Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia von SCHLINGMANN, Karl P, SASSEN, Martin C, METZGER, Daniel L, RAHMAN, Shamima, TAJIMA, Toshihiro, SHU, San-Ging, WALDEGGER, Siegfried, SEYBERTH, Hannsjoerg W, KONRAD, Martin, WEBER, Stefanie, PECHMANN, Ulla, KUSCH, Kerstin, PELKEN, Lutz, LOTAN, Daniel, SYRROU, Maria, PREBBLE, Jeffrey J, COLE, David E. C

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Classification and rescue of ROMK mutations underlying hyperprostaglandin E syndrome/antenatal Bartter syndrome von Peters, Melanie, Ermert, Saskia, Jeck, Nikola, Derst, Christian, Pechmann, Ulla, Weber, Stefanie, Schlingmann, Karl P., Seyberth, Hannsjoerg W., Waldegger, Siegfried, Konrad, Martin

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

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Bartter's and Gitelman's syndrome von Seyberth, Hannsjörg W, Weber, Stefanie, Kömhoff, Martin

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Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene von Weber, S, Hoffmann, K, Jeck, N, Saar, K, Boeswald, M, Kuwertz-Broeking, E, Meij, I I, Knoers, N V, Cochat, P, Suláková, T, Bonzel, K E, Soergel, M, Manz, F, Schaerer, K, Seyberth, H W, Reis, A, Konrad, M

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Pathophysiology and clinical presentations of salt-losing tubulopathies von Seyberth, Hannsjörg W.

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An improved terminology and classification of Bartter-like syndromes von Seyberth, Hannsjörg W

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Salt wasting and deafness resulting from mutations in two chloride channels von SCHLINGMANN, Karl P, KONRAD, Martin, JECK, Nikola, WALDEGGER, Petra, REINALTER, Stephan C, HOLDER, Martin, SEYBERTH, Hannsjörg W, WALDEGGER, Siegfried

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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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Loop Disorders: Insights Derived from Defined Genotypes von Jeck, Nikola, Seyberth, Hannsjörg W.

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Problems of prescription drug use in children von Seyberth, Hannsjörg W

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A new mutation (intron 9 +1 G>T) in the SLC12A3 gene is linked to Gitelman syndrome in Gypsies von Coto, Eliecer, Rodriguez, Julian, Jeck, Nikola, Alvarez, Victoria, Stone, Rosario, Loris, Cesar, Rodriguez, Luis M., Fischbach, Michel, Seyberth, Hannsjörg W., Santos, Fernando

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Increased systolic blood pressure with rofecoxib in congenital furosemide-like salt loss von Kömhoff, Martin, Klaus, Günter, Nazarowa, Sofia, Reinalter, Stephan C., Seyberth, Hannsjörg W.

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Effect of prostaglandin endoperoxides and metabolites on bone resorption in vitro von RAISZ, LAWRENCE G, DIETRICH, JOHN W, SIMMONS, HOLLIS A, SEYBERTH, HANNSJOERG W, HUBBARD, WALTER, OATES, JOHN A

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Effects of Celecoxib and Diclofenac on Blood Pressure, Renal Function, and Vasoactive Prostanoids in Young and Elderly Subjects von Dilger, Karin, Herrlinger, Charlotte, Peters, Jörg, Seyberth, Hannsjörg W., Schweer, Horst, Klotz, Ulrich

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Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome3q27 and is associated with mutations in the PCLN-1 gene von Weber, Stefanie, Hoffmann, Katrin, Jeck, Nikola, Saar, Kathrin, Boeswald, Martin, Kuwertz-Broeking, Eberhard, Meij, Ivan IC, Knoers, Nine VAM, Cochat, Pierre, Sulakova, Tereza, Bonzel, Klaus E, Soergel, Marianne, Manz, Friedrich, Schaerer, Karl, Seyberth, Hannsjoerg W, Reis, Andre, Konrad, Martin

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Localization of cyclooxygenase-1 and -2 in adult and fetal human kidney : implication for renal function von KOMHOFF, M, GRÖNE, H.-J, KLEIN, T, SEYBERTH, H. W, NOSING, R. M

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Problems of Prescription Drug Use in Children von Seyberth, Hannsjörg W.

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METHOD FOR DIAGNOSING A DEFECTIVE MAGNESIUM CHANNEL von SCHLINGMANN, KARL, PETER, LANG, FLORIAN, KONRAD, MARTIN, LANG, UNDINE, SEYBERTH, HANNSJOERG, W

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Verfahren zur Diagnose eines gestörten Magnesiumkanals von SEYBERTH, HANNSJOERG W, LANG, FLORIAN, KONRAD, MARTIN, LANG, UNDINE, SCHLINGMANN, KARL PETER

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