These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

187 related articles for article (PubMed ID: 19785597)

  • 1. Increased pachyonychia congenita severity in patients with concurrent keratin and filaggrin mutations.
    Gruber R; Wilson NJ; Smith FJ; Grabher D; Steinwender L; Fritsch PO; Schmuth M
    Br J Dermatol; 2009 Dec; 161(6):1391-5. PubMed ID: 19785597
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pachyonychia congenita patients with mutations in KRT6A have more extensive disease compared with patients who have mutations in KRT16.
    Spaunhurst KM; Hogendorf AM; Smith FJ; Lingala B; Schwartz ME; Cywinska-Bernas A; Zeman KJ; Tang JY
    Br J Dermatol; 2012 Apr; 166(4):875-8. PubMed ID: 22098151
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two novel de novo mutations of KRT6A and KRT16 genes in two Chinese pachyonychia congenita pedigrees with fissured tongue or diffuse plantar keratoderma.
    Du ZF; Xu CM; Zhao Y; Liu WT; Chen XL; Chen CY; Fang H; Ke HP; Zhang XN
    Eur J Dermatol; 2012; 22(4):476-80. PubMed ID: 22668561
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of clinically useful predictive genetic variants in pachyonychia congenita.
    Samuelov L; Sarig O; Adir N; Pavlovsky M; Smith FJ; Schwartz J; Hansen CD; Sprecher E
    Clin Exp Dermatol; 2021 Jul; 46(5):867-873. PubMed ID: 33486795
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A new KRT16 mutation associated with a phenotype of pachyonychia congenita.
    Paris F; Hurtado C; Azón A; Aguado L; Vizmanos JL
    Exp Dermatol; 2013 Dec; 22(12):838-9. PubMed ID: 24118415
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The molecular genetic analysis of the expanding pachyonychia congenita case collection.
    Wilson NJ; O'Toole EA; Milstone LM; Hansen CD; Shepherd AA; Al-Asadi E; Schwartz ME; McLean WH; Sprecher E; Smith FJ
    Br J Dermatol; 2014 Aug; 171(2):343-55. PubMed ID: 24611874
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A KRT16 mutation in the first Chinese pedigree with Pachyonychia congenita and review of the literatures.
    Xu Q; Zhang Q; Tang L; Jin L; Wang X; Kan L; Zheng X; Yang S
    J Cosmet Dermatol; 2019 Dec; 18(6):1930-1934. PubMed ID: 30859684
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A large mutational study in pachyonychia congenita.
    Wilson NJ; Leachman SA; Hansen CD; McMullan AC; Milstone LM; Schwartz ME; McLean WH; Hull PR; Smith FJ
    J Invest Dermatol; 2011 May; 131(5):1018-24. PubMed ID: 21326300
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation p.Leu128Pro in the 1A domain of K16 causes pachyonychia congenita with focal palmoplantar keratoderma in a Chinese family.
    Dai L; Wu J; Guo H; Huang Y; Zhang K; Liu D; Fu L; Wu Y; Guan X; Bai Y; Liao Q
    Eur J Pediatr; 2014 Jun; 173(6):737-41. PubMed ID: 24357266
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A review of the clinical phenotype of 254 patients with genetically confirmed pachyonychia congenita.
    Eliason MJ; Leachman SA; Feng BJ; Schwartz ME; Hansen CD
    J Am Acad Dermatol; 2012 Oct; 67(4):680-6. PubMed ID: 22264670
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel FLG mutations associated with ichthyosis vulgaris in the Chinese population.
    Xiong Z; Luo S; Xu X; Zhang L; Peng H; Li W; Xue J; Chen X; Hu Z; Xia K
    Clin Exp Dermatol; 2012 Mar; 37(2):177-80. PubMed ID: 22299762
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Revisiting pachyonychia congenita: a case-cohort study of 815 patients.
    Samuelov L; Smith FJD; Hansen CD; Sprecher E
    Br J Dermatol; 2020 Mar; 182(3):738-746. PubMed ID: 31823354
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genotype-phenotype correlations among pachyonychia congenita patients with K16 mutations.
    Fu T; Leachman SA; Wilson NJ; Smith FJ; Schwartz ME; Tang JY
    J Invest Dermatol; 2011 May; 131(5):1025-8. PubMed ID: 21160496
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Filaggrin haploinsufficiency is highly penetrant and is associated with increased severity of eczema: further delineation of the skin phenotype in a prospective epidemiological study of 792 school children.
    Brown SJ; Relton CL; Liao H; Zhao Y; Sandilands A; McLean WH; Cordell HJ; Reynolds NJ
    Br J Dermatol; 2009 Oct; 161(4):884-9. PubMed ID: 19681860
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Keratin 16-null mice develop palmoplantar keratoderma, a hallmark feature of pachyonychia congenita and related disorders.
    Lessard JC; Coulombe PA
    J Invest Dermatol; 2012 May; 132(5):1384-91. PubMed ID: 22336941
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pathophysiology of pachyonychia congenita-associated palmoplantar keratoderma: new insights into skin epithelial homeostasis and avenues for treatment.
    Zieman AG; Coulombe PA
    Br J Dermatol; 2020 Mar; 182(3):564-573. PubMed ID: 31021398
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ichthyosis vulgaris: novel FLG mutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup.
    Oji V; Seller N; Sandilands A; Gruber R; Gerss J; Hüffmeier U; Hamm H; Emmert S; Aufenvenne K; Metze D; Luger T; Loser K; Hausser I; Traupe H; McLean WH
    Br J Dermatol; 2009 Apr; 160(4):771-81. PubMed ID: 19183181
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Exacerbation of ichthyosis vulgaris phenotype by co-inheritance of STS and FLG mutations in a Chinese family with ichthyosis: a case report.
    Wang X; Tan L; Shen N; Lu Y; Zhang Y
    BMC Med Genet; 2018 Jul; 19(1):120. PubMed ID: 30021537
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Generalized bullae in a young girl with KRT6A-related pachyonychia congenita.
    Liu J; Zhong W; Yu B; Lin Z; Zheng Y; Hu X
    Pediatr Dermatol; 2020 Sep; 37(5):974-976. PubMed ID: 32662074
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pachyonychia congenita: a case report of a successful treatment with rosuvastatin in a patient with a KRT6A mutation.
    Abdollahimajd F; Rajabi F; Shahidi-Dadras M; Saket S; Youssefian L; Vahidnezhad H; Uitto J
    Br J Dermatol; 2019 Sep; 181(3):584-586. PubMed ID: 30307612
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.