177 related articles for article (PubMed ID: 32161960)
1. 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]
2. 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]
3. 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]
4. 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]
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. 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]
7. 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]
8. 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]
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. 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]
11. 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]
12. 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]
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. 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]
15. 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]
16. Analysis of the genes involved in Mendelian forms of low-renin hypertension in Chinese early-onset hypertensive patients.
Liu K; Qin F; Sun X; Zhang Y; Wang J; Wu Y; Ma W; Wang W; Wu X; Qin Y; Zhang H; Zhou X; Wu H; Hui R; Zou Y; Jiang X; Song L
J Hypertens; 2018 Mar; 36(3):502-509. PubMed ID: 28915228
[TBL] [Abstract][Full Text] [Related]
17. Phenotype-genotype analysis in two Chinese families with Liddle syndrome.
Gong L; Chen J; Shao L; Song W; Hui R; Wang Y
Mol Biol Rep; 2014 Mar; 41(3):1569-75. PubMed ID: 24474657
[TBL] [Abstract][Full Text] [Related]
18. Clinical and genetic characteristics of the patients with hypertension and hypokalemia carrying a novel
Chen M; Lv X; Li J; Guo M; Ma S
Scand J Clin Lab Invest; 2022; 82(7-8):576-580. PubMed ID: 36336351
[TBL] [Abstract][Full Text] [Related]
19. [Liddle's syndrome caused by a novel mutation of the gamma-subunit of epithelial sodium channel gene SCNN1G in Chinese].
Shi JY; Chen X; Ren Y; Long Y; Tian HM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):132-5. PubMed ID: 20376790
[TBL] [Abstract][Full Text] [Related]
20. A Rare Case of Familiar Hypertension Presenting with Hypertensive Encephalopathy in an Elderly Patient: A Diagnostic Dilemma: A Presentation of Liddle's Syndrome due to Novel Mutation in SCNN1G Gene.
Suman S; Sudhir M; Nitin S; Vikas M; Simran K; Preet SM
Saudi J Kidney Dis Transpl; 2021; 32(4):1163-1165. PubMed ID: 35229818
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
