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Pediatric heart transplantation from donation after circulatory death using normothermic regional perfusion and cold storage from a distant donor: First US experience.
Biniwale R, Lahar S, Balasubramanya S, Caraccio C, Ngang B, Barone H, Stimpson E, Dela Cruz K, Alejos JC, Williams R, Halnon N, Reardon L, Si MS, Shemin R, Ardehali A, Van Arsdell G. Biniwale R, et al. Among authors: si ms. JTCVS Tech. 2023 May 30;20:158-161. doi: 10.1016/j.xjtc.2023.05.010. eCollection 2023 Aug. JTCVS Tech. 2023. PMID: 37555030 Free PMC article. No abstract available.
High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects.
Zodanu GKE, Hwang JH, Mehta Z, Sisniega C, Barsegian A, Kang X, Biniwale R, Si MS, Satou GM, Halnon N, Ucla Congenital Heart Defect BioCore Faculty, Grody WW, Van Arsdell GS, Nelson SF, Touma M. Zodanu GKE, et al. Among authors: si ms. Int J Mol Sci. 2024 May 17;25(10):5469. doi: 10.3390/ijms25105469. Int J Mol Sci. 2024. PMID: 38791509 Free PMC article.
Intrahepatic Transcriptomics Differentiate Advanced Fibrosis and Clinical Outcomes in Adults With Fontan Circulation.
Bravo-Jaimes K, Wu X, Reardon LC, Lluri G, Lin JP, Moore JP, van Arsdell G, Biniwale R, Si MS, Naini BV, Venick R, Saab S, Wray CL, Ponder R, Rosenthal C, Klomhaus A, Böstrom KI, Aboulhosn JA, Kaldas FM. Bravo-Jaimes K, et al. Among authors: si ms. J Am Coll Cardiol. 2024 Feb 20;83(7):726-738. doi: 10.1016/j.jacc.2023.12.005. J Am Coll Cardiol. 2024. PMID: 38355242
Intrahepatic transcriptomics differentiate advanced fibrosis and clinical outcomes in adults with the Fontan circulation.
Bravo-Jaimes K, Wu X, Reardon LC, Lluri G, Lin JP, Moore JP, Arsdell GV, Biniwale R, Si MS, Naini BV, Venick R, Saab S, Wray CL, Ponder R, Rosenthal C, Klomhaus A, Böstrom KI, Aboulhosn JA, Kaldas FM. Bravo-Jaimes K, et al. Among authors: si ms. medRxiv [Preprint]. 2023 Jun 7:2023.06.05.23290997. doi: 10.1101/2023.06.05.23290997. medRxiv. 2023. PMID: 37333414 Free PMC article. Updated. Preprint.
Whole-Exome Sequencing Identifies Homozygote Nonsense Variants in LMOD2 Gene Causing Infantile Dilated Cardiomyopathy.
Sono R, Larrinaga TM, Huang A, Makhlouf F, Kang X, Su J, Lau R, Arboleda VA, Biniwale R, Fishbein GA, Khanlou N, Si MS, Satou GM, Halnon N, Ucla Congenital Heart Defects-BioCore Faculty, Van Arsdell GS, Gregorio CC, Nelson S, Touma M. Sono R, et al. Among authors: si ms. Cells. 2023 May 23;12(11):1455. doi: 10.3390/cells12111455. Cells. 2023. PMID: 37296576 Free PMC article.
146 results