Latest papers

TDP43-positive intraneuronal inclusions in a patient with motor neuron disease and Parkinson's disease.

Identifying poor adaptation to a new diagnosis of motor neuron disease: A pilot study into the value of an early patient-led interview.

[New evidence of the prion nature of amyotrophic leukospongiosis].

Primary lateral sclerosis may occur within familial amyotrophic lateral sclerosis pedigrees.

[Phoniatric and laryngologic symptoms in motor neuron disease (MND)]

Familial amyotrophic lateral sclerosis with a novel G85S mutation of superoxide dismutase 1 gene: clinical features of lower motor neuron disease.

Pseudobulbar syndrome in two patients with human immunodeficiency virus infection.

[Follow-up study of patients with chronic motor axonal neuropathy].

Application of robots at patients with paresis of the upper limb as a consequence of central motor neuron lesion for supporting physiotherapy during rehabilitation.

[Guillain-Barré syndrome in childhood].

Spastic hypertonia and movement disorders: pathophysiology, clinical presentation, and quantification.

Role of oral medications in spasticity management.

Physical activity as an exogenous risk factor in motor neuron disease (MND): a review of the evidence.

Evidence-Based Treatment Of Chronic Immune-Mediated Neuropathies

Vertebral artery dissection presenting with multilevel combined sensorimotor radiculopathy: a case report and literature review.

Intravenous administration of self-complementary AAV9 enables transgene delivery to adult motor neurons.

Cranial nerves palsy as an initial feature of an early onset distal hereditary motor neuropathy--a new distal hereditary motor neuropathy phenotype.

Linear longitudinal decline in fractional anisotropy in patients with amyotrophic lateral sclerosis: preliminary results.

IVIg dose increase in multifocal motor neuropathy

Ocular fixation instabilities in motor neurone disease