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Epidermolysis in a sentence

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Sentence count:18Posted:2017-07-05Updated:2020-07-24
Similar words: hemolysisepidermisepidermicglycolysishydrolysiselectrolysisanalysisparalysis
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1. Objective:Analysis characteristic and regularity of epidermolysis bullosa type eruption.
2. Analysis characteristic and regularity of epidermolysis bullosa type eruption.
3. Conclusion:Incidence of epidermolysis bullosa type eruption ought to be observed...
4. Epidermolysis bullosa acquisita(EBA) is an autoimmune subepidermal bullous disease. This disease is rare in childhood.
5. Preclinical progress has been achieved in the treatment of wounds, epidermolysis bullosa and ichthyosis.
6. Objective:To study molecule in basement membrane by electron microscopy and indirect immunofluorescence in patients with inherited epidermolysis bullosa.
7. Objective To investigate the experience of the specialized nursing of toxic epidermolysis, improve specialized nursing care and accelerate patients get well soon.
8. I have finally learned how to say, that I have a rare orphan genetic skin disorder named recessive dystrophic epidermolysis bullosa.
9. Bart syndrome is a genetic disorder characterized by the association of congenital localized absence of skin, epidermolysis bullosa, lesions of the mouth mucosa, and dystrophic nails.
10. Methods A retrospective study was performed on 31 patients with drug-induced bullosa epidermolysis.
11. Objective To study the gene mutation in a pedigree with Dowling - Meara type epidermolysis bullosa simplex ( DM - EBS ).
12. With regard to the death rate, exfoliative dermatitis was the highest, next was epidermolysis bullosa and Stevens-Johnson syndrome was the lowest.
13. Objective : To investigate the clinical features, diagnosis and therapy of patients with epidermolysis bullosa sim - plex Weber - Cockayne ( EBS - WC ).
14. Objective To explore the causes, clinical features and appropriate therapies of drug-induced bullosa epidermolysis.
15. Conclusions The causes and clinical features of drug-induced bullosa epidermolysis are extremely complicated.
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16. Conclusions The splicing mutation of COL7A1 gene is the underlying cause of and specific rather than common polymorphism for the family with dystrophic epidermolysis bullosa pruriginosa subtype.
17. Objective : To identify gene mutation in a family with Weber - Cockayne type epidermolysis bullosa simplex ( WC - EBS ).
18. Objective : To identify gene mutation in a family with Weber - Cockayne type epidermolysis bullosa simplex ( EBS - WC ).
More similar words: hemolysisepidermisepidermicglycolysishydrolysiselectrolysisanalysisparalysisepidemicpsychoanalysischemical analysisepidemiologyspidercost-benefit analysisbenefit-cost analysisepidemiologistsupply-side economicsin the final analysistaxidermyelysiumelysiantepidpolystyreneintrepidpolysyllabicepididymisside by sidetrepidationthermossermon
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