A) Inability to walk B) Additional clinical features C) Complete lack of tremor D) Age of onset exclusively under 30
A) Amyotrophic lateral sclerosis B) Huntington's disease C) Progressive supranuclear palsy D) Multiple sclerosis
A) Synucleinopathies and tauopathies B) Acute and chronic C) Genetic and metabolic D) Primary and secondary
A) Supranuclear gaze palsy B) Pick's disease C) Shy–Drager syndrome D) Corticobasal degeneration
A) Symmetrical onset B) Unilateral tremor C) Excellent response to levodopa D) Late-onset postural instability
A) SPECT B) MRI C) CT scan D) PET scan
A) Corticobasal degeneration B) Dementia with Lewy bodies C) Pick's disease D) Progressive supranuclear palsy
A) Ataxia and dysarthria B) Resting tremor and rigidity C) Alien limb and apraxia D) Memory loss and hallucinations
A) They respond significantly better B) They are less likely to respond C) They show identical response D) They react negatively to all medication
A) Multidisciplinary treatment of symptoms B) High-dose levodopa monotherapy C) Curative surgery D) Preventative gene therapy
A) Supranuclear gaze palsy B) Spontaneous recovery C) Increased dopamine production D) Reduced axial muscle rigidity
A) Stable without progression B) More slowly progressive C) More rapidly progressive D) Reversible |