Nghĩa của từ epidermolysis bằng Tiếng Việt
@Chuyên ngành kỹ thuật
@Lĩnh vực: y học
-chứng bong biểu bì
@Chuyên ngành kỹ thuật
@Lĩnh vực: y học
-chứng bong biểu bì
Đặt câu có từ "epidermolysis"
1. Objective:Analysis characteristic and regularity of epidermolysis bullosa type eruption.
2. Partial superficial epidermolysis of areola occurred in 2 cases.
3. Conclusion:Incidence of epidermolysis bullosa type eruption ought to be observed...
4. Recessive dystrophic epidermolysis bullosa with junctional blisters includes both the classical epidermolysis bullosa hereditaria letalis Herlitz (Herlitz-Pearson type) and a recently separated more benign adult type.
5. Analysis characteristic and regularity of epidermolysis bullosa type eruption.
6. Although epidermolysis bullosa acquisita is thought to be an autoimmune disease, epidermolysis bullosa is a group of inherited diseases in which epithelial adhesion protein defects lead to epithelial fragility and Bullae …
7. The two genetic disorders of Connective tissue are epidermolysis bullosa (EB) and Marfan syndrome
8. Conclusions The causes and clinical features of drug-induced bullosa epidermolysis are extremely complicated.
9. The relationship between these results and the phenomenology of epidermolysis bullosa hereditaria in skin is discussed.
10. Methods A retrospective study was performed on 31 patients with drug-induced bullosa epidermolysis.
11. Objective : To identify gene mutation in a family with Weber - Cockayne type epidermolysis bullosa simplex ( WC - EBS ).
12. Objective To explore the causes, clinical features and appropriate therapies of drug-induced bullosa epidermolysis.
13. Objective:To study molecule in basement membrane by electron microscopy and indirect immunofluorescence in patients with inherited epidermolysis bullosa.
14. Learn more about the different types of Blistering diseases, such as, dermatitis herpetiformis, epidermolysis bullosa, and bullous pemphigoid.
15. In epidermolysis bullosa hereditaria (e.b.h.) simplex, the mode of formation of the bulla is particularly remarkable.
16. In particular, epidermolysis bullosa hereditaria, the collodion baby phenotype and harlequin ichthyosis represent serious clinical challenges with neonatal onset.
17. 7 patients with epidermolysis bullosa hereditaria as well as 3 relatives were examined upon their coagulation system.
18. Objective : To identify gene mutation in a family with Weber - Cockayne type epidermolysis bullosa simplex ( EBS - WC ).
19. With regard to the death rate, exfoliative dermatitis was the highest, next was epidermolysis bullosa and Stevens-Johnson syndrome was the lowest.
20. Objective To investigate the experience of the specialized nursing of toxic epidermolysis, improve specialized nursing care and accelerate patients get well soon.
21. Pustular psoriasis of the palms and soles, epidermolysis bullosa hereditaria, hand-foot-mouth-disease, acrodermatitis enteropathica and scabies in children are possible differential diagnoses for vesicles on the palms and soles.
22. With vesicles, oozing or bullae: Pustular psoriasis of the palms and soles, epidermolysis bullosa hereditaria, hand-foot-mouth-disease, acrodermatitis enteropathica and scabies in children are possible differential diagnoses for vesicles on the palms and soles.
23. Several Aetiologies for BOSs have been documented, ranging from stenosis secondary to trachea-oesophageal fistula repair (18 50%), caustic ingestion (38%), achalasia (5%), epidermolysis bullosa (<1%) and gastrooesophageal reflux, to name a few.[3,4] All have showed a good 1-year follow-up success rate with balloon dilatation techniques.[1-5]