1.
Keratin Gene Mutation of an EHK Family;
表皮松解性角化过度家系基因突变研究
2.
Mutation Analysis of KRT9 Gene in a Chinese Family with Epidermolytic Palmoplantar Keratoderma;
表皮松解性掌跖角化症一家系的基因突变研究
3.
Screening and Analysis of Keratin 9 Gene (KRT9) Mutation in 4 Chinese Families with Epidermolytic Palmoplantar Keratoderma;
4个中国人表皮松解性掌跖角化症家系KRT9基因突变的研究
4.
hyperplastic epidermolysis bullosa
增生性大疱性表皮松解
5.
epidermolysis bullosa acquisita, EBA
获得性大疱性表皮松解症
6.
Laboratory Diagnoses of Epidermolysis Bullosa Acquisita;
获得性大疱性表皮松解症的实验诊断
7.
A Case of Epidermolysis Bullosa Drug Eruption Accompanied with Gastric Perforation
大疱性表皮松解性药疹伴胃穿孔1例
8.
Nursing Care for A Patient with Severe Brain Injury Combined with Epidermolysis Bullosa
1例重度颅脑损伤伴大疱性表皮松解型药疹患者的护理
9.
A case of recessive dystrophic epidermolysis bullosa
隐性遗传营养不良型大疱性表皮松解症1例
10.
Toxic bullosa epidermalysis associated with metamizole sodium tablets
安乃近片相关中毒性大疱性表皮松解症
11.
follicular hyperkeratosis
毛囊性角质化过度症
12.
Dominant Dystrophic Epidermolysis Bullosa: Mutation Analysis;
显性营养不良型大疱性表皮松解症的基因突变研究
13.
The Report of One Clan with Dystrophic Epidermolysis Bullosa Dominant;
遗传性营养不良型大疱性表皮松解症一家系报告
14.
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
15.
A family report of albopapuloid epidermolysis bullosa dystrophica dominant
白色丘疹样显性营养不良型大疱性表皮松解症一家系报告
16.
By decreasing the release of these chemicals in the skin, fluocinolone reduces inflammation and relieves itch.
透过减少这些化学物质在皮肤层,氟轻松能减轻炎症和解除痕痒。
17.
Analysis of Intravenous Immunoglobulin for the Treatment of Toxic Epidermal Necrolysis;
中毒性表皮坏死松解症免疫球蛋白治疗临床分析
18.
Mutation Analysis of COL7A1 Gene in Two Chinese Families with Dystrophic Epidermolysis Bullosa Pruriginosa;
痒疹样营养不良型大疱性表皮松解症两家系基因突变分析