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- A case of pretibial epidermolysis bullosa with pemphigus foliaceus is reported. 报告胫前大疱性表皮松解症并发落叶型天疱疮1例。
- Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa. 目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因突变,为进一步开展基因诊断和基因治疗奠定基础。
- Objective To study the gene mutation in a pedigree with Dowling-Meara type epidermolysis bullosa simplex (DM-EBS). 目的研究 Dowling-Meara亚型单纯型大疱性表皮松解症 (DM-EBS)一家系的基因突变。
- Objective: To identify gene mutation in a family with Weber-Cockayne type epidermolysis bullosa simplex (WC-EBS). 鉴定单纯型大疱性表皮松解症Weber-Cockayne亚型一家系中的基因突变位点。
- Objective:To identify gene mutation in a family with Weber-Cockayne type epidermolysis bullosa simplex(EBS-WC). 目的:研究Weber-Cockayne亚型单纯型大疱性表皮松解症(EBS-WC)一家系的基因突变,并进行产前诊断。
- Objective:Analysis characteristic and regularity of epidermolysis bullosa type eruption. 目的:探讨大疱性表皮松解型药疹的发生特点及一般规律。
- Preclinical progress has been achieved in the treatment of wounds, epidermolysis bullosa and ichthyosis. 前期的临床实验在治疗创伤，大疱性表皮松解症和鱼鳞病上已经取得了进展.
- Conclusion:Incidence of epidermolysis bullosa type eruption ought to be observed... 结论:应用上述药品时应注意观察大疱性表皮松解型药疹的发生。
- The most epidermolysis bullosa inducing drugs were antibiotics and CNS drugs. 28 patients died with the number ... 致死病例28例,致死药物以解热镇痛药居首位。
- Our results showed that 81 drugs were reported to cause 155 cases of epidermolysis bullosa. 结果:共查得81种药物引起的大疱性表皮松解症155例,诱发药物以抗微生物药和中枢神经系统药占绝大多数;
- Objective: (1) To study the gene mutation in a pedigree with Dowling-Meara type epidermolysis bullosa simplex(DW-EBS) of monogenic disease. 寻找单基因病痒疹样亚型单纯型大疱性表皮松解症(DM-EBS)一家系的基因突变位点。
- Objective:To investigate the clinical features,diagnosis and therapy of patients with epidermolysis bullosa sim-plex Weber-Cockayne(EBS-WC). 目的:探讨单纯型大疱性表皮松解症Weber-Cockayne(EBS-WC)亚型的临床特征、诊断及治疗。
- Mechanisms of Fibroblast Cell Therapy for Dystrophic Epidermolysis Bullosa: High Stability of Collagen VII Favors Long-term Skin Integrity. 成纤维细胞治疗营养不良性大疱性表皮松解症机制：VII-胶原蛋白的高度稳定性有利于保持长期皮肤完整。
- Methods:Electron microscopy and indirect immunofluorescence were performed on skin samples from 7 patients with epidermolysis bullosa. 方法:分析7个组织病理表现为表皮下疱的先天性大疱性表皮松解症患者的透射电镜和免疫荧光表现。
- I have finally learned how to say, that I have a rare orphan genetic skin disorder named recessive dystrophic epidermolysis bullosa. 现在我终于学会解释自己的病了：这是一种罕见的遗传性皮肤病，叫隐性遗传营养不良型大疱性表皮松解症。
- Based on the distincthereditary style.DEB is divided into dominant dystrophic epidermoIysis bullosa(DDEB) and recessive dystrophic epidermolysis bullosa (RDEB). 根据遗传方式的不同，可将DEB分为常染色体显性遗传型(DDEB)和常染色体隐性遗传型(RDEB)。
- Based on the distincthereditary style. DEB is divided into dominant dystrophic epidermoIysis bullosa(DDEB) and recessive dystrophic epidermolysis bullosa (RDEB). 根据遗传方式的不同，可将DEB分为常染色体显性遗传型(DDEB)和常染色体隐性遗传型(RDEB)。
- Results Among the 18 cases,there were 13 cases with drug eruption serious erythema multiforme,one case with drug eruption epidermolysis bullosa,4 cases with druy eruption measles. 结果18例卡马西平药疹中重症多形红斑型13例(72%25),大疱性表皮松解型1例(6%25),麻疹样发疹型4例(22%25),重症型多有肝、肾功能损害,病程长,皮质类固醇激素治疗有效。
- The development, causes of death and treatment of epidermolysis bullosa was retrospectively reviewed by retrieving the articles published in medical periodicals during 1970 1999. 目的:了解药源性大疱性表皮松解症的发生情况、致死原因及治疗方法。
- Objective To identify additional epidermolysis bullosa simplex(EBS) mutations for studying the correlation between genotype and phenotype of EBS, and to provide hasis for genetic counselling, as well as for gene diagnosis and gene therapy. 目的鉴定更多的单纯型大疱性表皮松解症（EBS）突变以研究EBS基因型和表型关系，为EBS的遗传咨询及基因诊断和基因治疗奠定基础。
