WPRIM Management System> DCMS> Chinese Journal of Dermatology> 2022> 55> 8

Volume: 55 Issue: 8

1. TP63 gene mutation analysis in a case of ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Page:696—699
2. Gene therapy for recessive dystrophic epidermolysis bullosa Page:739—743
3. A case of ADULT syndrome without finger/toe deformities caused by a TP63 mutation Page:709—712
4. Hereditary hemorrhagic telangiectasia complicated by aortic sinus aneurysm caused by a pathogenic mutation in the ACVRL1 gene: a family survey Page:716—720
5. Diagnosis of acanthosis nigricans in a family by targeted sequencing Page:693—695
6. Inhibitory effect of mucopolysaccharide polysulfate cream on hypertrophic scar formation in a rabbit ear model and its mechanisms of action Page:720—726
7. Identification of pathogenic genes in a family with oculocutaneous albinism Page:706—709
8. Mutation analysis of the KRT5 gene in a Chinese pedigree with Dowling-Degos disease Page:703—705
9. Some thoughts on hereditary dermatoses Page:651—652
10. Mutation analysis of the COL7A1 gene in 4 cases of recessive dystrophic epidermolysis bullosa Page:653—658
11. Effect of HaCaT cells with CRISPR-Cas9-induced KRT5 mutation on co-cultured human melanocytes Page:659—664
12. Clinical and pathological analysis of 8 cases of mucoepidermoid carcinoma Page:665—668
13. Analysis of skin and mucosal infections and their management after primary tumor resection in patients with paraneoplastic pemphigus Page:669—675
14. Retrospective analysis of efficacy and safety of minocycline alone or in combination with low-dose glucocorticoids in the treatment of 15 cases of pemphigus erythematosus and 9 cases of pemphigus herpetiformis Page:676—681
15. Rare subtypes of epidermolysis bullosa: three case reports and their pedigree analysis Page:682—685
16. Mutation analysis of the PNPLA1 gene in three families with congenital ichthyosiform erythroderma Page:685—689
17. Mutation analysis of the ADAR gene in two cases of dyschromatosis symmetrica hereditaria and a survey of their families Page:690—692
18. A novel pathogenic mutation in the NEMO gene in a family with incontinentia pigmenti Page:700—703
19. Analysis of clinical phenotype and gene variants in a patient with classic tuberous sclerosis complex Page:713—716
20. Treatment of some genodermatoses Page:735—739

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