Clinical characteristics and prognosis of a Chinese cohort with systemic light chain amyloidosis: a single-center study
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
https://link.springer.com/content/pdf/10.1007/s12185-023-03617-8.pdf
Reference43 articles.
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2. McCausland KL, White MK, Guthrie SD, et al. Light Chain (AL) amyloidosis: The journey to diagnosis. Patient. 2018;11(2):207–16.
3. Lousada I, Comenzo RL, Landau H, et al. Light chain amyloidosis: patient experience survey from the amyloidosis research consortium. Adv Ther. 2015;32(10):920–8.
4. Hester LL, Gifkins DM, et al. Diagnostic delay and characterization of the clinical prodrome in AL amyloidosis among 1523 US adults diagnosed between 2001 and 2019. Eur J Haematol. 2021;107(4):428–35.
5. Kyle RA, Greipp PR. Amyloidosis (AL). Clinical and laboratory features in 229 cases. Mayo Clin Proc. 1983;58(10):665–83.
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