Results 31 to 40 of about 1,229,635 (199)
Stroke: Vascular and Interventional Neurology, 2023 Introduction Moyamoya disease was first described in the 1950’s. After over six decades, however, the underlying etiology of Moyamoya still remains unknown.
Nolan Brown +7 more
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Navigating Diagnostic Complexities and Treatment Strategies of Moyamoya Syndrome: A Case Report. [PDF]
CureusMoyamoya syndrome (MMS) is characterized by progressive narrowing of intracranial arteries and the development of collateral vessel networks, often presenting with recurrent ischemic or hemorrhagic strokes.
Kwan LL +4 more
europepmc +2 more sources
Clinical and radiological recurrence after childhood arterial ischemic stroke [PDF]
, 2006 Background: Data on rates and risk factors for clinical and radiological recurrence of childhood arterial ischemic stroke (AIS) might inform secondary prevention strategies.
Wade, Angela +7 more
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Frontiers in Neurology, 2019 Background: Sickle cell disease (SCD) can be complicated by moyamoya syndrome. Brain magnetic resonance angiography (MRA) is a non-invasive method to diagnose this syndrome and, steno-occlusion and moyamoya vessels (MMV) scores have been proposed to ...
Paul Kauv +10 more
doaj +1 more source
, 2021 Moyamoya syndrome is a chronic and progressive narrowing of the arteries in the brain caused by different mechanisms than the genetic mutation that leads to moyamoya disease.
Elfallal, Samer +5 more
core +1 more source
Frontiers in Neurology, 2021 Background: Moyamoya disease is a rare cerebrovascular occlusive disease, which is characterized by stenosis and gradual occlusion of the internal carotid arteries, causing the progression of characteristic collateral vessels.
Ning Zou +3 more
doaj +1 more source
Moyamoya Syndrome with Primary Antiphospholipid Syndrome [PDF]
Medical Principles and Practice, 2006 <i>Objectives:</i> To report a rare case of moyamoya syndrome with primary antiphospholipid syndrome (APS). <i>Clinical Presentation and Intervention:</i> A 41-year-old woman was admitted with sudden onset of left-sided hemiparesis.
Mohammed Ali, Shuja-Ud-Din +3 more
openaire +2 more sources
Distinctive facial features in idiopathic Moyamoya disease in Caucasians: a first systematic analysis [PDF]
PeerJ, 2018 Background Craniofacial dysmorphic features are morphological changes of the face and skull which are associated with syndromic conditions. Moyamoya angiopathy is a rare cerebral vasculopathy that can be divided into Moyamoya syndrome, which is ...
Markus Kraemer +5 more
doaj +2 more sources
Surgical Management of Moyamoya Syndrome [PDF]
Skull Base, 2005 Moyamoya syndrome, a vasculopathy characterized by chronic progressive stenosis at the apices of the intracranial internal carotid arteries, is an increasingly recognized entity which is associated with cerebral ischemia. Diagnosis is made on the basis of clinical and radiographic findings, including a characteristic stenosis of the internal carotid ...
Edward R, Smith, R Michael, Scott
openaire +2 more sources
Data_Sheet_1_Increased Autoimmunity in Individuals With Down Syndrome and Moyamoya Disease.DOCX
, 2021 Objective: To determine if elevated rates of autoimmune disease are present in children with both Down syndrome and moyamoya disease given the high rates of autoimmune disease reported in both conditions and unknown etiology of angiopathy in this ...
Jonathan D. Santoro (6737372) +11 more
core +1 more source