European stroke organisation (ESO) guidelines on moyamoya angiopathy endorsed by vascular european reference network (VASCERN)

A Bersano, N Khan, B Fuentes, F Acerbi… - European Stroke …, 2023 - journals.sagepub.com
The European Stroke Organisation (ESO) guidelines on Moyamoya Angiopathy (MMA),
developed according to ESO standard operating procedure and Grading of …

Stroke in the Developing Brain: Neurophysiological Implications of Stroke Timing, Location, and Comorbid Factors

NM Hill, LA Malone, LR Sun - Pediatric Neurology, 2023 - Elsevier
Background Pediatric stroke, which is unique in that it represents a static insult to a
developing brain, often leads to long-term neurological disability. Neuroplasticity in infants …

Exploring autonomic alterations during seizures in temporal lobe epilepsy: Insights from a heart-rate variability analysis

SM You, BH Cho, HE Bae, YK Kim, JR Kim… - Journal of Clinical …, 2023 - mdpi.com
Epilepsy's impact on cardiovascular function and autonomic regulation, including heart-rate
variability, is complex and may contribute to sudden unexpected death in epilepsy (SUDEP) …

Psychiatric manifestations in moyamoya disease: more than a puff of smoke? a systematic review and a case-reports meta-analysis

LF Saccaro, C Mallet, A Wullschleger… - Frontiers in Psychiatry, 2024 - frontiersin.org
Introduction Moyamoya disease (MMD) is a life-threatening condition characterized by
stenosis of intracranial arteries. Despite the frequency and the impact of psychiatric …

Moyamoya disease in Southeast Asians: genetic and autopsy data, new cases, systematic review, and meta-analysis of all patients from the literature

D Strunk, P Bauer, K Keyvani, RR Diehl, R Veltkamp… - Journal of …, 2024 - Springer
Background Moyamoya disease (MMD) is a rare disorder causing ischemic and
hemorrhagic juvenile stroke. It is associated with the founder susceptibility variant p …

Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case Series

P Currao, M Balzarini, D Pruna… - Journal of Child …, 2025 - journals.sagepub.com
Neurofibromatosis type 1 (NF1) is a multisystemic neurocutaneous disease caused by a
heterozygous mutation of the NF1 gene that encodes neurofibromin. Complications include …

Moyamoya Disease: Clinical and Radiological Characteristics in Adult Greek Patients

S Vassilopoulou, A Tountopoulou, E Korompoki… - Journal of Clinical …, 2023 - mdpi.com
Background and purpose: The aim of our study is to present, for the first time, the clinical,
radiological, and neurocognitive characteristics of Greek adult patients with Moyamoya …

Post-infectious Moyamoya Syndrome: A Review of Existing Scientific Literature From 2000 to 2023

HM Qadri, RA Bashir, A Amir, MJ Chaudhry, MF Alam… - Cureus, 2024 - pmc.ncbi.nlm.nih.gov
Moyamoya disease (MMD) is considered a primary disorder of an unknown etiology. In
contrast, Moyamoya syndrome (MMS) refers to MMD associated with other underlying …

Epidemiology, causes, and morbidities of stroke in the young

AM Janas, M Barry, S Lee - Current opinion in pediatrics, 2023 - journals.lww.com
Epidemiology, causes, and morbidities of stroke in the young Page 1 CURRENT OPINION
Epidemiology, causes, and morbidities of stroke in the young Anna M. Janasa, Megan Barryb …

Remote ischemic conditioning prevents ischemic cerebrovascular events in children with moyamoya disease: a randomized controlled trial

SF Huang, JL Xu, CH Ren, N Sim, C Han… - World Journal of …, 2024 - Springer
Background Moyamoya disease (MMD) is a significant cause of childhood stroke and
transient ischemic attacks (TIAs). This study aimed to assess the safety and efficacy of …