Neuropathology of variants of progressive supranuclear palsy : Current Opinion in Neurology
Neuropathology of variants of progressive supranuclear palsy : Current Opinion in Neurology …

Human voluntary movement is controlled by the pyramidal motor system, a long CNS
pathway comprising corticospinal and lower motor neurons. Hereditary spastic paraplegias …

This article proposes a new measure called Apparent Fibre Density (AFD) for the analysis of
high angular resolution diffusion-weighted images using higher-order information provided …

Objective: While the hallmark of amyotrophic lateral sclerosis (ALS) is corticospinal tract in
combination with lower motor neuron degeneration, the clinical involvement of both …

The hereditary spastic paraplegias (HSPs) are a heterogeneous group of neurologic
disorders with the common feature of prominent lower-extremity spasticity, resulting from a …

Objective To evaluate progressive white matter (WM) degeneration in amyotrophic lateral
sclerosis (ALS). Methods Sixty-six patients with ALS and 43 healthy controls were enrolled …

Background Primary lateral sclerosis is a progressive upper-motor-neuron disorder
associated with markedly longer survival than ALS. In contrast to ALS, the genetic …

Cognitive decline is a burdensome extra-motor symptom associated with Parkinson's
disease (PD). This study aimed at investigating intrinsic functional connectivity (iFC) of the …

Motoneuron disease is a term encompassing three phenotypes defined largely by the
balance of upper versus lower motoneuron involvement, namely amyotrophic lateral …

Objective Neuropathological studies in amyotrophic lateral sclerosis (ALS) have shown a
dissemination in a regional sequence in four anatomically defined patterns. The aim of this …