Results 51 to 60 of about 5,183,178 (176)

Moyamoya disease and syndrome: a review

, 2022
Moyamoya disease is a chronic occlusive cerebrovascular disease that is non-inflammatory and non-atherosclerotic. It is characterized by endothelial hyperplasia and fibrosis of the intracranial portion of the carotid artery and its proximal branches ...
Luana A. Maranha Gatto (5379989), Zeferino Demartini Jr. (12702587), Renato Puppi Munhoz (6304718), Gelson Luis Koppe (4618165), Alex Roman (12702593), Bernardo CA. Teixeira (12702590)   +5 more
core   +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

Updates in the management of moyamoya disease

Interdisciplinary Neurosurgery, 2021
Moyamoya is a rare, steno-occlusive cerebrovascular disorder that often presents as ischemic or hemorrhagic intracerebral events. This review provides an overview of various surgical revascularization techniques used in treating Moyamoya disease ...
Angie Zhang, Nolan Brown, Barry Cheaney, II, Jessica K. Campos, R. Chase Ransom, Frank P.K. Hsu   +5 more
doaj   +1 more source

Pediatric new‐onset seizure‐like events: Yield of diagnostic work‐up

Epileptic Disorders, EarlyView.
Abstract Objective To assess the diagnostic yield of ancillary investigations in children presenting with new‐onset seizure‐like events (SLEs) at a tertiary first seizure clinic (FSC). Methods We conducted a retrospective cohort study including 1213 children evaluated for new‐onset SLEs at a tertiary FSC.
Geertruida Slinger, Lotte Noorlag, Willem M. Otte, Maeike Zijlmans, Rosalie L. Neijzen, Sandra M. A. van der Salm, Floor E. Jansen, Kees P. J. Braun, Eric van Diessen   +8 more
wiley   +1 more source

The Endothelial CXCR Family in Vascular Health and Disease

iNew Medicine, EarlyView.
ABSTRACT Endothelial cells (ECs) form the dynamic interface between blood and tissue, serving as key regulators of vascular homeostasis, inflammation, and repair. Among the molecular systems governing endothelial behavior, the C‐X‐C motif chemokine receptor (CXCR) family—originally characterized in immunology for its roles in leukocyte trafficking and ...
Zhiming Wu, Yandi Wu, Suowen Xu, Yu Huang, Li Wang   +4 more
wiley   +1 more source

ULTRASONOGRAPHIC CHANGES AFTER INDIRECT REVASCULARIZATION SURGERY IN PEDIATRIC PATIENTS WITH MOYAMOYA DISEASE

, 2017
The marked cerebral hypoperfusion of moyamoya disease (MMD) can be treated with encephaloduroarteriosynangiosis (EDAS), an indirect revascularization surgery.
Yeh, Shin-Joe;Tang, Sung-Chun;Tsai, Li-Kai;Chen, Ya-Fang;Liu, Hon-Man;Chen, Ying-An;Hsieh, Yu-Lin;Yang, Shih-Hung;Tien, Yu-Hsuan;Yang, Chi-Cheng;Kuo, Meng-Fai;Jeng, Jiann-Shing, 鄭建興;陳雅芳;楊士弘;蔡力凱;葉馨喬;廖漢文;郭夢菲;湯頌君   +1 more
core   +1 more source

Response to Letter to the Editor: Impact of 1024‐Matrix Size on Perforating Artery Visualization in Cerebral CTA Using a 64‐Slice CT Scanner

Journal of Medical Radiation Sciences, EarlyView.
This response addresses a Letter to the Editor commenting on our article on 1024‐matrix reconstruction for perforating artery visualisation in cerebral CTA using a 64‐slice CT scanner (https://doi.org/10.1002/jmrs.70055). It acknowledges that integration with iterative or deep‐learning reconstruction, workflow and PACS burden, and downstream clinical ...
Hokuto Nagumo, Yuki Nagata, Mayumi Maruko, Jun Sakai, Yusuke Fujiwara, Joma Oikawa   +5 more
wiley   +1 more source

Mood disorder in association with moyamoya disease

, 2012
MOYAMOYA DISEASE IS an inherited vaso-occlusive disease in which dilated collateral vessels appear hazy on angiography.1 Neuropsychiatric manifestations associated with moyamoya disease are uncommon.2 We describe a case of a 16-year-old boy with atypical
Behere, Rishikesh V., Ramasamy Sureshkumar, Ganesan Venkatasubramanian, Rao, Naren P., Bangalore Gangadhar, Shivarama Varambally, Varambally, Shivarama, Gangadhar, Bangalore, Naren P. Rao, Mathew John, John, Mathew, Venkatasubramanian, Ganesan, Rishikesh V. Behere, Sureshkumar, Ramasamy   +13 more
core   +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

Association of enlarged perivascular space burden with silent cerebral infarcts in children with sickle cell disease

British Journal of Haematology, EarlyView.
Enlarged perivascular spaces (ePVS) in the basal ganglia and centrum semiovale are highly prevalent in children with sickle cell disease (SCD). Enlarged PVS in the basal ganglia are associated with the presence of silent cerebral infarcts, another marker of neurological disease, in children with SCD. Summary Children with sickle cell disease (SCD) have
Kristine A. Karkoska, Jahnavi Gollamudi, Brady J. Williamson, Russell P. Sawyer, Daniel Woo, Achala Vagal, Hyacinth I. Hyacinth   +6 more
wiley   +1 more source