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Journal Abstract Search

447 related items for PubMed ID: 18238750

  • 1. Macromelia masquerading as an acromegaloid syndrome in an adult with Klippel-Trénaunay syndrome.
    Lowman E, Mooradian AD.
    Endocr Pract; 2008; 14(1):109-11. PubMed ID: 18238750
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  • 6. 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
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  • 8. 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 13; 20(6):1082-4. PubMed ID: 16361829
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  • 14. Klippel-Trénaunay Syndrome: Need for Careful Clinical Classification.
    Volz KR, Kanner CD, Evans J, Evans KD.
    J Ultrasound Med; 2016 Sep 13; 35(9):2057-65. PubMed ID: 27492391
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  • 15. Persistent fetal vasculature and spontaneous hyphema in a patient with Klippel-Trénaunay-Weber syndrome.
    Dhir L, Quinn AG.
    J AAPOS; 2010 Apr 13; 14(2):190-2. PubMed ID: 20451865
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  • 17. 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 13; 51(3):391-8. PubMed ID: 15337982
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  • 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 13; 92(2):173-4. PubMed ID: 24938246
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  • 20. An atypical case of Klippel-Trénaunay syndrome presenting with crossed-bilateral limb hypertrophy and postaxial polydactyly: a case report.
    Al-Najjar RM, Fonseca R.
    BMC Pediatr; 2019 Apr 06; 19(1):95. PubMed ID: 30954069
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