9 results on '"Bergametti, Francoise"'
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2. Genetics of cavernous angiomas
3. Recent insights into cerebral cavernous malformations: the molecular genetics of CCM
4. End‐Truncated LAMB1 Causes a Hippocampal Memory Defect and a Leukoencephalopathy.
5. Novel CCM2 missense variants abrogating the CCM1–CCM2 interaction cause cerebral cavernous malformations
6. Loss of α1β1 Soluble Guanylate Cyclase, the Major Nitric Oxide Receptor, Leads to Moyamoya and Achalasia
7. De novo mutations in CBL causing early-onset paediatric moyamoya angiopathy
8. Loss of BRCC3 Deubiquitinating Enzyme Leads to Abnormal Angiogenesis and Is Associated with Syndromic Moyamoya
9. Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease.
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