| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Tingting Song, Xiancun Liu, Rui Han, Lihua Huang, Jingjing Zhang, Haiyang X. Effects of end-tidal carbon dioxide levels in patients undergoing direct revascularization for Moyamoya disease and risk factors associated with postoperative complications. Medicine. vol 100. issue 7. 2021-02-26. PMID:33607783. |
a history of transient ischemic attack, severity of disease, urinary output, hematocrit, hypocapnia, and hypotension during direct revascularization (superficial temporal artery to middle cerebral artery [sta-mca]) in patients with moyamoya disease (mmd) may lead to a poor prognosis, however, to our knowledge evidence for end-tidal carbon dioxide (etco2) targets is lacking. |
2021-02-26 |
2023-08-13 |
Not clear |
| Mridula Goswami, Ramanandvignesh Pandian, Sadhna Sharm. Moyamoya Disease-"A Puff of Smoke": A Rare Pediatric Case Report. International journal of clinical pediatric dentistry. vol 13. issue 5. 2021-02-25. PMID:33623348. |
moyamoya disease (mmd) is a rare neurovascular disorder that is characterized by chronic progressive stenosis at the apices and bilateral occlusion of the intracranial internal carotid arteries. |
2021-02-25 |
2023-08-13 |
Not clear |
| Jamie Ah Ong, Sharon Yy Low, Wan Tew Seow, Chun Peng Goh, Tseng Tsai Yeo, Ning Chou, David Cy Low, Vincent Ng. Revascularisation surgery for paediatric moyamoya disease: The Singapore experience. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. vol 82. issue Pt B. 2021-02-22. PMID:33246909. |
moyamoya disease (mmd) is characterized by the spontaneous occlusion of the distal internal carotid arteries and resultant neo-angiogenesis of fragile collateral blood vessels. |
2021-02-22 |
2023-08-13 |
Not clear |
| Masanori Iwanishi, Choka Azuma, Yuji Tezuka, Yukako Yamamoto, Jun Ito-Kobayashi, Miki Washiyama, Toru Kusakabe, Shingo Kikugaw. Observation of p.R4810K, a Polymorphism of the Mysterin Gene, the Susceptibility Gene for Moyamoya Disease, in Two Female Japanese Diabetic Patients with Familial Partial Lipodystrophy 1. Internal medicine (Tokyo, Japan). vol 59. issue 20. 2021-02-18. PMID:33055470. |
mysterin, which was recently shown to play an important role in maintaining cellular fat storage, has been identified to be the susceptibility gene for moyamoya disease (mmd). |
2021-02-18 |
2023-08-13 |
Not clear |
| Nobuhiko Arai, Takashi Horiguchi, Satoshi Takahashi, Tadaki Nakahara, Takenori Akiyama, Masahiro Jinzaki, Kazunari Yoshid. Hemodynamic stress distribution identified by SPECT reflects ischemic symptoms of Moyamoya disease patients. Neurosurgical review. vol 43. issue 5. 2021-02-15. PMID:31444715. |
this study aimed to validate the hypothesis that the ratio of cerebral blood flow (cbf) at rest in the lenticular nucleus (ln) territory to that in the middle cerebral artery (mca) territory is higher in symptomatic moyamoya disease (mmd) patients than in asymptomatic mmd patients. |
2021-02-15 |
2023-08-13 |
Not clear |
| Jingjing Liu, Qinlan Xu, Hongchuan Niu, Rong Wang, Xun Ye, Xianzeng Li. Postoperative incidence of seizure and cerebral infarction in pediatric patients with epileptic type moyamoya disease: a meta-analysis of single rate. Chinese neurosurgical journal. vol 7. issue 1. 2021-02-11. PMID:33526093. |
surgery is a conventional mature treatment for moyamoya disease (mmd). |
2021-02-11 |
2023-08-13 |
Not clear |
