Background Gitelman syndrome is a salt-losing tubulopathy caused by mutations in the SLC12A3 gene, which encodes the thiazide-sensitive sodium-chloride cotransporter. Previous studies suggested an intermediate phenotype for heterozygous carriers. Methods To evaluate the phenotype of heterozygous carriers of pathogenic SLC12A3 mutations, we performed a cross-sectional study of patients with Gitelman syndrome, heterozygous carriers, and healthy noncarriers. Participants measured their BP at home for three consecutive days before hospital admission for blood and urine sampling and an oral glucose tolerance test. Results We enrolled 242 participants, aged 18–75 years, including 81 heterozygous carriers, 82 healthy noncarriers, and 79 pati...
Our understanding of Gitelman syndrome (GS) and Bartter syndrome has continued to evolve with the us...
Gitelmans syndrome (GS) is an inherited recessive disorder caused by homozygous or compound heterozy...
Gitelman's syndrome is characterised by persistent hypokalaemia, hypomagnesaemia and hypocalciuria (...
Background Gitelman syndrome is a salt-losing tubulopathy caused by mutations in the SLC12A3 gene, w...
Abstract Background Gitelman syndrome (GS) is an autosomal recessive tubulopathy caused by mutations...
Introduction: Gitelman syndrome (GS) is a tubulopathy exhibited by salt loss. GS cases are most ofte...
Gitelman's syndrome (GS) is an inherited recessive disorder caused by homozygous or compound heteroz...
Gitelman's syndrome (GS) is a salt-losing tubulopathy characterized by hypokalemic alkalosis with hy...
Gitelman syndrome is a rare autosomal recessive hereditary salt-losing tubulopathy, that manifests a...
Abstract Background Gitelman syndrome (GS) is a rare autosomal recessive renal tubular disease, caus...
Abstract Gitelman syndrome (GS), also referred to as familial hypokalemia-hypomagnesemia, is charact...
Contains fulltext : 70157.pdf ( ) (Open Access)Gitelman syndrome (GS), also referr...
Abstract Background Gitelman syndrome (GS) is a rare autosomal recessively inherited salt-wasting tu...
Abstract Background Gitelman syndrome (GS) is an autosomal recessive disorder caused by genic mutati...
Gitelman's syndrome is characterised by persistent hypokalaemia, hypomagnesaemia and hypocalciuria (...
Our understanding of Gitelman syndrome (GS) and Bartter syndrome has continued to evolve with the us...
Gitelmans syndrome (GS) is an inherited recessive disorder caused by homozygous or compound heterozy...
Gitelman's syndrome is characterised by persistent hypokalaemia, hypomagnesaemia and hypocalciuria (...
Background Gitelman syndrome is a salt-losing tubulopathy caused by mutations in the SLC12A3 gene, w...
Abstract Background Gitelman syndrome (GS) is an autosomal recessive tubulopathy caused by mutations...
Introduction: Gitelman syndrome (GS) is a tubulopathy exhibited by salt loss. GS cases are most ofte...
Gitelman's syndrome (GS) is an inherited recessive disorder caused by homozygous or compound heteroz...
Gitelman's syndrome (GS) is a salt-losing tubulopathy characterized by hypokalemic alkalosis with hy...
Gitelman syndrome is a rare autosomal recessive hereditary salt-losing tubulopathy, that manifests a...
Abstract Background Gitelman syndrome (GS) is a rare autosomal recessive renal tubular disease, caus...
Abstract Gitelman syndrome (GS), also referred to as familial hypokalemia-hypomagnesemia, is charact...
Contains fulltext : 70157.pdf ( ) (Open Access)Gitelman syndrome (GS), also referr...
Abstract Background Gitelman syndrome (GS) is a rare autosomal recessively inherited salt-wasting tu...
Abstract Background Gitelman syndrome (GS) is an autosomal recessive disorder caused by genic mutati...
Gitelman's syndrome is characterised by persistent hypokalaemia, hypomagnesaemia and hypocalciuria (...
Our understanding of Gitelman syndrome (GS) and Bartter syndrome has continued to evolve with the us...
Gitelmans syndrome (GS) is an inherited recessive disorder caused by homozygous or compound heterozy...
Gitelman's syndrome is characterised by persistent hypokalaemia, hypomagnesaemia and hypocalciuria (...