168 related articles for article (PubMed ID: 35774371)
1. A Novel Frame-Shift Mutation in
Lu YT; Liu XC; Zhou ZM; Zhang D; Sun L; Zhang Y; Fan P; Zhang L; Liu YX; Luo F; Zhou XL
Front Cardiovasc Med; 2022; 9():896564. PubMed ID: 35774371
[TBL] [Abstract][Full Text] [Related]
2. Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused by a Novel SCNN1B Mutation.
Fan P; Zhang D; Pan XC; Yang KQ; Zhang QY; Lu YT; Zhang Y; Liu XY; Ma WJ; Zhang HM; Song L; Cai J; Liu YX; Zhou XL
Kidney Blood Press Res; 2020; 45(4):603-611. PubMed ID: 32698182
[TBL] [Abstract][Full Text] [Related]
3. A frameshift mutation in the
Lu Y; Liu X; Sun L; Zhang D; Fan P; Yang K; Zhang L; Liu Y; Zhou X
Mol Med Rep; 2024 Feb; 29(2):. PubMed ID: 38099339
[TBL] [Abstract][Full Text] [Related]
4. A novel nonsense mutation in the β-subunit of the epithelial sodium channel causing Liddle syndrome.
Mareš Š; Filipovský J; Vlková K; Pešta M; Černá V; Hrabák J; Mlíková Seidlerová J; Mayer O
Blood Press; 2021 Oct; 30(5):291-299. PubMed ID: 34223773
[TBL] [Abstract][Full Text] [Related]
5. Liddle syndrome due to a novel mutation in the γ subunit of the epithelial sodium channel (ENaC) in family from Russia: a case report.
Kozina AA; Trofimova TA; Okuneva EG; Baryshnikova NV; Obuhova VA; Krasnenko AY; Tsukanov KY; Klimchuk OI; Surkova EI; Shatalov PA; Ilinsky VV
BMC Nephrol; 2019 Oct; 20(1):389. PubMed ID: 31655555
[TBL] [Abstract][Full Text] [Related]
6. Liddle syndrome misdiagnosed as primary aldosteronism resulting from a novel frameshift mutation of SCNN1B.
Fan P; Lu CX; Zhang D; Yang KQ; Lu PP; Zhang Y; Meng X; Hao SF; Luo F; Liu YX; Zhang HM; Song L; Cai J; Zhang X; Zhou XL
Endocr Connect; 2018 Dec; 7(12):1528-1534. PubMed ID: 30496127
[TBL] [Abstract][Full Text] [Related]
7. Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome.
Yang KQ; Lu CX; Fan P; Zhang Y; Meng X; Dong XQ; Luo F; Liu YX; Zhang HM; Wu HY; Cai J; Zhang X; Zhou XL
Clin Exp Hypertens; 2018; 40(2):107-111. PubMed ID: 28718682
[TBL] [Abstract][Full Text] [Related]
8. Truncated Epithelial Sodium Channel β Subunit Responsible for Liddle Syndrome in a Chinese Family.
Fan P; Lu CX; Yang KQ; Lu PP; Hao SF; Luo F; Zhang HM; Song L; Wu HY; Cai J; Zhang X; Zhou XL
Kidney Blood Press Res; 2019; 44(5):942-949. PubMed ID: 31437854
[TBL] [Abstract][Full Text] [Related]
9. A novel frameshift mutation of epithelial sodium channel β-subunit leads to Liddle syndrome in an isolated case.
Yang KQ; Lu CX; Xiao Y; Liu YX; Jiang XJ; Zhang X; Zhou XL
Clin Endocrinol (Oxf); 2015 Apr; 82(4):611-4. PubMed ID: 25378078
[TBL] [Abstract][Full Text] [Related]
10. A Family with Liddle Syndrome Caused by a Novel Stop-Gain Mutation in the γ Subunit of Epithelial Sodium Channels.
Wang X; Cao C; Yao Q; Guo L; Li C; Li J
Nephron; 2022; 146(6):647-651. PubMed ID: 35661050
[TBL] [Abstract][Full Text] [Related]
11. A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia.
Fan P; Zhao YM; Zhang D; Liao Y; Yang KQ; Tian T; Lou Y; Luo F; Ma WJ; Zhang HM; Song L; Cai J; Liu YX; Zhou XL
Am J Hypertens; 2019 Jul; 32(8):752-758. PubMed ID: 30977777
[TBL] [Abstract][Full Text] [Related]
12. Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension.
Fan P; Pan XC; Zhang D; Yang KQ; Zhang Y; Tian T; Luo F; Ma WJ; Liu YX; Wang LP; Zhang HM; Song L; Cai J; Zhou XL
Am J Hypertens; 2020 Jul; 33(7):670-675. PubMed ID: 32161960
[TBL] [Abstract][Full Text] [Related]
13. Liddle Syndrome: Review of the Literature and Description of a New Case.
Tetti M; Monticone S; Burrello J; Matarazzo P; Veglio F; Pasini B; Jeunemaitre X; Mulatero P
Int J Mol Sci; 2018 Mar; 19(3):. PubMed ID: 29534496
[TBL] [Abstract][Full Text] [Related]
14. Liddle Syndrome due to a Novel c.1713 Deletion in the Epithelial Sodium Channel β-Subunit in a Normotensive Adolescent.
Brower RK; Ghlichloo IA; Shabgahi V; Elsholz D; Menon RK; Vyas AK
AACE Clin Case Rep; 2021; 7(1):65-68. PubMed ID: 33851023
[TBL] [Abstract][Full Text] [Related]
15. A family with Liddle syndrome caused by a novel missense mutation in the PY motif of the beta-subunit of the epithelial sodium channel.
Gao L; Wang L; Liu Y; Zhou X; Hui R; Hu A
J Pediatr; 2013 Jan; 162(1):166-70. PubMed ID: 22809657
[TBL] [Abstract][Full Text] [Related]
16. Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome.
Polfus LM; Boerwinkle E; Gibbs RA; Metcalf G; Muzny D; Veeraraghavan N; Grove M; Shete S; Wallace S; Milewicz D; Hanchard N; Lupski JR; Hashmi SS; Gupta-Malhotra M
Cold Spring Harb Mol Case Stud; 2016 Nov; 2(6):a001255. PubMed ID: 27900368
[TBL] [Abstract][Full Text] [Related]
17. A novel epithelial sodium channel gamma-subunit de novo frameshift mutation leads to Liddle syndrome.
Wang Y; Zheng Y; Chen J; Wu H; Zheng D; Hui R
Clin Endocrinol (Oxf); 2007 Nov; 67(5):801-4. PubMed ID: 17634077
[TBL] [Abstract][Full Text] [Related]
18. Liddle syndrome misdiagnosed as primary aldosteronism is caused by inaccurate aldosterone-rennin detection while a novel
Yang Y; Wu C; Qu D; Xu X; Chen L; Sun Q; Zhao X
Blood Press; 2022 Dec; 31(1):139-145. PubMed ID: 35723567
[TBL] [Abstract][Full Text] [Related]
19. Reverse Phenotypes of Patients with Genetically Confirmed Liddle Syndrome.
Granhøj J; Nøhr TK; Hinrichs GR; Rasmussen M; Svenningsen P
Clin J Am Soc Nephrol; 2024 May; 19(5):610-619. PubMed ID: 38265765
[TBL] [Abstract][Full Text] [Related]
20. [Liddle syndrome as a rare cause of hypertension - a case report].
Bielawska-Niekludow J; Rybi-Szumińska A; Wasilewska A
Pol Merkur Lekarski; 2019 Nov; 47(281):190-192. PubMed ID: 31812974
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]