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Page 1
Moyamoya Disease: A Review of Clinical Research.
Hishikawa T, Sugiu K, Date I. Hishikawa T, et al. Acta Med Okayama. 2016 Aug;70(4):229-36. doi: 10.18926/AMO/54497. Acta Med Okayama. 2016. PMID: 27549666 Free article. Review.
About 5 decades have passed since the concept of moyamoya disease (MMD) was established in Japan. ...
About 5 decades have passed since the concept of moyamoya disease (MMD) was established in Japan. ...
Cutaneous manifestations in Moyamoya angiopathy: A review.
Mitri F, Bersano A, Hervé D, Kraemer M. Mitri F, et al. Eur J Neurol. 2021 May;28(5):1784-1793. doi: 10.1111/ene.14754. Epub 2021 Mar 1. Eur J Neurol. 2021. PMID: 33486780 Review.
BACKGROUND AND PURPOSE: Moyamoya angiopathy (MA) is a progressive cerebrovascular disease with a poorly understood pathophysiology. ...This results in early-onset ischemic or hemorrhagic strokes. The disease may be idiopathic (known as Moyamoya dise …
BACKGROUND AND PURPOSE: Moyamoya angiopathy (MA) is a progressive cerebrovascular disease with a poorly understood pathophysio …
Review of past research and current concepts on the etiology of moyamoya disease.
Houkin K, Ito M, Sugiyama T, Shichinohe H, Nakayama N, Kazumata K, Kuroda S. Houkin K, et al. Neurol Med Chir (Tokyo). 2012;52(5):267-77. doi: 10.2176/nmc.52.267. Neurol Med Chir (Tokyo). 2012. PMID: 22688062 Free article. Review.
Research on moyamoya disease has progressed remarkably in the past several decades. ...However, despite extensive research, the mechanism of moyamoya disease is still unknown. Consequently, the cardinal treatment of this disease has not yet been …
Research on moyamoya disease has progressed remarkably in the past several decades. ...However, despite extensive research, th …
Radiation-induced moyamoya syndrome.
Desai SS, Paulino AC, Mai WY, Teh BS. Desai SS, et al. Int J Radiat Oncol Biol Phys. 2006 Jul 15;65(4):1222-7. doi: 10.1016/j.ijrobp.2006.01.038. Epub 2006 Apr 19. Int J Radiat Oncol Biol Phys. 2006. PMID: 16626890 Review.
Radiation-induced moyamoya syndrome occurred in 27.7% of patients by 2 years, 53.2% of patients by 4 years, 74.5% of patients by 6 years, and 95.7% of patients by 12 years after RT. CONCLUSIONS: Patients who received RT to the parasellar region at a young age (< …
Radiation-induced moyamoya syndrome occurred in 27.7% of patients by 2 years, 53.2% of patients by 4 years, 74.5% of patients …
Surgical management of Moyamoya disease and syndrome: Current concepts and personal experience.
Thines L, Petyt G, Aguettaz P, Bodenant M, Himpens FX, Lenci H, Henon H, Gauthier C, Hossein-Foucher C, Cordonnier C, Lejeune JP. Thines L, et al. Rev Neurol (Paris). 2015 Jan;171(1):31-44. doi: 10.1016/j.neurol.2014.08.007. Epub 2014 Dec 30. Rev Neurol (Paris). 2015. PMID: 25555850 Review.
In this focus, we review, in the light of the recent literature, the modalities and indications of surgical cerebral revascularization for Moyamoya (MM) disease or syndrome. We also report our experience in the surgical management of adult MM. ...They are associated …
In this focus, we review, in the light of the recent literature, the modalities and indications of surgical cerebral revascularization for …
Moyamoya Vasculopathy in PHACE Syndrome: Six New Cases and Review of the Literature.
Tortora D, Severino M, Accogli A, Martinetti C, Vercellino N, Capra V, Rossi A, Pavanello M. Tortora D, et al. World Neurosurg. 2017 Dec;108:291-302. doi: 10.1016/j.wneu.2017.08.176. Epub 2017 Sep 5. World Neurosurg. 2017. PMID: 28887276 Review.
At the moment, there are no established surgical guidelines for high-risk vasculopathies, including quasi-moyamoya, in this syndrome. CASE DESCRIPTION: We described the clinicoradiologic features of a small series of 6 patients with PHACE syndrome and quasi-moyamoya …
At the moment, there are no established surgical guidelines for high-risk vasculopathies, including quasi-moyamoya, in this syndrome. …
Cerebrovascular neurosurgery 2014.
Salem M, Gross BA, Du R, Thomas AJ. Salem M, et al. J Clin Neurosci. 2015 May;22(5):775-8. doi: 10.1016/j.jocn.2015.01.002. Epub 2015 Feb 15. J Clin Neurosci. 2015. PMID: 25691077 Review.
Continued advances in our understanding of the management of cerebrovascular disease were made in 2014. A randomized trial for management of unruptured brain arteriovenous malformation (ARUBA) (Mohr et al. ...Lancet 2014;383:333-41) were also reported. Results from the Jap …
Continued advances in our understanding of the management of cerebrovascular disease were made in 2014. A randomized trial for manage …
Cardiac manifestations in a western moyamoya disease population: a single-center descriptive study and review.
Larson AS, Savastano L, Klaas J, Lanzino G. Larson AS, et al. Neurosurg Rev. 2021 Jun;44(3):1429-1436. doi: 10.1007/s10143-020-01327-x. Epub 2020 Jun 7. Neurosurg Rev. 2021. PMID: 32507930 Review.
An embryological association between moyamoya disease (MMD) and cardiac manifestations has been proposed. ...A total of 181 MMD patients were included in our analysis, 139 (76.8%) of whom were Caucasian. Ten patients had cardiac manifestations (5.5%). …
An embryological association between moyamoya disease (MMD) and cardiac manifestations has been proposed. ...A total of 181 MM …
[Moyamoya disease].
Papanagiotou P, Grunwald IQ, Politi M, Roth C, Reith W. Papanagiotou P, et al. Radiologe. 2005 May;45(5):466-70. doi: 10.1007/s00117-005-1222-1. Radiologe. 2005. PMID: 15864518 Review. German.
Moyamoya disease is an idiopathic progressive vasculopathy characterized by slowly progressive narrowing involving the distal internal carotid artery and the proximal circle of Willis. ...These enlarged collaterals appear as a "puff of smoke" on angiography, which g …
Moyamoya disease is an idiopathic progressive vasculopathy characterized by slowly progressive narrowing involving the distal …
The Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease and a Review of the Pertinent Literature.
Zhang Q, Liu Y, Yu L, Duan R, Ma Y, Ge P, Zhang D, Zhang Y, Wang R, Wang S, Zhao Y, Cao Y, Liu X, Deng X, Zhao J, Zhang X. Zhang Q, et al. World Neurosurg. 2017 Mar;99:701-708.e1. doi: 10.1016/j.wneu.2016.12.119. Epub 2017 Jan 5. World Neurosurg. 2017. PMID: 28063898 Review.
BACKGROUND: Quasi-moyamoya disease (MMD) is characterized by moyamoya vasculopathy and well-recognized comorbidity. ...The p.R4810K heterozygous variant was identified in 5 patients, including 3 patients with atherosclerosis, 1 patient with Graves d …
BACKGROUND: Quasi-moyamoya disease (MMD) is characterized by moyamoya vasculopathy and well-recognized comorbidity. ... …
95 results