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10.1007/s00467-008-0968-x http://scihub22266oqcxt.onion/10.1007/s00467-008-0968-x 18818955!7811505!18818955     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=18818955&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\18818955.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Pediatr+Nephrol 2009 ; 24 (4): 697-705 Nephropedia Template TP {{tp|p=18818955|t=2009. Inherited forms of renal hypomagnesemia: an update |pdf=|usr=}}{{18818955}} gab.com Text Inherited forms of renal hypomagnesemia: an update JO: Pediatr Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=18818955 #FOAvip The kidney plays an important role in ion homeostasis in the human body. Several hereditary disorders characterized by perturbations in renal magnesium reabsorption leading to hypomagnesemia have been described over the past 50 years, with the most important of these being Gitelman syndrome, familial hypomagnesemia with hypercalciuria and nephrocalcinosis, familial hypomagnesemia with secondary hypocalcemia, autosomal dominant hypomagnesemia with hypocalciuria, and autosomal recessive hypomagnesemia. Only recently, following positional cloning strategies in affected families, have mutations in renal ion channels and transporters been identified in these diseases. In this short review, I give an update on these hypomagnesemic disorders. Elucidation of the genetic etiology and, for most of these disorders, also the underlying pathophysiology of the disease, has greatly increased our understanding of the normal physiology of renal magnesium handling. This is yet another example of the importance of studying rare disorders in order to unravel physiological and pathophysiological processes in the human body. Twit Text FOAVip Inherited forms of renal hypomagnesemia: an update ????Pediatr Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=18818955 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=18818955 #FOAvip English Wikipedia <ref>{{Cite pmid|18818955}}</ref> Inherited forms of renal hypomagnesemia: an update #MMPMID18818955 Knoers NV Pediatr Nephrol 2009[Apr]; 24 (4): 697-705 PMID18818955show ga The kidney plays an important role in ion homeostasis in the human body. Several hereditary disorders characterized by perturbations in renal magnesium reabsorption leading to hypomagnesemia have been described over the past 50 years, with the most important of these being Gitelman syndrome, familial hypomagnesemia with hypercalciuria and nephrocalcinosis, familial hypomagnesemia with secondary hypocalcemia, autosomal dominant hypomagnesemia with hypocalciuria, and autosomal recessive hypomagnesemia. Only recently, following positional cloning strategies in affected families, have mutations in renal ion channels and transporters been identified in these diseases. In this short review, I give an update on these hypomagnesemic disorders. Elucidation of the genetic etiology and, for most of these disorders, also the underlying pathophysiology of the disease, has greatly increased our understanding of the normal physiology of renal magnesium handling. This is yet another example of the importance of studying rare disorders in order to unravel physiological and pathophysiological processes in the human body. |Gitelman Syndrome/genetics/physiopathology[MESH] |Humans[MESH] |Hypocalcemia/genetics/physiopathology[MESH] |Kidney Tubules/metabolism[MESH] |Kidney/*metabolism[MESH] |Magnesium Deficiency/*genetics/physiopathology[MESH] |Magnesium/*blood[MESH] |Metal Metabolism, Inborn Errors/*genetics/physiopathology[MESH]Inherited forms of renal hypomagnesemia: an update (epmc).pdf DeepDyve Pubget Overpricing