青年中文青年中文

epidermolysis的意思

epidermolysis中文翻譯:

n.[醫]表皮松解

相似詞語短語

epidermatoid───adj.表皮樣的

epidermoid───adj.(生物)表皮樣的,像表皮的

outermost layer of the epidermis───表皮的最外層

epidermal sebaceous cyst───表皮皮脂腺囊腫

epidermose───表皮的

epidermal inclusion cyst───表皮包涵囊腫

epidermal setae───表皮剛毛

enepidermic───adj.對皮膚用藥的

epidermal growth factor───[生理]表皮生長因子,[生理]上皮生長因子;上表皮生長因素

ectoderm epidermis───外胚層表皮

雙語使用場景

Objective: Analysis characteristic and regularity of epidermolysis bullosa type eruption.───目的:探討大皰性表皮松解型藥疹的發生特點及一般規律。

Preclinical progress has been achieved in the treatment of wounds, epidermolysis bullosa and ichthyosis.───前期的臨床實驗在治療創傷,大皰性表皮松解癥和魚鱗病上已經取得了進展。

EBA) is an autoimmune subepidermal bullous disease. This disease is rare in childhood.───兒童獲得性大皰表皮松解癥(EBA)是一種自身免疫性表皮下大皰病,比較少見。

Conclusion: Incidence of epidermolysis bullosa type eruption ought to be observed. . .───結論:應用上述藥品時應注意觀察大皰性表皮松解型藥疹的發生。

Conclusions The causes and clinical features of drug-induced bullosa epidermolysis are extremely complicated.───結論大皰性表皮松解型藥疹病因、臨床表現復雜;

Analysis characteristic and regularity of epidermolysis bullosa type eruption.───探討大皰性表皮松解型藥疹的發生特點及一般規律。

Methods: Electron microscopy and indirect immunofluorescence were performed on skin samples from 7 patients with epidermolysis bullosa.───方法:分析7個組織病理表現為表皮下皰的先天性大皰性表皮松解癥患者的透射電鏡和免疫熒光表現。

I have finally learned how to say, that I have a rare orphan genetic skin disorder named recessive dystrophic epidermolysis bullosa.───現在我終于學會解釋自己的病了:這是一種罕見的遺傳性皮膚病,叫隱性遺傳營養不良型大皰性表皮松解癥。

英語使用場景

I have finally learned how to say, that I have a rare orphan genetic skin disorder named recessive dystrophic epidermolysis bullosa.

Preclinical progress has been achieved in the treatment of wounds, epidermolysis bullosa and ichthyosis.

Objective To investigate the experience of the specialized nursing of toxic epidermolysis, improve specialized nursing care and accelerate patients get well soon.

Objective:To study molecule in basement membrane by electron microscopy and indirect immunofluorescence in patients with inherited epidermolysis bullosa.

Conclusion:Incidence of epidermolysis bullosa type eruption ought to be observed...

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.

Analysis characteristic and regularity of epidermolysis bullosa type eruption.

Objective:Analysis characteristic and regularity of epidermolysis bullosa type eruption.

Epidermolysis bullosa acquisita(EBA) is an autoimmune subepidermal bullous disease. This disease is rare in childhood.