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    Results: 1 to 20 of 27

    1.

    Cutaneous features of pseudoxanthoma elasticum in a patient with generalized arterial calcification of infancy due to a homozygous missense mutation in the ENPP1 gene.

    Li Q, Schumacher W, Jablonski D, Siegel D, Uitto J.

    Br J Dermatol. 2012 May;166(5):1107-11. doi: 10.1111/j.1365-2133.2012.10811.x. Epub 2012 Apr 4.

    PMID:
    22229486
    [PubMed - in process]
    2.

    Successful management of severe infant bullous pemphigoid with omalizumab.

    Dufour C, Souillet AL, Chaneliere C, Jouen F, Bodemer C, Jullien D, Cambazard F, Joly P, Reix P.

    Br J Dermatol. 2012 May;166(5):1140-2. doi: 10.1111/j.1365-2133.2011.10748.x. Epub 2012 Mar 2. No abstract available.

    PMID:
    22098309
    [PubMed - in process]
    3.

    An exploratory (1) H-nuclear magnetic resonance metabolomics study reveals altered urine spectral profiles in infants with atopic dermatitis.

    Assfalg M, Bortoletti E, D'Onofrio M, Pigozzi R, Molinari H, Boner AL, Peroni DG, Piacentini GL.

    Br J Dermatol. 2012 May;166(5):1123-5. doi: 10.1111/j.1365-2133.2011.10711.x. Epub 2012 Feb 6. No abstract available.

    PMID:
    22032695
    [PubMed - in process]
    4.

    Congenital insensitivity to pain with anhidrosis: a case with preserved itch sensation to histamine and partial pain sensation.

    Tanaka T, Satoh T, Tanaka A, Yokozeki H.

    Br J Dermatol. 2012 Apr;166(4):888-91. doi: 10.1111/j.1365-2133.2011.10706.x. Epub 2012 Feb 6.

    PMID:
    22032467
    [PubMed - in process]
    5.

    Infant epidermal skin physiology: adaptation after birth.

    Fluhr JW, Darlenski R, Lachmann N, Baudouin C, Msika P, De Belilovsky C, Hachem JP.

    Br J Dermatol. 2012 Mar;166(3):483-90. doi: 10.1111/j.1365-2133.2011.10659.x. Epub 2012 Jan 19.

    PMID:
    21967466
    [PubMed - indexed for MEDLINE]
    6.

    Clinical characteristics and risk of melanoma development from giant congenital melanocytic naevi in Korea: a nationwide retrospective study.

    Yun SJ, Kwon OS, Han JH, Kweon SS, Lee MW, Lee DY, Kim MB, Kim YC, Yoon TY, Chung KY, Kim IH, Kim KH, Suh KS, Lee SJ, Seo YJ, Kim KH, Park HJ, Roh MR, Ahn KJ, Yoon TJ, Kim MH, Li KS, Park JS, Shin BS, Ko JY, Ahn HH, Kim HJ, Park SD, Jang SJ, Won YH.

    Br J Dermatol. 2012 Jan;166(1):115-23. doi: 10.1111/j.1365-2133.2011.10636.x.

    PMID:
    21923752
    [PubMed - indexed for MEDLINE]
    7.

    Absence of clinical and dermoscopic differences between congenital and noncongenital melanocytic naevi in a cohort of 2-year-old children.

    Stinco G, Argenziano G, Favot F, Valent F, Patrone P.

    Br J Dermatol. 2011 Dec;165(6):1303-7. doi: 10.1111/j.1365-2133.2011.10538.x. Epub 2011 Nov 17.

    PMID:
    21790516
    [PubMed - indexed for MEDLINE]
    8.

    Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma.

    Fukuda S, Hamada T, Ishii N, Sakaguchi S, Sakai K, Akiyama M, Shimizu H, Masuda K, Izu K, Teye K, Tsuruta D, Karashima T, Nakama T, Yasumoto S, Hashimoto T.

    Br J Dermatol. 2012 Jan;166(1):218-21. doi: 10.1111/j.1365-2133.2011.10516.x. Epub 2011 Sep 29. No abstract available.

    PMID:
    21729033
    [PubMed - indexed for MEDLINE]
    9.

    Short- and medium-term efficacy of specific hydrotherapy in inherited ichthyosis.

    Bodemer C, Bourrat E, Mazereeuw-Hautier J, Boralevi F, Barbarot S, Bessis D, Blanchet-Bardon C, Bourdon-Lanoy E, Stalder JF, Ribet V, Guerrero D, Sibaud V.

    Br J Dermatol. 2011 Nov;165(5):1087-94. doi: 10.1111/j.1365-2133.2011.10510.x.

