340 related articles for article (PubMed ID: 24034083)
1. Features of a Chinese family with cerebral cavernous malformation induced by a novel CCM1 gene mutation.
Wang X; Liu XW; Lee N; Liu QJ; Li WN; Han T; Wei KK; Qiao S; Chi ZF
Chin Med J (Engl); 2013; 126(18):3427-32. PubMed ID: 24034083
[TBL] [Abstract][Full Text] [Related]
2. A novel CCM1 gene mutation causes cerebral cavernous malformation in a Chinese family.
Zhao Y; Xie L; Li P; Song J; Qu T; Fan W; Chen H; Chen D; Lu D; Zhou L; Mao Y
J Clin Neurosci; 2011 Jan; 18(1):61-5. PubMed ID: 20884211
[TBL] [Abstract][Full Text] [Related]
3. Spectrum of genotype and clinical manifestations in cerebral cavernous malformations.
Gault J; Sain S; Hu LJ; Awad IA
Neurosurgery; 2006 Dec; 59(6):1278-84; discussion 1284-5. PubMed ID: 17277691
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Identification of a c.601C>G mutation in the CCM1 gene in a kindred with multiple skin, spinal and cerebral cavernous malformations.
Haghighi A; Fathi D; Shahbazi M; Motahari MM; Friedman B
J Neurol Sci; 2013 Nov; 334(1-2):97-101. PubMed ID: 24007869
[TBL] [Abstract][Full Text] [Related]
7. Variable expression of cerebral cavernous malformations in carriers of a premature termination codon in exon 17 of the Krit1 gene.
Lucas M; Costa AF; García-Moreno JM; Solano F; Gamero MA; Izquierdo G
BMC Neurol; 2003 Jul; 3():5. PubMed ID: 12877753
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [Identification of a novel inheritable CCM1 gene mutation of 671del AT in a Chinese family with cerebral cavernous malformation].
Mao Y; Zhao Y; Zhou LF; Huang CX; Shou XF; Gong JL
Zhonghua Yi Xue Za Zhi; 2003 Sep; 83(18):1572-5. PubMed ID: 14642111
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. C329X in KRIT1 is a founder mutation among CCM patients in Sardinia.
Cau M; Loi M; Melis M; Congiu R; Loi A; Meloni C; Serrenti M; Addis M; Melis MA
Eur J Med Genet; 2009; 52(5):344-8. PubMed ID: 19454328
[TBL] [Abstract][Full Text] [Related]
12. Deep intronic KRIT1 mutation in a family with clinically silent multiple cerebral cavernous malformations.
Riant F; Odent S; Cecillon M; Pasquier L; de Baracé C; Carney MP; Tournier-Lasserve E
Clin Genet; 2014 Dec; 86(6):585-8. PubMed ID: 24251678
[TBL] [Abstract][Full Text] [Related]
13. Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex.
Stahl S; Gaetzner S; Voss K; Brackertz B; Schleider E; Sürücü O; Kunze E; Netzer C; Korenke C; Finckh U; Habek M; Poljakovic Z; Elbracht M; Rudnik-Schöneborn S; Bertalanffy H; Sure U; Felbor U
Hum Mutat; 2008 May; 29(5):709-17. PubMed ID: 18300272
[TBL] [Abstract][Full Text] [Related]
14. Biallelic somatic and germ line CCM1 truncating mutations in a cerebral cavernous malformation lesion.
Gault J; Shenkar R; Recksiek P; Awad IA
Stroke; 2005 Apr; 36(4):872-4. PubMed ID: 15718512
[TBL] [Abstract][Full Text] [Related]
15. A novel KRIT1 gene mutation in a patient with cerebral and multiple spinal cavernous malformations.
Lee YW; Lee ST; Cha JG; Park JH; Jeon BR; Lee YK; Kim JW; Ki CS
Ann Clin Lab Sci; 2010; 40(3):290-4. PubMed ID: 20689144
[TBL] [Abstract][Full Text] [Related]
16. Value of gradient-echo magnetic resonance imaging in the diagnosis of familial cerebral cavernous malformation.
Lehnhardt FG; von Smekal U; Rückriem B; Stenzel W; Neveling M; Heiss WD; Jacobs AH
Arch Neurol; 2005 Apr; 62(4):653-8. PubMed ID: 15824268
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Spectrum and expression analysis of KRIT1 mutations in 121 consecutive and unrelated patients with Cerebral Cavernous Malformations.
Cavé-Riant F; Denier C; Labauge P; Cécillon M; Maciazek J; Joutel A; Laberge-Le Couteulx S; Tournier-Lasserve E
Eur J Hum Genet; 2002 Nov; 10(11):733-40. PubMed ID: 12404106
[TBL] [Abstract][Full Text] [Related]
20. CCM1 gene deletion identified by MLPA in cerebral cavernous malformation.
Gaetzner S; Stahl S; Sürücü O; Schaafhausen A; Halliger-Keller B; Bertalanffy H; Sure U; Felbor U
Neurosurg Rev; 2007 Apr; 30(2):155-9; discussion 159-60. PubMed ID: 17187287
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
