Alexia Rinsant
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View article: #173 Description of a familial renal ApoCII amyloidosis associated with a p.Lys41Thr mutation
#173 Description of a familial renal ApoCII amyloidosis associated with a p.Lys41Thr mutation Open
Background and Aims Nasr et al. recently published the first series of 25 patients with hereditary renal apolipoprotein C-II amyloidosis (AApoCII). Twelve of them carried a APOC2(NM_000483.5):c.122A>C/p.(Lys41Thr) variant but only 3 had…
View article: A mouse model of cardiac immunoglobulin light chain amyloidosis reveals insights into tissue accumulation and toxicity of amyloid fibrils
A mouse model of cardiac immunoglobulin light chain amyloidosis reveals insights into tissue accumulation and toxicity of amyloid fibrils Open
View article: A mouse model of cardiac AL amyloidosis unveils mechanisms of tissue accumulation and toxicity of amyloid fibrils
A mouse model of cardiac AL amyloidosis unveils mechanisms of tissue accumulation and toxicity of amyloid fibrils Open
AL amyloidosis is one of the most common types of systemic amyloidosis, caused by the deposition in tissues of fibrillar aggregates of abnormal immunoglobulin (Ig) light chain (LC), leading to organ dysfunction. The most frequent and sever…
View article: Randall-Type Monoclonal IgE Kappa Light-Heavy Chain Deposition Disease
Randall-Type Monoclonal IgE Kappa Light-Heavy Chain Deposition Disease Open
View article: Acquired cutis laxa from heavy chain deposition disease
Acquired cutis laxa from heavy chain deposition disease Open
View article: Immunoglobulin light chain toxicity in a mouse model of monoclonal immunoglobulin light-chain deposition disease
Immunoglobulin light chain toxicity in a mouse model of monoclonal immunoglobulin light-chain deposition disease Open
Light chain deposition disease (LCDD) is a rare disorder characterized by glomerular and peritubular amorphous deposits of a monoclonal immunoglobulin (Ig) light chain (LC), leading to nodular glomerulosclerosis and nephrotic syndrome. We …
View article: Glomerulosclerosis and kidney failure in a mouse model of monoclonal immunoglobulin light-chain deposition disease
Glomerulosclerosis and kidney failure in a mouse model of monoclonal immunoglobulin light-chain deposition disease Open
Light chain deposition disease (LCDD) is a rare disorder characterized by glomerular and peritubular amorphous deposits of a monoclonal immunoglobulin (Ig) light chain (LC), leading to nodular glomerulosclerosis and nephrotic syndrome. We …
View article: DNAJB9 Is a Specific Immunohistochemical Marker for Fibrillary Glomerulonephritis
DNAJB9 Is a Specific Immunohistochemical Marker for Fibrillary Glomerulonephritis Open