BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 33058925)

  • 1. Ocular manifestations in phakomatosis pigmentovascularis: Current concepts on pathogenesis, diagnosis, and management.
    Abdolrahimzadeh S; Pugi DM; de Paula A; Scuderi G
    Surv Ophthalmol; 2021; 66(3):482-492. PubMed ID: 33058925
    [TBL] [Abstract][Full Text] [Related]  

  • 2. CHOROIDAL MELANOMA IN PHAKOMATOSIS PIGMENTOVASCULARIS WITH OVERLAPPING STURGE-WEBER SYNDROME AND KLIPPEL-TRENAUNAY SYNDROME.
    Fry MV; Williams BK; Kim HJ; Di Nicola M
    Retin Cases Brief Rep; 2023 Mar; 17(2):130-133. PubMed ID: 33907078
    [TBL] [Abstract][Full Text] [Related]  

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

  • 4. 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; 2015():786519. PubMed ID: 26451379
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Phacomatosis pigmentovascularis of cesioflammea type in 7 patients: combination of ocular pigmentation (melanocytosis or melanosis) and nevus flammeus with risk for melanoma.
    Shields CL; Kligman BE; Suriano M; Viloria V; Iturralde JC; Shields MV; Say EA; Shields JA
    Arch Ophthalmol; 2011 Jun; 129(6):746-50. PubMed ID: 21670341
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Glaucoma in phakomatosis pigmentovascularis.
    Teekhasaenee C; Ritch R
    Ophthalmology; 1997 Jan; 104(1):150-7. PubMed ID: 9022120
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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; 80(1):51-3. PubMed ID: 24448125
    [TBL] [Abstract][Full Text] [Related]  

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

  • 10. A case of Sturge-Weber syndrome in association with phacomatosis pigmentovascularis and developmental glaucoma.
    Gupta A; Dubey S; Agarwal M
    J AAPOS; 2007 Aug; 11(4):398-9. PubMed ID: 17512229
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Klippel-Trenaunay and Sturge-Weber overlap syndrome with phakomatosis pigmentovascularis.
    Chhajed M; Pandit S; Dhawan N; Jain A
    J Pediatr Neurosci; 2010 Jul; 5(2):138-40. PubMed ID: 21559162
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Phakomatosis pigmentovascularis cesioflammea: a case report].
    Viada Peláez MC; Stefano PC; Cirio A; Cervini AB
    Arch Argent Pediatr; 2018 Feb; 116(1):e121-e124. PubMed ID: 29333836
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital Triangular Alopecia Associated with Phakomatosis Pigmentovascularis Type II along with Klippel Trenaunay Syndrome.
    Gupta A; Khurana A; Malhotra P; Sardana K
    Indian Dermatol Online J; 2020; 11(1):91-93. PubMed ID: 32055518
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 15(11):. PubMed ID: 36384883
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An update on ophthalmological perspectives in oculodermal melanocytosis (Nevus of Ota).
    Abdolrahimzadeh S; Pugi DM; Manni P; Iodice CM; Di Tizio F; Persechino F; Scuderi G
    Graefes Arch Clin Exp Ophthalmol; 2023 Feb; 261(2):291-301. PubMed ID: 35851619
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Phakomatosis pigmentovascularis type IIb: A case with Klippel-Trenáunay syndrome and extensive dermal melanocytosis as nevus of Ota, nevus of Ito and ectopic Mongolian spots.
    Namiki T; Takahashi M; Nojima K; Ueno M; Hanafusa T; Tokoro S; Yokozeki H
    J Dermatol; 2017 Mar; 44(3):e32-e33. PubMed ID: 27374914
    [No Abstract]   [Full Text] [Related]  

  • 17. 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; 65(2):e46-e49. PubMed ID: 21763548
    [No Abstract]   [Full Text] [Related]  

  • 18. Phakomatosis pigmentovascularis type IIIb: a case associated with Sturge-Weber and Klippel-Trenaunay syndromes.
    Diociaiuti A; Guidi B; Aguilar Sanchez JA; Feliciani C; Capizzi R; Amerio P
    J Am Acad Dermatol; 2005 Sep; 53(3):536-9. PubMed ID: 16112377
    [No Abstract]   [Full Text] [Related]  

  • 19. SUBMILLIMETER CHOROIDAL MELANOMA DETECTION BY ENHANCED DEPTH IMAGING OPTICAL COHERENCE TOMOGRAPHY IN A PATIENT WITH OCULODERMAL MELANOCYTOSIS.
    Daitch Z; Shields CL; Say EA; Mashayekhi A; Shields JA
    Retin Cases Brief Rep; 2016; 10(1):6-10. PubMed ID: 26110523
    [TBL] [Abstract][Full Text] [Related]  

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

    [Next]    [New Search]
    of 8.