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The British Journal of Dermatology|December 12, 2019
Revisiting pachyonychia congenita: a case-cohort study of 815 patientsL Samuelov, F J D Smith, C D Hansen, et al.
The British Journal of Dermatology|March 28, 2017
Report of the 13th Annual International Pachyonychia Congenita Consortium SymposiumL Rittié, R L Kaspar, E Sprecher, et al.
The British Journal of Dermatology|December 7, 2017
Chronic pain in pachyonychia congenita: evidence for neuropathic originS Brill, E Sprecher, F J D Smith, et al.
The British Journal of Dermatology|September 30, 2009
Increased pachyonychia congenita severity in patients with concurrent keratin and filaggrin mutationsR Gruber, N J Wilson, F J D Smith, et al.
Clinical and Experimental Dermatology|October 6, 2018
Novel and recurrent mutations in keratin 1 cause epidermolytic ichthyosis and palmoplantar keratodermaF J D Smith, I M Kreuser-Genis, C S Jury, et al.
The British Journal of Dermatology|July 28, 2011
Transgrediens pachyonychia congenita (PC): case series of a nonclassical PC presentationK Harris, P R Hull, C D Hansen, et al.
The British Journal of Dermatology|December 31, 2013
Heterozygous frameshift mutation in keratin 5 in a family with Galli-Galli diseaseA K Reisenauer, S V Wordingham, J York, et al.
The British Journal of Dermatology|November 22, 2011
Pachyonychia congenita patients with mutations in KRT6A have more extensive disease compared with patients who have mutations in KRT16K M Spaunhurst, A M Hogendorf, F J D Smith, et al.
Clinical and Experimental Dermatology|October 28, 2016
Isolated recessive nail dysplasia caused by FZD6 mutations: report of three families and review of the literatureC Kasparis, D Reid, N J Wilson, et al.
Clinical and Experimental Dermatology|December 18, 2013
A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by DSP mutationsA Vahlquist, M Virtanen, M Hellström-Pigg, et al.
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