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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

384 related items for PubMed ID: 21801157

  • 1. Diffuse and focal palmoplantar keratoderma can be caused by a keratin 6c mutation.
    Akasaka E, Nakano H, Nakano A, Toyomaki Y, Takiyoshi N, Rokunohe D, Nishikawa Y, Korekawa A, Matsuzaki Y, Mitsuhashi Y, Sawamura D.
    Br J Dermatol; 2011 Dec; 165(6):1290-2. PubMed ID: 21801157
    [Abstract] [Full Text] [Related]

  • 2. Collapse of the keratin filament network through the expression of mutant keratin 6c observed in a case of focal plantar keratoderma.
    Kubo A, Oura Y, Hirano T, Aoyama Y, Sato S, Nakamura K, Takae Y, Amagai M.
    J Dermatol; 2013 Jul; 40(7):553-7. PubMed ID: 23662636
    [Abstract] [Full Text] [Related]

  • 3. Keratin K6c mutations cause focal palmoplantar keratoderma.
    Wilson NJ, Messenger AG, Leachman SA, O'Toole EA, Lane EB, McLean WH, Smith FJ.
    J Invest Dermatol; 2010 Feb; 130(2):425-9. PubMed ID: 19609311
    [Abstract] [Full Text] [Related]

  • 4. 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 Feb; 22(4):476-80. PubMed ID: 22668561
    [Abstract] [Full Text] [Related]

  • 5. Mutations in AAGAB underlie autosomal dominant punctate palmoplantar keratoderma.
    Dinani N, Ali M, Liu L, McGrath J, Mellerio J.
    Clin Exp Dermatol; 2017 Apr; 42(3):316-319. PubMed ID: 28239884
    [Abstract] [Full Text] [Related]

  • 6. Mutations in a keratin 6 isomer (K6c) cause a type of focal palmoplantar keratoderma.
    Bowden PE.
    J Invest Dermatol; 2010 Feb; 130(2):336-8. PubMed ID: 20081885
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening.
    Lovgren ML, McAleer MA, Irvine AD, Wilson NJ, Tavadia S, Schwartz ME, Cole C, Sandilands A, Smith FJD, Zamiri M.
    Br J Dermatol; 2017 May; 176(5):1345-1350. PubMed ID: 27534273
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. 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
    [Abstract] [Full Text] [Related]

  • 18. Acral keratoderma.
    Nesbitt LT, Rothschild H, Ichinose H, Stein W, Levy L.
    Arch Dermatol; 1975 Jun; 111(6):763-8. PubMed ID: 1137423
    [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
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 20.