Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Seizures and KRIT1[original query] |
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Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity. Cerebrovascular diseases (Basel, Switzerland) 2014 38 (6): 433-40. Choquet Hélène, Pawlikowska Ludmila, Nelson Jeffrey, McCulloch Charles E, Akers Amy, Baca Beth, Khan Yasir, Hart Blaine, Morrison Leslie, Kim Helen, |
Genome-wide Genotyping of Cerebral Cavernous Malformation Type 1 Individuals to Identify Genetic Modifiers of Disease Severity. Methods in molecular biology (Clifton, N.J.) 2020 6 2152 77-84. Choquet Hélène, Kim Hel |
Polymorphisms in genes related to oxidative stress and inflammation: Emerging links with the pathogenesis and severity of Cerebral Cavernous Malformation disease. Free radical biology & medicine 2021 6 172 403-417. Perrelli Andrea, Retta Saverio Frances |
Molecular genetic features and clinical manifestations in Chinese familial cerebral cavernous malformation: from a novel KRIT1/CCM1 mutation (c.1119dupT) to an overall view. Frontiers in neuroscience 2023 5 17 1184333. Yanming Chen, Xuchen Dong, Ye Wang, Haijun Lv, Nan Chen, Zhongyong Wang, Si Chen, Ping Chen, Sheng Xiao, Jizong Zhao, Jun Do |
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 : the official journal of National Stroke Association 2024 8 107947. Gustavo da Fontoura Galvão, Luisa Menezes Trefilio, Andreza Lemos Salvio, Elielson Veloso da Silva, Soniza Vieira Alves-Leon, Fabrícia Lima Fontes-Dantas, Jorge Marcondes de Sou |
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