Add to ORKGhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000247977300353&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=8e1609b174ce4e31116a60747a720701PediatricsUrology & NephrologySCI(E)0MEETING ABSTRACT91492-14922
Abstract Background Gitelman syndrome (GS) is a rare autosomal recessively inherited salt-wasting tu...
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-C...
Gitelman's syndrome is characterised by persistent hypokalaemia, hypomagnesaemia and hypocalciuria (...
Loss of function of mutated solute carrier family 12 member 3 (SLC12A3) gene is the most frequent et...
Abstract Background Gitelman syndrome (GS) is an autosomal recessive disorder caused by genic mutati...
Abstract Background Gitelman syndrome (GS) is an autosomal recessive disorder and mild variant of cl...
<i>Background:</i> Gitelman syndrome (GS) is an autosomal recessive renal tubulopathy caused by inac...
Abstract Background Gitelman syndrome (GS) is a rare autosomal recessive renal tubular disease, caus...
Gitelman's syndrome (GS) is a salt-losing tubulopathy with an autosomal recessive inheritance caused...
Gitelman's syndrome (GS) is a salt-losing tubulopathy characterized by hypokalemic alkalosis with hy...
Gitelman's syndrome is characterised by persistent hypokalaemia, hypomagnesaemia and hypocalciuria (...
Abstract Background Gitelman syndrome is an autosomal recessive inherited renal disorder characteriz...
We report a case of Gitelman syndrome (GS) in a dizygotic twin who presented at 12 years of age with...
The present study reported clinical characteristics and the results of gene mutation analysis of 3 C...
Gitelman syndrome (GS) is a recessive salt-losing tubulopathy that is caused by mutations in the SLC...
Abstract Background Gitelman syndrome (GS) is a rare autosomal recessively inherited salt-wasting tu...
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-C...
Gitelman's syndrome is characterised by persistent hypokalaemia, hypomagnesaemia and hypocalciuria (...
Loss of function of mutated solute carrier family 12 member 3 (SLC12A3) gene is the most frequent et...
Abstract Background Gitelman syndrome (GS) is an autosomal recessive disorder caused by genic mutati...
Abstract Background Gitelman syndrome (GS) is an autosomal recessive disorder and mild variant of cl...
<i>Background:</i> Gitelman syndrome (GS) is an autosomal recessive renal tubulopathy caused by inac...
Abstract Background Gitelman syndrome (GS) is a rare autosomal recessive renal tubular disease, caus...
Gitelman's syndrome (GS) is a salt-losing tubulopathy with an autosomal recessive inheritance caused...
Gitelman's syndrome (GS) is a salt-losing tubulopathy characterized by hypokalemic alkalosis with hy...
Gitelman's syndrome is characterised by persistent hypokalaemia, hypomagnesaemia and hypocalciuria (...
Abstract Background Gitelman syndrome is an autosomal recessive inherited renal disorder characteriz...
We report a case of Gitelman syndrome (GS) in a dizygotic twin who presented at 12 years of age with...
The present study reported clinical characteristics and the results of gene mutation analysis of 3 C...
Gitelman syndrome (GS) is a recessive salt-losing tubulopathy that is caused by mutations in the SLC...
Abstract Background Gitelman syndrome (GS) is a rare autosomal recessively inherited salt-wasting tu...
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-C...
Gitelman's syndrome is characterised by persistent hypokalaemia, hypomagnesaemia and hypocalciuria (...