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7. Hypokalemic rhabdomyolysis in congenital tubular disorders: a case series and a systematic review. von Vigier RO; Ortisi MT; La Manna A; Bianchetti MG; Bettinelli A Pediatr Nephrol; 2010 May; 25(5):861-6. PubMed ID: 20033223 [TBL] [Abstract][Full Text] [Related]
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10. Inherited renal tubular defects with hypokalemia. Muthukrishnan J; Modi KD; Kumar PJ; Jha R Saudi J Kidney Dis Transpl; 2009 Mar; 20(2):274-7. PubMed ID: 19237818 [TBL] [Abstract][Full Text] [Related]
12. The hypokalemia mystery: distinguishing Gitelman and Bartter syndromes from 'pseudo-Bartter syndrome'. Jdiaa SS; Walsh SB; Bockenhauer D; Fakhredine SW; Koubar SH Nephrol Dial Transplant; 2021 Dec; 37(1):29-30. PubMed ID: 32494811 [No Abstract] [Full Text] [Related]
13. Hypokalaemia and failure to thrive: report of a misleading onset. Conti G; Vitale A; Tedeschi S; Syrén ML; Pantano R; Chimenz R; Fede S; La Torre F; Coviello D; Fede C J Paediatr Child Health; 2010 May; 46(5):276-7. PubMed ID: 20412406 [TBL] [Abstract][Full Text] [Related]
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15. Gitelman syndrome presenting with cerebellar ataxia: a case report. Gokalp C; Cetin C; Bedir S; Duman S Acta Neurol Belg; 2020 Apr; 120(2):443-445. PubMed ID: 30756313 [No Abstract] [Full Text] [Related]
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19. Genetic screening for Bartter syndrome and Gitelman syndrome pathogenic genes among individuals with hypertension and hypokalemia. Bao M; Cai J; Yang X; Ma W Clin Exp Hypertens; 2019; 41(4):381-388. PubMed ID: 29953267 [TBL] [Abstract][Full Text] [Related]
20. Early onset children's Gitelman syndrome with severe hypokalaemia: a case report. Chen H; Ma R; Du H; Liu J; Jin L BMC Pediatr; 2020 Aug; 20(1):366. PubMed ID: 32758191 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]