Fan Y - Search Results

1

Concomitant presentation of Anderson-Tawil syndrome and myasthenia gravis in an adult patient: A case report.

Fan R, Ji R, Zou W, Wang G, Wang H, Penney DJ, Luo JJ, Fan Y. Fan R, et al. Among authors: fan y. Exp Ther Med. 2016 Oct;12(4):2435-2438. doi: 10.3892/etm.2016.3673. Epub 2016 Sep 6. Exp Ther Med. 2016. PMID: 27698745 Free PMC article.

2

Mutations in NEXN, a Z-disc gene, are associated with hypertrophic cardiomyopathy.

Wang H, Li Z, Wang J, Sun K, Cui Q, Song L, Zou Y, Wang X, Liu X, Hui R, Fan Y. Wang H, et al. Among authors: fan y. Am J Hum Genet. 2010 Nov 12;87(5):687-93. doi: 10.1016/j.ajhg.2010.10.002. Epub 2010 Oct 21. Am J Hum Genet. 2010. PMID: 20970104 Free PMC article.

3

A Novel Exonic Splicing Mutation in the TAZ (G4.5) Gene in a Case with Atypical Barth Syndrome.

Fan Y, Steller J, Gonzalez IL, Kulik W, Fox M, Chang R, Westerfield BA, Batra AS, Wang RY, Gallant NM, Pena LS, Wang H, Huang T, Bhuta S, Penny DJ, McCabe ER, Kimonis VE. Fan Y, et al. JIMD Rep. 2013;11:99-106. doi: 10.1007/8904_2013_228. Epub 2013 Apr 19. JIMD Rep. 2013. PMID: 23606313 Free PMC article.

4

Functional changes in pulmonary arterial endothelial cells associated with BMPR2 mutations.

Wang H, Ji R, Meng J, Cui Q, Zou W, Li L, Wang G, Sun L, Li Z, Huo L, Fan Y, Penny DJ. Wang H, et al. Among authors: fan y. PLoS One. 2014 Sep 4;9(9):e106703. doi: 10.1371/journal.pone.0106703. eCollection 2014. PLoS One. 2014. PMID: 25187962 Free PMC article.

5

Early onset severe pulmonary arterial hypertension with 'two-hit' digenic mutations in both BMPR2 and KCNA5 genes.

Wang G, Knight L, Ji R, Lawrence P, Kanaan U, Li L, Das A, Cui B, Zou W, Penny DJ, Fan Y. Wang G, et al. Among authors: fan y. Int J Cardiol. 2014 Dec 20;177(3):e167-9. doi: 10.1016/j.ijcard.2014.08.124. Epub 2014 Aug 28. Int J Cardiol. 2014. PMID: 25189502 No abstract available.

6

Novel homozygous BMP9 nonsense mutation causes pulmonary arterial hypertension: a case report.

Wang G, Fan R, Ji R, Zou W, Penny DJ, Varghese NP, Fan Y. Wang G, et al. Among authors: fan y, fan r. BMC Pulm Med. 2016 Jan 22;16:17. doi: 10.1186/s12890-016-0183-7. BMC Pulm Med. 2016. PMID: 26801773 Free PMC article.

7

Variant R94C in TNNT2-Encoded Troponin T Predisposes to Pediatric Restrictive Cardiomyopathy and Sudden Death Through Impaired Thin Filament Relaxation Resulting in Myocardial Diastolic Dysfunction.

Ezekian JE, Clippinger SR, Garcia JM, Yang Q, Denfield S, Jeewa A, Dreyer WJ, Zou W, Fan Y, Allen HD, Kim JJ, Greenberg MJ, Landstrom AP. Ezekian JE, et al. Among authors: fan y. J Am Heart Assoc. 2020 Mar 3;9(5):e015111. doi: 10.1161/JAHA.119.015111. Epub 2020 Feb 26. J Am Heart Assoc. 2020. PMID: 32098556 Free PMC article.

8

Hereditary pulmonary arterial hypertension burden in pediatrics: A single referral center experience.

Ishizuka M, Zou W, Whalen E, Ely E, Coleman RD, Lopez-Terrada DH, Penny DJ, Fan Y, Varghese NP. Ishizuka M, et al. Among authors: fan y. Front Pediatr. 2023 Mar 29;11:1050706. doi: 10.3389/fped.2023.1050706. eCollection 2023. Front Pediatr. 2023. PMID: 37063688 Free PMC article.

9

Genetic testing of the FBN1 gene in Chinese patients with Marfan/Marfan-like syndrome.

Yang H, Luo M, Chen Q, Fu Y, Zhang J, Qian X, Sun X, Fan Y, Zhou Z, Chang Q. Yang H, et al. Among authors: fan y. Clin Chim Acta. 2016 Aug 1;459:30-35. doi: 10.1016/j.cca.2016.05.021. Epub 2016 May 24. Clin Chim Acta. 2016. PMID: 27234404

10

Genetic testing of 10 patients with features of Loeys-Dietz syndrome.

Luo M, Yang H, Yin K, Chen Q, Zhang J, Fan Y, Zhou Z, Chang Q. Luo M, et al. Among authors: fan y. Clin Chim Acta. 2016 May 1;456:144-148. doi: 10.1016/j.cca.2016.02.005. Epub 2016 Feb 11. Clin Chim Acta. 2016. PMID: 26877057

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