Results 201 to 204 of about 2,405 (204)

Spectrum and expression analysis of KRIT1 mutations in 121 consecutive and unrelated patients with Cerebral Cavernous Malformations

European Journal of Human Genetics, 2002
Anne Joutel, Elisabeth Tournier-Lasserve
exaly  

Familial cerebral cavernous malformation: Report of a novel KRIT1 mutation in a Portuguese family

Seizure: the Journal of the British Epilepsy Association, 2017
exaly  

Comprehensive analysis of Novel mutations in CCM1/KRIT1 and CCM2/MGC4607 and their clinical implications in Cerebral Cavernous malformations

Journal of Stroke and Cerebrovascular Diseases
Jorge M De Souza, Gustavo Galvão, Fontes-Dantas Fl   +2 more
exaly  

KRIT1: A Traffic Warden at the Busy Crossroads Between Redox Signaling and the Pathogenesis of Cerebral Cavernous Malformation Disease

Antioxidants and Redox Signaling
Andrea Perrelli, Chiara Ferraris, Angela J Glading   +2 more
exaly