Periodic electroencephalographic discharges and epileptic spasms involve cortico-striatal-thalamic loops on Arterial Spin Labeling Magnetic Resonance Imaging

M Eisermann, L Fillon, A Saitovitch… - Brain …, 2022 - academic.oup.com
Periodic discharges are a rare peculiar electroencephalogram pattern, occasionally
associated with motor or other clinical manifestations, usually observed in critically ill …

Acute hemichorea in a young type 1 diabetic

JB Lin, AA Sng, FS Wang, AP Tan… - International Journal of …, 2020 - Taylor & Francis
Abstract Purpose/Aim: Acute movement disorder is an uncommon presenting symptom in
patients with diabetes mellitus. We report a 20-year-old lady with poorly controlled type 1 …

Disappearance of hemichorea as the initial presentation of moyamoya disease after revascularization surgery regardless of residual hypoperfusion evaluated by …

K Onodera, H Sato, M Lepic, K Suzuki, H Ooigawa… - Neurochirurgie, 2023 - Elsevier
Background and importance Although hypoperfusion of the basal ganglia or the frontal
subcortical matter is suspected, the pathology of chorea in moyamoya disease remains …

Corticostriatal hypermetabolism in moyamoya disease-induced hemichorea: two case reports and a literature review

W Xian, X Zhang, X Shi, G Luo, C Yi, Z Pei - Frontiers in Neurology, 2021 - frontiersin.org
Moyamoya disease (MMD) is a rare cause of chorea, and its pathophysiological mechanism
remains unclear. We explore the use of cerebral positron emission tomography (PET) to …

[HTML][HTML] Oro-mandibular dystonia in pediatric moyamoya disease: Two cases report

Y Koga, D Kashiwazaki, E Hori, N Akioka… - Surgical Neurology …, 2021 - ncbi.nlm.nih.gov
Background: In this report, we describe rare two pediatric cases that developed oro-
mandibular dystonia due to moyamoya disease. Case Description: A 7-year-old boy …

[HTML][HTML] Late-onset, first-ever involuntary movement after successful surgical revascularization for pediatric moyamoya disease–Report of two cases

S Hasegawa, T Tanaka, S Yamamoto… - Surgical Neurology …, 2023 - ncbi.nlm.nih.gov
Background: A small number of children with Moyamoya disease develop involuntary
movements as an initial presentation at the onset, which usually resolves after effective …

Asymmetric lenticulostriate arteries in patients with moyamoya disease presenting with movement disorder: three new cases

J Xu, S Li, GB Rajah, W Zhao, C Ren, Y Ding… - Neurological …, 2020 - Taylor & Francis
Objective Unilateral movement disorder associated with moyamoya disease is a rare finding
and the mechanism remains to be fully elucidated. Theories postulated include contralateral …

Late-onset chorea after cerebral revascularization as a clinical manifestation of moyamoya disease

P Enríquez-Ruano, CE Navarro, N Penagos… - Neurological …, 2021 - Springer
Dear Editor, Moyamoya disease is a cerebral arteriopathy with an incidence of 0.086 per
100,000 inhabitants [1], being more common in women and Asian population. It has a broad …

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M Eisermann, L Fillon, A Saitovitch, J Boisgontier… - 2022 - scholar.archive.org
Periodic discharges are a rare peculiar EEG pattern, occasionally associated with motor or
other clinical manifestations, usually observed in critically ill patients. Their underlying …

[HTML][HTML] Truncal dystonia with isolated middle cerebral artery ischemia: A case report of revascularization therapy for dystonia

S Matsumoto, Y Yamamoto, K Fujita… - Surgical Neurology …, 2022 - ncbi.nlm.nih.gov
Background: Dystonia is a rare movement disorder with some cases being difficult to treat.
Although dystonia can occur as a symptom of moyamoya disease, few studies have reported …