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Self-reverting mutations partially correct the blood phenotype in a Diamond Blackfan anemia patient.
Venugopal P, Moore S, Lawrence DM, George AJ, Hannan RD, Bray SC, To LB, D'Andrea RJ, Feng J, Tirimacco A, Yeoman AL, Young CC, Fine M, Schreiber AW, Hahn CN, Barnett C, Saxon B, Scott HS. Venugopal P, et al. Among authors: young cc. Haematologica. 2017 Dec;102(12):e506-e509. doi: 10.3324/haematol.2017.166678. Epub 2017 Sep 29. Haematologica. 2017. PMID: 28971907 Free PMC article. No abstract available.
A novel germline SAMD9L mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemia.
Cheah JJC, Brown AL, Schreiber AW, Feng J, Babic M, Moore S, Young CC, Fine M, Phillips K, Guandalini M, Wilson P, Poplawski N, Hahn CN, Scott HS. Cheah JJC, et al. Among authors: young cc. Haematologica. 2019 Jul;104(7):e318-e321. doi: 10.3324/haematol.2018.207316. Epub 2019 Mar 28. Haematologica. 2019. PMID: 30923096 Free PMC article. No abstract available.
Impact of duration of dual anti-platelet therapy on risk of complications after stent-assisted coiling of unruptured aneurysms.
Ringer AJ, Hanel RA, Baig AA, Siddiqui AH, Lopes DK, Barros G, Bass DI, Levitt MR, Young CC, Naylor RM, Lanzino G, Crowley RW, Serrone JC, Kan PT, Binning MJ, Veznedaroglu E, Boulos A, Tawk R; Endovascular Neurosurgery Research Group (ENRG). Ringer AJ, et al. Among authors: young cc. J Neurointerv Surg. 2024 Aug 13:jnis-2024-021977. doi: 10.1136/jnis-2024-021977. Online ahead of print. J Neurointerv Surg. 2024. PMID: 39137967
741 results