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cover and contents
Abstract
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59)
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2024, Vol.57(7): 0–0
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Expert consensus on hematoporphyrin monomethyl ether-mediated photodynamic therapy for treating port-wine stains （2024）
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262)
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2024, Vol.57(7): 581–589 doi: https://doi.org/10.35541/cjd.20230584
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Treatment of port-wine stains: current status and prospects
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2024, Vol.57(7): 590–594 doi: https://doi.org/10.35541/cjd.20240047
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Efficacy and influencing factors of hematoporphyrin monomethyl ether-mediated photodynamic therapy in the treatment of adult patients with port-wine stains: a retrospective study
Abstract
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2024, Vol.57(7): 595–600 doi: https://doi.org/10.35541/cjd.20240045
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Untargeted metabolomics analysis-based metabolic characterization of hemangioma-derived endothelial cells
Abstract
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2024, Vol.57(7): 601–609 doi: https://doi.org/10.35541/cjd.20230452
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Efficacy of 595-nm pulsed dye laser in the treatment of port‐wine stains in 155 infants and toddlers: a retrospective analysis
Abstract
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76)
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2024, Vol.57(7): 610–615 doi: https://doi.org/10.35541/cjd.20240062
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Efficacy of hematoporphyrin monomethyl ether-mediated photodynamic therapy in the treatment of facial port-wine stains in 15 children with Sturge-Weber syndrome
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2024, Vol.57(7): 616–622 doi: https://doi.org/10.35541/cjd.20240065
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Application of reflectance confocal microscopy combined with optical coherence tomography in the observation of histological changes and evaluation of therapeutic efficacy in melasma: a retrospective analysis
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2024, Vol.57(7): 623–631 doi: https://doi.org/10.35541/cjd.20240079
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Drug survival rate and safety of dupilumab in the treatment of atopic dermatitis in elderly patients: a retrospective cohort analysis
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2024, Vol.57(7): 632–636 doi: https://doi.org/10.35541/cjd.20230732
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Clinical characteristics of and NF1 gene mutation analysis in 22 patients with neurofibromatosis type 1
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2024, Vol.57(7): 637–644 doi: https://doi.org/10.35541/cjd.20240027
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A case of nodular hypertrophic port-wine stains treated with long-pulsed 1 064-nm Nd:YAG laser
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2024, Vol.57(7): 645–646 doi: https://doi.org/10.35541/cjd.20210945
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Two sisters suffering from connective tissue nevus
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2024, Vol.57(7): 646–648 doi: https://doi.org/10.35541/cjd.20210890
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A case of systemic sclerosis with secondary normotensive renal crisis and hemolytic uremic syndrome
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2024, Vol.57(7): 648–649 doi: https://doi.org/10.35541/cjd.20220444
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A case of ichthyosis hystric Curth-Macklin type caused by a novel mutation in the KRT1 gene
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2024, Vol.57(7): 650–651 doi: https://doi.org/10.35541/cjd.20220294
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A case of congenital unilateral nevoid telangiectasia with Bier spots
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2024, Vol.57(7): 652–653 doi: https://doi.org/10.35541/cjd.20220118
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Dupilumab for the treatment of epidermolysis bullosa pruriginosa in a child
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2024, Vol.57(7): 654–655 doi: https://doi.org/10.35541/cjd.20220778
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Diagnosis and treatment of port-wine stains-associated syndromes
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2024, Vol.57(7): 656–660 doi: https://doi.org/10.35541/cjd.20240048
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Port-wine stains: mechanisms underlying the development and progression
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43)
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2024, Vol.57(7): 661–664 doi: https://doi.org/10.35541/cjd.20240052
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Treatment of Merkel cell carcinoma
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2024, Vol.57(7): 665–667 doi: https://doi.org/10.35541/cjd.20210536
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Long non-coding RNA-mediated competitive endogenous RNA regulatory network in keloids
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2024, Vol.57(7): 668–671 doi: https://doi.org/10.35541/cjd.20210471
