Results 41 to 50 of about 9,757 (189)

Induced pluripotent stem cell line from a mouse model of human azoospermia with a frameshift mutation Tex11_1260Ins(TT)

open access: yesStem Cell Research, 2022
Infertility is a common disease that impacts 15% of reproductive age couples worldwide, and genetic causes are implicated in about half of those cases. Non-obstructive azoospermia is a severe form of male infertility that features spermatogenic failure ...
Kien T.D. Tran   +4 more
doaj   +1 more source

Distribution of CFTR and IVS8polyT genotypes in the two groups of patients divided according to the histopathological results: obstructive azoospermia and nonobstructive azoospermia/oligozoospermia.

open access: yes, 2014
[−] means no CF mutation detected on single chromosome.Distribution of CFTR and IVS8polyT genotypes in the two groups of patients divided according to the histopathological results: obstructive azoospermia and nonobstructive azoospermia/oligozoospermia.
Marija Mircevska (658227)   +5 more
core   +1 more source

Relationship between testicular sperm extraction and varicocelectomy in patients with varicocele and nonobstructive azoospermia

open access: yes, 2013
To evaluate the effect of varicocelectomy on sperm retrieval at testicular sperm extraction (TESE) and at spermiograms in patients with nonobstructive ...
COSTANTINI, Claudio   +4 more
core   +1 more source

Overexpression of hsa-miR-30a-5p and nonobstructive azoospermia: A case-control study [PDF]

open access: yes, 2022
Background: Some previous human and animal studies have supported the idea that KDM3A down-regulation might be the main cause of male infertility, especially in nonobstructive azoospermia (NOA).
Motovali-Bashi, M. (Majid)   +11 more
core   +1 more source

MBOAT1 homozygous missense variant causes nonobstructive azoospermia

open access: yesAsian Journal of Andrology, 2022
Nonobstructive azoospermia (NOA) is a common cause of infertility and is defined as the complete absence of sperm in ejaculation due to defective spermatogenesis. The aim of this study was to identify the genetic etiology of NOA in an infertile male from
Yang-Yang Wan   +7 more
doaj   +1 more source

The significance of karyotyping and azoospermia factor analysis in patients with nonobstructive azoospermia or oligozoospermia

open access: yes, 2023
[[abstract]]Objective We present our study about the significance of karyotyping and azoospermia factor(AZF) analysis in patients with azoospermia or oligozoospermia.
Che, Shin-Wen;Chen, Shin-Wen;陳持平;Chen, Chih-Ping;Ch, Schu-Rern;Chern, Schu-Rern;Kuo, Yu-Ling;Kuo, Yu-Ling;Chien-Ling, Chien-Ling C;Chiu, Chien-Ling
core  

Sperm Retrieval and Intracytoplasmic Sperm Injection in Men With Nonobstructive Azoospermia, and Treated and Untreated Varicocele

open access: yes, 2009
Purpose: We evaluated the impact of varicocelectomy on the sperm retrieval success rate using microsurgical testicular sperm extraction and intracytoplasmic sperm injection in men with clinical varicocele and nonobstructive ...
Ergen, Ali   +5 more
core   +1 more source

Identification of pathogenic mutations from nonobstructive azoospermia patients

open access: yesBiology of Reproduction, 2022
Abstract It is estimated that approximately 25% of nonobstructive azoospermia (NOA) cases are caused by single genetic anomalies, including chromosomal aberrations and gene mutations. The identification of these mutations in NOA patients has always been a research hot spot in the area of human infertility.
Hanwei, Jiang   +5 more
openaire   +2 more sources

Surgical management of nonobstructive azoospermia [PDF]

open access: yes, 2018
Nonobstructive azoospermia (NOA) is characterized by the complete absence of sperm in the ejaculate due to testicular failure. The evaluation and management of patients with NOA offer a challenge to the reproductive urologist.
Tanrikut, Cigdem   +2 more
core   +1 more source

Multidimensional Determinants of Quality of Life in Men With Klinefelter Syndrome: A Narrative Review of Workshop Evidence

open access: yesAndrology, EarlyView.
ABSTRACT Background Klinefelter syndrome (KS), typically characterized by a 47, XXY karyotype, is the most common sex chromosomal aneuploidy in males, with a prevalence of approximately one in 600–660 individuals. Despite its frequency, the syndrome remains significantly underdiagnosed, with 50%–75% of affected individuals never receiving a clinical ...
Francesca Allosso   +2 more
wiley   +1 more source

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