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Updated: Aug 23, 2026

Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
Published on: June 9, 2018
Therapeutic options in systemic AL amyloidosis
I I van Gameren1, H Lokhorst, B P C Hazenberg
1Department of Rheumatology, University Hospital Groningen, The Netherlands. iivangameren@xs4all.nl
Abstract:
Systemic amyloid light chain (AL) amyloidosis is a severe disease with unfavourable prognosis. Since the late 1970s different therapeutic modalities in AL amyloidosis have been investigated, trying to prolong survival. This review deals with the therapeutic modalities in AL amyloidosis to date, and highlights future perspectives.
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