epidermolysis bullosa

Nine Cases in One Family of Epidermolysis Bullosa

大疱性表皮松解症同一家族9例报告

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）。

Study of Gene Mutation of Dominant Dystrophic Epidermolysis Bullosa of One Case

1例DEB的基因突变研究

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

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

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

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

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

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。

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

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

Epidermolysis Bullosa Necrotic Dermatitis Medicamentosa ( with Analysis 35 Cases )

大疱性表皮松解坏死型药物性皮炎（附35例分析）

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。

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

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）

Cyclosporine controls epidermolysis bullosa acquisita co - occuring with acquired factor VIII deficiency

环孢菌素控制获得性大疱性表皮松解症同时伴发获得性Ⅷ因子缺乏

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。

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

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

A new mutation in the linker 12 domain of keratin 5 in a Chinese family with Weber-Cockayne epidermolysis bullosa simplex

一中国家系Weber-Cockayne单纯性大疱性表皮松解症角蛋白5连接子12结构域的新变异

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。

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。

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

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。

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）

A Case of Dominant Dystrophia Epidermolysis Bullosa Pasini

Pasini型大疱性表皮松解症1例

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；

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。