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You searched for: Author/Creator Matsuda, Mitsuhiro

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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)

4. A sporadic elder case of erythrokeratodermia variabilis with a single base‐pair transversion in GJB3 gene successfully treated with systemic vitamin A derivative. Issue 11 (9th October 2014)

6. Anti‐desmoglein 1 antibody‐positive mother and antibody‐negative child with Darier's disease. Issue 2 (8th September 2022)

7. 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)

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)

10. 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)