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The management of light chain (AL) amyloidosis in Europe: clinical characteristics, treatment patterns, and efficacy outcomes between 2004 and 2018.
Palladini G, Schönland S, Merlini G, Milani P, Jaccard A, Bridoux F, Dimopoulos MA, Ravichandran S, Hegenbart U, Roeloffzen W, Cibeira MT, Agis H, Minnema MC, Bergantim R, Hájek R, João C, Leonidakis A, Cheliotis G, Sonneveld P, Kastritis E, Wechalekar A. Palladini G, et al. Among authors: wechalekar a. Blood Cancer J. 2023 Jan 25;13(1):19. doi: 10.1038/s41408-023-00789-8. Blood Cancer J. 2023. PMID: 36697388 Free PMC article.
Perspectives in treatment of AL amyloidosis.
Wechalekar AD, Hawkins PN, Gillmore JD. Wechalekar AD, et al. Br J Haematol. 2008 Feb;140(4):365-77. doi: 10.1111/j.1365-2141.2007.06936.x. Epub 2007 Dec 19. Br J Haematol. 2008. PMID: 18162121 Free article. Review.
Solid organ transplantation in AL amyloidosis.
Sattianayagam PT, Gibbs SD, Pinney JH, Wechalekar AD, Lachmann HJ, Whelan CJ, Gilbertson JA, Hawkins PN, Gillmore JD. Sattianayagam PT, et al. Among authors: wechalekar ad. Am J Transplant. 2010 Sep;10(9):2124-31. doi: 10.1111/j.1600-6143.2010.03227.x. Am J Transplant. 2010. PMID: 20883547 Free article.
ASCT for AL: all's well that ends well.
Wechalekar AD. Wechalekar AD. Blood. 2011 Oct 20;118(16):4298-9. doi: 10.1182/blood-2011-08-375105. Blood. 2011. PMID: 22021449 Free article. No abstract available.
270 results