Results 111 to 120 of about 9,652 (216)

Cerebellar Venous Infarction Combined with Developmental Venous Anomaly and Contralateral Sinus Thrombosis

Вестник рентгенологии и радиологии
Developmental venous anomalies (DVA) are among the most common malformations, accounting for about 55% of all cerebral vascular anomalies. Most of them are asymptomatic, detected incidentally by brain magnetic resonance imaging and do not require ...
A. P. Demyanov, M. B. Dolgushin, T. M. Rostovtseva   +2 more
doaj   +1 more source

Incidence of subjective anosmia after interhemispheric approach to anterior skull pathology [PDF]

, 2008
Oral Poster Paper IIINTRODUCTION: Interhemispheric approach to anterior skull base pathology may cause damage to the olfactory nerve by traction with subsequent anosmia. This deficit may affect patient’s daily activities and work.
Leung, GKK, Li, LF
core  

[Cerebral cavernous malformations].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 2005
Cerebral cavernous malformations exist in sporadic and familial forms. They have considerable genetic and clinical heterogeneity. Better understanding of these disorders may improve management.This review is based on personal experience and recent literature.Cerebral cavernous malformations are venous malformations that can be detected with gradient ...
Jeanette, Koht, Geir J, Braathen, Dirk, Neubert, Michael Bjørn, Russell   +3 more
openaire   +1 more source

Ventriculoperitoneal shunt failure and infection: a retrospective review at Queen Mary Hospital [PDF]

, 2008
Oral Poster Paper IBACKGROUND: Ventriculoperitoneal shunting is a commonly performed procedure for diversion of cerebrospinal fluid. However shunt failure and infection results in significant morbidity and repeated operations.
Leung, G, Wong, PHD
core  

Intracranial cavernous angiomas [PDF]

, 2010
Objective: To describe the clinical presentation, diagnosis, and management of patients presenting with intracranial cavernous angiomas (CAs) at a tertiary care hospital in Pakistan.Study Design: Case series.
Bhatti, Atta-ul-Aleem, Enam, Ather, Kazim, Syed Faraz   +2 more
core   +1 more source

A novel PDCD10 gene mutation in cerebral cavernous malformations: a case report and review of the literature

Journal of Pain Research, 2019
Weiwei Yu, Haiqiang Jin, Qian You, Ding Nan, Yining HuangDepartment of Neurology, Peking University First Hospital, Beijing 100034, People’s Republic of ChinaAbstract: Cerebral cavernous malformations (CCMs) are one of the most common types of ...
Yu W, Jin H, You Q, Nan D, Huang Y
doaj  

Biology of vascular malformations of the brain [PDF]

, 2009
,, Al-Shahi Salman, Rustam, Awad, Issam A, Golanov, Eugene, Leblanc, Gabrielle G, Young, William L   +5 more
core   +1 more source

Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss families [PDF]

, 2018
Cavernous malformations (CCMs) are benign, well-circumscribed, and mulberry-like vascular malformations that may be found in the central nervous system in up to 0.5% of the population. Cavernous malformations can be sporadic or inherited.
Andermann, F., Baumann, C., Baumgartner, R., Bonassin, F., Georgiadis, D., Graeni, C., Merlo, A., Rouleau, G., Siegel, A., Stepper, F., Sturzenegger, M., Verlaan, D.   +11 more
core  

Blue rubber-bleb nevus syndrome: report of a familial case with a dural arteriovenous fistula [PDF]

, 2003
We report a case of a 45-year-old woman known to have a familial form of blue rubber-bleb nevus syndrome (BRBNS). The patient developed severe occipital headaches and bilateral retroauricular bruits.
Barbosa, V, Carvalho, S, Machado, E, Santos, N   +3 more
core  

Plasma biomarkers in patients with familial cavernous malformation and their first-degree relatives: a cross-sectional study

Scientific Reports
Familial cerebral cavernous malformation (FCCM), especially severe cases, impose a heavy physical and psychological burden on patients and their families.
Chunwang Li, Shuna Huang, Qixuan Li, Lingyun Zhuo, Yaqing Kang, Penghui Liu, Weilin Huang, Ke Ma, Xinru Lin, Weiheng Zhuang, Darong Chen, Huimin Wang, Lingjun Yan, Dengliang Wang, Yuanxiang Lin, Dezhi Kang, Fuxin Lin   +16 more
doaj   +1 more source