This review charts the progress of anti‐glycolipid antibodies in neuropathy, from their
original discovery 20 years ago in immunoglobulin M paraproteinaemic neuropathy through …

PURPOSE: To review the clinical features, complications, and treatment of Waldenström's
macroglobulinemia, a low-grade lymphoproliferative disorder that produces monoclonal …

The clinical and laboratory phenotype of a paraproteinaemic neuropathy syndrome termed
chronic sensory ataxic neuropathy with anti-disialosyl IgM antibodies is described in a series …

Approximately 10% of patients with peripheral neuropathy of otherwise unknown etiology
have an associated monoclonal gammopathy. Both the neuropathies and the monoclonal …

This multicentre randomised double blind crossover trial tested the short term efficacy of
intravenous immunoglobulin (IVIg) 2.0 g/kg given over 24 or 48 hours in patients with …

Using an enzyme-linked immunosorbent assay and a thin-layer chromatography-
immunostaining procedure, we detected serum antibodies against acidic glycolipids in 36 of …

Increased titers of antibodies to GM1 ganglioside in humans are associated with lower motor
neuron disease and predominantly motor neuropathy with or without conduction block. To …

High titers of IgM anti‐GM1 antibodies are commonly found in the serum of patients with
some lower motor neuron disorders and peripheral neuropathies. Enzyme‐linked …

Monoclonal gammopathies are disorders characterized by the proliferation of a single clone
of plasma cells producing a homogeneous monoclonal protein (M-protein, M-component …

High titers of serum antibodies to neural antigens occur in several forms of neuropathy.
These include neuropathies associated with monoclonal gammopathy, inflammatory …