Amyloidosis is a rare disorder that is characterized by the variable accumulation of an extracellular eosinophilic proteinaceous substanceamyloidin nearly all the tissues of the body. Amyloid (from the Greek amylon, starch, and eidos, resemblance) is a complex protein mixture dominated by a fibrillar component that can be identified by electron microscopy
Primary systemic amyloidosis is an immunoglo-bulin light chain disorder that is 1/5th as com-mon as ...
Primary Systemic Amyloidosis (AL) is the most frequent form of systemic amyloidosis and its morbilil...
SYNOPSIS Among 8,758 necropsies there are 93 cases of systemic amyloidosis. Of these, 14 are associa...
The clinical and pathological features of amyloidosis are examined in the light of a classification ...
Amyloidosis is a morphological concept (2) the diagnosis of which has been based on histo-logical cr...
Multiple myeloma and its variants, Waldenstrom's macroglobulinemia, the heavy chain diseases (HCDs),...
Primary amyloidosis is a plasma cell dyscrasia characterised by excess production of abnormal immuno...
Amyloidosis is a heterogeneous group of disorders charac-terized by extracellular deposition of uniq...
Amyloidosis is a protein misfolding disorder in which soluble proteins aggregate as insoluble amyloi...
A conception of amyloidosis as merely a compli-cation of chronic syphilitic, tuberculous or septic d...
Primary systemic amyloidosis is a rare disease. We report three cases of primary systemic amyloidosi...
ONLY in recent years has there been some unanimity of opinion in regard to the classification of amy...
Amyloidosis is a heterogeneous group of disorders associated with pathological deposition of amyloid...
Amyloidosis AL is a disease which is caused by abnormal production of protein and accumulation at bo...
Amyloidosis is a benign, slowly progressive condition characterized by the presence of extracellular...
Primary systemic amyloidosis is an immunoglo-bulin light chain disorder that is 1/5th as com-mon as ...
Primary Systemic Amyloidosis (AL) is the most frequent form of systemic amyloidosis and its morbilil...
SYNOPSIS Among 8,758 necropsies there are 93 cases of systemic amyloidosis. Of these, 14 are associa...
The clinical and pathological features of amyloidosis are examined in the light of a classification ...
Amyloidosis is a morphological concept (2) the diagnosis of which has been based on histo-logical cr...
Multiple myeloma and its variants, Waldenstrom's macroglobulinemia, the heavy chain diseases (HCDs),...
Primary amyloidosis is a plasma cell dyscrasia characterised by excess production of abnormal immuno...
Amyloidosis is a heterogeneous group of disorders charac-terized by extracellular deposition of uniq...
Amyloidosis is a protein misfolding disorder in which soluble proteins aggregate as insoluble amyloi...
A conception of amyloidosis as merely a compli-cation of chronic syphilitic, tuberculous or septic d...
Primary systemic amyloidosis is a rare disease. We report three cases of primary systemic amyloidosi...
ONLY in recent years has there been some unanimity of opinion in regard to the classification of amy...
Amyloidosis is a heterogeneous group of disorders associated with pathological deposition of amyloid...
Amyloidosis AL is a disease which is caused by abnormal production of protein and accumulation at bo...
Amyloidosis is a benign, slowly progressive condition characterized by the presence of extracellular...
Primary systemic amyloidosis is an immunoglo-bulin light chain disorder that is 1/5th as com-mon as ...
Primary Systemic Amyloidosis (AL) is the most frequent form of systemic amyloidosis and its morbilil...
SYNOPSIS Among 8,758 necropsies there are 93 cases of systemic amyloidosis. Of these, 14 are associa...