Results 31 to 40 of about 1,142,799 (204)

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, Kirkham, F.J., Wade, A., Prengler, M., Prengler, Mara, Ganesan, Vijeya, Kirkham, Fenella J., Ganesan, V.   +7 more
core   +1 more source

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), Brian G. Skotko (9032567), Michael S. Rafii (7918070), Anthony C. Wang (11405363), Eugenia Ho (11405366), Ramon A. Durazo-Arvizu (10277724), Deepti Nagesh (11405369), Melanie A. Manning (11405378), Sarah Lee (520785), Mellad Khoshnood (11405372), Runi Tanna (11405375), Gary K. Steinberg (11405381)   +11 more
core   +1 more source

Co-occurrence of Moyamoya syndrome and Kartagener syndrome caused by the mutation of DNAH5 and DNAH11: a case report

BMC Neurology, 2020
Background Kartagener syndrome is an autosomal recessive inherited disorder of primary ciliary dyskinesia. Moyamoya syndrome refers to a moyamoya angiopathy associated with other neurological and/or extra-neurological symptoms, or due to a well ...
Lili Zhang, Xungang Feng, Junhu Zhang, Yanlei Hao, Yuzhong Wang   +4 more
doaj   +1 more source

Abstract Number ‐ 281: Clinical and Epidemiological Characteristics of Moyamoya Disease Presenting with Concomitant Autoimmune Conditions

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, Rohin Singh, Daniel Harrison, Megan Bauman, Andreas Seas, Shane Shahrestani, Julian Gendreau, Oren Gottfried   +7 more
doaj   +1 more source

Brain infarction following elective laparoscopic cholecystectomy in a patient with sickle cell disease and previously undetected Moyamoya syndrome

Journal of Pediatric Surgery Case Reports, 2018
Objective: We report a 7 year-old boy, known case of sickle cell disease, who underwent laparoscopic cholecystectomy for gallstones. He sustained brain insult due to undiagnosed MoyaMoya syndrome.
Jamal Al Hudhaif, Adel Ahmed Al Fayez, Azzah Saleh Alzahrani, Mohammed Al Rajhi   +3 more
doaj   +1 more source

Atypical Posterior Reversible Encephalopathy Syndrome in a Postpartum Woman With Moyamoya Disease: A Case Report and Literature Review

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, Guixiang Guo, Fangchao Wan, Xin Li   +3 more
doaj   +1 more source

Moyamoya in Hispanics: not only in Japanese

Neurology International, 2014
Moyamoya disease was first described in 1957 as hypoplasia of the bilateral internal carotid arteries, the characteristic appearance of the associated network of abnormally dilated collateral vessels on angiography was later likened to something hazy ...
Sarmad Said, Chad J. Cooper, Haider Alkhateeb, Juan M. Galvis, German T. Hernandez, Hasan J. Salameh   +5 more
doaj   +1 more source

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, Quoc Bao Huynh, Dagmar Wieczorek, Brunilda Balliu, Barbara Mikat, Stefan Boehringer   +5 more
doaj   +2 more sources

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, Shefeek Abubacker, Ahamed, Ghassan, Baidas, Mohammad, Naeem   +3 more
openaire   +2 more sources

Moyamoya angiopathy in a case of Klinefelter syndrome.

, 2021
20.500.12530/87852Moyamoya angiopathy, a rare cerebrovascular condition, can be primary (moyamoya disease) or secondary (moyamoya syndrome). Genetic factors, such as the ring finger protein 213 (RNF213), have been associated with moyamoya disease ...
Ray, Adrija, Benito-León, Julián, Roy, Dipayan, Ghosh, Ritwik, Das, Shambaditya   +4 more
core   +1 more source