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10.1093/ndt/gfu198

http://scihub22266oqcxt.onion/10.1093/ndt/gfu198
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25165187!ä!25165187

suck abstract from ncbi


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pmid25165187      Nephrol+Dial+Transplant 2014 ; 29 Suppl 4 (ä): iv63-71
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  • Inherited disorders of renal hypomagnesaemia #MMPMID25165187
  • Konrad M; Schlingmann KP
  • Nephrol Dial Transplant 2014[Sep]; 29 Suppl 4 (ä): iv63-71 PMID25165187show ga
  • The kidney plays a key role in the maintenance of normal magnesium balance. The distal tubule of the kidney, namely the thick ascending limb of the loop of Henle and the distal convoluted tubule, is crucial for the regulation of serum magnesium levels and body magnesium content. The identification of molecular defects related to rare inherited magnesium losing disorders has contributed greatly to a better understanding of the process of renal magnesium handling. Since the number of genetic defects related to magnesium metabolism is still increasing, it might be expected that our knowledge on magnesium physiology will further improve. This knowledge will hopefully lead to therapeutic strategies that enable specific therapies for patients suffering from the symptoms and possible sequelae of chronic magnesium depletion.
  • |Humans[MESH]
  • |Hypercalciuria/*genetics[MESH]
  • |Magnesium Deficiency/blood/*genetics[MESH]
  • |Magnesium/*blood[MESH]
  • |Metal Metabolism, Inborn Errors/blood/*genetics[MESH]
  • |Nephrocalcinosis/*genetics[MESH]


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