W. Emser

TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis

Benchmarking the stability of human detergent-solubilised voltage-gated sodium channels for structural studies using eel as a reference

Restless legs syndrome/Willis–Ekbom disease diagnostic criteria: updated International Restless Legs Syndrome Study Group (IRLSSG) consensus criteria – history, rationale, description, and significance

Diffusion tensor imaging: Concepts and applications

Restless Legs Syndrome

Randomized trials of dopamine agonists in restless legs syndrome: A systematic review, quality assessment, and meta-analysis

Sodium channelopathies of skeletal muscle result from gain or loss of function

Updating P300: An integrative theory of P3a and P3b

Ferric Carboxymaltose in Patients with Heart Failure and Iron Deficiency

The severity range of restless legs syndrome (RLS) and augmentation in a prospective patient cohort: Association with ferritin levels

Linkage of Familial Amyotrophic Lateral Sclerosis With Frontotemporal Dementia to Chromosome 9q21-q22

Rapidly progressive aphasic dementia and motor neuron disease

Physical Trauma and Family History of Neurodegenerative Diseases in Amyotrophic Lateral Sclerosis: A Population-Based Case-Control Study

The Physiology, Signaling, and Pharmacology of Dopamine Receptors

The Treatment of Restless Legs Syndrome and Periodic Limb Movement Disorder in Adults—An Update for 2012: Practice Parameters with an Evidence-Based Systematic Review and Meta-Analyses

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

Tau protein isoforms, phosphorylation and role in neurodegenerative disorders11These authors contributed equally to this work.

Epidemiology of mutations in superoxide dismutase in amyotrophic lateal sclerosis

Amyotrophic Lateral Sclerosis

The new mutation, E46K, of α‐synuclein causes parkinson and Lewy body dementia

Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosis

Circadian rhythms in the eye: The physiological significance of melatonin receptors in ocular tissues

Le potentiel évoqué cognitif P300 (II) : variabilité interindividuelle et application clinique en psychopathologie

Intrinsic disorder in proteins associated with neurodegenerative diseases

Posterior leukoencephalopathy without severe hypertension

Classification of Intrinsically Disordered Regions and Proteins

Frontotemporal lobar degeneration

Familial amyotrophic lateral sclerosis with a point mutation of SOD-1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles.

Extrapineal melatonin: sources, regulation, and potential functions

Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22.

Etiology and pathogenesis of prion diseases.

Melatonin decreases the amplitude of the b-wave of the human electroretinogram

The P300 component of event-related potentials in schizophrenic patients

Effective cabergoline treatment in idiopathic restless legs syndrome

Parasitic Myositis by Echinococcus alveolaris

Improved therapy of myotonia with the lidocaine derivative tocainide

Familial occurrence of amyotrophic lateral sclerosis, parkinsonism, and dementia