Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

33 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Molecular pathogenesis of Marfan syndrome.
Ramachandra CJ, Mehta A, Guo KW, Wong P, Tan JL, Shim W. Ramachandra CJ, et al. Int J Cardiol. 2015;187:585-91. doi: 10.1016/j.ijcard.2015.03.423. Epub 2015 Mar 31. Int J Cardiol. 2015. PMID: 25863307 Review.
The KCNH2-IVS9-28A/G mutation causes aberrant isoform expression and hERG trafficking defect in cardiomyocytes derived from patients affected by Long QT Syndrome type 2.
Mura M, Mehta A, Ramachandra CJ, Zappatore R, Pisano F, Ciuffreda MC, Barbaccia V, Crotti L, Schwartz PJ, Shim W, Gnecchi M. Mura M, et al. Among authors: ramachandra cj. Int J Cardiol. 2017 Aug 1;240:367-371. doi: 10.1016/j.ijcard.2017.04.038. Epub 2017 Apr 12. Int J Cardiol. 2017. PMID: 28433559
33 results