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Mouse Model of Human Congenital Heart Disease: Progressive Atrioventricular Block Induced by a Heterozygous Nkx2-5 Homeodomain Missense Mutation.
Chowdhury R, Ashraf H, Melanson M, Tanada Y, Nguyen M, Silberbach M, Wakimoto H, Benson DW, Anderson RH, Kasahara H. Chowdhury R, et al. Among authors: ashraf h. Circ Arrhythm Electrophysiol. 2015 Oct;8(5):1255-64. doi: 10.1161/CIRCEP.115.002720. Epub 2015 Jul 30. Circ Arrhythm Electrophysiol. 2015. PMID: 26226998 Free PMC article.
Compound loss of muscleblind-like function in myotonic dystrophy.
Lee KY, Li M, Manchanda M, Batra R, Charizanis K, Mohan A, Warren SA, Chamberlain CM, Finn D, Hong H, Ashraf H, Kasahara H, Ranum LP, Swanson MS. Lee KY, et al. Among authors: ashraf h. EMBO Mol Med. 2013 Dec;5(12):1887-900. doi: 10.1002/emmm.201303275. Epub 2013 Oct 8. EMBO Mol Med. 2013. PMID: 24293317 Free PMC article.
A mouse model of human congenital heart disease: high incidence of diverse cardiac anomalies and ventricular noncompaction produced by heterozygous Nkx2-5 homeodomain missense mutation.
Ashraf H, Pradhan L, Chang EI, Terada R, Ryan NJ, Briggs LE, Chowdhury R, Zárate MA, Sugi Y, Nam HJ, Benson DW, Anderson RH, Kasahara H. Ashraf H, et al. Circ Cardiovasc Genet. 2014 Aug;7(4):423-433. doi: 10.1161/CIRCGENETICS.113.000281. Epub 2014 Jul 15. Circ Cardiovasc Genet. 2014. PMID: 25028484 Free PMC article.
Cardiac Amyloid for the Internist.
Ashraf H, Hafeez A, Vilaro J. Ashraf H, et al. Cureus. 2021 Jan 26;13(1):e12915. doi: 10.7759/cureus.12915. Cureus. 2021. PMID: 33654598 Free PMC article.
A 68-Year-Old Man With Shock and Hypoxia.
Latner JP, Ashraf H, Kalra SS, Patel D. Latner JP, et al. Among authors: ashraf h. Chest. 2022 Feb;161(2):e117-e119. doi: 10.1016/j.chest.2021.04.078. Chest. 2022. PMID: 35131064 No abstract available.
685 results