| Alessandro Raso, Roberto Biassoni, Samantha Mascelli, Paolo Nozza, Elisabetta Ugolotti, Eddi Di Marco, Patrizia De Marco, Elisa Merello, Armando Cama, Marco Pavanello, Valeria Capr. Moyamoya vasculopathy shows a genetic mutational gradient decreasing from East to West. Journal of neurosurgical sciences. vol 64. issue 2. 2021-02-03. PMID:27787485. |
moyamoya disease (mmd) is a chronic, occlusive cerebrovascular disease characterized by bilateral steno-occlusive changes at the terminal portion of the internal carotid arteries and an abnormal vascular network at the base of the brain determining stroke in children. |
2021-02-03 |
2023-08-13 |
Not clear |
| Constantin Roder, Till-Karsten Hauser, Ulrike Ernemann, Marcos Tatagiba, Nadia Khan, Benjamin Bende. Arterial wall contrast enhancement in progressive moyamoya disease. Journal of neurosurgery. vol 132. issue 6. 2021-01-26. PMID:31125967. |
the purpose of this study was to evaluate chronological patterns of arterial wall contrast enhancement in contrast-enhanced high-resolution mri (ce-hr-mri) in patients with moyamoya disease (mmd). |
2021-01-26 |
2023-08-13 |
Not clear |
| Priyanka Sarkar, Kavitha Thirumuruga. New insights into TNFα/PTP1B and PPARγ pathway through RNF213- a link between inflammation, obesity, insulin resistance, and Moyamoya disease. Gene. vol 771. 2021-01-21. PMID:33333224. |
one such ischemic carotid artery disease is moyamoya disease (mmd) associated with diabetes type i and ii, but the causality was unclear. |
2021-01-21 |
2023-08-13 |
Not clear |
| Xiaocheng Lu, Yabo Huang, Peng Zhou, Pinjing Hui, Zhong Wan. Decreased cortical perfusion in areas with blood-brain barrier dysfunction in Moyamoya disease. Acta neurochirurgica. vol 162. issue 10. 2021-01-19. PMID:32700079. |
recently, several studies have focused on the relationship between blood-brain barrier (bbb) impairment and the etiology of moyamoya disease (mmd). |
2021-01-19 |
2023-08-13 |
Not clear |
| Faith D Moore, Tamer Riz. Moyamoya Disease in a Six Month Caucasian Female. Cureus. vol 12. issue 12. 2021-01-12. PMID:33425553. |
moyamoya disease (mmd) is a progressive cerebral arteriopathy characterized by stenosis and/or occlusion of the internal carotid arteries and the arteries around the circle of willis, with the development of "moyamoya" vessels, which are an attempt at revascularization at the base of the brain. in this paper we describe a 6 month, 3-week-old girl who presented with seizures and strokes due to moyamoya disease. the diagnosis of early onset mmd was made due to the magnetic resonance angiography results showing severe stenosis of the terminal/supraclinoid carotid arteries bilaterally with moyamoya vessels, and a completely novel de novo mutation in the rnf213 gene. |
2021-01-12 |
2023-08-13 |
Not clear |
| Yukihiro Goto, Hideki Oka, Akihiko Hin. Managing intervention for severe intraventricular hemorrhage casting in moyamoya disease: Report of two cases. International journal of surgery case reports. vol 73. 2021-01-10. PMID:32721887. |
when severe intraventricular hemorrhage (ivh) casting in moyamoya disease (mmd) is mentioned, experts advocate not to evacuate the ivh in acute phase. |
2021-01-10 |
2023-08-13 |
Not clear |
| Kikutaro Tokairin, Ken Kazumata, Shuho Gotoh, Taku Sugiyama, Hiroyuki Kobayash. Neuroendoscope-Assisted Aneurysm Trapping for Ruptured Intraventricular Aneurysms in Moyamoya Disease Patients. World neurosurgery. vol 141. 2021-01-07. PMID:32492540. |
intracranial hematomas associated with abnormal collateral vessels are observed in certain populations of adult patients with moyamoya disease (mmd). |
2021-01-07 |
2023-08-13 |
Not clear |
