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3. Antenatal Bartter syndrome: a rare cause of unexplained severe polyhydramnios. Bhat YR; Vinayaka G; Vani R; Prashanth KA; Sreelakshmi K Ann Trop Paediatr; 2011; 31(2):153-7. PubMed ID: 21575321 [TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of Bartter syndrome: amniotic fluid aldosterone. Rachid M; Dreux S; Pean de Ponfilly G; Vargas-Poussou R; Czerkiewicz I; Chevenne D; Oury JF; Deschênes G; Muller F Ann Biol Clin (Paris); 2017 Apr; 75(2):204-208. PubMed ID: 28377333 [TBL] [Abstract][Full Text] [Related]
5. Elevated aldosterone in amniotic fluid and maternal blood has diagnostic potential in pregnancies complicated with a fetus of Bartter syndrome. Nakanishi T; Suzumori N; Mizuno H; Suzuki K; Sato T; Tanemura M; Suzuki Y; Suzumori K Fetal Diagn Ther; 2005; 20(6):481-4. PubMed ID: 16260879 [TBL] [Abstract][Full Text] [Related]
6. A Rare Cause of Refractory Severe Polyhydramnios: Antenatal Bartter Syndrome. Nam G; Cho A; Park MH Medicina (Kaunas); 2021 Mar; 57(3):. PubMed ID: 33809664 [No Abstract] [Full Text] [Related]
7. Prenatal diagnosis of Bartter syndrome. Shalev H; Ohaly M; Meizner I; Carmi R Prenat Diagn; 1994 Oct; 14(10):996-8. PubMed ID: 7899275 [TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of Bartter syndrome with biochemical examination of amniotic fluid: case report. Dane B; Yayla M; Dane C; Cetin A Fetal Diagn Ther; 2007; 22(3):206-8. PubMed ID: 17228161 [TBL] [Abstract][Full Text] [Related]
10. [Fetal polyuria and decrease of electrolytes in amniotic fluid as principal markers of neonatal Bartter's syndrome]. Di Pietro A; Proverbio MR; Tammaro V; Riccio E; Santoro C; Sarnelli C; Cicale F Pediatr Med Chir; 1997; 19(4):267-8. PubMed ID: 9508653 [TBL] [Abstract][Full Text] [Related]
11. Electrolyte composition of the amniotic fluid in Bartter syndrome. Massa G; Proesmans W; Devlieger H; Vandenberghe K; Van Assche A; Eggermont E Eur J Obstet Gynecol Reprod Biol; 1987 Apr; 24(4):335-40. PubMed ID: 3582718 [TBL] [Abstract][Full Text] [Related]
12. Biochemical examination of mother's urine is useful for prenatal diagnosis of Bartter syndrome. Matsushita Y; Suzuki Y; Oya N; Kajiura S; Okajima K; Uemura O; Suzumori K Prenat Diagn; 1999 Jul; 19(7):671-3. PubMed ID: 10419618 [TBL] [Abstract][Full Text] [Related]
13. [Bartter syndrome--a rare cause of severe polyhydramnios]. Media J; Hoseth GE Ugeskr Laeger; 2006 Dec; 168(50):4425-6. PubMed ID: 17217871 [TBL] [Abstract][Full Text] [Related]
14. Bartter syndrome: An infrequent tubulopathy of prenatal onset. Gómez de la F CL; Novoa P JM; Caviedes R N Rev Chil Pediatr; 2019 Aug; 90(4):437-442. PubMed ID: 31859717 [TBL] [Abstract][Full Text] [Related]
17. Severe Bartter syndrome type 1: Prompt postnatal management thanks to antenatal identification of SLC12A1 pathogenic variants. D'Angelantonio D; Majore S; Di Netta T; Zotta F; Parise G; Savino E; Rosignoli S; Bizzarri B; Signore F; Grammatico P; Bottillo I Arch Pediatr; 2022 Oct; 29(7):530-533. PubMed ID: 36058813 [TBL] [Abstract][Full Text] [Related]
18. [The neonatal form of Bartter's syndrome: current findings in etiology and physiopathology]. Proesmans WC Verh K Acad Geneeskd Belg; 1992; 54(3):253-93. PubMed ID: 1413986 [TBL] [Abstract][Full Text] [Related]
19. Two neonates with Bartter syndrome. Afzal T; Fatima S; Shirazi IH; Halim A J Pak Med Assoc; 2018 Nov; 68(11):1721-1723. PubMed ID: 30410160 [TBL] [Abstract][Full Text] [Related]
20. [Differential diagnosis of a polyhydramnion in hyperprostaglandin E syndrome: a case report]. Marek S; Tekesin I; Hellmeyer L; Kömhoff M; Seyberth HW; Maier RF; Schmidt S Z Geburtshilfe Neonatol; 2004 Dec; 208(6):232-5. PubMed ID: 15647987 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]