Resultats de la cerca - Hannsjörg W. Seyberth

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  1. 1
    Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects

    Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects per Hannsjörg W. Seyberth, Karl P. Schlingmann

    Publicat 2011
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  2. 2
    Immunolocalization of the Four Prostaglandin E2 Receptor Proteins EP1, EP2, EP3, and EP4 in Human Kidney

    Immunolocalization of the Four Prostaglandin E2 Receptor Proteins EP1, EP2, EP3, and EP4 in Human Kidney per RUTA MORATH, Thomas Klein, Hannsjörg W. Seyberth, Rolf M. Nüsing

    Publicat 1999
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  3. 3
    Atrial natriuretic peptide and other vasoactive hormones in nephrotic syndrome

    Atrial natriuretic peptide and other vasoactive hormones in nephrotic syndrome per Tivadar Tulassay, Wolfgang Rascher, R. Lang, Hannsjörg W. Seyberth, K Schärer

    Publicat 1987
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  4. 4
    Mutations in the Chloride Channel Gene, CLCNKB, Leading to a Mixed Bartter-Gitelman Phenotype

    Mutations in the Chloride Channel Gene, CLCNKB, Leading to a Mixed Bartter-Gitelman Phenotype per Nikola Jeck, Martin Konrad, Melanie Peters, Stefanie Weber, Klaus E. Bonzel, Hannsjörg W. Seyberth

    Publicat 2000
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  5. 5
    Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome

    Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome per Stephan C. Reinalter, Nikola Jeck, Christoph Brochhausen, Bernhard Watzer, Rolf M. Nüsing, Hannsjörg W. Seyberth, Martin Kömhoff

    Publicat 2002
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  6. 6
    Salt Wasting and Deafness Resulting from Mutations in Two Chloride Channels

    Salt Wasting and Deafness Resulting from Mutations in Two Chloride Channels per Karl P. Schlingmann, Martin Konrad, Nikola Jeck, Petra Waldegger, Stephan C. Reinalter, Martin Holder, Hannsjörg W. Seyberth, Siegfried Waldegger

    Publicat 2004
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  7. 7
    Disruption of TRPM6/TRPM7 complex formation by a mutation in the <i>TRPM6</i> gene causes hypomagnesemia with secondary hypocalcemia

    Disruption of TRPM6/TRPM7 complex formation by a mutation in the <i>TRPM6</i> gene causes hypomagnesemia with secondary hypocalcemia per Vladimir Chubanov, Siegfried Waldegger, Michael Mederos y Schnitzler, Helga Vitzthum, Martin Sassen, Hannsjörg W. Seyberth, Martin Konrad, Thomas Gudermann

    Publicat 2004
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  8. 8
    Regulation of CLC-Ka/barttin by the ubiquitin ligase Nedd4-2 and the serum- and glucocorticoid-dependent kinases

    Regulation of CLC-Ka/barttin by the ubiquitin ligase Nedd4-2 and the serum- and glucocorticoid-dependent kinases per Hamdy M. Embark, Christoph Böhmer, Mònica Palmada, Jeyaganesh Rajamanickam, Amanda W. Wyatt, Sabine Wallisch, Giovambattista Capasso, Petra Waldegger, Hannsjörg W. Seyberth, Siegfried Waldegger, Florian Läng

    Publicat 2004
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  9. 9
    Novel Paracellin-1 Mutations in 25 Families with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

    Novel Paracellin-1 Mutations in 25 Families with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis per Stefanie Weber, Linda Schneider, Melanie Peters, Joachim Misselwitz, Gabriele Rönnefarth, M. Böswald, Klaus E. Bonzel, Tomáš Seeman, Tereza Šuláková, Eberhard Kuwertz-Bröking, Alojz Gregorič, Jean‐Bernard Palcoux, Velibor Tasić, Friedrich Manz, K Schärer, Hannsjörg W. Seyberth, Martin Konrad

    Publicat 2001
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  10. 10
    Novel Molecular Variants of the Na-K-2Cl Cotransporter Gene Are Responsible for Antenatal Bartter Syndrome

    Novel Molecular Variants of the Na-K-2Cl Cotransporter Gene Are Responsible for Antenatal Bartter Syndrome per Rosa Vargas‐Poussou, Delphine Feldmann, Martin Vollmer, Martin Konrad, Lisa E. Kelly, Lambertus P. van den Heuvel, Lamia Tebourbi, M. Brandis, Lothar Károlyi, Steven Hébert, Henny H. Lemmink, Georges Deschênes, Friedhelm Hildebrandt, Hannsjörg W. Seyberth, Lisa M. Guay‐Woodford, Nine V.A.M. Knoers, Corinne Antignac

    Publicat 1998
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  11. 11
    Polyhydramnios, Transient Antenatal Bartter’s Syndrome, and<i>MAGED2</i>Mutations

    Polyhydramnios, Transient Antenatal Bartter’s Syndrome, and<i>MAGED2</i>Mutations per Kamel Laghmani, Bodo B. Beck, Sung-Sen Yang, Elie Seaayfan, Andrea Wenzel, Björn Reusch, Helga Vitzthum, Dario Priem, Sylvie Demaretz, K. E. Bergmann, L. Duin, Heike Göbel, Christoph J. Mache, Hölger Thiele, Malte P. Bartram, Carlos Dombret, Janine Altmüller, Peter Nürnberg, Thomas Benzing, Elena Levtchenko, Hannsjörg W. Seyberth, Günter Klaus, Gökhan Yiğit, Shih‐Hua Lin, Albert Timmer, Tom J. de Koning, Sicco A. Scherjon, Karl P. Schlingmann, Mathieu J.M. Bertrand, Markus M. Rinschen, Olivier De Backer, Martin Konrad, Martin Kömhoff

    Publicat 2016
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  12. 12
    Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes [published erratum appears in Hum Mol Genet 1997 Apr;6(4):650]

    Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. Internati... per Lothar Károlyi, Martin Konrad, Arnold Köckerling, Andreas Ziegler, D Zimmermann, Bernd Roth, Christian Wieg, Karl‐Heinz Grzeschik, Manuela C. Koch, Hannsjörg W. Seyberth, Rosa Vargas, Lionel Forestier, G Jean, M Deschaux, Gian Franco Rizzoni, Patrick Niaudet, Corinne Antignac, Delphine Feldmann, Frederique Lorridon, Emmanuel Cougoureux, Jean-Luc Alessandri, Louis David, Pascal Saunier, Georges Deschênes, Friedhelm Hildebrandt, Martin Vollmer, Willem Proesmans, M. Brandis, Lambertus P. van den Heuvel, Henny H. Lemmink, Willy M. Nillesen, L.A.H. Monnens, Nine Knoers, Lisa M. Guay‐Woodford, Christopher J. Wright, Gilbert Madrigal, Steven Hébert

    Publicat 1997
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