Results 41 to 50 of about 15,778 (214)

Moyamoya-like cerebrovascular disease in a child with a novel mutation in myosin heavy chain 11 [PDF]

, 2017
Heterozygous mutations in the MYH11 gene affecting the C-terminal coiled-coil region of the smooth muscle myosin heavy chain, a contractile protein of smooth muscle cells (SMC), have been described to cause thoracic aortic aneurysm or aortic dissection ...
Brogan, P, Eleftheriou, D, Ganesan, V, Hong, Y, Keylock, A, Mulhern, C, Omoyinmi, E, Roebuck, D, Saunders, D   +8 more
core   +1 more source

Moyamoya Periventricular Choroidal Collateral Registry―A Multicenter Cohort Study of Moyamoya Disease with Choroidal Anastomosis: Study Protocol

Neurologia Medico-Chirurgica
Recent cohort studies on hemorrhagic and asymptomatic moyamoya disease have revealed that choroidal anastomosis, a type of fragile periventricular collateral pathway (periventricular anastomosis) typical of the disease, is an independent predictor of ...
Takeshi FUNAKI, Susumu MIYAMOTO, The Moyamoya P-ChoC Registry Group   +2 more
doaj   +1 more source

The roles of endoglin gene in cerebrovascular diseases. [PDF]

, 2017
Endoglin (ENG, also known as CD105) is a transforming growth factor β (TGFβ) associated receptor and is required for both vasculogenesis and angiogenesis.
Ma, Li, Su, Hua, Zhang, Rui, Zhu, Wan
core   +2 more sources

Research progress on the inflammatory pathogenesis of moyamoya disease

Guangxi Yike Daxue xuebao
Moyamoya disease is a specific cerebrovascular disease characterized by progressive narrowing of the terminal part of the internal carotid artery and its major branches, and these changes lead to chronic cerebrovascular occlusion and the formation of an ...
Chaojue HUANG, Yuyang CHEN, Hui LIANG, Chang LIU, Daqin FENG   +4 more
doaj   +1 more source

Silent Moyamoya disease - A rare case report

Radiology Case Reports, 2021
Moyamoya is a rare cerebrovascular disorder marked by chronic, gradual blockage of the circle of Willis arteries, leading to characteristic collateral vessels, specifically cerebral angiography.
Juna Musa, MD Mcs, Masum Rahman, MD, Ali Guy, Clinical assistant professor, Angela Guy, PHD candidate, Kristi Saliaj, MD, Abu Bakar Siddik, MD, Fjolla Hyseni, MD, Ketjana Elezi, Pharmacist, Ina Kola, MD, Anisa Cobo, MD, Ilir Ahmetgjekaj, PhD.   +10 more
doaj   +1 more source

Early manifestation of Moyamoya syndrome in a 2-year-old child with Down syndrome

Radiology Case Reports, 2021
Moyamoya is a rare occlusive cerebrovascular disease characterized by progressive stenosis of the terminal portion of the internal carotid artery and the circle of Willis.
Abasin Tajmalzai, MD, Asadullah Shirzai, MD, Din Mohammad Najah, MD   +2 more
doaj   +1 more source

Fibroblast growth factors 1 and 2 in cerebrospinal fluid are associated with HIV disease, methamphetamine use, and neurocognitive functioning. [PDF]

, 2016
BackgroundHuman immunodeficiency virus (HIV) and methamphetamine use commonly affect neurocognitive (NC) functioning. We evaluated the relationships between NC functioning and two fibroblast growth factors (FGFs) in volunteers who differed in HIV ...
Bharti, Ajay R, Cherner, Mariana, Ellis, Ronald J, Everall, Ian P, Grant, Igor, Heaton, Robert K, Letendre, Scott L, Masliah, Eliezer, Potter, Michael, Rosario, Debra, Woods, Steven Paul   +10 more
core   +2 more sources

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

Arteriopathy diagnosis in childhood arterial ischemic stroke: results of the vascular effects of infection in pediatric stroke study. [PDF]

, 2014
Background and purposeAlthough arteriopathies are the most common cause of childhood arterial ischemic stroke, and the strongest predictor of recurrent stroke, they are difficult to diagnose.
A. Abdalla, A. James Barkovich, A. Kirton, A. Yeh, A.K. Chan, B.H. Bjornson, C. Amlie-Lefond, C.K. Fox, Carlos Leiva-Salinas, G.S. Kovacevic, Gabrielle A. deVeber, Guangming Zhu, Heather J. Fullerton, J. Condie, J. Elbers, J.L. Carpenter, J.Y. Yager, Katherine Sear, L. Titomanlio, L.C. Jordan, L.P. Zou, M.A. Tan, M.F. Rafay, M.I. Hernandez Chavez, M.J. Lim, M.J. Rivkin, M.T. Mackay, Max Wintermark, Michael M. Dowling, Mitchell S.V. Elkind, N. Dlamini, Nancy K. Hills, Neil R. Friedman, O. Farooq, P. Humphreys, P. Pergami, Qinghua Hou, R. Forsyth, R. Kneen, Rebecca N. Ichord, S. Pavlakis, S.L. Benedict, S.M. Sultan, Timothy J. Bernard, V.C. Wong, W.D. Lo   +45 more
core   +1 more source

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