay with HPLC for Therapeutic Drug Monitoring of Mycophenolic Acid in Pediatric Renal-Transplant Recipients on Mycophenolate Mofetil Therapy

    Comparison of the Emit Immunoassay with HPLC for Therapeutic Drug Monitoring of Mycophenolic Acid in Pediatric Renal-Transplant Recipients on Mycophenolate Mofetil Therapy nork Lutz T. Weber, Maria Shipkova, Victor W. Armstrong, Natalie Wagner, Ekkehard Schütz, Otto Mehls, Lothar Bernd Zimmerhackl, Michael Oellerich, Burkhard Tönshoff

    Argitaratua 2002
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  7. 7
    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 nork 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

    Argitaratua 2009
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  8. 8
    Pharmacokinetics of mycophenolic acid (MPA) and determinants of MPA free fraction in pediatric and adult renal transplant recipients. German Study group on Mycophenolate Mofetil Therapy in Pediatric Renal Transplant Recipients.

    Pharmacokinetics of mycophenolic acid (MPA) and determinants of MPA free fraction in pediatric and adult renal transplant recipients. German Study group on Mycophenolate Mofetil Th... nork Lutz T. Weber, Maria Shipkova, T. Lamersdorf, P. D. Niedmann, M. Wiesel, A Mandelbaum, Lothar Bernd Zimmerhackl, Ekkehard Schütz, Otto Mehls, Michael Oellerich, Victor W. Armstrong, Burkhard Tönshoff

    Argitaratua 1998
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  9. 9
    Protocol and rationale for a randomized controlled SGLT2 inhibitor trial in pediatric and young adult populations with chronic kidney disease: DOUBLE PRO-TECT Alport

    Protocol and rationale for a randomized controlled SGLT2 inhibitor trial in pediatric and young adult populations with chronic kidney disease: DOUBLE PRO-TECT Alport nork Oliver Groß, Jan Boeckhaus, Lutz T. Weber, Hiddo J.L. Heerspink, James Simon, Rees Ahmed, Christoph Gerst, Ulrike Duerr, Florian Walker, Ralf Tostmann, Jürgen Helm, Thomas Asendorf, Tim Friede

    Argitaratua 2024
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  10. 10
    Three-layered proteomic characterization of a novel<i>ACTN4</i>mutation unravels its pathogenic potential in FSGS

    Three-layered proteomic characterization of a novel<i>ACTN4</i>mutation unravels its pathogenic potential in FSGS nork Malte P. Bartram, Sandra Habbig, Caroline Pahmeyer, Martin Höhne, Lutz T. Weber, Hölger Thiele, Janine Altmüller, Nina Kottoor, Andrea Wenzel, Marcus Krüeger, Bernhard Schermer, Thomas Benzing, Markus M. Rinschen, Bodo B. Beck

    Argitaratua 2016
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  11. 11
    Long-term follow-up after rituximab for steroid-dependent idiopathic nephrotic syndrome

    Long-term follow-up after rituximab for steroid-dependent idiopathic nephrotic syndrome nork Markus J. Kemper, Jutta Gellermann, Sandra Habbig, Rafael T. Krmar, Katalin Dittrich, T. Jungraithmayr, Lars Pape, L. Patzer, H. Billing, Lutz T. Weber, Martina Pohl, Kelli Rosenthal, A. Rosahl, D. E. Mueller-Wiefel, Jörg Dötsch

    Argitaratua 2011
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  12. 12
    Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid–Resistant Nephrotic Syndrome

    Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid–Resistant Nephrotic Syndrome nork Anja Büscher, Bodo B. Beck, Anette Melk, Julia Hoefele, Birgitta Kranz, Daniel Bamborschke, Sabrina Baig, Bärbel Lange-Sperandio, Theresa Jungraithmayr, Lutz T. Weber, Markus J. Kemper, Burkhard Tönshoff, Peter F. Hoyer, Martin Konrad, Stefanie Weber

    Argitaratua 2015
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  13. 13
    Mutations in Multiple PKD Genes May Explain Early and Severe Polycystic Kidney Disease

    Mutations in Multiple PKD Genes May Explain Early and Severe Polycystic Kidney Disease nork Carsten Bergmann, Jennifer von Bothmer, Nadina Ortiz Brüchle, Andreas Venghaus, Valeska Frank, Henry Fehrenbach, Tobias Hampel, Lars Pape, Annegret Buske, Jón J. Jónsson, Nanette Sarioglu, Antónia Santos, José Carlos Ferreira, Jan U. Becker, Reinhold Cremer, Julia Hoefele, Marcus R. Benz, Lutz T. Weber, Reinhard Buettner, Klaus Zerres

