Results 51 to 60 of about 21,247 (273)

A rare cranial disease: Prolactinoma-associated moyamoya syndrome

Ulusal Romatoloji Dergisi
Moyamoya disease is a rare chronic progressive cerebrovascular disease. The etiology of moyamoya disease has not been established yet. If an underlying cause is detected, moyamoya disease is called moyamoya syndrome.
Ayberk Bayramgil, İrem İşlek, Erkingül Shugaiv, Meryem Can   +3 more
doaj   +1 more source

Embedded 3D‐Coaxial Bioprinting of Stenotic Brain Vessels with a Mechanically Enhanced Extracellular Matrix Bioink for Investigating Hemodynamic Force‐Induced Endothelial Responses

Advanced Functional Materials, EarlyView.
In this study, a physically enhanced vascular dECM bioink and used 3D‐coaxial bioprinting are developed to fabricate mature brain blood vessels for cerebral atherosclerosis research. This model demonstrates that vascular geometry‐induced hemodynamic changes trigger vascular inflammation, ensuring its potential for cerebrovascular research.
Wonbin Park, Min‐Ju Choi, Jae‐Seong Lee, Minjun Ahn, Wonil Han, Ge Gao, Dong‐Woo Cho, Byoung Soo Kim   +7 more
wiley   +1 more source

Genetics of Moyamoya disease [PDF]

Journal of Human Genetics, 2010
Moyamoya disease (MMD) is a disease pattern consisting of bilateral stenosis of the intracranial internal carotid arteries (ICA) accompanied by a network of abnormal collateral vessels that bypass the stenosis. Once symptomatic, insufficient cerebral blood flow or rupture of the fragile collaterals may cause stroke or hemorrhage, resulting in severe ...
Boris Krischek, Marcos Tatagiba, Constantin Roder, Nikhil R. Nayak, Ituro Inoue, Nadia Khan   +5 more
openaire   +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.
Ganesan, V., Kirkham, F.J., Prengler, M., Wade, A.   +3 more
core  

Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations [PDF]

, 2018
Smooth muscle dysfunction syndrome (SMDS) due to heterozygous ACTA2 arginine 179 alterations is characterized by patent ductus arteriosus, vasculopathy (aneurysm and occlusive lesions), pulmonary arterial hypertension, and other complications in smooth ...
A Kikuchi, Alan C Braverman, AN Moosa, Anji Yetman, Anna L Mitchell, Anne Child, Anthony Estrera, AT Yetman, Birgit Lorenz, BL Loeys, Cori Feist, Denver Sallee, Dianna M Milewicz, DJ Schneider, DM Milewicz, Ellen S Regalado, ES Regalado, ES Roach, FM Roulez, Glen Iannucci, Hiroko Morisaki, HU Moller, J de Grazia, J Richer, JL Anderson, John R Ostergaard, Julie De Backer, Julie Richer, Kathryn C Chatfield, Kathryn W Holmes, Lauren Mellor-Crummey, LC Ades, Lesley Ades, LW Fung, M Al-Mohaissen, M Elizabeth Brickner, M Keir, MC Brodsky, ME Meuwissen, MM Georgescu, MR Amans, Mustafa Tekin, NJ Ullrich, P Munot, Patricia Musolino, Paul Mark, Reed Pyeritz, RV Lacro, S Prabhu, Shaine A Morris, Sherene Shalhub, Susan Benedict, T Logeswaran, Takayuki Morisaki, Timothy J Bradley, Y Arlachov   +55 more
core   +3 more sources

“MR Fingerprinting for Imaging Brain Hemodynamics and Oxygenation”

Journal of Magnetic Resonance Imaging, EarlyView.
ABSTRACT Over the past decade, several studies have explored the potential of magnetic resonance fingerprinting (MRF) for the quantification of brain hemodynamics, oxygenation, and perfusion. Recent advances in simulation models and reconstruction frameworks have also significantly enhanced the accuracy of vascular parameter estimation.
T. Coudert, A. Delphin, A. Barrier, E. L. Barbier, B. Lemasson, J. M. Warnking, T. Christen   +6 more
wiley   +1 more source

Cerebral infarction following intracranial hemorrhage in pediatric Moyamoya disease - A case report and brief review of literature

Annals of Indian Academy of Neurology, 2012
Moyamoya disease is a clinical entity characterized by progressive cerebrovascular occlusion with spontaneous development of a collateral vascular network called Moyamoya vessels. This disease mainly manifests as cerebral ischemia.
Soumya Patra, Radheshyam Purkait, Tapankumar Sinhamahapatra, Abhijit Misra   +3 more
doaj   +1 more source

Moyamoya: An Uncommon Variant Of Stroke In Childrena

Journal of Bahria University Medical and Dental College, 2021
Moyamoya is a rare cause of stroke in children. It is an infrequent cerebrovascular disorder of unknown etiology. We are reporting a case of a 7-year-old girl who presented with an acute history of left-sided weakness.
Rida Zaheer, Ayesha Ahmed, Shazia Shakoor, Shakeel Ahmed   +3 more
doaj   +1 more source

Atypical postoperative radiographical findings in a patient with moyamoya disease: A case report

Radiology Case Reports, 2019
Moyamoya disease is a chronic cerebrovascular disease characterized by spontaneous and progressive stenosis or occlusion of the internal carotid artery and its branches.
Masaki Ikegami, MD, Tomoya Kamide, MD, PhD, Toshiki Ikeda, MD, PhD, Yuichiro Kikkawa, MD, PhD, Hiroki Kurita, MD, PhD   +4 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