Results 11 to 20 of about 8,444 (208)

Case Report: A novel heterozygous nonsense mutation in KRIT1 cause hereditary cerebral cavernous malformation [PDF]

Frontiers in Oncology, 2023
Cerebral cavernous malformation (CCM) is a vascular malformation of the central nervous system and mainly characterized by enlarged capillary cavities without intervening brain parenchyma. Genetic studies have identified three disease-causing genes (CCM1/
Zhenxing Liu, Kaikai Guo, Xuebin Hu, Xianqin Zhang   +3 more
doaj   +2 more sources

Case report: Thrombolysis in patients with acute ischemic stroke and cerebral cavernous malformation [PDF]

Frontiers in Neurology, 2023
Lin J, Weng X, Zheng J, Wu S, Bao Q, Peng F, Huang Y.   +6 more
exaly   +2 more sources

Intracranial Hemorrhage Rate and Lesion Burden in Patients With Familial Cerebral Cavernous Malformation [PDF]

Journal of the American Heart Association, 2023
Shantel Weinsheimer, Cynthia Tsang, Obiora Okoye   +2 more
exaly   +2 more sources

Impact of socioeconomics and race on clinical follow-up and trial enrollment and adherence in cerebral cavernous malformation [PDF]

Journal of Stroke and Cerebrovascular Diseases, 2023
Stephanie Hage, Matthew Hagan, Agnieszka Stadnik   +2 more
exaly   +2 more sources

Progress on clinical characteristics and pathogenesis of cerebral cavernous malformation in children

Chinese Journal of Contemporary Neurology and Neurosurgery, 2023
Cerebral cavernous malformation is the second most common vascular malformation of the central nervous system. The main clinical manifestations in children include epileptic seizure, spontaneous cerebral hemorrhage, and focal neurological deficits.
HAN Guo⁃qing, PU Ke, LI Qing⁃guo
doaj   +1 more source

Dural based cavernoma of cerebral convexity – A rare case report

Interdisciplinary Neurosurgery, 2023
Cerebral cavernous malformations occur in about 0.4–0.5 % of the population. They account for about 5–13 % of all vascular malformations of the central nervous system, commonly occurring in the cerebral parenchyma.
H. Mohamed Naleer, V. Vivek, Rav Tej Bathala, Venkata Shashank Davuluri, Jishnu, K. Ganesh, Lawrence D. Cruze   +6 more
doaj   +1 more source

A Chinese Family With Cerebral Cavernous Malformation Caused by a Frameshift Mutation of the CCM1 Gene: A Case Report and Review of the Literature

Frontiers in Neurology, 2022
BackgroundFamilial cerebral cavernous malformation (FCCM) is a vascular malformation disease closely linked to three identified genes: KRIT1/CCM1, MGC4607/CCM2 and PDCD10/CCM3.
Wenyu Liu, Wenyu Liu, Ming Liu, Ming Liu, Di Lu, Di Lu, Jiwei Wang, Jiwei Wang, Zexin Cao, Zexin Cao, Xuchen Liu, Xuchen Liu, Zichao Feng, Zichao Feng, Bin Huang, Bin Huang, Xinyu Wang, Xinyu Wang   +17 more
doaj   +1 more source

Case report: A second case of cerebral cavernous malformation after high-dose chemotherapy for medulloblastoma [PDF]

Frontiers in Oncology
Pionelli MG, Mazio F, Errico ME, Russo C, Cristofano A, Covelli EM, Donofrio V, Capasso M, Capozza MA, De Gregorio F, Ruotolo S, Abate ME, Cinalli G.   +12 more
exaly   +2 more sources

Cerebral cavernous malformations and epilepsy [PDF]

Neurosurgical Focus, 2006
✓Seizures and epilepsy are frequent clinical manifestations of cerebral cavernous malformations (CCMs) and represent the most common symptomatic presentation of supratentorial lesions. Clinicians often diagnose CCMs in patients after a first seizure, or in some cases after obtaining neuroimaging studies in patients suffering from chronic epilepsy ...
Issam, Awad, Pascal, Jabbour
openaire   +2 more sources

Diagnosis and treatment status of suprasellar optic pathway cavernous malformations

Journal of International Medical Research, 2023
Cerebral cavernous malformations constitute a subtype of cerebral vascular malformation typically located in the cerebral cortex. However, their occurrence in the suprasellar optic pathway is relatively rare.
Songbai Xu, Liu Yang
doaj   +1 more source