These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
393 related articles for article (PubMed ID: 32113992)
1. Novel CCM1 (KRIT1) Mutation Detection in Brazilian Familial Cerebral Cavernous Malformation: Different Genetic Variants in Inflammation, Oxidative Stress, and Drug Metabolism Genes Affect Disease Aggressiveness. Fontes-Dantas FL; da Fontoura Galvão G; Veloso da Silva E; Alves-Leon S; Cecília da Silva Rêgo C; Garcia DG; Marques SA; Blanco Martinez AM; Reis da Silva M; Marcondes de Souza J World Neurosurg; 2020 Jun; 138():535-540.e8. PubMed ID: 32113992 [TBL] [Abstract][Full Text] [Related]
2. Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity. Choquet H; Pawlikowska L; Nelson J; McCulloch CE; Akers A; Baca B; Khan Y; Hart B; Morrison L; Kim H; Cerebrovasc Dis; 2014; 38(6):433-40. PubMed ID: 25472749 [TBL] [Abstract][Full Text] [Related]
3. Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1. Choquet H; Trapani E; Goitre L; Trabalzini L; Akers A; Fontanella M; Hart BL; Morrison LA; Pawlikowska L; Kim H; Retta SF Free Radic Biol Med; 2016 Mar; 92():100-109. PubMed ID: 26795600 [TBL] [Abstract][Full Text] [Related]
4. First Report of Concomitant Pathogenic Mutations Within MGC4607/CCM2 and KRIT1/CCM1 in a Familial Cerebral Cavernous Malformation Patient. da Fontoura Galvão G; Veloso da Silva E; Fontes-Dantas FL; Filho RC; Alves-Leon S; Marcondes de Souza J World Neurosurg; 2020 Oct; 142():481-486.e1. PubMed ID: 32615293 [TBL] [Abstract][Full Text] [Related]
5. A novel CCM1/KRIT1 heterozygous deletion mutation (c.1919delT) in a Chinese family with familial cerebral cavernous malformation. Yang C; Wu B; Zhong H; Li Y; Zheng X; Xu Y Clin Neurol Neurosurg; 2018 Jan; 164():44-46. PubMed ID: 29169046 [TBL] [Abstract][Full Text] [Related]
6. Comprehensive analysis of Novel mutations in CCM1/KRIT1 and CCM2/MGC4607 and their clinical implications in Cerebral Cavernous malformations. Galvão GDF; Trefilio LM; Salvio AL; da Silva EV; Alves-Leon SV; Fontes-Dantas FL; de Souza JM J Stroke Cerebrovasc Dis; 2024 Nov; 33(11):107947. PubMed ID: 39181174 [TBL] [Abstract][Full Text] [Related]
7. Polymorphisms in genes related to oxidative stress and inflammation: Emerging links with the pathogenesis and severity of Cerebral Cavernous Malformation disease. Perrelli A; Retta SF Free Radic Biol Med; 2021 Aug; 172():403-417. PubMed ID: 34175437 [TBL] [Abstract][Full Text] [Related]
8. Association of cardiovascular risk factors with disease severity in cerebral cavernous malformation type 1 subjects with the common Hispanic mutation. Choquet H; Nelson J; Pawlikowska L; McCulloch CE; Akers A; Baca B; Khan Y; Hart B; Morrison L; Kim H Cerebrovasc Dis; 2014; 37(1):57-63. PubMed ID: 24401931 [TBL] [Abstract][Full Text] [Related]
9. Novel KRIT1/CCM1 mutation in a patient with retinal cavernous hemangioma and cerebral cavernous malformation. Reddy S; Gorin MB; McCannel TA; Tsui I; Straatsma BR Graefes Arch Clin Exp Ophthalmol; 2010 Sep; 248(9):1359-61. PubMed ID: 20306072 [TBL] [Abstract][Full Text] [Related]
10. Exome capture sequencing identifies a novel CCM1 mutation in a Chinese family with multiple cerebral cavernous malformations. Mao CY; Yang J; Zhang SY; Luo HY; Song B; Liu YT; Wu J; Sun SL; Yang ZH; Du P; Wang YH; Shi CH; Xu YM Int J Neurosci; 2016 Dec; 126(12):1071-6. PubMed ID: 26643368 [TBL] [Abstract][Full Text] [Related]
