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Marianne C Astor, Kristian Løvås, Anette S B Wolff, Bjørn Nedrebø, Eirik Bratland, Jon Steen-Johnsen and Eystein S Husebye

Borochowitz Z Boettger MB Beck GE Englehardt RK Carmi R . Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia . Nature Genetics 2002 31 171 – 174 . ( doi:10.1038/ng901 ). 9 Voets T Nilius B Hoefs S van der

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Efstratios Kardalas, Stavroula A Paschou, Panagiotis Anagnostis, Giovanna Muscogiuri, Gerasimos Siasos and Andromachi Vryonidou

hypokalemia. Finally, hypomagnesemia is very important. More than 50% of clinically significant hypokalemia has concomitant magnesium deficiency and is clinically most frequently observed in individuals receiving loop or thiazide diuretic therapy. Concomitant