epidermolysis
1. epidermolysis bullosa hereditaria lethalis
(拉)先天性大疱性致死性表皮松解
2. epidermolysis bullosa simplex
(拉)单纯性大疱性表皮松解
3. epidermolysis bullosa acquisita
(拉)后天性大疱性表皮松解
4. epidermolysis bullosa lethalis
(拉)致死性大疱性表皮松解
5. 23rd of April, Went to Leshan to visit two children diagnosed with Hereditary epidermolysis bullosa, Wan Lihong and Wan Yuqing .
4月23日,到乐山看望两个“遗传性大疱性表皮松解症”的孩子(万丽红、万雨晴)。
6. Study on gene mutation in a dystrophic epidermolysis bullosa family
一营养不良型大疱表皮松解症家系的基因突变
7. toxic bullosa epidermolysis
中毒性大疱性表皮松解
8. Epidermolysis Bullosa (EB) is a rare genetic disease characterized by the presence of extremely fragile skin and recurrent blister formation, resulting from minor mechanical friction or trauma.
什么是'大疱性表皮松解症单纯,斑驳的色素沉着-罕见的遗传性皮肤疾病起泡'?
9. congenital epidermolysis bullosa
先天性大疱性表皮松解
10. Congenital junctional epidermolysis bullosa
先天性结合部大疱性表皮松解
11. generalized epidermolysis bullosa simplex
全身性单纯性大疱性表皮松解
12. 6.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.
13. Autosomal dominant epidermolysis bullosa simplex
单纯常染色体显性大疱性表皮松解
14. epidermolysis simplex
单纯性表皮松解症
15. dysplastic epidermolysis bullosa dystrophica
发育不良性营养不良性大疱性表皮松解
16. epidermolysis bullosa of oral cavity
口腔大疱性表皮松解症
17. acquired epidermolysis bullosa
后天性大疱性表皮松解
18. epidermolysis acquisita
后天性表皮松解症
19. epidermolysis bullosa hyperplastica
增生性大疱性表皮松解
20. hyperplastic epidermolysis
增生性表皮松解
21. Polydysplastic epidermolysis bullosa
多发育不良性大疱性表皮松解
22. polydysplastic epidermolysis bullosa dystrophica
多种发育不良性营养不良性大疱性表皮松解
23. epidermolysis bullosa polydysplastica
多种增生不良型大疱型表皮松解症
24. epidermolysis bullosa
大疱性表皮松解
25. Epidermolysis bullosa letalis with pyloric atresia
大疱性表皮松解伴幽门闭锁
26. Epidermolysis bullosa by drug
大疱性表皮松解型药疹
27. epidermolysis bollosa
大疱性表皮松解症
28. Keywords pretibial epidermolysis bullosa;pemphigus;foliaceus;
大疱性表皮松解症;胫前;天疱疮;落叶型;
29. 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。
30. localized epidermolysis bullosa simplex
局限性单纯性大疱性表皮松解
31. epidermolysis bullosa dystrophica generalisata Pasini
帕西尼普通营养不良性大疱性表皮松解
32. epidermolysis acuta toxica
急性中毒性表皮松解
33. epidermolysis acute toxica
急性毒性表皮松解
34. Adult junctional epidermolysis bullosa
成人结合部大疱性表皮松解
35. 4. 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。
36. Epidermolysis bullosa simplex of the hands and feet
手和脚单纯大疱性表皮松解
37. 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。
38. 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。
39. dominant epidermolysis bullosa simplex with mottled pigmentation
显性单纯性伴有斑点状色素沉着的大疱性表皮松解症
40. dominant epidermolysis bullosa simplex WeberCockayne
显性单纯性大疱性表皮松解, 韦-科二氏(综合征)
41. dominant epidermolysis bullosa simplex
显性单纯性大疱性表皮松解症
42. dominant epidermolysis bullosa simplex Ogna
显性单纯性大疱性表皮松解症, 奥格纳(氏)变型
43. dominant epidermolysis bullosa simplex kobner
显性单纯性大疱性表皮松解症, 科布内(氏)变型
44. dominant epidermolysis bullosa Bart
显性大疱性表皮松解症, 巴特氏(综合征)
45. dominant epidermolysis bullosa herpetiformis Dowling-Meara
显性疱疹样大疱性表皮松解症, 多-米二氏(综合征)