11. Novel loss of function mutation in KRIT1/CCM1 is associated with distinctly progressive cerebral and spinal cavernous malformations after radiochemotherapy for intracranial malignant germ cell tumor. Russo A; Neu MA; Theruvath J; Kron B; Wingerter A; Hey-Koch S; Tanyildizi Y; Faber J Childs Nerv Syst; 2017 Aug; 33(8):1275-1283. PubMed ID: 28488085 [TBL] [Abstract][Full Text] [Related]
12. KRIT1 loss-of-function induces a chronic Nrf2-mediated adaptive homeostasis that sensitizes cells to oxidative stress: Implication for Cerebral Cavernous Malformation disease. Antognelli C; Trapani E; Delle Monache S; Perrelli A; Daga M; Pizzimenti S; Barrera G; Cassoni P; Angelucci A; Trabalzini L; Talesa VN; Goitre L; Retta SF Free Radic Biol Med; 2018 Feb; 115():202-218. PubMed ID: 29170092 [TBL] [Abstract][Full Text] [Related]
13. A Novel KRIT1/CCM1 Gene Insertion Mutation Associated with Cerebral Cavernous Malformations in a Chinese Family. Wang H; Pan Y; Zhang Z; Li X; Xu Z; Suo Y; Li W; Wang Y J Mol Neurosci; 2017 Feb; 61(2):221-226. PubMed ID: 28160210 [TBL] [Abstract][Full Text] [Related]
14. Correlation of the venous angioarchitecture of multiple cerebral cavernous malformations with familial or sporadic disease: a susceptibility-weighted imaging study with 7-Tesla MRI. Dammann P; Wrede K; Zhu Y; Matsushige T; Maderwald S; Umutlu L; Quick HH; Hehr U; Rath M; Ladd ME; Felbor U; Sure U J Neurosurg; 2017 Feb; 126(2):570-577. PubMed ID: 27153162 [TBL] [Abstract][Full Text] [Related]
15. High-throughput sequencing of the entire genomic regions of CCM1/KRIT1, CCM2 and CCM3/PDCD10 to search for pathogenic deep-intronic splice mutations in cerebral cavernous malformations. Rath M; Jenssen SE; Schwefel K; Spiegler S; Kleimeier D; Sperling C; Kaderali L; Felbor U Eur J Med Genet; 2017 Sep; 60(9):479-484. PubMed ID: 28645800 [TBL] [Abstract][Full Text] [Related]
16. A novel KRIT1/CCM1 mutation accompanied by a NOTCH3 mutation in a Chinese family with multiple cerebral cavernous malformations. Li C; Liu P; Huang W; Wang H; Ma K; Zhuo L; Kang Y; He Q; Lin Y; Kang D; Lin F Neurogenetics; 2023 Apr; 24(2):137-146. PubMed ID: 36892712 [TBL] [Abstract][Full Text] [Related]
17. A Novel CCM1/KRIT1 Heterozygous Nonsense Mutation (c.1864C>T) Associated with Familial Cerebral Cavernous Malformation: a Genetic Insight from an 8-Year Continuous Observational Study. Yang C; Nicholas VH; Zhao J; Wu B; Zhong H; Li Y; Xu Y J Mol Neurosci; 2017 Apr; 61(4):511-523. PubMed ID: 28255959 [TBL] [Abstract][Full Text] [Related]
18. Clinical, magnetic resonance imaging, and genetic study of 5 Italian families with cerebral cavernous malformation. Battistini S; Rocchi R; Cerase A; Citterio A; Tassi L; Lando G; Patrosso MC; Galli R; Brunori P; Sgrò DL; Pitillo G; Lo Russo G; Marocchi A; Penco S Arch Neurol; 2007 Jun; 64(6):843-8. PubMed ID: 17562932 [TBL] [Abstract][Full Text] [Related]
19. KRIT1 Gene in Patients with Cerebral Cavernous Malformations: Clinical Features and Molecular Characterization of Novel Variants. Ricci C; Cerase A; Riolo G; Manasse G; Battistini S J Mol Neurosci; 2021 Sep; 71(9):1876-1883. PubMed ID: 33651268 [TBL] [Abstract][Full Text] [Related]
20. Familial cerebral cavernous malformation: Report of a novel KRIT1 mutation in a Portuguese family. Rosário Marques I; Antunes F; Ferreira N; Grunho M Seizure; 2017 Dec; 53():72-74. PubMed ID: 29145060 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]