Results 121 to 130 of about 4,624 (210)

Novel Development of a Large Cerebral Cavernous Malformation in an Adolescent With a History of Familial Cerebral Cavernous Malformation Syndrome

open access: yesCureus
Cerebral cavernous malformations (CCM) are capillary vascular malformations of the central nervous system (CNS). These lesions can be either familial or sporadic. We present a case of a 16-year-old girl with familial CCM syndrome who presented with a six-
Mary G McIntosh, Laura L Hayes
semanticscholar   +1 more source

Doctor of Philosophy [PDF]

open access: yes, 2011
dissertationCerebral cavernous malformation (CCM), or cavernous angioma, is a common disease that can occur sporadically or familially with autosomal dominant inheritance. CCMs are vascular malformations, predominantly in the brain, consisting of dilated,
Chan, Aubrey C.
core  

CCM2 Molecular Signaling Pathway [PDF]

open access: yes, 2009
Cerebral cavernous malformations (CCM) are a central nervous system vascular malformation often responsible for hemorrhagic strokes. Molecular genetic studies have identified three genes (CCMl KRITI, CCM2 Malcavernin, and CCM3 PDCDIO) and four possible ...
Boylan, Arianne J.
core   +1 more source

UEG Week 2024 Poster Presentations

open access: yes
United European Gastroenterology Journal, Volume 12, Issue S8, Page 665-1360, October 2024.
wiley   +1 more source

Improved differentiation of cavernous malformation and acute intraparenchymal hemorrhage on CT using an AI algorithm

open access: yesScientific Reports
This study aimed to evaluate the utility of an artificial intelligence (AI) algorithm in differentiating between cerebral cavernous malformation (CCM) and acute intraparenchymal hemorrhage (AIH) on brain computed tomography (CT).
Jung Youn Kim   +3 more
doaj   +1 more source

Biology of vascular malformations of the brain [PDF]

open access: yes, 2009
,   +5 more
core   +1 more source

Genetics and Molecular Biology of Cerebral Cavernous Malformations and CCM Italia

open access: yes, 2012
Loss-of-function mutations of the KRIT1 gene (CCM1) have been associated with the pathogenesis of Cerebral Cavernous Malformations (CCM), a major cerebrovascular disease characterized by abnormally enlarged and leaky capillaries that predispose to seizures, focal neurological deficits, and fatal intracerebral haemorrhage.
openaire   +1 more source

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