BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

97 related articles for article (PubMed ID: 24238821)

  • 1. Status epilepsy in CCM with KRIT1 gene change.
    Craft EV; Vasudevan PC
    Eur J Paediatr Neurol; 2014 Mar; 18(2):241-2. PubMed ID: 24238821
    [No Abstract]   [Full Text] [Related]  

  • 2. Large Cystic Cavernous Malformation in Infant with Novel KRIT1 Gene Abnormality.
    Lu VM; Daniels DJ
    World Neurosurg; 2019 Oct; 130():304-305. PubMed ID: 31326642
    [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. Search for loss of heterozygosity and mutation analysis of KRIT1 gene in CCM patients.
    Marini V; Ferrera L; Pigatto F; Origone P; Garrè C; Dorcaratto A; Viale G; Alberti F; Mareni C
    Am J Med Genet A; 2004 Sep; 130A(1):98-101. PubMed ID: 15368504
    [No Abstract]   [Full Text] [Related]  

  • 5. Cerebral cavernous malformations: mutations in Krit1.
    Verlaan DJ; Davenport WJ; Stefan H; Sure U; Siegel AM; Rouleau GA
    Neurology; 2002 Mar; 58(6):853-7. PubMed ID: 11914398
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cerebral cavernous malformation: clinical report of two families with variable phenotype associated with KRIT1 mutation.
    Balasubramanian M; Jain V; Glover RC; Robertson LK; Mordekar SR
    Eur J Paediatr Neurol; 2013 Nov; 17(6):661-5. PubMed ID: 23806994
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mystery Case: Cutaneous lesions in KRIT1-associated cerebral cavernous malformations.
    Brownlee WJ; Roxburgh R
    Neurology; 2014 Sep; 83(14):e133-4. PubMed ID: 25267988
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 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. Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
    Limaye N; Revencu N; Van Regemorter N; Garzon M; Bonduelle M; Chung W; Daras MD; Fahey MC; Garrett C; Gillerot Y; Gillessen-Kaesbach G; Giménez-Arnau A; Guzzetta F; Battaglia D; Heimda K; Lissens W; Taub E; Van Maldergem L; Van Paesschen W; Wieczorek D; Wood NW; Boon L; Vikkula M
    Hum Genet; 2007 Dec; 122(5):549. PubMed ID: 18380023
    [No Abstract]   [Full Text] [Related]  

  • 11. Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
    Limaye N; Revencu N; Van Regemorter N; Garzon M; Bonduelle M; Chung W; Daras MD; Fahey MC; Garrett C; Gillerot Y; Gillessen-Kaesbach G; Giménez-Arnau A; Guzzetta F; Battaglia D; Heimda K; Lissens W; Taub E; Van Maldergem L; Van Paesschen W; Wieczorek D; Wood NW; Boon L; Vikkula M
    Hum Genet; 2007 Dec; 122(5):549-50. PubMed ID: 18383587
    [No Abstract]   [Full Text] [Related]  

  • 12. Blue papules in a patient with neurologic symptoms.
    Wang CM; Motaparthi K; Grekin SJ; Hsu S
    JAMA Dermatol; 2013 Jan; 149(1):97-102. PubMed ID: 23324766
    [No Abstract]   [Full Text] [Related]  

  • 13. Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
    Limaye N; Revencu N; Van Regemorter N; Garzon M; Bonduelle M; Chung W; Daras MD; Fahey MC; Garrett C; Gillerot Y; Gillessen-Kaesbach G; Giménez-Arnau A; Guzzetta F; Battaglia D; Heimdal K; Lissens W; Taub E; Van Maldergem L; Van Paesschen W; Wieczorek D; Wood NW; Boon L; Vikkula M
    Hum Genet; 2007 Dec; 122(5):551. PubMed ID: 18383595
    [No Abstract]   [Full Text] [Related]  

  • 14. KRIT1 loss of function causes a ROS-dependent upregulation of c-Jun.
    Goitre L; De Luca E; Braggion S; Trapani E; Guglielmotto M; Biasi F; Forni M; Moglia A; Trabalzini L; Retta SF
    Free Radic Biol Med; 2014 Mar; 68(100):134-47. PubMed ID: 24291398
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Identification of a novel KRIT1 mutation in an Italian family with cerebral cavernous malformation by the protein truncation test.
    Marini V; Ferrera L; Dorcaratto A; Viale G; Origone P; Mareni C; Garrè C
    J Neurol Sci; 2003 Aug; 212(1-2):75-8. PubMed ID: 12810002
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A splice-site mutation in CCM1/KRIT1 is associated with retinal and cerebral cavernous hemangioma.
    Kitzmann AS; Pulido JS; Ferber MJ; Highsmith WE; Babovic-Vuksanovic D
    Ophthalmic Genet; 2006 Dec; 27(4):157-9. PubMed ID: 17148043
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Recent insights into cerebral cavernous malformations: the molecular genetics of CCM.
    Riant F; Bergametti F; Ayrignac X; Boulday G; Tournier-Lasserve E
    FEBS J; 2010 Mar; 277(5):1070-5. PubMed ID: 20096038
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cerebral cavernous malformations associated with cutaneous angiokeratomas and hemangiomas.
    Whitworth WW; Hick RW; Nelson KC; Sidhu-Malik NK
    Cutis; 2015 Nov; 96(5):329-32. PubMed ID: 26682556
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
    Limaye N; Revencu N; Van Regemorter N; Garzon M; Bonduelle M; Chung W; Daras MD; Fahey MC; Garrett C; Gillerot Y; Gillessen-Kaesbach G; Giménez-Arnau A; Guzzetta F; Battaglia D; Heimdal K; Lissens W; Taub E; Van Maldergem L; Van Paesschen W; Wieczorek D; Wood NW; Boon L; Vikkula M
    Hum Genet; 2007 Dec; 122(5):552. PubMed ID: 18383597
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.