Multifocal motor neuropathy (MMN) is characterized by slowly progressive,predominantly distal,asymmetric limb weakness and partial conduction blocks (CB) of motor axons. Cranial nerve involvement and respiratory failure are uncommon. We report two patients who exhibited unilateral hypoglossal and abducens palsy as presenting signs. Other remarkable features were autonomic instability and respiratory failure due to bilateral phrenic nerve involvement. Treatment with intravenous (IV) immunoglobulin (Ig) resulted in an improvement. Patient 2,who showed IgM reactivity against ganglioside GM1,has been receiving maintenance therapy with IVIg for 7years. We speculate that cranial weakness of our patients could be due to CB similar to those detecte...
Objective To describe a patient with multifocal motor neuropathy with conduction block who had annu...
We report a patient with motor neuropathy in whom plasma exchange (PE) was followed by a pronounced ...
A patient with a progressive lower motor neuron syndrome and neurophysiological evidence of motor ax...
Multifocal motor neuropathy (MMN) is characterized by slowly progressive,predominantly distal,asymme...
Multifocal motor neuropathy (MMN) is an immune-mediated neuropathy. Wasting and weakness typically d...
Background: Multifocal motor neuropathy (MMN) occasionally presents with cranial nerve involvement. ...
Multifocal motor neuropathy (MMN) is a chronic demyelinating neuropathy mainly characterized by mult...
We report a case with symptoms of facial swelling, bilateral facial paralysis, dysphagia and aspirat...
INTRODUCTION: Cramp-fasciculation syndrome is a peripheral nerve hyperexcitability disorder, which c...
Multifocal motor neuropathy is characterized by slowly progressive, asymmetrical weakness of the arm...
Multifocal motor neuropathy (MMN) is a rare and disabling disease. Several experimental studies and ...
Several articles on multifocal motor neuropathy (MMN) have appeared in 2007 and 2008, broadening the...
Initially described only about 20 years ago, multifocal motor neuropathy (MMN) is a predominantly di...
Motor neuropathy with multifocal conduction blocks represents a recently identified autoimmune disor...
Multifocal motor neuropathy (MMN) is a purely motor multineuropathy characterized by multifocal cond...
Objective To describe a patient with multifocal motor neuropathy with conduction block who had annu...
We report a patient with motor neuropathy in whom plasma exchange (PE) was followed by a pronounced ...
A patient with a progressive lower motor neuron syndrome and neurophysiological evidence of motor ax...
Multifocal motor neuropathy (MMN) is characterized by slowly progressive,predominantly distal,asymme...
Multifocal motor neuropathy (MMN) is an immune-mediated neuropathy. Wasting and weakness typically d...
Background: Multifocal motor neuropathy (MMN) occasionally presents with cranial nerve involvement. ...
Multifocal motor neuropathy (MMN) is a chronic demyelinating neuropathy mainly characterized by mult...
We report a case with symptoms of facial swelling, bilateral facial paralysis, dysphagia and aspirat...
INTRODUCTION: Cramp-fasciculation syndrome is a peripheral nerve hyperexcitability disorder, which c...
Multifocal motor neuropathy is characterized by slowly progressive, asymmetrical weakness of the arm...
Multifocal motor neuropathy (MMN) is a rare and disabling disease. Several experimental studies and ...
Several articles on multifocal motor neuropathy (MMN) have appeared in 2007 and 2008, broadening the...
Initially described only about 20 years ago, multifocal motor neuropathy (MMN) is a predominantly di...
Motor neuropathy with multifocal conduction blocks represents a recently identified autoimmune disor...
Multifocal motor neuropathy (MMN) is a purely motor multineuropathy characterized by multifocal cond...
Objective To describe a patient with multifocal motor neuropathy with conduction block who had annu...
We report a patient with motor neuropathy in whom plasma exchange (PE) was followed by a pronounced ...
A patient with a progressive lower motor neuron syndrome and neurophysiological evidence of motor ax...