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 · 775 citations

Trpm Gene Family, Natural Sciences, Genetics +8

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 · 369 citations · Full text

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

Renal Pathology, Renal Inflammation, Pathology +22

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 · 324 citations

Adrenal Gland, Urology, Prostaglandin Synthesis +7

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 · 280 citations · Full text

Biology, Chloride Transporters, Deafness Resulting +11