Primary systemic amyloidosis is an immunoglo-bulin light chain disorder that is 1/5th as com-mon as multiple myeloma. Amyloidosis is regularly seen in the practice of a hematologist and has recently undergone major advances in terms of the ability to evaluate responses as well as new therapeutic options that were not avail-able when this topic was covered as an educa-tion session at the American Society of Hematol-ogy meeting 5 years ago. Waldenström macroglo-bulinemia (WM) is rarer than amyloidosis (1500 per year WM versus 3000 per year amyloid in the US), and recent consensus panels have estab-lished the definition of the disease, the diagnos-tic criteria, criteria for initiation of therapy and
Primary amyloidosis is a plasma cell dyscrasia characterised by excess production of abnormal immuno...
International audienceSystemic AL amyloidosis is a rare complication of monoclonal gammopathies. Ren...
International audienceImmunoglobulin M (IgM)-related amyloidosis remains a rare and little-known com...
Consensus Panel 6 (CP6) of the 11th International Workshop on Waldenström's Macroglobulinemia (...
Amyloidosis associated with immunoglobulin M clones is a distinct clinical entity that poses specifi...
Waldenström’s macroglobulinaemia is a B-cell disorder characterised by bone marrow infiltration with...
Systemic amyloidosis is a heterogeneous group of diseases associated with protein misfolding into in...
The diagnosis of Waldenström macroglobulinaemia (WM) can be challenging given the variety of signs a...
Systemic amyloidosis is a heterogeneous group of diseases associated with protein misfolding into in...
Amyloidosis is a group of diseases characterized by an irreversible and extracellular deposition of ...
: The treatment of patients with systemic light chain (AL) amyloidosis is a challenge to hematologis...
Immunoglobulin M (IgM)-related amyloidosis remains a rare and little-known complication of monoclona...
BACKGROUND: Amyloidosis has been a mystery for centuries, but research of the last decennia has clar...
Systemic light-chain amyloidosis (AL) is caused by misfolded immunoglobulin light-chain proteins tha...
How we treat Waldenström’s macroglobulinemia Waldenström’s macroglobuline-mia (WM) is a distinct cli...
Primary amyloidosis is a plasma cell dyscrasia characterised by excess production of abnormal immuno...
International audienceSystemic AL amyloidosis is a rare complication of monoclonal gammopathies. Ren...
International audienceImmunoglobulin M (IgM)-related amyloidosis remains a rare and little-known com...
Consensus Panel 6 (CP6) of the 11th International Workshop on Waldenström's Macroglobulinemia (...
Amyloidosis associated with immunoglobulin M clones is a distinct clinical entity that poses specifi...
Waldenström’s macroglobulinaemia is a B-cell disorder characterised by bone marrow infiltration with...
Systemic amyloidosis is a heterogeneous group of diseases associated with protein misfolding into in...
The diagnosis of Waldenström macroglobulinaemia (WM) can be challenging given the variety of signs a...
Systemic amyloidosis is a heterogeneous group of diseases associated with protein misfolding into in...
Amyloidosis is a group of diseases characterized by an irreversible and extracellular deposition of ...
: The treatment of patients with systemic light chain (AL) amyloidosis is a challenge to hematologis...
Immunoglobulin M (IgM)-related amyloidosis remains a rare and little-known complication of monoclona...
BACKGROUND: Amyloidosis has been a mystery for centuries, but research of the last decennia has clar...
Systemic light-chain amyloidosis (AL) is caused by misfolded immunoglobulin light-chain proteins tha...
How we treat Waldenström’s macroglobulinemia Waldenström’s macroglobuline-mia (WM) is a distinct cli...
Primary amyloidosis is a plasma cell dyscrasia characterised by excess production of abnormal immuno...
International audienceSystemic AL amyloidosis is a rare complication of monoclonal gammopathies. Ren...
International audienceImmunoglobulin M (IgM)-related amyloidosis remains a rare and little-known com...