    Argitaratua 2011
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  14. 14
    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 nork 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

    Argitaratua 2019
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  15. 15
    Urinary Dickkopf-related protein 3 as a novel biomarker for kidney function decline in children with Alport syndrome

    Urinary Dickkopf-related protein 3 as a novel biomarker for kidney function decline in children with Alport syndrome nork Jan Boeckhaus, Burkhard Tönshoff, Lutz T. Weber, Lars Pape, Kay Latta, Henry Fehrenbach, Baerbel Lange‐Sperandio, Matthias Kettwig, Sabine König, Ulrike John-Kroegel, Jutta Gellermann, Matthias Galiano, Shekib A. Jami, Dennis Pieper, Gry H. Dihazi, Angelika Hafke, Stefan Kohl, Max C. Liebau, Jens König, Dieter Haffner, Oliver Groß, Manuel Wallbach

    Argitaratua 2025
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  16. 16
    Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD)

    Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD) nork Kathrin Burgmaier, Samuel Kilian, Bert Bammens, Thomas Benzing, Heiko Billing, Anja Büscher, Matthias Galiano, Franziska Grundmann, Günter Klaus, Djalila Mekahli, Laurence Michel‐Calemard, Gordana Miloševski‐Lomić, Bruno Ranchin, Katja Sauerstein, Susanne Schaefer, Rukshana Shroff, Rosalie Sterenborg, Sarah Verbeeck, Lutz T. Weber, Dorota Wicher, Elke Wühl, Jörg Dötsch, Franz Schaefer, Max C. Liebau

    Argitaratua 2019
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  17. 17
    KANK deficiency leads to podocyte dysfunction and nephrotic syndrome

    KANK deficiency leads to podocyte dysfunction and nephrotic syndrome nork Heon Yung Gee, Fujian Zhang, Shazia Ashraf, Stefan Kohl, Carolin E. Sadowski, Virginia Vega-Warner, Weibin Zhou, Svjetlana Lovric, Humphrey Fang, Margaret Nettleton, Jun‐yi Zhu, Julia Hoefele, Lutz T. Weber, Ľudmila Podracká, A Böör, Henry Fehrenbach, Jeffrey W. Innis, Joseph Washburn, Shawn Levy, Richard P. Lifton, Edgar A. Otto, Zhe Han, Friedhelm Hildebrandt

    Argitaratua 2015
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  18. 18
    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 nork 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

    Argitaratua 2018
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  19. 19
    Rationale, design and objectives of ARegPKD, a European ARPKD registry study

    Rationale, design and objectives of ARegPKD, a European ARPKD registry study nork Kathrin Ebner, Markus Feldkoetter, Gema Ariceta, Carsten Bergmann, Reinhard Buettner, Anke Doyon, Ali Düzova, Heike Goebel, Dieter Haffner, Barbara Hero, Bernd Höppe, Thomas Illig, Augustina Jankauskiené, Norman Klopp, Jens König, Mieczysław Litwin, Djalila Mekahli, Bruno Ranchin, Anja Sander, Sara Testa, Lutz T. Weber, Dorota Wicher, Ayşe Yüzbaşıoğlu, Klaus Zerres, Jörg Dötsch, Franz Schaefer, Max C. Liebau

    Argitaratua 2015
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  20. 20
    ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling

    ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling nork Heon Yung Gee, Pawaree Saisawat, Shazia Ashraf, Toby W. Hurd, Virginia Vega-Warner, Humphrey Fang, Bodo B. Beck, Olivier Gribouval, Weibin Zhou, Katrina A. Diaz, S. Natarajan, Roger C. Wiggins, Svjetlana Lovric, Gil Chernin, Dominik S. Schoeb, Buğsu Övünç, Yaacov Frishberg, Neveen A. Soliman, Hanan Fathy, Heike Goebel, Julia Hoefele, Lutz T. Weber, Jeffrey W. Innis, Christian Faul, Zhe Han, Joseph Washburn, Corinne Antignac, Shawn Levy, Edgar A. Otto, Friedhelm Hildebrandt

    Argitaratua 2013
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