Cost-effective diagnosis of male oxidative stress using the nitroblue tetrazolium test: useful application for the developing world
Zinc therapy improves deleterious effects of chronic copper administration on mice testes: histopathological evaluation
Processes involved in assisted reproduction technologies significantly increase sperm DNA fragmentation and phosphatidylserine translocation
The effect of mahogunin gene mutant on reproduction in male mice: a new sight for infertility?
Body mass index has no impact on sperm quality but on reproductive hormones levels
Effect of alcohol intake and cigarette smoking on sperm parameters and pregnancy
Reproductive function in middle-aged males: healthy men versus male partners of infertile couples
Sperm DNA fragmentation in couples with unexplained recurrent spontaneous abortions
Relationship between dyslipidaemia and semen quality and serum sex hormone levels: an infertility study of 167 Japanese patients
Differential expression of mRNA aromatase in ejaculated spermatozoa from infertile men in relation to either asthenozoospermia or teratozoospermia
ACP1 genetic polymorphism and spermatic parameters in men with varicocele
Infertility in rats subjected to genitofemoral nerve section is not associated with testicular damage
SEMG1 may be the candidate gene for idiopathic asthenozoospermia
Effect of the metabolic syndrome on male reproductive function: a case-controlled pilot study
Effect of Coenzyme Q10 supplementation on antioxidant enzymes activity and oxidative stress of seminal plasma: a double-blind randomised clinical trial
Combination of running exercise and high dose of anabolic androgenic steroid, nandrolone decanoate, increases protamine deficiency and DNA damage in rat spermatozoa
Ovotesticular disorder of sexual development due to 47,XYY/46,XY/45,X mixed gonadal dysgenesis in a phenotypic male presenting as cyclical haematuria: clinical presentation and assessment of long-term outcomes
Identification of fatty acids in canine seminal plasma
Novel and rare CFTR gene mutations in Turkish patients with congenital aplasia of vas deferens