Results 41 to 50 of about 2,246 (161)
Surgical treatment of the patient with sturge-weber syndrome-a case report [PDF]
, 2017 Gnatek Adrian, Osica Piotr, Janas-Naze Anna. Surgical treatment of the patient with sturge-weber syndrome-a case report. Journal of Education, Health and Sport. 2017;7(11):176-182. eISSN 2391-8306. DOI http://dx.doi.org/10.5281/zenodo.1049076 http://ojs.
Gnatek Adrian +2 more
core +3 more sources
Українська Інтервенційна Нейрорадіологія та Хірургія, 2023 Cavernous hemangiomas (CH) are benign vascular lesions of the central nervous system, which are thin-walled vascular sinusoids without smooth muscle with hemosiderin deposits.
M.S. Gudym, I.M. Bortnik, M.B. Vyval
doaj
III cranial nerve cavernous malformation: A case report and review of the literature [PDF]
, 2020 Background: Cavernous malformations generally occur in brain parenchyma but rarely these lesions arise from cranial nerves (CNs). Case Description: This paper described a case of a woman presented with III CN dysfunction due to the presence of a right ...
Altieri, R. +6 more
core +1 more source
Research Progress on the Posterior Midline Lumbar Spinous Process‐Splitting Approach
Orthopaedic Surgery, Volume 17, Issue 4, Page 990-998, April 2025.The lumbar spinous process‐splitting approach primarily involves three methods of splitting the spinous process: (A and B) Classic spinous process‐splitting technique: The spinous process is longitudinally split along the midline, with the base detached from the lamina to preserve the bilateral attachment of the paraspinal muscles.
Yizhong Ma +4 more
wiley +1 more source
Cerebral Cavernous Malformation: From Genetics to Pharmacotherapy
Brain and Behavior, Volume 15, Issue 1, January 2025.CCM1, CCM2, CCM3, MAP3K3, and PIK3CA genes mediate CCM pathogenesis by regulating the RhoA–ROCK, MAP3K3–KLF2/4, and PIK3CA–AKT–mTOR pathways, affecting processes such as cell migration, intercellular junctions, cell proliferation, inflammation, autophagy, EndMT, angiogenesis, and oxidative stress.
Zhuangzhuang Zhang +3 more
wiley +1 more source
Case Reports in Psychiatry, Volume 2025, Issue 1, 2025.Background: Neuroleptic malignant syndrome (NMS) is an idiosyncratic and life‐threatening side effect that usually occurs in response to dopamine receptor antagonist medications. Despite increased awareness, the diagnosis of NMS remains challenging due to its wide differential diagnoses, which can lead to delayed treatment and increased mortality or ...
Forouzan Elyasi +4 more
wiley +1 more source
Clinical study on CyberKnife for treating giant cavernous hemangioma in cavernous sinus region
Chinese Journal of Contemporary Neurology and Neurosurgery, 2015 Objective To investigate the efficacy and safety of CyberKnife for giant cavernous hemangioma in cavernous sinus. Methods The data of 7 cases of giant cavernous hemangioma in cavernous sinus region confirmed by imaging examination and treated with ...
Lu SUN +8 more
doaj
Chinese Journal of Contemporary Neurology and Neurosurgery, 2020 Objective To investigate the expression and mechanism of exosomal intercellular adhesion molecule ⁃ 1 (ICAM ⁃ 1) in patients with intracranial cavernous hemangioma (CCM) associated epilepsy.
Bin LI, Hui ZHOU, Ai⁃qin JIN
doaj
Cerebral vascular malformations: pathogenesis and therapy
MedComm, Volume 5, Issue 12, December 2024.CVMs management based on imaging genomics and liquid biopsy. In the future, somatic or de novo germline mutation information could be used to direct neurosurgical and medical management of CVMs. Somatic or germline variants can be acquired from imaging genomics or liquid biopsies preoperatively.
Qiheng He +11 more
wiley +1 more source
Familiäre Kavernome des Zentralnervensystems: Eine klinische und genetische Studie an 15 deutsche Familien [PDF]
, 2018 Zusammenfassung: 1928 beschrieb Hugo Friedrich Kufs erstmalig eine Familie mit zerebralen, retinalen und kutanen Kavernomen. Mittlerweile wurden über 300 weitere Familien beschrieben.
Andermann, E. +18 more
core