Fan P - Search Results

1

Identification of a novel frameshift mutation in the SCNN1B causing Liddle syndrome.

Qu Y, Lu Y, Zhang D, Liu X, Fan P, Chen J, Zhang H, Yang K, Tian T, Zhou Y, Zhang Q, Zhang Y, Wang L, Huang Z, Liu Y, Hu A, Zhou X. Qu Y, et al. Among authors: fan p. Sci Bull (Beijing). 2023 Feb 26;68(4):383-387. doi: 10.1016/j.scib.2023.02.006. Epub 2023 Feb 7. Sci Bull (Beijing). 2023. PMID: 36774301 No abstract available.

2

Recent advancements in the molecular genetics of left ventricular noncompaction cardiomyopathy.

Dong X, Fan P, Tian T, Yang Y, Xiao Y, Yang K, Liu Y, Zhou X. Dong X, et al. Among authors: fan p. Clin Chim Acta. 2017 Feb;465:40-44. doi: 10.1016/j.cca.2016.12.013. Epub 2016 Dec 15. Clin Chim Acta. 2017. PMID: 27989498 Review.

3

Outcomes of percutaneous coronary intervention and coronary artery bypass grafting in patients with Takayasu arteritis.

Yang Y, Tian T, Yang K, Zhang Y, Meng X, Fan P, Feng L, Mu C, Gao L, Zhou X. Yang Y, et al. Among authors: fan p. Int J Cardiol. 2017 Aug 15;241:64-69. doi: 10.1016/j.ijcard.2017.02.041. Epub 2017 Feb 13. Int J Cardiol. 2017. PMID: 28237733

4

Left Ventricular Non-Compaction: A Cardiomyopathy With Acceptable Prognosis in Children.

Tian T, Yang Y, Zhou L, Luo F, Li Y, Fan P, Dong X, Liu Y, Cui J, Zhou X. Tian T, et al. Among authors: fan p. Heart Lung Circ. 2018 Jan;27(1):28-32. doi: 10.1016/j.hlc.2017.01.013. Epub 2017 Mar 1. Heart Lung Circ. 2018. PMID: 28343948

5

Clinical characteristics and outcomes of left ventricular pseudoaneurysm: A retrospective study in a single-center of China.

Meng X, Yang YK, Yang KQ, Zhang Y, Lu PP, Fan P, Ma LH, Zhou XL. Meng X, et al. Among authors: fan p. Medicine (Baltimore). 2017 May;96(18):e6793. doi: 10.1097/MD.0000000000006793. Medicine (Baltimore). 2017. PMID: 28471977 Free PMC article.

6

A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation.

Yang KQ, Lu CX, Zhang Y, Yang YK, Li JC, Lan T, Meng X, Fan P, Tian T, Wang LP, Liu YX, Zhang X, Zhou XL. Yang KQ, et al. Among authors: fan p. Sci Rep. 2017 May 25;7(1):2407. doi: 10.1038/s41598-017-02455-z. Sci Rep. 2017. PMID: 28546535 Free PMC article.

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. Yang KQ, et al. Among authors: fan p. Clin Exp Hypertens. 2018;40(2):107-111. doi: 10.1080/10641963.2017.1334799. Epub 2017 Jul 18. Clin Exp Hypertens. 2018. PMID: 28718682 Review.

8

Aortic Aneurysm in Takayasu Arteritis.

Yang KQ, Meng X, Zhang Y, Fan P, Wang LP, Zhang HM, Wu HY, Jiang XJ, Cai J, Zhou XL, Hui RT, Zheng DY, Liu LS. Yang KQ, et al. Among authors: fan p. Am J Med Sci. 2017 Dec;354(6):539-547. doi: 10.1016/j.amjms.2017.08.018. Epub 2017 Sep 1. Am J Med Sci. 2017. PMID: 29208249

9

Cardiac Valve Involvement in Takayasu Arteritis Is Common: A Retrospective Study of 1,069 Patients Over 25 Years.

Zhang Y, Yang K, Meng X, Tian T, Fan P, Zhang H, Ma W, Song L, Wu H, Cai J, Luo F, Zhou X, Zheng D, Liu L. Zhang Y, et al. Among authors: fan p. Am J Med Sci. 2018 Oct;356(4):357-364. doi: 10.1016/j.amjms.2018.06.021. Epub 2018 Jun 30. Am J Med Sci. 2018. PMID: 30360804

10

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. Fan P, et al. Endocr Connect. 2018 Dec;7(12):1528-1534. doi: 10.1530/EC-18-0484. Endocr Connect. 2018. PMID: 30496127 Free PMC article.

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