Improving genetic diagnostic yield in familial and sporadic cerebral cavernous malformations: detection of copy number and deep Intronic variants. [PDF]
Sikta N +18 more
europepmc +1 more source
Late-onset familial cerebral cavernous malformation without a family history: a case description. [PDF]
Zhang Z, Sun W, Wang Z, Wei L.
europepmc +1 more source
Silencing <i>KRIT1</i> Partially Reverses the Effects of Disturbed Flow on the Endothelial Cell Transcriptome. [PDF]
Meecham A +10 more
europepmc +1 more source
Recurrent somatic copy number alterations in resected cerebral cavernous malformations. [PDF]
Ressler AK +11 more
europepmc +1 more source
Temporal transcriptomic dynamics in rat spinal cord after tibial fracture unveil crosstalk between spinal cord and bone. [PDF]
Deng J +8 more
europepmc +1 more source
Data publication with the structural biology data grid supports live analysis [PDF]
Brett, Tom J, et al,, Tolia, Niraj H
core +2 more sources
Familial Cerebral Cavernous Malformations : A Clinical Series and Literature Review. [PDF]
Dogu H +5 more
europepmc +1 more source
Somatic Genetic Testing Provides Diagnosis of Verrucous Venous Malformation in an Individual with Discrepant Radiology, Pathology, and Clinical Findings. [PDF]
Britt A +9 more
europepmc +1 more source
Multiple cavernous malformations presenting in a patient with Poland syndrome: A case report [PDF]
core +1 more source
Cerebral Cavernous Malformation disease: characterization of new pathogenic mechanisms and development of nanotechnology-based therapeutic approaches [PDF]
Perrelli, Andrea +1 more
core

