Objective To detect the mutations of Krit-1 gene that cause familial cerebral cavernous malformation (CCM) in the Han ethnic origin.
目的探查汉族家族性中枢神经系统海绵状血管畸形(CCM)的突变基因。
Endovascular treatments were studied in 10 cases of cerebral vascular disease, including intracranial aneurysms, cerebral vascular malformation, carotid-cavernous fistula.
总结了血管内介入治疗颅内动脉瘤、脑血管畸形、颈内动脉—海绵窦瘘共10例的体会。
Endovascular treatments were studied in 10 cases of cerebral vascular disease, including intracranial aneurysms, cerebral vascular malformation, carotid-cavernous fistula.
总结了血管内介入治疗颅内动脉瘤、脑血管畸形、颈内动脉—海绵窦瘘共10例的体会。
应用推荐