ichthyosis的例句大全

OBJECTIVE: To study retrospectively the effect and ADRs of etretinate in 49 patients of keratinization, including psoriasis 33 cases, pityriasis rubra pilaris 6 cases, ichthyosis 3 cases and lichen planus 7 cases.

目的：回顾性研究了依曲替酯治疗49例角化性疾病（银屑病33例，毛发红糠疹6例，鱼鳞病3例和扁平苔藓7例）的疗效及不良反应等。

Diagnosing X-linked Ichthyosis by Monoplast Single-round Duplex PCR

单细胞单轮二重PCR诊断X-连锁鱼鳞病

Investigation of STS Gene in a Pedigree with X-Linked Ichthyosis

X性联锁遗传鱼鳞病一家系的STS基因研究

Ichthyosis bullosa of Siemens: Its correct diagnosis facilitated by molecular genetic testing

分子遗传学检测使Siemens大疱性鱼鳞病易于正确诊断

First report of gene mutation in a Chinese patient with ichthyosis bullosa of Siemens

Siemens大疱性鱼鳞病基因突变国内首次报道

Pathological observation of ichthyosis hystrix Lambert type with light and electron microscopes

Lambert型豪猪状鱼鳞病的光镜及电镜分析

We studied disseminated superficial actinic porokeratosis ( DSAP) and ichthyosis vulgaris ( IV).

我们研究了播散性浅表光化性汗孔角化症（DSAP）和寻常型鱼鳞病（IV）。

Transglutaminase 1 gene mutations in a family with lamellar ichthyosis

板层状鱼鳞病TGM1基因突变研究

Objective To detect the mutations of GJB2 and GJB6 genes in the first Chinese case of keratitis, ichthyosis and deafness ( KID) syndrome.

目的检测国内首例先天性角膜炎、鱼鳞病、耳聋综合征（KID）患者的GJB2基因和GJB6基因突变。

Barrier dysfunction and pathogenesis of neutral lipid storage disease with ichthyosis ( Chanarin-Dorfman syndrome)

伴鱼鳞病的中性脂质贮存异常的发病机制和屏障功能障碍（Chanarin-Dorfman综合征）

Objective To detect the mutations of transglutaminase 1 ( TGM1) gene in a family with lamellar ichthyosis.

目的探讨一个板层状鱼鳞病家系转谷氨酰胺酶1基因（TGM1）的突变。

Results: 97 cases were randomly divided into three groups. After 28 days treatment, respectively the efficacy rates were 100%, 100% for ichthyosis vulgaris and rhagadia manus and pedalis in test group, vs.

结果：97例患者随机分为试验组、对照组和开放组，28d治疗后，试验组鱼鳞病和手足皲裂的有效率均为100%、对照组则分别为91.7%和27.3%。

Serum essential fatty acid analyses in patients with psoriasis and ichthyosis

银屑病和鱼鳞病患者血清必需脂肪酸分析

Gene Mutations in Two Sporadic Cases of Epidermolytic Hyperkeratosis Ichthyosis

表皮松解性角化过度型鱼鳞病二例及其基因突变的研究

Keratitis ichthyosis and deafness syndrome: first report in China

角膜炎·鱼鳞病·耳聋综合征&国内首例报告

Objective To study the nursing experience of children with severe ichthyosis.

目的探讨重症鱼鳞病患儿的临床护理经验。

Objective To identify gene mutations of two cases of epidermolytic hyperkeratosis ichthyosis.

目的研究二例表皮松解性角化过度型鱼鳞病患者基因突变情况。

A case of X-linked ichthyosis with interatrial septal defect

伴房间隔缺损的X-连锁鱼鳞病1例

Analysis on the Genotype and Clinical Phenotype Correlations of Four Style Heritage Ichthyosis

四种遗传性鱼鳞病基因型与临床表型的相关性分析

Nursing for 23 children with severe ichthyosis

重症鱼鳞病患儿的护理23例