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Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): A consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis
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Immunoglobulin M monoclonal gammopathies of undetermined significance and indolent Waldenstrom's macroglobulinemia recognize the same determinants of evolution into symptomatic lymphoid disorders: Proposal for a common prognostic scoring system
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Prognostic validation of the international classification of immunoglobulin M gammopathies: A survival advantage for patients with immunoglobulin m monoclonal gammopathy of undetermined significance?
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Systemic AL amyloidosis due to non-Hodgkin's lymphoma: an unusual clinicopathologic association
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Outcome in systemic AL amyloidosis in relation to changes in concentration of circulating free immunoglobulin light chains following chemotherapy
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Immunoglobulin light chain variable (V) region genes influence clinical presentation and outcome in light chain-associated amyloidosis (AL)
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Clinicopathological definition of Waldenstrom's macroglobulinemia: Consensus panel recommendations from the second international workshop on Waldenstrom's macroglobulinemia
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Prognostic factors in symptomatic Waldenstrom's macroglobulinemia
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Prognostic factors and response to fludarabine therapy in Waldenstrom's macroglobulinemia: An update of a US intergroup trial (SW0G S9003)
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Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis.
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A long-term study of prognosis in monoclonal gammopathy of undetermined significance
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NEW ENGLAND JOURNAL OF MEDICINE (2002)
Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a French family
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Waldenstrom's macroglobulinemia associated with AA amyloidosis
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