Moyamoya disease: diagnosis and interventions

M Ihara, Y Yamamoto, Y Hattori, W Liu… - The Lancet …, 2022 - thelancet.com
Moyamoya disease is a rare cause of stroke, radiologically characterised by progressive
stenosis of the terminal portion of the internal carotid arteries and compensatory capillary …

Ring finger protein 213 assembles into a sensor for ISGylated proteins with antimicrobial activity

F Thery, L Martina, C Asselman, Y Zhang… - Nature …, 2021 - nature.com
ISG15 is an interferon-stimulated, ubiquitin-like protein that can conjugate to substrate
proteins (ISGylation) to counteract microbial infection, but the underlying mechanisms …

Cerebral arteriopathies of childhood and stroke–A focus on systemic arteriopathies and pediatric fibromuscular dysplasia (FMD)

M Hausman-Kedem, P Krishnan… - Vascular …, 2024 - journals.sagepub.com
Systemic vascular involvement in children with cerebral arteriopathies is increasingly
recognized and often highly morbid. Fibromuscular dysplasia (FMD) represents a cerebral …

Luminal and wall changes in intracranial arterial lesions for predicting stroke occurrence

HJ Kim, EH Choi, JW Chung, JH Kim, YS Kim, WK Seo… - Stroke, 2020 - Am Heart Assoc
Background and Purpose: Luminal imaging (degree of stenosis) currently serves as the gold
standard to predict stroke recurrence and guide therapeutic strategies in patients with …

Current treatment for childhood arterial ischaemic stroke

PB Sporns, HJ Fullerton, S Lee, A Kirton… - The Lancet Child & …, 2021 - thelancet.com
Paediatric arterial ischaemic stroke is an important cause of neurological morbidity in
children, with consequences including motor disorders, intellectual impairment, and …

Twig-like middle cerebral artery: Embryological persistence or secondary consequences?

T Ota, M Komiyama - Interventional Neuroradiology, 2021 - journals.sagepub.com
We would like to comment on twig-like middle cerebral artery (MCA) in relation to the
interesting article “Hemorrhagic events associated with unfused or twig-like configuration of …

Role of the RNF213 Variant in Vascular Outcomes in Patients With Intracranial Atherosclerosis

HJ Kim, EH Choi, JW Chung, JH Kim… - Journal of the …, 2021 - Am Heart Assoc
Background The RNF213 (ring finger protein 213 gene) variant R4810K is a susceptibility
allele not only for Moyamoya disease (MMD) but also for intracranial atherosclerosis (ICAS) …

Genome-wide association study of intracranial artery stenosis followed by phenome-wide association study

S Dofuku, K Sonehara, S Miyawaki, S Sakaue… - Translational Stroke …, 2023 - Springer
The genetic background of intracranial artery stenosis (ICAS), a major cause of ischemic
stroke, remains elusive. We performed the world's first genome-wide association study …

Effect of the RNF213 p.R4810K Variant on the Progression of Intracranial Artery Stenosis: A 15-Year Follow-up Study

S Okazaki, T Yoshimoto, M Ohara, M Takagaki… - Neurology …, 2022 - AAN Enterprises
Background and Objectives Intracranial artery stenosis is the predominant etiology of
ischemic stroke in the Asian population. Furthermore, the presence of the RNF213 p …

Research progress of moyamoya disease combined with renovascular hypertension

E Liu, H Zhao, C Liu, X Tan, C Luo, S Yang - Frontiers in Surgery, 2022 - frontiersin.org
Moyamoya disease (MMD) is an idiopathic cerebrovascular disease which was first
described by Suzuki and Takaku in 1969. Moyamoya disease is a non-atherosclerotic …