Results 181 to 190 of about 3,837 (194)
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A British family with familial cerebral cavernous malformation due to a rare mutation of the CCM2 gene

Acta Neurologica Belgica, 2020
Muhammed Noushad   +3 more
openaire   +1 more source

STK25 Protein Mediates TrkA and CCM2 Protein-dependent Death in Pediatric Tumor Cells of Neural Origin

Journal of Biological Chemistry, 2012
Derek F Ceccarelli   +2 more
exaly  

Familial cerebral cavernous malformations associated with a splice-site CCM2 deletion

Journal of Neurology, 2009
Adolfo Jiménez-Huete   +7 more
openaire   +1 more source

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   +2 more
exaly  

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