577 related articles for article (PubMed ID: 27153162)
1. 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]
2. Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations.
Rinaldi C; Bramanti P; Scimone C; Donato L; Alafaci C; D'Angelo R; Sidoti A
J Neurol Sci; 2017 Sep; 380():31-37. PubMed ID: 28870584
[TBL] [Abstract][Full Text] [Related]
3. [Gene mutations in patients with hereditary cavernous malformations].
Belousova OB; Bulygina ES; Okishev DN; Prohorchuk EB; Tsygankova SV; Pronin IN; Shishkina LV; Ryzhova MV; Skryabin KG; Konovalov AN
Zh Nevrol Psikhiatr Im S S Korsakova; 2017; 117(6):66-72. PubMed ID: 28745674
[TBL] [Abstract][Full Text] [Related]
4. Familial versus sporadic cavernous malformations: differences in developmental venous anomaly association and lesion phenotype.
Petersen TA; Morrison LA; Schrader RM; Hart BL
AJNR Am J Neuroradiol; 2010 Feb; 31(2):377-82. PubMed ID: 19833796
[TBL] [Abstract][Full Text] [Related]
5. Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations.
Scimone C; Bramanti P; Alafaci C; Granata F; Piva F; Rinaldi C; Donato L; Greco F; Sidoti A; D'Angelo R
J Mol Neurosci; 2017 Feb; 61(2):189-198. PubMed ID: 28000143
[TBL] [Abstract][Full Text] [Related]
6. Genetic Screening of Pediatric Cavernous Malformations.
Merello E; Pavanello M; Consales A; Mascelli S; Raso A; Accogli A; Cama A; Valeria C; De Marco P
J Mol Neurosci; 2016 Oct; 60(2):232-8. PubMed ID: 27561926
[TBL] [Abstract][Full Text] [Related]
7. Sporadic cerebral cavernous malformations: report of further mutations of CCM genes in 40 Italian patients.
D'Angelo R; Alafaci C; Scimone C; Ruggeri A; Salpietro FM; Bramanti P; Tomasello F; Sidoti A
Biomed Res Int; 2013; 2013():459253. PubMed ID: 24058906
[TBL] [Abstract][Full Text] [Related]
8. The venous angioarchitecture of sporadic cerebral cavernous malformations: a susceptibility weighted imaging study at 7 T MRI.
Dammann P; Wrede KH; Maderwald S; El Hindy N; Mueller O; Chen B; Zhu Y; Hütter BO; Ladd ME; Schlamann M; Sandalcioglu IE; Sure U
J Neurol Neurosurg Psychiatry; 2013 Feb; 84(2):194-200. PubMed ID: 23085932
[TBL] [Abstract][Full Text] [Related]
9. Biallelic somatic and germline mutations in cerebral cavernous malformations (CCMs): evidence for a two-hit mechanism of CCM pathogenesis.
Akers AL; Johnson E; Steinberg GK; Zabramski JM; Marchuk DA
Hum Mol Genet; 2009 Mar; 18(5):919-30. PubMed ID: 19088123
[TBL] [Abstract][Full Text] [Related]
10. DNA promoter methylation of CCM genes in human cerebral cavernous malformations: Importance of confirming MSP data through sequencing.
Saban D; Larisch J; Nickel AC; Pierscianek D; Dammann P; Sure U; Zhu Y
Eur J Med Genet; 2020 Dec; 63(12):104090. PubMed ID: 33122157
[TBL] [Abstract][Full Text] [Related]
11. Molecular diagnosis in cerebral cavernous malformations.
Mondejar R; Lucas M
Neurologia; 2017 Oct; 32(8):540-545. PubMed ID: 26304651
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Genomic causes of multiple cerebral cavernous malformations in a Japanese population.
Tsutsumi S; Ogino I; Miyajima M; Ikeda T; Shindo N; Yasumoto Y; Ito M; Arai H
J Clin Neurosci; 2013 May; 20(5):667-9. PubMed ID: 23485406
[TBL] [Abstract][Full Text] [Related]
14. Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 gene.
Garaci F; Marsili L; Riant F; Marziali S; Cécillon M; Pasquarelli R; Sangiuolo F; Floris R; Novelli G; Tournier-Lasserve E; Brancati F
Neuroradiol J; 2015 Jun; 28(3):289-93. PubMed ID: 26246098
[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. Clinical features of cerebral cavernous malformations patients with KRIT1 mutations.
Denier C; Labauge P; Brunereau L; Cavé-Riant F; Marchelli F; Arnoult M; Cecillon M; Maciazek J; Joutel A; Tournier-Lasserve E; ;
Ann Neurol; 2004 Feb; 55(2):213-20. PubMed ID: 14755725
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Lesions from patients with sporadic cerebral cavernous malformations harbor somatic mutations in the CCM genes: evidence for a common biochemical pathway for CCM pathogenesis.
McDonald DA; Shi C; Shenkar R; Gallione CJ; Akers AL; Li S; De Castro N; Berg MJ; Corcoran DL; Awad IA; Marchuk DA
Hum Mol Genet; 2014 Aug; 23(16):4357-70. PubMed ID: 24698976
[TBL] [Abstract][Full Text] [Related]
19. Postzygotic mosaicism in cerebral cavernous malformation.
Rath M; Pagenstecher A; Hoischen A; Felbor U
J Med Genet; 2020 Mar; 57(3):212-216. PubMed ID: 31446422
[TBL] [Abstract][Full Text] [Related]
20. Mutation prevalence of cerebral cavernous malformation genes in Spanish patients.
Mondéjar R; Solano F; Rubio R; Delgado M; Pérez-Sempere A; González-Meneses A; Vendrell T; Izquierdo G; Martinez-Mir A; Lucas M
PLoS One; 2014; 9(1):e86286. PubMed ID: 24466005
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
