BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 32613723)

  • 1. Klippel-Trenaunay and Sturge-Weber Overlap Syndrome with KRAS and GNAQ mutations.
    He R; Liao S; Yao X; Huang R; Zeng J; Zhang J; Yu J
    Ann Clin Transl Neurol; 2020 Jul; 7(7):1258-1264. PubMed ID: 32613723
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Co-occurrence of Sturge-Weber syndrome and Klippel-Trenaunay-Weber syndrome phenotype: Consideration of the historical aspect.
    Sakaguchi Y; Takenouchi T; Uehara T; Kishi K; Takahashi T; Kosaki K
    Am J Med Genet A; 2017 Oct; 173(10):2831-2833. PubMed ID: 28782176
    [No Abstract]   [Full Text] [Related]  

  • 3. Association of Somatic GNAQ Mutation With Capillary Malformations in a Case of Choroidal Hemangioma.
    Bichsel CA; Goss J; Alomari M; Alexandrescu S; Robb R; Smith LE; Hochman M; Greene AK; Bischoff J
    JAMA Ophthalmol; 2019 Jan; 137(1):91-95. PubMed ID: 30422215
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Klippel-Trenaunay syndrome.
    Cohen MM
    Am J Med Genet; 2000 Jul; 93(3):171-5. PubMed ID: 10925375
    [No Abstract]   [Full Text] [Related]  

  • 5. Somatic GNAQ Mutation is Enriched in Brain Endothelial Cells in Sturge-Weber Syndrome.
    Huang L; Couto JA; Pinto A; Alexandrescu S; Madsen JR; Greene AK; Sahin M; Bischoff J
    Pediatr Neurol; 2017 Feb; 67():59-63. PubMed ID: 27919468
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ.
    Shirley MD; Tang H; Gallione CJ; Baugher JD; Frelin LP; Cohen B; North PE; Marchuk DA; Comi AM; Pevsner J
    N Engl J Med; 2013 May; 368(21):1971-9. PubMed ID: 23656586
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phakomatosis pigmentovascularis type IIb with Klippel-Trenaunay syndrome: Association with GNAQ mutation in vascular endothelial cells.
    Minami Y; Okamoto T; Hirotsu Y; Amemiya K; Osada A; Tsukamoto K; Omata M; Kawamura T
    J Dermatol; 2022 Dec; 49(12):e444-e445. PubMed ID: 35906786
    [No Abstract]   [Full Text] [Related]  

  • 8. Klippel-Trenaunay syndrome and Sturge-Weber syndrome: variations on a theme?
    Vissers W; Van Steensel M; Steijlen P; Renier W; Van De Kerkhof P; Van Der Vleuten C
    Eur J Dermatol; 2003; 13(3):238-41. PubMed ID: 12804981
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Association on Sturge Weber and Klippel Trenaunay Weber syndromes. Apropos of 2 cases].
    Guízar Vázquez J; Navarrete Cadena C; Barrón Uribe C; Velázquez E; Armendares S
    Bol Med Hosp Infant Mex; 1979; 36(3):415-24. PubMed ID: 218598
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The somatic GNAQ mutation c.548G>A (p.R183Q) is consistently found in Sturge-Weber syndrome.
    Nakashima M; Miyajima M; Sugano H; Iimura Y; Kato M; Tsurusaki Y; Miyake N; Saitsu H; Arai H; Matsumoto N
    J Hum Genet; 2014 Dec; 59(12):691-3. PubMed ID: 25374402
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Sturge--Weber-Klippel--Trenaunay syndrome (case report)].
    Rafai MA; Otmani HE; Boulaajaj FZ; Sibai M; Moutaouakkil F; Chlihi A; Slassi I
    J Mal Vasc; 2008 Feb; 33(1):35-8. PubMed ID: 18343067
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sturge-Weber-Klippel-Trenaunay syndrome: what's in a name?
    Happle R
    Eur J Dermatol; 2003; 13(3):223. PubMed ID: 12804977
    [No Abstract]   [Full Text] [Related]  

  • 13. [Sturge-Weber-Dimitri syndrome associated with Klippel-Trenaunay syndrome].
    Belli L; Delmar A; Abulafia J; González Rescigno GR; Estrada E; Repetto A; Calvo E
    Med Cutan Ibero Lat Am; 1980; 8(1-3):59-63. PubMed ID: 6267388
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An infantile case of Sturge-Weber syndrome in association with Klippel-Trenaunay-Weber syndrome and phakomatosis pigmentovascularis.
    Lee CW; Choi DY; Oh YG; Yoon HS; Kim JD
    J Korean Med Sci; 2005 Dec; 20(6):1082-4. PubMed ID: 16361829
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Two reports of phacomatosis pigmentovascularis type IIb, one in association with Sturge-Weber syndrome and Klippel-Trenaunay syndrome.
    Finklea LB; Mohr MR; Warthan MM; Darrow DH; Williams JV
    Pediatr Dermatol; 2010; 27(3):303-5. PubMed ID: 20609155
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Computational analysis for GNAQ mutations: New insights on the molecular etiology of Sturge-Weber syndrome.
    Martins L; Giovani PA; Rebouças PD; Brasil DM; Haiter Neto F; Coletta RD; Machado RA; Puppin-Rontani RM; Nociti FH; Kantovitz KR
    J Mol Graph Model; 2017 Sep; 76():429-440. PubMed ID: 28779688
    [TBL] [Abstract][Full Text] [Related]  

  • 17. GNAQ R183Q somatic mutation contributes to aberrant arteriovenous specification in Sturge-Weber syndrome through Notch signaling.
    Huang L; Sun H; Liu Y; Xu L; Hu M; Yang Y; Wang N; Wu Y; Guo W
    FASEB J; 2023 Sep; 37(9):e23148. PubMed ID: 37606556
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Brief communication: nevus unis lateris and Klippel-Trenaunay-Weber syndrome with the Sturge Weber anomalady in a consanguineous Puerto Rican family.
    Rivera-Reyes LR; Toro-Solá MA
    Bol Asoc Med P R; 1979 Feb; 71(2):69-71. PubMed ID: 222308
    [No Abstract]   [Full Text] [Related]  

  • 19. Endothelial
    Huang L; Bichsel C; Norris AL; Thorpe J; Pevsner J; Alexandrescu S; Pinto A; Zurakowski D; Kleiman RJ; Sahin M; Greene AK; Bischoff J
    Arterioscler Thromb Vasc Biol; 2022 Jan; 42(1):e27-e43. PubMed ID: 34670408
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sturge-Weber syndrome.
    Comi AM
    Handb Clin Neurol; 2015; 132():157-68. PubMed ID: 26564078
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.