Pharmacokinetics of different routes of administration of misoprostol von Tang, Oi Shan, Schweer, Horst, Seyberth, H.W., Lee, Sharon W.H., Ho, Pak Chung

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Localization of cyclooxygenase-1 and -2 in adult and fetal human kidney: implication for renal function von Komhoff, M, Grone, H. J, Klein, T, Seyberth, H. W, Nusing, R. M

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Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6 , a new member of the TRPM gene family von Sassen, Martin, Kratz, Markus, Haddad, Elie, Syrrou, Maria, Konrad, Martin, Weber, Stefanie, Niemann Nejsum, Lene, Klingel, Karin, Nielsen, Søren, Ristoff, Ellinor, Peters, Melanie, Vitzthum, Helga, Dinour, Dganit, Waldegger, Siegfried, Seyberth, Hannsjörg W, Schlingmann, Karl P

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Disruption of TRPM6/TRPM7 Complex Formation by a Mutation in the TRPM6 Gene Causes Hypomagnesemia with Secondary Hypocalcemia von Chubanov, Vladimir, Waldegger, Siegfried, Michael Mederos y Schnitzler, Vitzthum, Helga, Sassen, Martin C., Seyberth, Hannsjörg W., Konrad, Martin, Gudermann, Thomas, Jan, Lily Y.

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Survey of unlicensed and off label drug use in paediatric wards in European countries von Conroy, Sharon, Choonara, Imti, Impicciatore, Piero, Mohn, Angelika, Arnell, Henrik, Rane, Anders, Knoeppel, Carmen, Seyberth, Hannsjoerg, Pandolfini, Chiara, Raffaelli, Maria Pia, Rocchi, Francesca, Bonati, Maurizio, Jong, Geert't, de Hoog, Matthijs, van den Anker, John

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Effective NSAID treatment indicates that hyperprostaglandinism is affecting the clinical severity of childhood hypophosphatasia von Girschick, H J, Schneider, P, Haubitz, I, Hiort, O, Collmann, H, Beer, M, Shin, Y S, Seyberth, H W

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Metabolic basis of high density lipoproteins and apolipoprotein A-I increase by HMG-CoA reductase inhibition in healthy subjects and a patient with coronary artery disease von Schaefer, J.R., Schweer, H., Ikewaki, K., Stracke, H., Seyberth, H.J., Kaffarnik, H., Maisch, B., Steinmetz, A.

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Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome von KONRAD, M, VOLLMER, M, GUAY-WOODFORD, L, KNOERS, N. V. A. M, SEYBERTH, H. W, FELDMANN, D, HILDEBRANDT, F, LEMMINK, H. H, VAN DEN HEUVEL, L. P. W. J, JECK, N, VARGAS-POUSSOU, R, LAKINGS, A, RUF, R, DESCHENES, G, ANTIGNAC, C

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Hypokalemic Salt-Losing Tubulopathy With Chronic Renal Failure and Sensorineural Deafness von Jeck, Nikola, Reinalter, Stephan C, Henne, Thomas, Marg, Wolfgang, Mallmann, Rudolf, Pasel, Katharina, Vollmer, Martin, Klaus, Gunter, Leonhardt, Andreas, Seyberth, Hannsjorg W, Konrad, Martin

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Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain von Lemmink, Henny H., Knoers, Nine V.A.M., Károlyi, Lothar, van Dijk, Henk, Niaudet, Patrick, Antignac, Corinne, Guay-Woodford, Lisa M., Goodyer, Paul R., Carel, Jean-Claude, Hermes, Ad, Seyberth, Hansjörg W., Monnens, Leo A.H., van den Heuvel, Lambert P.W.J.

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Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis von WEBER, Stefanie, SCHNEIDER, Linda, GREGORIC, Alojz, PALCOUX, Jean-Bernard, TASIC, Velibor, MANZ, Friedrich, SCHÄRER, Karl, SEYBERTH, Hannsjörg W, KONRAD, Martin, PETERS, Melanie, MISSELWITZ, Joachim, RÖNNEFARTH, Gabriele, BÖSWALD, Michael, BONZEL, Klaus E, SEEMAN, Tomas, SULAKOVA, Tereza, KUWERTZ-BRÖKING, Eberhard

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Effects of selective COX‐2 inhibition on prostanoids and platelet physiology in young healthy volunteers von GRAFF, J., SKARKE, C., KLINKHARDT, U., WATZER, B., HARDER, S., SEYBERTH, H., GEISSLINGER, G., NÜSING, R. M.

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Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus von Marr, Nannette, Bichet, Daniel G, Lonergan, Michele, Arthus, Marie-Francoise, Jeck, Nikola, Seyberth, Hannsjörg W., Rosenthal, Walter, van Os, Carel H., Oksche, Alexander, Deen, Peter M. T.

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Mutations in the chloride channel gene, CLCNKB, leading to a mixed bartter-gitelman phenotype von JECK, Nikola, KONRAD, Martin, PETERS, Melanie, WEBER, Stefanie, BONZEL, Klaus E, SEYBERTH, Hannsjörg W

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Immunolocalization of the four prostaglandin E2 receptor proteins EP1, EP2, EP3, and EP4 in human kidney von MORATH, R, KLEIN, T, SEYBERTH, H. W, NÜSING, R. M

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Pharmacokinetics of a novel oral slow-release form of misoprostol von Fiala, C., Aronsson, A., Granath, F., Stephansson, O., Seyberth, H.W., Watzer, B., Gemzell-Danielsson, K.

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Renal cortical regulation of COX-1 and functionally related products in early renovascular hypertension (rat) von Theilig, F, Debiec, H, Nafz, B, Ronco, P, Nüsing, R, Seyberth, H W, Pavenstädt, H, Bouby, N, Bachmann, S

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Treatment of childhood hypophosphatasia with nonsteroidal antiinflammatory drugs von Girschick, H.J, Seyberth, H.W, Huppertz, H.I

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Localization of the prostacyclin receptor in human kidney von Kömhoff, Martin, Lesener, Britta, Nakao, Kazuwa, Seyberth, Hannsjörg W., Nüsing, Rolf M.

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Impaired response to furosemide in hyperprostaglandin E syndrome: Evidence for a tubular defect in the loop of Henle von Köckerling, Arnold, Reinalter, Stephan C., Seyberth, Hannsjörg W.

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