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Cerebral vascular malformations adjacent to sensorimotor and visual cortex. Functional magnetic resonance imaging studies before and after therapeutic intervention.
Pathobiology of human cerebrovascular malformations: basic mechanisms and clinical relevance.
Cerebral cavernous malformations proteins inhibit Rho kinase to stabilize vascular integrity.
What genes can teach us about human cerebrovascular malformations.
Functional anatomy of the human supplementary sensorimotor area: results of extraoperative electrical stimulation.
Endothelial TLR4 and the microbiome drive cerebral cavernous malformations.
The cerebral cavernous malformation disease causing gene KRIT1 participates in intestinal epithelial barrier maintenance and regulation.
Cerebral cavernous malformations form an anticoagulant vascular domain in humans and mice.
Distinct cellular roles for PDCD10 define a gut-brain axis in cerebral cavernous malformation.
Cerebral Cavernous Malformation Proteins in Barrier Maintenance and Regulation.
Permissive microbiome characterizes human subjects with a neurovascular disease cavernous angioma.
Abortive intussusceptive angiogenesis causes multi-cavernous vascular malformations.
Cerebral Cavernous Malformation: From Mechanism to Therapy.