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pro vyhledávání: '"Lorenza Baldi"'
Autor:
Marina Pitto, Marie Louise Syren, Francesca Raimondo, Samuele Corbetta, Lorenza Baldi, Alberto Bettinelli, Paola Rebora, Andrea Savoia, Silvana Tedeschi
BACKGROUND Gitelman syndrome (GS) and Bartter syndrome (BS) are hereditary salt-losing tubulopathies (SLTs) resulting from defects of renal proteins involved in electrolyte reabsorption, as for sodium-chloride cotransporter (NCC) and furosemide-sensi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bf4d40a5b7d51bb3bccd290c1df6b40
http://hdl.handle.net/10281/61372
http://hdl.handle.net/10281/61372
