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Journal Abstract Search

212 related items for PubMed ID: 33170527

  • 1. The anatomic distribution of isolated and syndrome-associated port-wine stain.
    Elias AJ, Hand JL, Tollefson MM, Davis DMR.
    Pediatr Dermatol; 2021 Jan; 38(1):77-82. PubMed ID: 33170527
    [Abstract] [Full Text] [Related]

  • 2. 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, Groupe de Recherche Clinique en Dermatologie Pédiatrique.
    J Am Acad Dermatol; 2015 Mar; 72(3):473-80. PubMed ID: 25592619
    [Abstract] [Full Text] [Related]

  • 3. [Sturge-Weber syndrome in port-wine stain patients: a retrospective study on the clinical features and screening strategy].
    Wu Y, Yu RJ, Lin XX, Guo WY.
    Zhonghua Yan Ke Za Zhi; 2017 Oct 11; 53(10):753-757. PubMed ID: 29050188
    [Abstract] [Full Text] [Related]

  • 4. Clinical characteristics of infants with port-wine stain and glaucoma secondary to Sturge-Weber Syndrome.
    Yan H, Hu M, Cui Y, Li L, Liang T.
    BMC Ophthalmol; 2022 Jun 09; 22(1):260. PubMed ID: 35681114
    [Abstract] [Full Text] [Related]

  • 5. Ocular features in a patient presenting with a rare combination of multiple phakomatoses.
    Senthilkumar VA, Kohli P, Mishra C, Mamchisetti K.
    BMJ Case Rep; 2022 Nov 16; 15(11):. PubMed ID: 36384883
    [Abstract] [Full Text] [Related]

  • 6. Klippel-Trénaunay Syndrome: Need for Careful Clinical Classification.
    Volz KR, Kanner CD, Evans J, Evans KD.
    J Ultrasound Med; 2016 Sep 16; 35(9):2057-65. PubMed ID: 27492391
    [Abstract] [Full Text] [Related]

  • 7. 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 16; 83(4):1110-1117. PubMed ID: 32413446
    [Abstract] [Full Text] [Related]

  • 8. 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 16; 121(4):1173-1180. PubMed ID: 18349634
    [Abstract] [Full Text] [Related]

  • 9. [Clinical and Neuroimaging Analysis of 24 Cases of Sturge-Weber Syndrome].
    Li YM, Liu C, Cong TX, Zhang HY, Zhou H, Zhao Q, Jiang X.
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2020 Jul 16; 51(4):562-566. PubMed ID: 32691568
    [Abstract] [Full Text] [Related]

  • 10. Sturge-Weber syndrome and associated congenital vascular disorders: a review.
    Nathan N, Thaller SR.
    J Craniofac Surg; 2006 Jul 16; 17(4):724-8. PubMed ID: 16877925
    [Abstract] [Full Text] [Related]

  • 11. 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 16; 35(5):575-581. PubMed ID: 30020536
    [Abstract] [Full Text] [Related]

  • 12. Klippel-Trénaunay syndrome: the importance of "geographic stains" in identifying lymphatic disease and risk of complications.
    Maari C, Frieden IJ.
    J Am Acad Dermatol; 2004 Sep 16; 51(3):391-8. PubMed ID: 15337982
    [Abstract] [Full Text] [Related]

  • 13. Port-wine stain as a clue for two rare coexisting entities.
    Almeida FT, Caldas R, Duarte MDL, Brito C.
    BMJ Case Rep; 2018 Jul 13; 2018():. PubMed ID: 30007908
    [Abstract] [Full Text] [Related]

  • 14. 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 07; 20(9):. PubMed ID: 31067686
    [Abstract] [Full Text] [Related]

  • 15. An unusual case of Sturge-Weber syndrome in association with phakomatosis pigmentovascularis and Klippel-Trenaunay-Weber syndrome.
    Saricaoğlu MS, Güven D, Karakurt A, Sengun A, Ziraman I.
    Retina; 2002 Jun 07; 22(3):368-71. PubMed ID: 12055477
    [No Abstract] [Full Text] [Related]

  • 16. Sturge-Weber syndrome in patients with facial port-wine stain.
    Piram M, Lorette G, Sirinelli D, Herbreteau D, Giraudeau B, Maruani A.
    Pediatr Dermatol; 2012 Jun 07; 29(1):32-7. PubMed ID: 21906147
    [Abstract] [Full Text] [Related]

  • 17. Klippel-Trenaunay syndrome or not? An exploration of atypical presentations.
    Anthony L, Bayat I.
    BMJ Case Rep; 2024 Mar 12; 17(3):. PubMed ID: 38471707
    [Abstract] [Full Text] [Related]

  • 18. Klippel Trenaunay syndrome in association with Sturge Weber syndrome about one case.
    Sfaihi L, Aissa K, Fourati H, Kamoun F, Mnif Z, Kamoun T, Hachicha M.
    Tunis Med; 2014 Feb 12; 92(2):173-4. PubMed ID: 24938246
    [No Abstract] [Full Text] [Related]

  • 19. Hematoporphyrin monomethyl ether photodynamic therapy for the treatment of Sturge-Weber syndrome and large segmental facial port-wine stain.
    Li X, Diao P, Liu L, Zhou H, Yang Y, Han C, Jiang X.
    Dermatol Ther; 2022 May 12; 35(5):e15404. PubMed ID: 35199900
    [Abstract] [Full Text] [Related]

  • 20. [Own clinical experience in treatment of port-wine stain with KTP 532 nm laser].
    Latkowski IT, Wysocki MS, Siewiera IP.
    Wiad Lek; 2005 May 12; 58(7-8):391-6. PubMed ID: 16425790
    [Abstract] [Full Text] [Related]

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