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Journal Abstract Search

247 related items for PubMed ID: 30007908

  • 1. 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]

  • 2. 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]

  • 3. 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 16; 20(6):1082-4. PubMed ID: 16361829
    [Abstract] [Full Text] [Related]

  • 4. Phakomatosis Pigmentovascularis Type IIB: a case report.
    Colin TS, Kumarasinghe Sujith PW.
    J Dermatol; 2004 May 16; 31(5):415-8. PubMed ID: 15187311
    [Abstract] [Full Text] [Related]

  • 5. Sturge-Weber syndrome in association with Klippel-Trenaunay syndrome and phakomatosis pigmentovascularis type IIb.
    Mandal RK, Ghosh SK, Koley S, Roy AC.
    Indian J Dermatol Venereol Leprol; 2014 May 16; 80(1):51-3. PubMed ID: 24448125
    [Abstract] [Full Text] [Related]

  • 6. 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 16; 22(3):368-71. PubMed ID: 12055477
    [No Abstract] [Full Text] [Related]

  • 7. A port-wine stain in association with underlying syndrome.
    Jabr FI, Skeik N.
    Postgrad Med; 2014 Nov 16; 126(7):157-9. PubMed ID: 25548818
    [Abstract] [Full Text] [Related]

  • 8. Phakomatosis pigmentovascularis type IIb.
    Wang B, Yang M, Lv S, Xu N, Zhang Y, Wu S, Wang J, Li F.
    J Dtsch Dermatol Ges; 2019 Nov 16; 17(11):1179-1182. PubMed ID: 31765096
    [No Abstract] [Full Text] [Related]

  • 9. Klippel-Trenaunay Syndrome: A Case Report.
    Sah RK, Sharma S, Ghimire S, Bagale BB, Kayastha M, Chapagain RH.
    J Nepal Health Res Counc; 2016 May 16; 14(33):135-139. PubMed ID: 27885298
    [Abstract] [Full Text] [Related]

  • 10. Phakomatosis pigmentovascularis type IIb associated with Klippel-Trénaunay syndrome and congenital triangular alopecia.
    Turk BG, Turkmen M, Tuna A, Kilinc Karaarslan I, Ozdemir F.
    J Am Acad Dermatol; 2011 Aug 16; 65(2):e46-e49. PubMed ID: 21763548
    [No Abstract] [Full Text] [Related]

  • 11. CHOROIDAL MELANOMA IN PHAKOMATOSIS PIGMENTOVASCULARIS WITH KLIPPEL-TRENAUNAY SYNDROME.
    Shields CL, Di Nicola M, Pellegrini M, Shields JA.
    Retina; 2018 Nov 16; 38(11):2220-2227. PubMed ID: 28937525
    [Abstract] [Full Text] [Related]

  • 12. Phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome.
    Al Robaee A, Banka N, Alfadley A.
    Pediatr Dermatol; 2004 Nov 16; 21(6):642-5. PubMed ID: 15575847
    [Abstract] [Full Text] [Related]

  • 13. Phacomatosis pigmentovascularis type II.
    Du LC, Delaporte E, Catteau B, Destee A, Piette F.
    Eur J Dermatol; 1998 Dec 16; 8(8):569-72. PubMed ID: 9889430
    [Abstract] [Full Text] [Related]

  • 14. Ophthalmic Alterations in the Sturge-Weber Syndrome, Klippel-Trenaunay Syndrome, and the Phakomatosis Pigmentovascularis: An Independent Group of Conditions?
    Abdolrahimzadeh S, Scavella V, Felli L, Cruciani F, Contestabile MT, Recupero SM.
    Biomed Res Int; 2015 Dec 16; 2015():786519. PubMed ID: 26451379
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. 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 Mar 12; 27(3):303-5. PubMed ID: 20609155
    [Abstract] [Full Text] [Related]

  • 17. Combined capillary-venous-lymphatic malformations without overgrowth in patients with Klippel-Trénaunay syndrome.
    Brandigi E, Torino G, Messina M, Molinaro F, Mazzei O, Matucci T, López Gutiérrez JC.
    J Vasc Surg Venous Lymphat Disord; 2018 Mar 12; 6(2):230-236. PubMed ID: 29233587
    [Abstract] [Full Text] [Related]

  • 18. Naevus varicosus osteohypertrophicus. An early diagnostic approach.
    Dervendizi Sikova D, Pavlova LT, V'lckova Laskoska MT, Nikolovska ST, Caca Biljanovska N.
    Adv Exp Med Biol; 1999 Mar 12; 455():535-40. PubMed ID: 10599395
    [Abstract] [Full Text] [Related]

  • 19. Phakomatosis pigmentovascularis type IIB with neurologic abnormalities.
    Cho S, Choi JH, Sung KJ, Moon KC, Koh JK.
    Pediatr Dermatol; 2001 Mar 12; 18(3):263. PubMed ID: 11446368
    [No Abstract] [Full Text] [Related]

  • 20. Macromelia masquerading as an acromegaloid syndrome in an adult with Klippel-Trénaunay syndrome.
    Lowman E, Mooradian AD.
    Endocr Pract; 2008 Mar 12; 14(1):109-11. PubMed ID: 18238750
    [Abstract] [Full Text] [Related]

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