    PMID:
    21729027
    [PubMed - indexed for MEDLINE]
    10.

    Nodular lesions arising in a large congenital melanocytic naevus in a newborn with eruptive disseminated Spitz naevi.

    Feito-Rodríguez M, de Lucas-Laguna R, Bastian BC, Leboit P, González-Beato MJ, López-Gutiérrez JC, Requena L, Pizarro A.

    Br J Dermatol. 2011 Nov;165(5):1138-42. doi: 10.1111/j.1365-2133.2011.10502.x.

    PMID:
    21711345
    [PubMed - indexed for MEDLINE]
    11.

    Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): evidence of founder effects.

    Rodríguez-Pazos L, Ginarte M, Fachal L, Toribio J, Carracedo A, Vega A.

    Br J Dermatol. 2011 Oct;165(4):906-11. doi: 10.1111/j.1365-2133.2011.10454.x. Epub 2011 Aug 4.

    PMID:
    21668430
    [PubMed - indexed for MEDLINE]
    12.

    An exceptional mutational event leading to Chanarin-Dorfman syndrome in a large consanguineous family.

    Samuelov L, Fuchs-Telem D, Sarig O, Sprecher E.

    Br J Dermatol. 2011 Jun;164(6):1390-2. doi: 10.1111/j.1365-2133.2011.10252.x. Epub 2011 May 13.

    PMID:
    21332462
    [PubMed - indexed for MEDLINE]
    13.

    Primitive erythropoiesis in infantile haemangioma.

    Itinteang T, Tan ST, Brasch HD, Vishvanath A, Day DJ.

    Br J Dermatol. 2011 May;164(5):1097-100. doi: 10.1111/j.1365-2133.2010.10187.x.

    PMID:
    21518328
    [PubMed - indexed for MEDLINE]
    14.

    Malignant skin tumours in patients with inherited ichthyosis.

    Natsuga K, Akiyama M, Shimizu H.

    Br J Dermatol. 2011 Aug;165(2):263-8. doi: 10.1111/j.1365-2133.2011.10381.x. Epub 2011 Jul 11. Review.

    PMID:
    21517795
    [PubMed - indexed for MEDLINE]
    15.

    Infantile haemangioma: new aspects on the pathogenesis of the most common skin tumour in children.

    Hoeger PH.

    Br J Dermatol. 2011 Feb;164(2):234-5. doi: 10.1111/j.1365-2133.2011.10204.x. No abstract available.

    PMID:
    21271990
    [PubMed - indexed for MEDLINE]
    16.

    Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosis.

    Arin MJ, Oji V, Emmert S, Hausser I, Traupe H, Krieg T, Grimberg G.

    Br J Dermatol. 2011 Feb;164(2):442-7. doi: 10.1111/j.1365-2133.2010.10096.x.

    PMID:
    21271994
    [PubMed - indexed for MEDLINE]
    17.

    A study of the efficacy of carbon dioxide and pigment-specific lasers in the treatment of medium-sized congenital melanocytic naevi.

    August PJ, Ferguson JE, Madan V.

    Br J Dermatol. 2011 May;164(5):1037-42. doi: 10.1111/j.1365-2133.2011.10236.x. Epub 2011 Apr 11.

    PMID:
    21275945
    [PubMed - indexed for MEDLINE]
    18.

    Mutations in two genes on chromosome 13 resulting in a complex hair and skin phenotype due to two rare genodermatoses: KLICK and autosomal recessive woolly hair/hypotrichosis simplex.

    Horev L, Babay S, Ramot Y, Saad-Edin B, Moorad S, Ingber A, Maly A, Zlotogorski A.

    Br J Dermatol. 2011 May;164(5):1113-6. doi: 10.1111/j.1365-2133.2011.10229.x. No abstract available.

    PMID:
    21275938
    [PubMed - indexed for MEDLINE]
    19.

    Aquagenic palmoplantar keratoderma: a new sign of cystic fibrosis?

    Phillips R.

    Br J Dermatol. 2011 Jan;164(1):224-5. doi: 10.1111/j.1365-2133.2010.10069.x. No abstract available.

    PMID:
    20874787
    [PubMed - indexed for MEDLINE]
    20.

    Induction of p38, tumour necrosis factor-α and RANTES by mechanical stretching of keratinocytes expressing mutant keratin 10R156H.

    Obarzanek-Fojt M, Favre B, Huber M, Ryser S, Moodycliffe AM, Wipff PJ, Hinz B, Hohl D.

    Br J Dermatol. 2011 Jan;164(1):125-34. doi: 10.1111/j.1365-2133.2010.10013.x. Epub 2010 Nov 11.

    PMID:
    20804491
    [PubMed - indexed for MEDLINE]

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