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cover and contents
Abstract
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105)
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2022, Vol.55(8): 0–0
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Some thoughts on hereditary dermatoses
Abstract
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326)
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10
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2022, Vol.55(8): 651–652 doi: https://doi.org/10.35541/cjd.20220509
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Mutation analysis of the COL7A1 gene in 4 cases of recessive dystrophic epidermolysis bullosa
Abstract
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397)
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2022, Vol.55(8): 653–658 doi: https://doi.org/10.35541/cjd.20210455
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Effect of HaCaT cells with CRISPR-Cas9-induced KRT5 mutation on co-cultured human melanocytes
Abstract
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356)
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2022, Vol.55(8): 659–664 doi: https://doi.org/10.35541/cjd.20210748
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Clinical and pathological analysis of 8 cases of mucoepidermoid carcinoma
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543)
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2022, Vol.55(8): 665–668 doi: https://doi.org/10.35541/cjd.20210795
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Analysis of skin and mucosal infections and their management after primary tumor resection in patients with paraneoplastic pemphigus
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348)
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2022, Vol.55(8): 669–675 doi: https://doi.org/10.35541/cjd.20220003
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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
Abstract
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477)
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2022, Vol.55(8): 676–681 doi: https://doi.org/10.35541/cjd.20210751
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Rare subtypes of epidermolysis bullosa: three case reports and their pedigree analysis
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2022, Vol.55(8): 682–685 doi: https://doi.org/10.35541/cjd.20210479
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Mutation analysis of the PNPLA1 gene in three families with congenital ichthyosiform erythroderma
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2022, Vol.55(8): 685–689 doi: https://doi.org/10.35541/cjd.20220156
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Mutation analysis of the ADAR gene in two cases of dyschromatosis symmetrica hereditaria and a survey of their families
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345)
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2022, Vol.55(8): 690–692 doi: https://doi.org/10.35541/cjd.20210299
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Diagnosis of acanthosis nigricans in a family by targeted sequencing
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383)
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2022, Vol.55(8): 693–695 doi: https://doi.org/10.35541/cjd.20210695
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TP63 gene mutation analysis in a case of ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
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515)
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2022, Vol.55(8): 696–699 doi: https://doi.org/10.35541/cjd.20201051
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A novel pathogenic mutation in the NEMO gene in a family with incontinentia pigmenti
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270)
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2022, Vol.55(8): 700–703 doi: https://doi.org/10.35541/cjd.20210931
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Mutation analysis of the KRT5 gene in a Chinese pedigree with Dowling-Degos disease
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366)
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2022, Vol.55(8): 703–705 doi: https://doi.org/10.35541/cjd.20210028
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Identification of pathogenic genes in a family with oculocutaneous albinism
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2022, Vol.55(8): 706–709 doi: https://doi.org/10.35541/cjd.20210393
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A case of ADULT syndrome without finger/toe deformities caused by a TP63 mutation
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445)
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2022, Vol.55(8): 709–712 doi: https://doi.org/10.35541/cjd.20210554
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Analysis of clinical phenotype and gene variants in a patient with classic tuberous sclerosis complex
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2022, Vol.55(8): 713–716 doi: https://doi.org/10.35541/cjd.20210541
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Hereditary hemorrhagic telangiectasia complicated by aortic sinus aneurysm caused by a pathogenic mutation in the ACVRL1 gene： a family survey
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328)
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2022, Vol.55(8): 716–720 doi: https://doi.org/10.35541/cjd.20210566
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Inhibitory effect of mucopolysaccharide polysulfate cream on hypertrophic scar formation in a rabbit ear model and its mechanisms of action
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376)
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2022, Vol.55(8): 720–726 doi: https://doi.org/10.35541/cjd.20210690
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KRT5 gene mutation-induced epidermolysis bullosa simplex with mottled pigmentation in a family
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285)
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2022, Vol.55(8): 727–729 doi: https://doi.org/10.35541/cjd.20210317
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Mutation analysis of the COL7A1 gene in a family with Bart syndrome
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295)
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2022, Vol.55(8): 729–730 doi: https://doi.org/10.35541/cjd.20201123
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Rhabdomyolysis after high-intensity exercise in a patient with acne receiving isotretinoin treatment
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2022, Vol.55(8): 731–732 doi: https://doi.org/10.35541/cjd.20220314
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Congenital multiple fibrofolliculomas in an infant
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308)
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2022, Vol.55(8): 733–734 doi: https://doi.org/10.35541/cjd.20210054
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Treatment of some genodermatoses
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367)
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2022, Vol.55(8): 735–739 doi: https://doi.org/10.35541/cjd.20220001
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Gene therapy for recessive dystrophic epidermolysis bullosa
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453)
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2022, Vol.55(8): 739–743 doi: https://doi.org/10.35541/cjd.20210499
