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1. A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in Netherton syndrome. Issue 7 (20th May 2016)

2. A founder deletion of corneodesmosin gene (CDSN) is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases. Issue 2 (May 2017)

3. A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases. Issue 2 (May 2016)

5. Anti‐early endosome antigen 1 autoantibodies were detected in a pemphigus‐like patient but not in the majority of pemphigus diseases. Issue 5 (May 2016)

6. Atypical pemphigus with immunoglobulin G autoantibodies against desmoglein 3 and desmocollin 3. Issue 4 (2nd September 2015)

7. Case of paraneoplastic pemphigus with immunoglobulin (Ig)G and IgA antibodies to various antigens. Issue 8 (11th March 2016)

8. Corrigendum to 'Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia' [Journal of Dermatological Science 78 (2015) 82–85]. Issue 2 (August 2015)

9. Corrigendum to 'Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia' [Journal of Dermatological Science 78 (2015) 82–85]. Issue 2 (August 2015)