نتایج جستجو برای: oligoasthenoteratozoospermia

تعداد نتایج: 145  

Journal: :medical journal of islamic republic of iran 0
mohammad a. khalili from the research and clinical center for infertility, shahid sadoughi university of medical sciences, bou-ali avenue, yazd,l.r. iran. serajeddin vahidi abbas aflatounian mohammad a. karimzadeh hussain amir-arjmand

the latest micromanipulative technique, intracytoplasmic sperm injection (icsi), has been very successful in cases of severe male factor infertility. the main objective of this study is to report the results of our first experience with icsi in cases of male factor infertility, as well as patients who had failed their previous cycles with conventional in vitro fertilization (ivf). normal fertil...

Journal: :Human reproduction 2005
Adele De Palma Nunziatina Burrello Nunziata Barone Rosario D'Agata Enzo Vicari Aldo E Calogero

BACKGROUND Patients with oligoasthenoteratozoospermia (OAT) and normal karyotypes have an increased sperm aneuploidy rate. This may be due to an altered intratesticular environment that affects the chromosomal segregation mechanism(s). Alternatively, it may be due to a generalized meiotic and mitotic abnormality. In this case, patients with abnormal spermatogenesis should also have an increased...

2014
Jinu Lee Dong Ryul Lee Suman Lee

Monocarboxylic acid transporter 2 (MCT2) transports pyruvate and lactate outside and inside of sperms, mainly as energy sources and plays roles in the regulation of spermatogenesis. We investigated the association among genetic variations in the MCT2 gene, male infertility and MCT2 expression levels in sperm. The functional and genetic significance of the intron 2 (+28201A > G, rs10506398) and ...

Journal: :Human reproduction 2006
Han-Chul Lee Yu-Mi Jeong Sook Hwan Lee Kwang Yul Cha Seung-Hun Song Nam Keun Kim Kyo Won Lee Suman Lee

BACKGROUND Three typical folate metabolism enzymes-i.e. methylenetetrahydrofolate reductase (MTHFR), methionine synthase (MS) and MS reductase (MTRR) in the folate cycle-play a critical role in DNA synthesis and methylation reactions. We evaluated whether polymorphisms of these three enzymes are associated with non-obstructive male infertility. METHOD Three hundred and sixty patients with non...

Journal: :In vivo 2017
Cemallettin Cengiz Beyaz Sezgin Gunes Kadir Onem Tuba Kulac Ramazan Asci

Many genetic alterations have been identified to aid in understanding the genetic basis of male infertility, however, the cause of 30% of male infertility remains unknown. Some studies indicated that subdeletions of Y chromosome may be a reason for male infertility caused by testicular failure. In this regard, we aimed to investigate frequency of AZFc region subdeletions and their clinical effe...

2014
Rosita A Condorelli Aldo E Calogero Enzo Vicari Laura Mongioi' Giovanni Burgio Rossella Cannarella Filippo Giacone Linda Iacoviello Giuseppe Morgia Vincenzo Favilla Sebastiano Cimino Sandro La Vignera

The present study evaluated the conventional sperm parameters and the seminal concentration of CD45pos cells (pan-leukocyte marker) of infertile patients with idiopathic oligoasthenoteratozoospermia (OAT). The patients were arbitrarily divided into three groups treated with recombinant follicle-stimulating hormone FSH: α (Group A = 20 patients), recombinant FSH- β (Group B = 20 patients), and h...

Journal: :Human reproduction 2002
B Peterlin T Kunej J Sinkovec N Gligorievska B Zorn

BACKGROUND The objective of this study was to estimate the frequency of Y chromosome microdeletions in the Slovenian population of infertile men and to analyse the consequences of mutation in respect to clinical severity and prognosis. METHODS In a controlled clinical study at the university-based medical genetics service and infertility clinic, 226 infertile men undergoing ICSI were tested. ...

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