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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. 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]
7. 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]
8. Effect of indomethacin on amniotic fluid prostaglandin and aldosterone levels in a fetus with Bartter syndrome. Amsalem H; Valsky DV; Yagel S; Celnikier DH; Anteby EY Prenat Diagn; 2003 May; 23(5):431-3. PubMed ID: 12749044 [No Abstract] [Full Text] [Related]
9. 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. 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]
12. 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]
13. Bartter syndrome in two siblings--antenatal and neonatal observations. Proesmans W; Devlieger H; Van Assche A; Eggermont E; Vandenberghe K; Lemmens F; Sieprath P; Lijnen P Int J Pediatr Nephrol; 1985; 6(1):63-70. PubMed ID: 3888887 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Amniotic fluid biochemistry in isolated polyhydramnios: a series of 464 cases. Allaf B; Dreux S; Schmitz T; Czerkiewicz I; Le Vaillant C; Benachi A; Houfflin-Debarge V; Maréchaud M; Oury JF; Muller F Prenat Diagn; 2015 Dec; 35(13):1331-5. PubMed ID: 26426702 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]