153 related articles for article (PubMed ID: 36819197)
1. Case Report: Transient antenatal bartter syndrome in an extremely preterm infant with a novel
Yang H; Liu Z; Wu Y; Xu J; He Y; Wang R; Zhang W; Chen D
Front Pediatr; 2022; 10():1093268. PubMed ID: 36819197
[TBL] [Abstract][Full Text] [Related]
2. A novel MAGED2 variant in a Chinese preterm newborn with transient antenatal Bartter's syndrome with 4 years follow-up.
Ma M; Zhang M; Zhou Y; Yao F; Wei M; Li Z; Qiu Z
BMC Nephrol; 2021 Dec; 22(1):408. PubMed ID: 34895150
[TBL] [Abstract][Full Text] [Related]
3. Polyhydramnios, Transient Antenatal Bartter's Syndrome, and MAGED2 Mutations.
Laghmani K; Beck BB; Yang SS; Seaayfan E; Wenzel A; Reusch B; Vitzthum H; Priem D; Demaretz S; Bergmann K; Duin LK; Göbel H; Mache C; Thiele H; Bartram MP; Dombret C; Altmüller J; Nürnberg P; Benzing T; Levtchenko E; Seyberth HW; Klaus G; Yigit G; Lin SH; Timmer A; de Koning TJ; Scherjon SA; Schlingmann KP; Bertrand MJ; Rinschen MM; de Backer O; Konrad M; Kömhoff M
N Engl J Med; 2016 May; 374(19):1853-63. PubMed ID: 27120771
[TBL] [Abstract][Full Text] [Related]
4. Transient Antenatal Bartter's Syndrome: A Case Report.
Meyer M; Berrios M; Lo C
Front Pediatr; 2018; 6():51. PubMed ID: 29594084
[TBL] [Abstract][Full Text] [Related]
5. A Case Report and Literature Review of a Novel Mutation in the MAGED2 Gene of a Patient With Severe Transient Polyhydramnios.
Wu X; Huang L; Luo C; Liu Y; Niu J
Front Pediatr; 2021; 9():778814. PubMed ID: 34926352
[No Abstract] [Full Text] [Related]
6. Successful antenatal treatment of MAGED2-related Bartter syndrome and review of treatment options and efficacy.
Walsh CJ; Micke K; Elfman H; Bock M; Harper T; Zaretsky M; Galan HL; Behrendt N; Putra M
Prenat Diagn; 2024 Feb; 44(2):172-179. PubMed ID: 38159268
[TBL] [Abstract][Full Text] [Related]
7. Prevalence of Novel
Legrand A; Treard C; Roncelin I; Dreux S; Bertholet-Thomas A; Broux F; Bruno D; Decramer S; Deschenes G; Djeddi D; Guigonis V; Jay N; Khalifeh T; Llanas B; Morin D; Morin G; Nobili F; Pietrement C; Ryckewaert A; Salomon R; Vrillon I; Blanchard A; Vargas-Poussou R
Clin J Am Soc Nephrol; 2018 Feb; 13(2):242-250. PubMed ID: 29146702
[TBL] [Abstract][Full Text] [Related]
8. Identification of a novel intronic mutation of MAGED2 gene in a Chinese family with antenatal Bartter syndrome.
Yan X; Hu Y; Zhang X; Gao X; Zhao Y; Peng H; Ouyang L; Zhang C
BMC Med Genomics; 2024 Jan; 17(1):23. PubMed ID: 38238844
[TBL] [Abstract][Full Text] [Related]
9. Type 3 antenatal Bartter syndrome presenting with mild polyuria.
Otsubo Y; Kano Y; Suzumura H; Yoshihara S
BMJ Case Rep; 2021 Apr; 14(4):. PubMed ID: 33827883
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of MAGED2 gene mutation causing transient antenatal Bartter syndrome.
Takemori S; Tanigaki S; Nozu K; Yoshihashi H; Uchiumi Y; Sakaguchi K; Tsushima K; Kitamura A; Kobayashi C; Matsuhima M; Tajima A; Nagano C; Kobayashi Y
Eur J Med Genet; 2021 Oct; 64(10):104308. PubMed ID: 34400373
[TBL] [Abstract][Full Text] [Related]
11. A Case of a Novel MAGED2 Mutation Resulting in Non-transient Bartter's Syndrome in an Adult Female.
Albaba I; Azher S; Mehta S; Faddoul G
Cureus; 2023 May; 15(5):e38681. PubMed ID: 37288186
[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. MAGED2: a novel form of antenatal Bartter's syndrome.
Kömhoff M; Laghmani K
Curr Opin Nephrol Hypertens; 2018 Jul; 27(4):323-328. PubMed ID: 29677005
[TBL] [Abstract][Full Text] [Related]
14. Transient antenatal Bartter's Syndrome and X-linked polyhydramnios: insights from the genetics of a rare condition.
Quigley R; Saland JM
Kidney Int; 2016 Oct; 90(4):721-3. PubMed ID: 27633862
[TBL] [Abstract][Full Text] [Related]
15. Antenatal Bartter syndrome: a new compound heterozygous mutation in exon 2 of KCNJ1 gene.
Mani S; Nair J; Handa D
BMJ Case Rep; 2021 Oct; 14(10):. PubMed ID: 34663630
[TBL] [Abstract][Full Text] [Related]
16. 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. A variant of Bartter's syndrome. Bartter's syndrome associated with hydramnios, prematurity, hypercalciuria and nephrocalcinosis.
Ohlsson A; Sieck U; Cumming W; Akhtar M; Serenius F
Acta Paediatr Scand; 1984 Nov; 73(6):868-74. PubMed ID: 6395627
[TBL] [Abstract][Full Text] [Related]
18. [Neonatal variant of Bartter syndrome].
Bertram H; Seidenberg J; Ehrich JH; Brodehl J
Monatsschr Kinderheilkd; 1992 May; 140(5):281-5. PubMed ID: 1614456
[TBL] [Abstract][Full Text] [Related]
19. Nephrogenic diabetes insipidus.
Bockenhauer D; Bichet DG
Curr Opin Pediatr; 2017 Apr; 29(2):199-205. PubMed ID: 28134709
[TBL] [Abstract][Full Text] [Related]
20. Neonatal Bartter syndrome.
Parkash J; Muhammad Sohail Salat ; Khan IA
J Coll Physicians Surg Pak; 2006 Aug; 16(8):548-50. PubMed ID: 16899189
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
