Hyperkinetic Movement Disorder as the First Manifestation of Moyamoya Disease in a 15-Year-Old: A Case Report. [PDF]
ABSTRACT Physicians evaluating pediatric movement disorders, especially chorea, should consider a broad differential diagnosis, including vascular etiologies such as moyamoya disease. Prompt recognition, appropriate neuroimaging, and early diagnosis are crucial for guiding management and optimizing patient outcomes.
Okar L +4 more
europepmc +2 more sources
A 50 year old with a rapid neuropsychiatric deterioration and choreaform movements [PDF]
A 50-year-old man presented acutely to the hospital with behavioural disturbance, choreiform movements and profound nihilistic delusions. He reported recent drug and alcohol abuse, and also apparent involvement in several recent criminal activities, for ...
Campbell, Stewart +3 more
core +1 more source
Chorea, Pruritus and Polycythemia: Looking for Clues
Chorea is a movement disorder usually due to vascular, hereditary, metabolic or drug- induced causes, and has rarely been reported in association with polycythemia vera (PV).
Vânia Rodrigues +3 more
doaj +1 more source
Brain muscarinic cholinergic receptors in Huntington's disease [PDF]
Muscarinic cholinergic receptors and choline acetyltransferase (ChAT) activity were studied in postmortem brain tissue from patients with Huntington's disease and matched control subjects.
Agid, Y. +4 more
core +1 more source
Chorea is thought to be caused by deactivation of the indirect pathway in the basal ganglia circuit. However, few imaging studies have evaluated the basal ganglia circuit in actual patients with chorea.
Nobuyuki Ishii +5 more
doaj +1 more source
Charles West: a 19th century perspective on acquired childhood aphasia [PDF]
Dr Charles West was the founder (1852) of the first paediatric hospital in the English-speaking world. In a career spanning four decades, he devoted a great part of his energies to describing the nervous diseases of infants and children.
Hellal, Paula, Lorch, Marjorie
core +1 more source
Chorea: A Journey Throughout History
The original descriptions of chorea date from the Middle Ages, when an epidemic of “dancing mania” swept throughout Europe. The condition was initially considered a curse sent by a saint, but was named “Saint Vitus’s dance&rdquo ...
Thiago Cardoso Vale, Francisco Cardoso
doaj +1 more source
Clinical and genetic analysis of 29 Brazilian patients with Huntington’s disease-like phenotype [PDF]
Huntington’s disease (HD) is a neurodegenerative disorder characterized by chorea, behavioral disturbances and dementia, caused by a pathological expansion of the CAG trinucleotide in the HTT gene. Several patients have been recognized with the typical
Adrian Danek +38 more
core +3 more sources
A case report: chorea gravidarum [PDF]
Chorea gravidarum is the term given to chorea occurring during pregnancy. It is not an etiologically or pathologically distinct morbid entity, but a generic term for chorea of any etiology.
Sheela SR, Gomathy E , Anitha NPG
doaj
Oxidative stress parameters in plasma of Huntington's disease patients, asymptomatic Huntington's disease gene carriers and healthy subjects : a cross-sectional study [PDF]
BACKGROUND : Animal data and postmortem studies suggest a role of oxidative stress in the Huntington's disease (HD), but in vivo human studies have been scarce.
Babić, Tomislav +5 more
core +1 more source