46. dominant epidermolysis bullosa dys-trophica albopapuloidea Pasini
显性白色丘疹样营养障碍型大疱性表皮松解症, Pasini(综合征)
47. 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
48. Dominant dystrophic epidermolysis bullosa
显性营养不良性大疱性表皮松解
49. dominant epidermolysis bullosa dystrophica Cockayne-Touraine
显性营养障碍性大疱性表皮松解症, 考-托二氏(综合征)
50. dominant dystrophia epidermolysis bullosa
显性遗传营养不良型大疱性表皮松解
51. epidermolysis bullosa dystrophic dominant
显性遗传营养不良性大疱性表皮松解
52. 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)。
53. generalized atrophic benign epidermolysis bullosa
泛发性萎缩性良性大疱性表皮松解
54. 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。
55. albopapuloid epidermolysis bullosa dystrophica
白丘疹样营养不良性大疱性表皮松解
56. albopapular form of epidermolysis bullosa
白色丘疹形大疱性表皮松解
57. epidermolysis bullosa albo papuloid
白色丘疹样大疱性表皮松解
58. 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。
59. 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。
60. Objective To investigate the experience of the specialized nursing of toxic epidermolysis, improve specialized nursing care and accelerate patients get well soon.
目的总结中毒性表皮松解症(TEN)患者的护理经验,提高护理质量,有效地促进患者康复。
61. Objective To probe the potential risk factors in the process of remedy of children having drug-induced bullous epidermolysis complicated with septicemia and the effect of predictive nursing.
目的探讨儿童大疱表皮松解型药疹合并败血症在救治过程中存在的潜在危险因素和早期预见护理的效果。
62. 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。
63. 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。
64. 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。
65. Keywords SD-Ag;Epidermolysis bullosa by drug;Clinical study;
磺胺嘧啶银;大疱性表皮松解型药疹;临床研究;
66. Epidermolysis bullosa dystrophica neurotrophica
神经营养不良性大疱性表皮松解
67. junctional epidermolysis bullosa
结合性大疱性表皮松解
68. 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%),大疱性表皮松解型1例(6%),麻疹样发疹型4例(22%),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。
69. 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;
70. Results:Antibacterials is the first drugs that cause epidermolysis bullosa type eruption,the sceond is psychotropic drug and nerve drug.route of administration is mainly oral administration.
结果:抗菌药物引起的大疱性表皮松解型药疹居首位,其次为神经精神类药物。给药途径以口服为主。
71. 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。
72. Pretibial epidermolysis bullosa
胫骨前大疱性表皮松解
73. Epidermolysis bullosa hereditaria letalis
致命性大疱性表皮松解
74. epidermolysis bullosa fatalis
致死性大疱性表皮松解
75. 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。
76. Jordan Young is one of only five children in Britain with epidermolysis bullosa, a painful condition that means his skin suffers irritation every time it comes in contact with ordinary materials.
英国一名只有1岁大的小童由于罹患可致命的罕见皮肤失调的怪病,只能接触真丝和绸缎,就连尿片也必须以丝绸缝制。
77. Keywords adverse drug reaction;epidermolysis bullosa type eruption;literature;
药品不良反应;大疱性表皮松解型药疹;文献分析;
78. acquired(non-inherited)epidermolysis bullosa acquisita
获得性(非遗传性)大泡性表皮松解
79. epidermolysis bullosa acquisita,EBA
获得性大疱性表皮松解症
80. epidermolysis bullosa atrophicans
萎缩性大疱性表皮松解