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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Seizures and KRIT1[original query]
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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