Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

53,685 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Indicators and prediction models for the severity of Covid-19.
Huang J, Gao J, Zhu W, Feng R, Liu Q, Chen X, Huang J, Yang Z, Lin X, Zhang Z, Lin Y. Huang J, et al. Int J Clin Pract. 2021 Oct;75(10):e14571. doi: 10.1111/ijcp.14571. Epub 2021 Jul 6. Int J Clin Pract. 2021. PMID: 34170611 Free PMC article.
Case report of familial sudden cardiac death caused by a DSG2 p.F531C mutation as genetic background when carrying with heterozygous KCNE5 p.D92E/E93X mutation.
Lin Y, Huang J, He S, Feng R, Zhong Z, Liu Y, Ye W, Li X, Liao H, Fei H, Rao F, Shan Z, Deng C, Zhan X, Xue Y, Liu H, Zhang B, Wang K, Zhang Q, Wu S, Lin X. Lin Y, et al. Among authors: huang j. BMC Med Genet. 2018 Aug 21;19(1):148. doi: 10.1186/s12881-018-0580-2. BMC Med Genet. 2018. PMID: 30129429 Free PMC article.
Compound and heterozygous mutations of KCNQ1 in long QT syndrome with familial history of unexplained sudden death: Identified by analysis of whole exome sequencing and predisposing genes.
Lin Y, Zhao T, He S, Huang J, Liu Q, Yang Z, Qin J, Yu N, Lu H, Lin X. Lin Y, et al. Among authors: huang j. Ann Noninvasive Electrocardiol. 2020 Jan;25(1):e12694. doi: 10.1111/anec.12694. Epub 2019 Sep 29. Ann Noninvasive Electrocardiol. 2020. PMID: 31565860 Free PMC article.
Young and early-onset dilated cardiomyopathy with malignant ventricular arrhythmia and sudden cardiac death induced by the heterozygous LDB3, MYH6, and SYNE1 missense mutations.
Zhao T, Ma Y, Zhang Z, Xian J, Geng X, Wang F, Huang J, Yang Z, Luo Y, Lin Y. Zhao T, et al. Among authors: huang j. Ann Noninvasive Electrocardiol. 2021 Jul;26(4):e12840. doi: 10.1111/anec.12840. Epub 2021 May 5. Ann Noninvasive Electrocardiol. 2021. PMID: 33949037 Free PMC article.
Overlap phenotypes of the left ventricular noncompaction and hypertrophic cardiomyopathy with complex arrhythmias and heart failure induced by the novel truncated DSC2 mutation.
Lin Y, Huang J, Zhu Z, Zhang Z, Xian J, Yang Z, Qin T, Chen L, Huang J, Huang Y, Wu Q, Hu Z, Lin X, Xu G. Lin Y, et al. Among authors: huang j, huang y. Orphanet J Rare Dis. 2021 Nov 24;16(1):496. doi: 10.1186/s13023-021-02112-9. Orphanet J Rare Dis. 2021. PMID: 34819141 Free PMC article.
Reactivation of PPARα alleviates myocardial lipid accumulation and cardiac dysfunction by improving fatty acid β-oxidation in Dsg2-deficient arrhythmogenic cardiomyopathy.
Lin Y, Liu R, Huang Y, Yang Z, Xian J, Huang J, Qiu Z, Lin X, Zhang M, Chen H, Wang H, Huang J, Xu G. Lin Y, et al. Among authors: huang j, huang y. Acta Pharm Sin B. 2023 Jan;13(1):192-203. doi: 10.1016/j.apsb.2022.05.018. Epub 2022 May 21. Acta Pharm Sin B. 2023. PMID: 36815030 Free PMC article.
53,685 results
You have reached the last available page of results. Please see the User Guide for more information.