1 anti-GD1b ganglioside antibody in autoimmune ataxic neuropathies.

2 ole of human anti-GD1b antibodies in sensory ataxic neuropathies.

3 clonal antibodies from patients with chronic ataxic neuropathies and Miller Fisher syndrome were stud

4                                   Autoimmune ataxic neuropathies are a subset of the sensory ataxic n

5 oglobulin G (IgG) antibodies, and in chronic ataxic neuropathies associated with persistently elevate

6 Huttenlocher syndrome to adult-onset sensory ataxic neuropathy dysarthria and ophthalmoparesis.

7         The major known causes of autoimmune ataxic neuropathies include sensory variants of the Guil

8    The major site of pathology in autoimmune ataxic neuropathies is the dorsal root ganglion, but dor

9 reviously under the acronym CANOMAD: chronic ataxic neuropathy, ophthalmoplegia, IgM paraprotein, col

10          The combination of CPEO and sensory ataxic neuropathy (SANO, incomplete SANDO) was found in

11 xic neuropathies are a subset of the sensory ataxic neuropathies which are characterized by ataxia as

12 c neuropathy syndrome termed chronic sensory ataxic neuropathy with anti-disialosyl IgM antibodies is

13                                  The sensory ataxic neuropathy with dysarthria and ophthalmoparesis (

14                   The combination of sensory ataxic neuropathy with ophthalmoparesis (SANO) was obser