Results 31 to 40 of about 8,359 (251)

Kromosoomianomaaliad ja kromosoomivariandid infertiilsetel meestel [PDF]

open access: yes, 2006
Lastetust esineb umbes 15% peredest. Selle mehepoolsetest põhjustest moodustavad 30% geneetilised tegurid, eeskätt kromosoomihaigused. Eestis on viljatuse tsütogeneetilisi põhjusi seni vähe uuritud.
Lissitsina, Jelena   +2 more
core   +2 more sources

Obesity and Increased Risk for Oligozoospermia and Azoospermia [PDF]

open access: yesArchives of Internal Medicine, 2012
The global obesity epidemic parallels a decrease in male fertility. Yet, the association between body mass index (BMI) and sperm parameters remains controversial. A negative correlation between BMI and sperm concentration or total sperm count (TSC) was shown by several reports,1, 2 but not documented by others.3, 4 The purpose of this report was to ...
Sermondade, Nathalie   +5 more
openaire   +7 more sources

Genomic study of TEX15 variants: prevalence and allelic heterogeneity in men with spermatogenic failure

open access: yesFrontiers in Genetics, 2023
Introduction: Human spermatogenesis is a highly intricate process that requires the input of thousands of testis-specific genes. Defects in any of them at any stage of the process can have detrimental effects on sperm production and/or viability.
Sidra Qureshi   +18 more
doaj   +1 more source

Serum inhibin B as a marker of spermatogenesis [PDF]

open access: yes, 1998
Inhibin B is produced by Sertoli cells, provides negative feedback on FSH secretion, and may prove to be an important marker for the functioning of seminiferous tubules.
Jong, F.H. (Frank) de   +4 more
core   +3 more sources

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

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2022
Objective: We present our study about the significance of karyotyping and azoospermia factor(AZF) analysis in patients with azoospermia or oligozoospermia.
Shin-Wen Chen   +4 more
doaj  

Prevalence of Y chromosome deletions in a Brazilian population of nonobstructive azoospermic and severely oligozoospermic men [PDF]

open access: yes, 2003
We determined the prevalence of Y chromosome deletions in a population of 60 Brazilian nonobstructive azoospermic and severely oligozoospermic men. PCR-based screening of microdeletions was performed on lymphocyte DNA for the presence of 14 sequence ...
Avellar, Maria Christina Werneck   +6 more
core   +2 more sources

Relationship between Dairy Product Consumption and Oligospermia; a Case-Control Study

open access: yesMen's Health Journal, 2018
Introduction: Infertility affects an estimated 15% of couples globally and in Iran, a quarter of Introduction: One of the current debates regarding men’s reproductive health is the declining sperm count and the role of nutritional and environmental ...
Alireza Dizavi   +4 more
doaj   +1 more source

Meiotic recombination and male infertility: from basic science to clinical reality? [PDF]

open access: yes, 2011
Infertility is a common problem that affects approximately 15% of the population. Although many advances have been made in the treatment of infertility, the molecular and genetic causes of male infertility remain largely elusive. This review will present
Hann, Michael C.   +2 more
core   +1 more source

Approach to the Patient With Oligozoospermia [PDF]

open access: yesThe Journal of Clinical Endocrinology & Metabolism, 2013
Male infertility affects 1 in 20 men and is the sole or contributory factor in half of assisted reproductive treatments (ARTs). A reduced sperm density (oligozoospermia) is often accompanied by poor motility and morphology reflecting qualitative and quantitative defects in spermatogenesis.
openaire   +3 more sources

Study on occurrence of the IVS8-5T allele of the CFTR gene in Ukrainian males with spermatogenesis failure [PDF]

open access: yes, 2010
Aim. To study the IVS8-5T allele of the CFTR gene and it is involvement in spermatogenesis failure in men with azoospermia and oligozoospermia. Methods.
Fesai O. A.   +3 more
core   +1 more source

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