| b' Wing Mann Ho, Alice Stephanie G\\xc3\\xb6rke, Florian Dazinger, Bettina Pfausler, Elke R Gizewski, Ondra Petr, Claudius Thom\\xc3\\xa. Transcallosal, transchoroidal clipping of a hypothalamic collateral vessel aneurysm in Moyamoya disease. Acta neurochirurgica. vol 162. issue 8. 2021-01-05. PMID:32306162.' |
peripheral collateral vessel aneurysms in moyamoya disease (mmd) remain difficult to treat due to their deep location, small size, and vascular fragility. |
2021-01-05 |
2023-08-13 |
Not clear |
| Anthony Larson, Lorenzo Rinaldo, Giuseppe Lanzino, James P Klaa. High prevalence of pro-thrombotic conditions in adult patients with moyamoya disease and moyamoya syndrome: a single center study. Acta neurochirurgica. vol 162. issue 8. 2021-01-05. PMID:32462312. |
moyamoya disease (mmd) and moyamoya syndrome (mms) have been reported to be associated with pro-thrombotic states in some patients. |
2021-01-05 |
2023-08-13 |
Not clear |
| Yahui Zhao, Junlin Lu, Qian Zhang, Yan Zhang, Dong Zhang, Rong Wang, Yuanli Zha. Time Course of Neoangiogenesis After Indirect Bypass Surgery for Moyamoya Disease : Comparison of Short-term and Long-term Follow-up Angiography. Clinical neuroradiology. vol 30. issue 1. 2021-01-04. PMID:30511151. |
indirect bypass surgery, which induces spontaneous neoangiogenesis in ischemic brain tissue and improves cerebral blood flow, is an effective treatment for moyamoya disease (mmd). |
2021-01-04 |
2023-08-13 |
Not clear |
| Changwen Li, Nan Zhang, Shaojie Yu, Yong Xu, Yang Yao, Minghui Zeng, Dongxue Li, Chengyu Xi. Individualized Perioperative Blood Pressure Management for Adult Moyamoya Disease: Experience from 186 Consecutive Procedures. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association. vol 30. issue 1. 2021-01-04. PMID:33160127. |
in adult patients with moyamoya disease (mmd) underwent combined revascularization, cerebral infarction during the acute postoperative phase is common and can lead to neurological dysfunction after revascularization in mmd patients. |
2021-01-04 |
2023-08-13 |
Not clear |
| Jiwook Ryu, Eika Hamano, Masaki Nishimura, Tetsu Satow, Jun C Takahash. Difference in periventricular anastomosis in child and adult moyamoya disease: a vascular morphology study. Acta neurochirurgica. vol 162. issue 6. 2020-12-28. PMID:32356203. |
periventricular anastomosis (pa), which is a novel term for extended collateral vessels in moyamoya disease (mmd), is reportedly associated with a high risk of intracranial hemorrhage in adult patients. |
2020-12-28 |
2023-08-13 |
Not clear |
| Yuki Shinya, Satoru Miyawaki, Hirofumi Nakatomi, Masahiro Shin, Akira Teraoka, Nobuhito Sait. Hemorrhagic Onset Intracranial Artery Dissection of Middle Cerebral Artery Followed by Progressive Arterial Stenosis with Genetic Variant RNF213 p.Arg4810Lys (rs112735431). World neurosurgery. vol 141. 2020-12-28. PMID:32438004. |
rnf213 was recently identified as a susceptibility gene for moyamoya disease (mmd) and intracranial artery stenosis (icas). |
2020-12-28 |
2023-08-13 |
Not clear |
| Kikutaro Tokairin, Shuji Hamauchi, Masaki Ito, Ken Kazumata, Taku Sugiyama, Naoki Nakayama, Masahito Kawabori, Toshiya Osanai, Kiyohiro Houki. Vascular Smooth Muscle Cell Derived from IPS Cell of Moyamoya Disease - Comparative Characterization with Endothelial Cell Transcriptome. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association. vol 29. issue 12. 2020-12-08. PMID:32992193. |
moyamoya disease (mmd) is an occlusive cerebrovascular disease, causing stroke in children and young adults with unknown etiology. |
2020-12-08 |
2023-08-13 |
Not clear |