Add to ORKGBartter syndrome, first described in 1962 [1], is a group of closely related hereditary tubulopathies. All variants of the syndrome share several clinical characteristics including renal salt wasting, hypo
OBJECTIVE: Bartter\u27s syndrome is a rare genetic disorder characterized by renal salt wasting...
Bartter syndrome (BS) is an autosomal recessively inherited rare renal tubular disorder characterize...
Bartter syndrome comprises a group of rare autosomal-recessive salt-losing disorders with distinct p...
Síndrome de Bartter; Hipokalièmia heretada; Tubulopatia perdedora de salSíndrome de Bartter; Hipopot...
Tamara da Silva Cunha, Ita Pfeferman Heilberg Nephrology Division, Universidade Federal de Sã...
Bartter syndrome and Gitelman syndrome (GS) are autosomal recessive disorders usually caused by homo...
Variants of inherited hypokalemic tubulopathies follow autosomal recessive inheritance and share cha...
Bartter Syndrome (BS) is a rare, inherited renal tubulopathy characterised by hypokalaemic, hypochlo...
A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes....
Bartter syndrome (BS) and Gitelman syndrome (GS) are renal tubular disorders affecting sodium, potas...
BACKGROUND: We aim to review the clinical features of two renal tubular disorders characterized by s...
Bartter and Gitelman syndromes are rare inherited tubulopathies characterized by hypokalaemic, hypoc...
The kidney plays a key role in determining the long-term set points of fluid and electrolyte balance...
Bartter and Gitelman syndromes are rare inherited tubulopathies characterized by hypokalaemic, hypoc...
Abstract Bartter syndrome (BS) is a salt-losing hereditary tubulopathy characterized by hypokalemic ...
OBJECTIVE: Bartter\u27s syndrome is a rare genetic disorder characterized by renal salt wasting...
Bartter syndrome (BS) is an autosomal recessively inherited rare renal tubular disorder characterize...
Bartter syndrome comprises a group of rare autosomal-recessive salt-losing disorders with distinct p...
Síndrome de Bartter; Hipokalièmia heretada; Tubulopatia perdedora de salSíndrome de Bartter; Hipopot...
Tamara da Silva Cunha, Ita Pfeferman Heilberg Nephrology Division, Universidade Federal de Sã...
Bartter syndrome and Gitelman syndrome (GS) are autosomal recessive disorders usually caused by homo...
Variants of inherited hypokalemic tubulopathies follow autosomal recessive inheritance and share cha...
Bartter Syndrome (BS) is a rare, inherited renal tubulopathy characterised by hypokalaemic, hypochlo...
A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes....
Bartter syndrome (BS) and Gitelman syndrome (GS) are renal tubular disorders affecting sodium, potas...
BACKGROUND: We aim to review the clinical features of two renal tubular disorders characterized by s...
Bartter and Gitelman syndromes are rare inherited tubulopathies characterized by hypokalaemic, hypoc...
The kidney plays a key role in determining the long-term set points of fluid and electrolyte balance...
Bartter and Gitelman syndromes are rare inherited tubulopathies characterized by hypokalaemic, hypoc...
Abstract Bartter syndrome (BS) is a salt-losing hereditary tubulopathy characterized by hypokalemic ...
OBJECTIVE: Bartter\u27s syndrome is a rare genetic disorder characterized by renal salt wasting...
Bartter syndrome (BS) is an autosomal recessively inherited rare renal tubular disorder characterize...
Bartter syndrome comprises a group of rare autosomal-recessive salt-losing disorders with distinct p...