BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

288 related articles for article (PubMed ID: 28318403)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Hyperkeratotic cutaneous vascular malformation associated with familial cerebral cavernous malformations (FCCM) with KRIT1/CCM1 mutation.
    Feldmeyer L; Baumann-Vogel H; Tournier-Lasserve E; Riant F; Jung HH; French LE; Kamarashev J
    Eur J Dermatol; 2014; 24(2):255-7. PubMed ID: 24721395
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 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. 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]  

  • 11. Vertebral Intraosseous Vascular Malformations in a Familial Cerebral Cavernous Malformation Population: Prevalence, Histologic Features, and Associations With CNS Disease.
    Tandberg SR; Bocklage T; Bartlett MR; Morrison LA; Nelson J; Hart BL
    AJR Am J Roentgenol; 2020 Feb; 214(2):428-436. PubMed ID: 31825263
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Multiple cerebral cavernous malformations: Clinical course of confirmed, assumed and non-familial disease.
    Santos AN; Rauschenbach L; Saban D; Chen B; Darkwah Oppong M; Herten A; Gull HH; Rieß C; Deuschl C; Schmidt B; Jabbarli R; Wrede KH; Zhu Y; Frank B; Sure U; Dammann P
    Eur J Neurol; 2022 May; 29(5):1427-1434. PubMed ID: 35060255
    [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. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. A Japanese pedigree of familial cerebral cavernous malformations--a case report.
    Imada Y; Yuki K; Migita K; Sadatomo T; Kuwabara M; Yamada T; Kurisu K
    Hiroshima J Med Sci; 2014 Dec; 63(4):43-8. PubMed ID: 25707093
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 15.