Хайлтын үр дүнгүүд - Martin Konrad
- 52-н 1 - 20 үр дүнгүүдийг харуулж байна
- Дараагийн хуудас руу очих
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Disruption of TRPM6/TRPM7 complex formation by a mutation in the <i>TRPM6</i> gene causes hypomagnesemia with secondary hypocalcemia -н Vladimir Chubanov, Siegfried Waldegger, Michael Mederos y Schnitzler, Helga Vitzthum, Martin Sassen, Hannsjörg W. Seyberth, Martin Konrad, Thomas Gudermann
Хэвлэсэн 2004Artigo -
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First Reported Nosocomial Outbreak of Severe Acute Respiratory Syndrome Coronavirus 2 in a Pediatric Dialysis Unit -н Vera Schwierzeck, Jens König, Joachim Kühn, Alexander Mellmann, Carlos L. Correa-Martínez, Heymut Omran, Martin Konrad, Thomas Kaiser, Stefanie Kampmeier
Хэвлэсэн 2020Artigo -
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Percutaneous Endoscopic Gastrostomy in Children on Peritoneal Dialysis -н 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
Хэвлэсэн 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 -н 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
Хэвлэсэн 2017Artigo -
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Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference -н 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
Хэвлэсэн 2016Artigo -
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Loss of insulin-induced activation of TRPM6 magnesium channels results in impaired glucose tolerance during pregnancy -н 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
Хэвлэсэн 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... -н 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
Хэвлэсэн 2021Artigo -
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Immunosuppression and Renal Outcome in Congenital and Pediatric Steroid-Resistant Nephrotic Syndrome -н 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
Хэвлэсэн 2010Artigo -
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Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid–Resistant Nephrotic Syndrome -н 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
Хэвлэсэн 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 -н 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
Хэвлэсэн 2014Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Medicine
Internal medicine
Biology
Genetics
Gene
Endocrinology
Kidney
Chemistry
Magnesium
Organic chemistry
Hypomagnesemia
Mutation
Pediatrics
Kidney disease
Gastroenterology
Hypokalemia
Nephrocalcinosis
Disease
Intensive care medicine
Pathology
Bartter syndrome
Biochemistry
Nephrology
Phenotype
Cell biology
Gitelman syndrome
Hypercalciuria
Hypocalciuria
Reabsorption
Renal function