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searching for Pachyonychia congenita 5 found (29 total)

Steatocystoma multiplex (633 words) [view diff] exact match in snippet view article find links to article

et al. (1997). "Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex". J. Invest

List of patient-reported quality of life surveys (8,434 words) [view diff] case mismatch in snippet view article find links to article

hydroxychloroquine. Pachyonychia Congenita. The Pachyonychia Congenita Quality of Life (PCQoL) was developed in 2012 to determine the effect Pachyonychia Congenita has

Type II keratin (922 words) [view diff] exact match in snippet view article find links to article

skin disorders, including psoriasis, epidermolysis bullosa, and pachyonychia congenita. Type I keratin Schweizer, Jürgen; Bowden, Paul E.; Coulombe, Pierre

RNA interference (15,445 words) [view diff] exact match in snippet view article find links to article

NCT00689065 TD101 K6a (N171K mutation) Naked siRNA Pachyonychia congenita I Completed Pachyonychia Congenita Project NCT00716014 AGN211745 VEGFR1 Naked siRNA

RNA silencing (5,475 words) [view diff] exact match in snippet view article find links to article

domain Drug Indication Target Ocular and retinal disorders TD101 Pachyonychia congenita Keratin 6A N171K mutant Ocular and retinal disorders QPI-1007 Non-arteritic