Hannsjörg W. Seyberth

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family

Karl P. Schlingmann, Stefanie Weber, Melanie Peters et al. · Nature Genetics · 2002 · 784 citations

Life Sciences, Genetics, Molecular Genetics +11

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

Vladimir Chubanov, Siegfried Waldegger, Michael Mederos y Schnitzler et al. · Proceedings of the National Academy of Sciences · 2004 · 372 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +17

Localization of cyclooxygenase-1 and -2 in adult and fetal human kidney: implication for renal function

Martin Kömhoff, H.-J. Gröne, Thomas Klein et al. · American Journal of Physiology-Renal Physiology · 1997 · 362 citations

Life Sciences, Developmental Biology, Physiology +13

Bartter's syndrome: A disorder characterized by high urinary prostaglandins and a dependence of hyperreninemia on prostaglandin synthesis

John R. Gill, Jurgen C. Fro ̈lich, Robert E. Bowden et al. · The American Journal of Medicine · 1976 · 325 citations

Medicine, Endocrinology, Voiding Dysfunction +3

Salt Wasting and Deafness Resulting from Mutations in Two Chloride Channels

Karl P. Schlingmann, Martin Konrad, Nikola Jeck et al. · New England Journal of Medicine · 2004 · 284 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17