201 related articles for article (PubMed ID: 36473093)
1. A case report of a young boy with low renin and high aldosterone levels induced by Liddle syndrome who was previously misdiagnosed with primary aldosteronism.
Jin Y; Qiu W; Yao J
J Pediatr Endocrinol Metab; 2023 Feb; 36(2):212-215. PubMed ID: 36473093
[TBL] [Abstract][Full Text] [Related]
2. Liddle syndrome presenting with normal aldosterone levels: A case report.
Wang R; Zhang Y; Pan R; Zhang R; Zhao Y
Medicine (Baltimore); 2023 Nov; 102(47):e35944. PubMed ID: 38013303
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Liddle syndrome: A case report.
Jin Y; Qiu W; Yao J
Med Clin (Barc); 2021 Jun; ():. PubMed ID: 34147249
[TBL] [Abstract][Full Text] [Related]
5. The importance of genetic counseling and genetic screening: a case report of a 16-year-old boy with resistant hypertension and severe hypokalemia.
Kuang ZM; Wang Y; Wang JJ; Liu JH; Zeng R; Zhou Q; Yu ZQ; Jiang L
J Am Soc Hypertens; 2017 Mar; 11(3):136-139. PubMed ID: 28236585
[TBL] [Abstract][Full Text] [Related]
6. 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]
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. Resistant Hypertension: A Clinical Perspective.
Hannah-Shmouni F; Gubbi S; Spence JD; Stratakis CA; Koch CA
Endocrinol Metab Clin North Am; 2019 Dec; 48(4):811-828. PubMed ID: 31655778
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Liddle syndrome: clinical and genetic profiles.
Cui Y; Tong A; Jiang J; Wang F; Li C
J Clin Hypertens (Greenwich); 2017 May; 19(5):524-529. PubMed ID: 27896928
[TBL] [Abstract][Full Text] [Related]
11. Low-Renin Hypertension.
Athimulam S; Lazik N; Bancos I
Endocrinol Metab Clin North Am; 2019 Dec; 48(4):701-715. PubMed ID: 31655771
[TBL] [Abstract][Full Text] [Related]
12. Prevalence of Liddle Syndrome Among Young Hypertension Patients of Undetermined Cause in a Chinese Population.
Wang LP; Yang KQ; Jiang XJ; Wu HY; Zhang HM; Zou YB; Song L; Bian J; Hui RT; Liu YX; Zhou XL
J Clin Hypertens (Greenwich); 2015 Nov; 17(11):902-7. PubMed ID: 26075967
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Normokalemic hyperaldosteronism in patients with resistant hypertension.
Benchetrit S; Bernheim J; Podjarny E
Isr Med Assoc J; 2002 Jan; 4(1):17-20. PubMed ID: 11802302
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. [Diagnosis and treatment outcome in primary aldosteronism based on a retrospective analysis of 187 cases].
Szücs N; Gláz E; Varga I; Tóth M; Kiss R; Patócs A; Jakab C; Perner F; Járay J; Horányi J; Dabasi G; Molnár F; Major L; Füto L; Rácz K; Tulassay Z
Orv Hetil; 2006 Jan; 147(2):51-9. PubMed ID: 16509213
[TBL] [Abstract][Full Text] [Related]
19. [Liddle syndrome (or pseudo-hyperaldosteronism). Long-term development and erythrocyte potassium flow study in 4 cases].
Noblins M; Kleinknecht D; Dommergues JP; Nazaret C; Garay RP; Jullien M; Guillot M; Fries D; Charpentier B
Arch Fr Pediatr; 1992 Oct; 49(8):685-91. PubMed ID: 1288451
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
