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WPRIM Management System>
DCMS
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Chinese Journal of Dermatology
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2022
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55
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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