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Quoted phrase not found in phrase index: "Spermatogenic failure 49"
Page 1
Fertility problems in men carrying a translocation involved in breakpoints on chromosome 17p13: A retrospective, observational study.
Li R. Li R. Medicine (Baltimore). 2022 Dec 9;101(49):e32216. doi: 10.1097/MD.0000000000032216. Medicine (Baltimore). 2022. PMID: 36626513 Free PMC article.
Several breakpoints of chromosome 17 are related to important genes, which can lead to spermatogenic failure. This study aimed to identify the clinical features of 3 men with translocation karyotypes involving breakpoints on chromosome 17p13. ...The results suggest …
Several breakpoints of chromosome 17 are related to important genes, which can lead to spermatogenic failure. This study aimed …
High serum FSH is not a risk factor for low bone mineral density in infertile men.
Antonio L, Priskorn L, Olesen IA, Petersen JH, Vanderschueren D, Jørgensen N. Antonio L, et al. Bone. 2020 Jul;136:115366. doi: 10.1016/j.bone.2020.115366. Epub 2020 Apr 15. Bone. 2020. PMID: 32304878
METHODS: One hundred and thirty-seven men with a history of male factor infertility due to spermatogenic failure (SgF men) as well as a control group of 70 men from couples treated with IVF for female factor infertility (non-SgF men) were included in a long-term fol …
METHODS: One hundred and thirty-seven men with a history of male factor infertility due to spermatogenic failure (SgF men) as …
Decrease of anti-Mullerian hormone in genetic spermatogenic failure.
Plotton I, Garby L, Morel Y, Lejeune H. Plotton I, et al. Andrologia. 2012 Oct;44(5):349-54. doi: 10.1111/j.1439-0272.2010.01092.x. Epub 2011 Mar 25. Andrologia. 2012. PMID: 21486417
In a prospective clinical study from April 2008 to March 2009 in University Hospital, we measured AMH levels in 49 consecutive patients with azoospermia. AMH plasma levels were correlated with FSH, inhibin B, bioavailable testosterone plasma levels and testicular volume an …
In a prospective clinical study from April 2008 to March 2009 in University Hospital, we measured AMH levels in 49 consecutive patien …
Genetic variants in Piwi-interacting RNA pathway genes confer susceptibility to spermatogenic failure in a Chinese population.
Gu A, Ji G, Shi X, Long Y, Xia Y, Song L, Wang S, Wang X. Gu A, et al. Hum Reprod. 2010 Dec;25(12):2955-61. doi: 10.1093/humrep/deq274. Epub 2010 Oct 11. Hum Reprod. 2010. PMID: 20940137
We hypothesized that Piwi gene polymorphisms could be a risk factor for spermatogenic failure. METHODS: For this study, 490 patients with idiopathic azoospermia or oligozoospermia and 468 fertile controls were recruited from an infertility clinic. ...A significant t …
We hypothesized that Piwi gene polymorphisms could be a risk factor for spermatogenic failure. METHODS: For this study, 490 pa …
Assessing the cognitive and behavioral development of 3-year-old children born from fathers with severe male infertility.
Cheung S, Neri QV, Squires J, Rosenwaks Z, Palermo GD. Cheung S, et al. Am J Obstet Gynecol. 2021 May;224(5):508.e1-508.e11. doi: 10.1016/j.ajog.2020.11.030. Epub 2020 Nov 26. Am J Obstet Gynecol. 2021. PMID: 33248137 Free article.
Ages and Stages Questionnaires outcomes were also compared for the offspring conceived via in vitro fertilization and intracytoplasmic sperm injection by gender; however, no significant differences were observed. In addition, 5 separate subanalyses were then conducted excl …
Ages and Stages Questionnaires outcomes were also compared for the offspring conceived via in vitro fertilization and intracytoplasmic sperm …
First study of microdeletions in the Y chromosome of Algerian infertile men with idiopathic oligo- or azoospermia.
Chellat D, Rezgoune ML, McElreavey K, Kherouatou N, Benbouhadja S, Douadi H, Cherifa B, Abadi N, Satta D. Chellat D, et al. Urol Int. 2013;90(4):455-9. doi: 10.1159/000347046. Epub 2013 Mar 16. Urol Int. 2013. PMID: 23548818
Among the 80 infertile men screened for microdeletion, 1 subject was found to have microdeletions in the AZFc (sY254 and sY255) region. The deletion was found in azoospermic subjects (1/49, 2%). The overall AZF deletion frequency was low (1/80, 1.3%). AZF microdeletions we …
Among the 80 infertile men screened for microdeletion, 1 subject was found to have microdeletions in the AZFc (sY254 and sY255) region. The …
Diagnostic evaluation of oxidoreductive capability of sperm mitochondria.
Piasecka M, Gaczarzewicz D, Kurzawa R, Laszczyńska M, Kram A. Piasecka M, et al. Rocz Akad Med Bialymst. 2004;49 Suppl 1:108-10. Rocz Akad Med Bialymst. 2004. PMID: 15638390
The NADH-dependent NBT screening assay was used to identify and visualise: 1/ morphological defects of sperm midpiece, 2/ immature sperm forms with extensive cytoplasmic retention, reflecting developmental failure in spermatogenic remodelling process, 3/ cytoplasmic …
The NADH-dependent NBT screening assay was used to identify and visualise: 1/ morphological defects of sperm midpiece, 2/ immature sperm for …