BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

485 related articles for article (PubMed ID: 29476210)

  • 1. A child with Apert syndrome and Sturge-Weber syndrome: could fibronectin or the RAS/MAPK signaling pathway be the connection?
    Tan AP; Chong WK
    Childs Nerv Syst; 2018 Jun; 34(6):1247-1250. PubMed ID: 29476210
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Increased fibronectin expression in sturge-weber syndrome fibroblasts and brain tissue.
    Comi AM; Hunt P; Vawter MP; Pardo CA; Becker KG; Pevsner J
    Pediatr Res; 2003 May; 53(5):762-9. PubMed ID: 12621118
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fibronectin: characterization of a somatic mutation in Sturge-Weber syndrome (SWS).
    Zhou Q; Zheng JW; Yang XJ; Wang YA; Ye WM; Zhu HG; Zhang ZY
    Med Hypotheses; 2009 Aug; 73(2):199-200. PubMed ID: 19359105
    [TBL] [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. The Pathogenesis of Port Wine Stain and Sturge Weber Syndrome: Complex Interactions between Genetic Alterations and Aberrant MAPK and PI3K Activation.
    Nguyen V; Hochman M; Mihm MC; Nelson JS; Tan W
    Int J Mol Sci; 2019 May; 20(9):. PubMed ID: 31067686
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Retrospective review of screening for Sturge-Weber syndrome with brain magnetic resonance imaging and electroencephalography in infants with high-risk port-wine stains.
    Zallmann M; Mackay MT; Leventer RJ; Ditchfield M; Bekhor PS; Su JC
    Pediatr Dermatol; 2018 Sep; 35(5):575-581. PubMed ID: 30020536
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sturge-Weber syndrome: an update for the pediatrician.
    Dingenen E; Segers D; De Maeseneer H; Van Gysel D
    World J Pediatr; 2024 May; 20(5):435-443. PubMed ID: 38658498
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Sturge-Weber syndrome: altered blood vessel fibronectin expression and morphology.
    Comi AM; Weisz CJ; Highet BH; Skolasky RL; Pardo CA; Hess EJ
    J Child Neurol; 2005 Jul; 20(7):572-7. PubMed ID: 16159522
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sturge-Weber syndrome coexisting with episodes of rhabdomyolysis.
    Zhu M; Li X; Zhou M; Wan H; Wu Y; Hong D
    BMC Neurol; 2013 Nov; 13():169. PubMed ID: 24207015
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Forehead location and large segmental pattern of facial port-wine stains predict risk of Sturge-Weber syndrome.
    Boos MD; Bozarth XL; Sidbury R; Cooper AB; Perez F; Chon C; Paras G; Amlie-Lefond C
    J Am Acad Dermatol; 2020 Oct; 83(4):1110-1117. PubMed ID: 32413446
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sturge-Weber syndrome: deep venous occlusion and the radiologic spectrum.
    Slasky SE; Shinnar S; Bello JA
    Pediatr Neurol; 2006 Nov; 35(5):343-7. PubMed ID: 17074605
    [TBL] [Abstract][Full Text] [Related]  

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

  • 15. Sturge-Weber Syndrome: A Case Report.
    Timilsina S; Kunwor B; Thapa Chhetri S; Nepal S; Sedhai K
    JNMA J Nepal Med Assoc; 2023 Nov; 61(267):890-892. PubMed ID: 38289732
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A prospective study of risk for Sturge-Weber syndrome in children with upper facial port-wine stain.
    Dutkiewicz AS; Ezzedine K; Mazereeuw-Hautier J; Lacour JP; Barbarot S; Vabres P; Miquel J; Balguerie X; Martin L; Boralevi F; Bessou P; Chateil JF; Léauté-Labrèze C;
    J Am Acad Dermatol; 2015 Mar; 72(3):473-80. PubMed ID: 25592619
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sturge-weber Syndrome with Bilateral Fronto-parieto-temporal Lobe Atrophy and Bilateral Leptomeningeal Angiomatosis: A Rare Case.
    Kumar A; Panhwar IA; Rehan B; Shadani K
    J Coll Physicians Surg Pak; 2022 Aug; 32(8):S136-S138. PubMed ID: 36210673
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sturge-Weber syndrome and dermatomal facial port-wine stains: incidence, association with glaucoma, and pulsed tunable dye laser treatment effectiveness.
    Hennedige AA; Quaba AA; Al-Nakib K
    Plast Reconstr Surg; 2008 Apr; 121(4):1173-1180. PubMed ID: 18349634
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sturge-Weber syndrome: from the past to the present.
    Sudarsanam A; Ardern-Holmes SL
    Eur J Paediatr Neurol; 2014 May; 18(3):257-66. PubMed ID: 24275166
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Updates on Sturge-Weber Syndrome.
    Yeom S; Comi AM
    Stroke; 2022 Dec; 53(12):3769-3779. PubMed ID: 36263782
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.