533 related articles for article (PubMed ID: 25556204)
1. Increased number of white matter lesions in patients with familial cerebral cavernous malformations.
Golden MJ; Morrison LA; Kim H; Hart BL
AJNR Am J Neuroradiol; 2015 May; 36(5):899-903. PubMed ID: 25556204
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. Familial Cerebral Cavernous Malformations Are Associated with Adrenal Calcifications on CT Scans: An Imaging Biomarker for a Hereditary Cerebrovascular Condition.
Strickland CD; Eberhardt SC; Bartlett MR; Nelson J; Kim H; Morrison LA; Hart BL
Radiology; 2017 Aug; 284(2):443-450. PubMed ID: 28318403
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. CCM1 mutation screen of sporadic cases with cerebral cavernous malformations.
Verlaan DJ; Laurent SB; Sure U; Bertalanffy H; Andermann E; Andermann F; Rouleau GA; Siegel AM
Neurology; 2004 Apr; 62(7):1213-5. PubMed ID: 15079030
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Familial Cerebral Cavernous Malformation Syndrome with Concomitant Fourth Ventricular Ependymoma: True Association or Mere Coincidence?
Algattas H; Abou-Al-Shaar H; Mendelson M; Arnold GL; Felker J; Meade J; Greene S
Cancer Genet; 2020 Jun; 244():36-39. PubMed ID: 32434131
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Cutaneous findings of familial cerebral cavernous malformation syndrome due to the common Hispanic mutation.
Manole AK; Forrester VJ; Zlotoff BJ; Hart BL; Morrison LA
Am J Med Genet A; 2020 May; 182(5):1066-1072. PubMed ID: 32100472
[TBL] [Abstract][Full Text] [Related]
16. Familial cerebral cavernous malformations: Rio de Janeiro study and review of the recommendations for management.
Domingues F; Gasparetto EL; Andrade R; Noro F; Eiras A; Gault J; Correia CE; de Souza JM
Arq Neuropsiquiatr; 2008 Dec; 66(4):795-9. PubMed ID: 19099113
[TBL] [Abstract][Full Text] [Related]
17. Genotype-phenotype correlations in cerebral cavernous malformations patients.
Denier C; Labauge P; Bergametti F; Marchelli F; Riant F; Arnoult M; Maciazek J; Vicaut E; Brunereau L; Tournier-Lasserve E
Ann Neurol; 2006 Nov; 60(5):550-556. PubMed ID: 17041941
[TBL] [Abstract][Full Text] [Related]
18. KRIT1/cerebral cavernous malformation 1 protein localizes to vascular endothelium, astrocytes, and pyramidal cells of the adult human cerebral cortex.
Guzeloglu-Kayisli O; Amankulor NM; Voorhees J; Luleci G; Lifton RP; Gunel M
Neurosurgery; 2004 Apr; 54(4):943-9; discussion 949. PubMed ID: 15046662
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 mutations.
Gianfrancesco F; Cannella M; Martino T; Maglione V; Esposito T; Innocenzi G; Vitale E; Liquori CL; Marchuk DA; Squitieri F
Am J Med Genet B Neuropsychiatr Genet; 2007 Jul; 144B(5):691-5. PubMed ID: 17440989
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]