Purpose of review Progressive supranuclear palsy (PSP) is a 4R tau neuropathologic entity.
While historically defined by the presence of a vertical supranuclear gaze palsy and falls in …

Progressive supranuclear palsy-Richardson syndrome (PSP-RS) is a sporadic atypical
parkinsonian syndrome with levodopa-unresponsive axial-predominant parkinsonism, early …

Abstract Rapid onset Obesity, Hypothalamic dysfunction, Hypoventilation, and Autonomic
Dysregulation (ROHHAD) is a rare syndrome whose underlying pathophysiology and …

Objectives: To evaluate the ability of saccadic strategies developed during vestibular
compensation to reduce the effect of an impaired vestibulo-ocular reflex (VOR) on a retinal …

Background POLR3A pathogenic variants are associated with hypomyelination, hypodontia,
hypogonadism, and movement disorders. Cases We describe the range of movement …

Neuro-ophthalmological signs and symptoms are common in the emergency department but
are a frequent source of diagnostic uncertainties. However, neuro-ophthalmological signs …

Background Genetic prion diseases, including Gerstmann‐Sträussler‐Scheinker disease
(GSS), are extremely rare, fatal neurodegenerative disorders, often associated with …

Spinocerebellar ataxias (SCAs) represent a large group of heredodegenerative diseases,
with great phenotypic and genotypic heterogeneity. However, in the clinical neurological …

Saccadic slowing as a component of supranuclear saccadic gaze palsy is an important
diagnostic sign in multiple neurologic conditions, including degenerative, inflammatory …

Background: Vertical gaze palsy is a rare clinical manifestation of intracranial hypotension.
The typical features of intracranial hypotension include a postural headache, dural …