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Journal Abstract Search

139 related items for PubMed ID: 33314074

  • 1. Phakomatosis pigmentovascularis IIb (phakomatosis cesioflammea) associated with the absence of infrarenal inferior vena cava.
    Pan Y, Jiang X.
    Int J Dermatol; 2021 May; 60(5):647-649. PubMed ID: 33314074
    [No Abstract] [Full Text] [Related]

  • 2. Phakomatosis pigmentovascularis type IIb with a patent umbilical vein and inferior vena cava hypoplasia.
    Lo PY, Tzung TY.
    Br J Dermatol; 2003 Apr; 148(4):836-8. PubMed ID: 12752160
    [No Abstract] [Full Text] [Related]

  • 3. Phakomatosis pigmentovascularis and Lisch nodules. Relationship between Von Recklinghausen and phakomatosis pigmentovascularis?
    Ruiz Villaverde R, Viera Ramirez A, Linares Solano J, Naranjo Sintes R, Gutierrez Salmerón MT.
    J Eur Acad Dermatol Venereol; 2003 Jan; 17(1):53-5. PubMed ID: 12602970
    [Abstract] [Full Text] [Related]

  • 4. Phakomatosis cesioflammea with late-onset glaucoma and acquired nevus spilus-like lesion - 15 years of follow-up.
    Chiu HH, Chen GS, Wu CS, Ke CL, Cheng ST.
    Int J Dermatol; 2009 Apr; 48(4):416-8. PubMed ID: 19335431
    [Abstract] [Full Text] [Related]

  • 5. Phacomatosis pigmentovascularis of cesioflammea type.
    Villarreal DJ, Leal F.
    An Bras Dermatol; 2016 Apr; 91(5 suppl 1):54-56. PubMed ID: 28300894
    [Abstract] [Full Text] [Related]

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

  • 7. Clinical characteristics and treatment of 52 cases of phakomatosis pigmentovascularis.
    Shin H, Kim YG, Kim YE, Park H.
    J Dermatol; 2019 Oct; 46(10):843-848. PubMed ID: 31389056
    [Abstract] [Full Text] [Related]

  • 8. Phakomatosis pigmentovascularis type Ⅲa mainly manifested by zosteriform nevus spilus: A case report with dermoscopic features.
    Yang X, Lu D, Xu S.
    Photodiagnosis Photodyn Ther; 2022 Jun; 38():102890. PubMed ID: 35490960
    [Abstract] [Full Text] [Related]

  • 9. Congenital triangular alopecia in phakomatosis pigmentovascularis: report of 3 cases.
    Kim HJ, Park KB, Yang JM, Park SH, Lee ES.
    Acta Derm Venereol; 2000 May; 80(3):215-6. PubMed ID: 10954219
    [No Abstract] [Full Text] [Related]

  • 10. Port-wine-stain (nevus flammeus), congenital Becker's nevus, café-au-lait-macule and lentigines: phakomatosis pigmentovascularis type Ia--a new combination.
    Joshi A, Garg VK, Agrawal S, Agarwalla A, Thakur A.
    J Dermatol; 1999 Dec; 26(12):834-6. PubMed ID: 10659508
    [Abstract] [Full Text] [Related]

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

  • 12. 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; 17(11):1179-1182. PubMed ID: 31765096
    [No Abstract] [Full Text] [Related]

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

  • 14. 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]

  • 15. 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]

  • 16. Phakomatosis Pigmentovascularis.
    Tran C, Alward WLM.
    Ophthalmol Glaucoma; 2021 Jul 13; 4(3):250. PubMed ID: 34030827
    [No Abstract] [Full Text] [Related]

  • 17. A case of phakomatosis pigmentovascularis type II: port-wine stain and dermal melanocytosis with cutis marmorata telangiectatica congenita-like lesions.
    Namiki T, Arai M, Miura K, Yokozeki H.
    Eur J Dermatol; 2016 Jun 01; 26(3):302-3. PubMed ID: 26905386
    [No Abstract] [Full Text] [Related]

  • 18. [Phakomatosis pigmentovascularis cesioflammea: a case report].
    Viada Peláez MC, Stefano PC, Cirio A, Cervini AB.
    Arch Argent Pediatr; 2018 Feb 01; 116(1):e121-e124. PubMed ID: 29333836
    [Abstract] [Full Text] [Related]

  • 19. Phacomatosis cesioflammea with unilateral lipohypoplasia.
    Castori M, Rinaldi R, Angelo C, Zambruno G, Grammatico P, Happle R.
    Am J Med Genet A; 2008 Feb 15; 146A(4):492-5. PubMed ID: 18203153
    [Abstract] [Full Text] [Related]

  • 20. Picture of the month. Phakomatosis pigmentovascularis.
    Narchi H, Santos M, Tunnessen WW.
    Arch Pediatr Adolesc Med; 2001 Feb 15; 155(2):191-2. PubMed ID: 11177096
    [No Abstract] [Full Text] [Related]

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