Search Results - Martin Konrad
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Recent Advances in Molecular Genetics of Hereditary Magnesium-Losing Disorders by Martin Konrad, Stefanie Weber
Published 2003Revisão -
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Disruption of TRPM6/TRPM7 complex formation by a mutation in the <i>TRPM6</i> gene causes hypomagnesemia with secondary hypocalcemia by Vladimir Chubanov, Siegfried Waldegger, Michael Mederos y Schnitzler, Helga Vitzthum, Martin Sassen, Hannsjörg W. Seyberth, Martin Konrad, Thomas Gudermann
Published 2004Artigo -
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First Reported Nosocomial Outbreak of Severe Acute Respiratory Syndrome Coronavirus 2 in a Pediatric Dialysis Unit by Vera Schwierzeck, Jens König, Joachim Kühn, Alexander Mellmann, Carlos L. Correa-Martínez, Heymut Omran, Martin Konrad, Thomas Kaiser, Stefanie Kampmeier
Published 2020Artigo -
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Percutaneous Endoscopic Gastrostomy in Children on Peritoneal Dialysis by Christian von Schnakenburg, Reinhard Feneberg, Christian Plank, Miriam Zimmering, Klaus Arbeiter, Martin Bald, Henry Fehrenbach, Martin Griebel, Christoph Licht, Martin Konrad, Kirsten Timmermann, Markus J. Kemper
Published 2006Artigo -
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Biallelic mutations in CYP24A1 or SLC34A1 as a cause of infantile idiopathic hypercalcemia (IIH) with vitamin D hypersensitivity: molecular study of 11 historical IIH cases by Ewa Pronicka, Elżbieta Ciara, Paulina Halat, Agnieszka Janiec, Marek Wójcik, E Rowińska, Dariusz Rokicki, Paweł Płudowski, Ewa Wojciechowska, Aldona Wierzbicka, Janusz Książyk, Agnieszka Jacoszek, Martin Konrad, Karl P. Schlingmann, Mieczysław Litwin
Published 2017Artigo -
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Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference by Anne Blanchard, Detlef Böckenhauer, Davide Bolignano, Lorenzo A. Calò, Etienne Cosyns, Olivier Devuyst, David H. Ellison, Fiona E. Karet, Nine V.A.M. Knoers, Martin Konrad, Shih-Hua Lin, Rosa Vargas‐Poussou
Published 2016Artigo -
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Loss of insulin-induced activation of TRPM6 magnesium channels results in impaired glucose tolerance during pregnancy by Anil V. Nair, Berthold Hocher, Sjoerd Verkaart, Femke van Zeeland, Thiemo Pfab, Torsten Slowinski, Youpeng Chen, Karl P. Schlingmann, André Schaller, Sabina Gallati, René J.M. Bindels, Martin Konrad, Joost G.J. Hoenderop
Published 2012Artigo -
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Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubul... by Martin Konrad, Tom Nijenhuis, Gema Ariceta, Aurélia Bertholet‐Thomas, Lorenzo A. Calò, Giovambattista Capasso, Francesco Emma, Karl P. Schlingmann, Mandeep Singh, Francesco Trepiccione, Stephen B. Walsh, Kirsty Whitton, Rosa Vargas‐Poussou, Detlef Böckenhauer
Published 2021Artigo -
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Immunosuppression and Renal Outcome in Congenital and Pediatric Steroid-Resistant Nephrotic Syndrome by Anja Büscher, Birgitta Kranz, Rainer Büscher, Friedhelm Hildebrandt, Bernd Dworniczak, Petra Pennekamp, Eberhard Kuwertz-Bröking, Anne‐Margret Wingen, Ulrike John, Markus J. Kemper, L.A.H. Monnens, Peter F. Hoyer, Stefanie Weber, Martin Konrad
Published 2010Artigo -
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Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid–Resistant Nephrotic Syndrome by 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
Published 2015Artigo -
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Clinical Utility of Simultaneous Quantitation of 25-Hydroxyvitamin D and 24,25-Dihydroxyvitamin D by LC-MS/MS Involving Derivatization With DMEQ-TAD by Martin Kaufmann, John C. Gallagher, Munro Peacock, Karl‐Peter Schlingmann, Martin Konrad, Hector F. DeLuca, Rita Sigüeiro, Borja Lopez, Antonio Mouriño, M.A. Maestro, René St‐Arnaud, Joel S. Finkelstein, Donald P. Cooper, Glenville Jones
Published 2014Artigo
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