BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 25427202)

  • 1. A 2-year-old girl with skin fragility.
    Mir-Bonafe JF; Baselga-Torres E; Gonzalez-Sarmiento R
    JAMA Dermatol; 2015 Feb; 151(2):225-6. PubMed ID: 25427202
    [No Abstract]   [Full Text] [Related]  

  • 2. Painless erosions on the hands and feet of a 7-year-old boy.
    Schimmel J; Renzi M; Fawaz B; Halpern A
    Pediatr Dermatol; 2020 Mar; 37(2):371-372. PubMed ID: 32196738
    [No Abstract]   [Full Text] [Related]  

  • 3. Genetic heterogeneity in keratolytic winter erythema (Oudtshoorn skin disease).
    Huntington MK; Jassim AD
    Arch Dermatol; 2006 Aug; 142(8):1073-4. PubMed ID: 16924068
    [No Abstract]   [Full Text] [Related]  

  • 4. Generalized Skin Scaling in a Young Girl: A Quiz.
    Mo R; Wang H; Lin Z
    Acta Derm Venereol; 2019 Dec; 99(13):1322-1323. PubMed ID: 31612237
    [No Abstract]   [Full Text] [Related]  

  • 5. Homozygous deletion of six genes including corneodesmosin on chromosome 6p21.3 is associated with generalized peeling skin disease.
    Teye K; Hamada T; Krol RP; Numata S; Ishii N; Matsuda M; Ohata C; Furumura M; Hashimoto T
    J Dermatol Sci; 2014 Jul; 75(1):36-42. PubMed ID: 24794518
    [TBL] [Abstract][Full Text] [Related]  

  • 6. PLACK syndrome shows remarkable phenotypic homogeneity.
    Mohamad J; Samuelov L; Ben-Amitai D; Malchin N; Sarig O; Sprecher E
    Clin Exp Dermatol; 2019 Jul; 44(5):580-583. PubMed ID: 30656735
    [No Abstract]   [Full Text] [Related]  

  • 7. Increased expression of caspase-1 and interleukin-18 in peeling skin disease, and a novel mutation of corneodesmosin.
    Valentin F; Oji V; Hausser I; Liebau E; Tarinski T; Metze D; Breitkreutz D; Traupe H; Jonca N; Terheyden P
    Acta Derm Venereol; 2015 Nov; 95(8):1019-21. PubMed ID: 26014679
    [No Abstract]   [Full Text] [Related]  

  • 8. [Peeling skin disease: the responsibility of corneodesmosin].
    Dereure O
    Ann Dermatol Venereol; 2010 Dec; 137(12):841. PubMed ID: 21134591
    [No Abstract]   [Full Text] [Related]  

  • 9. Keratolysis exfoliativa (dyshidrosis lamellosa sicca): a distinct peeling entity.
    Chang YY; van der Velden J; van der Wier G; Kramer D; Diercks GF; van Geel M; Coenraads PJ; Zeeuwen PL; Jonkman MF
    Br J Dermatol; 2012 Nov; 167(5):1076-84. PubMed ID: 23039091
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Peeling skin syndrome.
    Bansal M; Mahajan S; Sankhwar S; Bansal A
    BMJ Case Rep; 2015 Jul; 2015():. PubMed ID: 26150647
    [No Abstract]   [Full Text] [Related]  

  • 11. Peeling skin syndrome associated with novel variant in FLG2 gene.
    Alfares A; Al-Khenaizan S; Al Mutairi F
    Am J Med Genet A; 2017 Dec; 173(12):3201-3204. PubMed ID: 28884927
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases.
    Teye K; Suga Y; Numata S; Soejima M; Ishii N; Krol RP; Ohata C; Matsuda M; Honma M; Ishida-Yamamoto A; Hamada T; Koda Y; Hashimoto T
    J Dermatol Sci; 2016 May; 82(2):134-7. PubMed ID: 26867961
    [No Abstract]   [Full Text] [Related]  

  • 13. KLICK syndrome: recognizable phenotype and hot-spot POMP mutation.
    Morice-Picard F; Jonca N; Pichery M; Mermin D; Leauté-Labrèze C; Taïeb A; Mazereeuw-Hautier J; Boralevi F
    J Eur Acad Dermatol Venereol; 2017 Mar; 31(3):e154-e156. PubMed ID: 27503413
    [No Abstract]   [Full Text] [Related]  

  • 14. Generalized Ichthyotic Peeling Skin Syndrome due to FLG2 Mutations.
    Bolling MC; Jan SZ; Pasmooij AMG; Lemmink HH; Franke LH; Yenamandra VK; Sinke RJ; van den Akker PC; Jonkman MF
    J Invest Dermatol; 2018 Aug; 138(8):1881-1884. PubMed ID: 29505760
    [No Abstract]   [Full Text] [Related]  

  • 15. Inflammatory peeling skin syndrome caused by a mutation in CDSN encoding corneodesmosin.
    Israeli S; Zamir H; Sarig O; Bergman R; Sprecher E
    J Invest Dermatol; 2011 Mar; 131(3):779-81. PubMed ID: 21191406
    [No Abstract]   [Full Text] [Related]  

  • 16. [19-year-old woman with nodular painless skin alterations].
    Giannakidou-Jordan E; Brenken C; Benker G; Bornstein SR; Barthel A
    Dtsch Med Wochenschr; 2014 Mar; 139(10):481-2. PubMed ID: 24570193
    [No Abstract]   [Full Text] [Related]  

  • 17. Transcriptomic Analysis of Two Cdsn-Deficient Mice Shows Gene Signatures Biologically Relevant for Peeling Skin Disease.
    Zaafouri S; Pichery M; Huchenq A; Valentin F; Oji V; Mazereeuw-Hautier J; Serre G; Jonca N
    J Invest Dermatol; 2018 Jun; 138(6):1431-1435. PubMed ID: 29277537
    [No Abstract]   [Full Text] [Related]  

  • 18. Identification of the first nonsense CDSN mutation with expression of a truncated protein causing peeling skin syndrome type B.
    Mallet A; Kypriotou M; George K; Leclerc E; Rivero D; Mazereeuw-Hautier J; Serre G; Huber M; Jonca N; Hohl D
    Br J Dermatol; 2013 Dec; 169(6):1322-5. PubMed ID: 23957618
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Peeling skin syndrome: genetic defects in late terminal differentiation of the epidermis.
    Bowden PE
    J Invest Dermatol; 2011 Mar; 131(3):561-4. PubMed ID: 21307953
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Severe dermatitis, multiple allergies and metabolic wasting (SAM) syndrome caused by de novo mutation in the DSP gene misdiagnosed as generalized pustular psoriasis and treatment of acitretin with gabapentin.
    Liang J; Li C; Zhang Z; Ni C; Yu H; Li M; Yao Z
    J Dermatol; 2019 Jul; 46(7):622-625. PubMed ID: 31106887
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.