azoospermia的例句大全

Objective: To treat obstructive azoospermia by percutaneous epididymal, testicular sperm aspiration ( PETSA) and intracytoplasmic sperm injection ( ICSI).

目的：应用经皮附睾、睾丸穿刺取精术（PETSA），结合单精子卵浆内显微注射（ICSI）技术治疗阻塞性无精子症。

Objective: To introduce the application of percutaneous epididymal sperm aspiration ( PESA) in the differential diagnosis between obstructive and non-obstructive azoospermia, and to investigate the association of the results of PESA with testis volume and the level of serum follicle stimulating hormone ( FSH).

目的：介绍经皮附睾穿刺取精术（PESA）在梗阻性和非梗阻性无精子症诊断中的应用，并探讨睾丸体积和血清卵泡刺激素（FSH）水平对其结果的影响。

Enzymatic digestion plus mechanical searching improves testicular sperm retrieval in non-obstructive azoospermia cases

酶消化与机械找精联合以改进非梗阻性无精症患者的睾丸取精术

Percutaneous epididymal and/ or testicular sperm aspiration and intracytoplasmic sperm injection in the treatment of obstructive azoospermia

经皮附睾、睾丸穿刺取精卵浆内显微注射治疗阻塞性无精子症

[ Conclusions] It is a recommendable method that simple testicular needle aspiration in the men diagnosis and treatment of the men with obstructive azoospermia.

结论简易式睾丸穿刺取精用于阻塞性无精子症的诊治是一种值得推广的方法。

Azoospermia factor microdeletion on Y chromosome in patients with idiopathic azoospermia or severe oligozoospermia

原发性无精、少弱精症患者Y染色体AZF微缺失检测

To investigate the relationship between microdeletion of azoospermia factor ( AZF) and male infertility.

对原发性无精子及少弱精症患者与AZF微缺失的关系。

The incidence rate of large Y in infertile men with oligospermia or azoospermia was 35.37% ( 52/ 147);

其中少弱畸精患者大Y发生率为35.37%（52/147）；

Conclusion ICSI is an effective treatment for infertility of severe oligo-astheno-teratospermia and obstructive azoospermia.

结论ICSI技术是治疗重度少、弱、畸精症及阻塞性无精症性不育的有效手段。

Evaluation of treatment of intracytoplasmic sperm injection for infertility of severe oligo-astheno-teratospermia and obstructive azoospermia

重度少、弱、畸精症及阻塞性无精症患者单精子卵胞浆内注射治疗结果分析

The analysis of correlation between karyotype and AZF microdeletion on Y chromosome for patients with azoospermia and severe oligozoospermia.

目的：研究男性原发性无精及严重少精症患者Y染色体AZF微缺失区域与临床表型的关系。

Objective To analyze the pattern and prevalence of partial copy deletion of deleted-in-azoospermia ( DAZ) gene in the azoospermia factor C ( AZFc) region of patients with idiopathic azoospermia or severe oligozoospermia.

目的分析原发无精症和严重少精症患者Y染色体无精症因子C区（azoospermia factor C，AZFc）DAZ基因（deleted-in-azoospermia，DAZ）部分拷贝缺失的类型与频率。

Screening of AZF microdeletion in the patients with azoospermia or severe oligozoospermia

严重少精、无精患者无精子因子（AZF）的检测及意义

The rates of which showed FSH, LH and T reducing together were 14.3% in azoospermia and 7.7% in severe oligospermia;

FSH、LH、T均呈降低者，无精症组14.3%，重度少精症组7.7%；

The rates of which showed FSH, LH increasing but T in the normal reference range were 38.1% in azoospermia and 23.1% in severe oligospermia;

FSH、LH升高而T在正常参考范围者，无精症组38.1%，重度少精症组23.1%；

Study on the Relationship between the Region of Y Chromosome AZF Microdeletion and Clinical Phenotype in Patients with Idiopathic Azoospermia and Oligospermia

无精症及严重少精症患者Y染色体AZF微缺失区域与临床表型关系的研究

Objective To investigate the relationship between chromosome abnormalities and Y chromosome microdeletion of azoospermia factor ( AZF) in patients with azoospermia and oligozoospermia.

目的探讨无精、少精及严重少精症与染色体核型异常和Y染色体无精子因子（AZF）微缺失的关系。

Methods Deletions in 25 azoospermic and 27 severe oligozoospermic Chinese patients were screened by STS PCR strategy. A total of 23 STSs in interval 6 of Yq, including 4 STSs in the deleted azoospermia gene ( DAZ) region were analyzed.

方法运用STS PCR法对25例无精症和27例严重少精症患者的Y染色体interval6的23个序列标签位点（STS）进行缺失筛查。

Methods The levels of seminal plasma PGE 2 and PGF 1 α were determined by radioimmunoassay ( RIA) in 130 men who were divided into normal control, infertility, oligospermia and azoospermia groups;

方法用放免法检测130例不同生育状态（正常生育对照组，不育组，少精组及无精组）精浆中PGE2和PGF1α的含量；

Conclusion The frequency of partial copy deletion of DAZ gene in Chinese idiopathic azoospermia or severe oligozoospermia patients is much higher than that of fertile controls, suggesting that the deletion of DAZ1/ DAZ2 may be one of the important genetic etiological factors of spermatogenesis damage.

实验组与对照组DAZ1/DAZ2共缺失率差异有极显著性。结论原发无精和严重少精症存在较高频率的AZFc区DAZ基因的部分缺失，这可能是中国男性原发不育的病因之一。