epidermolysis bullosa
英
美
网络 大疱性表皮松解症; 大疱性表皮裂解; 大疱性表皮松解; 表皮溶解水疱症; 松解症
双语例句
- Treatment for dystrophic epidermolysis bullosa using tissue-engineering technique and cell therapy
组织工程技术和细胞疗法治疗营养不良性大疱性表皮松解症 - Treatment of drug eruption of epidermolysis bullosa with high-power photon therapeutic device in one case
高光功率光子治疗仪治疗大疱性表皮松解萎缩坏死型药疹1例 - A Case of Epidermolysis Bullosa Drug Eruption Accompanied with Gastric Perforation Recovery of gastrointestinal motility following laparoscopy versus open operation for repair of gastric perforation
大疱性表皮松解性药疹伴胃穿孔1例胃穿孔腹腔镜修补术与开腹修补术术后胃肠动力恢复的对比研究 - 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。 - 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。 - Junctional epidermolysis bullosa. Identification of a new mutation in two Lebanese families ( Fren)
接合型大疱性表皮松解症在两个黎巴嫩家系中发现一个新的突变（法国） - Treatment of 14 Patients with Epidermolysis Bullosa Drug Eruption
14例大疱性表皮坏死松解型药疹治疗体会 - Inherited epidermolysis bullosa a study on molecule in basement membrane zone
先天性大疱性表皮松解症基底膜带分子的研究 - Immunofluorescence studies on the Skin Sections of Recessive Dystrophic Epidermolysis Bullosa Patients with Anti-P_ ( 200) Pemphigoid Sera
抗P（200）血清对隐性遗传性营养不良性大疱性表皮松解症皮肤的免疫荧光研究 - A Case of Dominant Dystrophia Epidermolysis Bullosa Pasini
Pasini型大疱性表皮松解症1例 - Analysis of clinical features, diagnosis and therapy in 17 patients with epidermolysis bullosa simplex Weber-Cockayne
单纯型大疱性表皮松解症Weber-Cockayne亚型临床特征、诊断和治疗分析 - Objective: To identify gene mutation of a dystrophic epidermolysis bullosa family.
目的：研究一营养不良型大疱表皮松解症家系的基因突变。 - Objective: To study molecule in basement membrane by electron microscopy and indirect immunofluorescence in patients with inherited epidermolysis bullosa.
目的：通过透射电镜和免疫荧光研究先天性大疱性表皮松解症患者的基底膜带分子。 - Both direct immunofluorescence staining ( DIF) of skin biopsy and indirect immunofluorescence test ( IIF) of serum offered valuable adjuncts to clinical and histological diagnosis in two patients with epidermolysis bullosa acquisita ( EBA).
采用皮肤活检直接免疫荧光法（DIF）和血清间接免疫荧光法（IIF）确诊两例获得性大疱性表皮松解症（EBA）。 - Nursing care of a case with epidermolysis bullosa atrophy-necrosis drug eruption
1例大疱性表皮松解萎缩坏死型药疹病人的护理 - Dystrophic Epidermolysis Bullosa: Analysis of Clinical and Genetic Features and Study on the Structure Deficiency of Basement Membrane Zone
营养不良型大疱性表皮松解症：临床、遗传特点分析及其基底膜带结构缺陷的研究 - 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。 - Keratin gene mutation in a pedigree of Dowling-Meara epidermolysis bullosa simplex
Dowling-Meara型单纯性大疱性表皮松解症一家系角蛋白基因突变研究 - With regard to the death rate, exfoliative dermatitis was the highest, next was epidermolysis bullosa and Stevens-Johnson syndrome was the lowest.
死亡率以剥脱性皮炎型最高，大疱表皮坏死松解型次之，重症多形红斑型最低。 - IgG and IgA BMZ Ab in epidermolysis bullosa acquisita sera specifically reacted with 290 000 dermal peptide.
获得性大疱性表皮松解症患者血清中IgG型和IgA型BMZ抗体特异性结合真皮提取物中290000多肽； - Analysis of Clinical Features and Diagnosis of Dominant Dystrophic Epidermolysis Bullosa Genealogy
显性营养不良型大疱性表皮松解症家系临床表现与诊断分析 - Nine Cases in One Family of Epidermolysis Bullosa
大疱性表皮松解症同一家族9例报告 - Objective To report a pedigree of generalized atrophic benign epidermolysis bullosa ( GABEB), a special type of junctional epidermolysis bullosa ( JEB).
目的报道我国首例泛发性萎缩性良性大疱性表皮松解症家系。 - Objective: To investigate the gene mutation in a pedigree of Dowling-Meara Epidermolysis Bullosa Simplex ( EBS), confirm the type of EBS.
目的：研究一家族性DowlingMeara型单纯性大疱性表皮松解症（EBS）中的遗传基础，分析患者的基因突变及确定EBS的亚型。 - Albopapuloid epidermolysis bullosa ── report of six cases
白色丘疹样大疱性表皮松解症&附6例报告 - Hallopeau-Siemens type of recessive dystrophic epidermolysis bullosa: a case report
常染色体隐性遗传的Hallopeau-Siemens型营养不良型大疱性表皮松解症1例 - 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。 - Recessive dystrophic epidermolysis bullosa ( Hallopeau-Siemens) with IgA nephropathy: 4 Cases ( Fren)
隐性营养不良型大疱性表皮松解伴IgA肾病：4例报道（法语）