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• W2793837538 abstract "Summary Background. — Immunoglobulinic (AL) amyloidosis is a complication of plasma cell dyscrasia, characterized by widespread deposition of amyloid fibrils derived from monoclonal light chains. Cardiac amyloid is the main prognostic factor, with a median survival of six months. Cardiac transplantation in AL amyloidosis is associated with high mortality, due to disease recurrence in the allograft and systemic progression. Suppression of light chain (LC) production" @default.
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• W2793837538 date "2008-01-01" @default.
• W2793837538 modified "2023-10-17" @default.
• W2793837538 title "Heart transplantation in systemic (AL) amyloidosis: A retrospective study of eight French patients Transplantation cardiaque et amylose AL en France : étude rétrospective de huit observations" @default.
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