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Novel regulatory variant in ABO intronic RUNX1 binding site inducing A3 phenotype.
Thun GA, Gueuning M, Sigurdardottir S, Meyer E, Gourri E, Schneider L, Merki Y, Trost N, Neuenschwander K, Engström C, Frey BM, Meyer S, Mattle-Greminger MP. Thun GA, et al. Among authors: meyer s, meyer e. Vox Sang. 2024 Apr;119(4):377-382. doi: 10.1111/vox.13580. Epub 2024 Jan 16. Vox Sang. 2024. PMID: 38226545
Plasma and platelet lipidome changes in Fabry disease.
Burla B, Oh J, Nowak A, Piraud N, Meyer E, Mei D, Bendt AK, Studt JD, Frey BM, Torta F, Wenk MR, Krayenbuehl PA. Burla B, et al. Among authors: meyer e. Clin Chim Acta. 2024 Aug 15;562:119833. doi: 10.1016/j.cca.2024.119833. Epub 2024 Jun 30. Clin Chim Acta. 2024. PMID: 38955246 Free article.
The protean presentations of XK disease (McLeod syndrome): a case series with new observations and updates on previously reported families.
Walker RH, Barreto M, Bateman JR, Bustamante ML, Chiu G, Feitell S, Frey BM, Guerra P, Guerrero S, Jung HH, Maldonado F, Meyer E, Miranda M, McFarland E, Oates P, Ochoa G, Olsson K, Paucar M, Proschle JA, Sammler EM, Troncoso M, Wu-Wallace R, Young L, Vege S, Westhoff CM, Danek A. Walker RH, et al. Among authors: meyer e. Front Neurosci. 2024 Sep 9;18:1408105. doi: 10.3389/fnins.2024.1408105. eCollection 2024. Front Neurosci. 2024. PMID: 39315078 Free PMC article.
Donor Regulatory T-Cell Therapy to Prevent Graft-Versus-Host Disease.
Meyer E, Pavlova A, Villar-Prados A, Bader CS, Xie B, Muffly L, Kim P, Sutherland KC, Bharadwaj S, Dahiya S, Frank MJ, Arai S, Johnston L, Miklos DB, Rezvani AR, Shiraz P, Sidana S, Shizuru JA, Weng WK, Agrawal V, Putnam A, Fernhoff NB, Tamaresis J, Lu Y, Pawar RD, McClellan JS, Lowsky R, Negrin RS. Meyer E, et al. Blood. 2025 Jan 10:blood.2024026446. doi: 10.1182/blood.2024026446. Online ahead of print. Blood. 2025. PMID: 39792934
2,630 results