Free Access
Med Sci (Paris)
Volume 28, Number 5, Mai 2012
Page(s) 497 - 502
Section Cellules germinales et infertilité mâle
Published online 30 May 2012
  1. World Health Organization. WHO laboratory manual for the examination of human semen and sperm-cervical mucus interaction. Cambridge : Cambridge University Press, 1999 : 138 p. [Google Scholar]
  2. Boivin J, Bunting L, Collins JA, Nygren KG. International estimates of infertility prevalence and treatment-seeking: potential need and demand for infertility medical care. Hum Reprod 2007 ; 22 : 1506–1512. [CrossRef] [PubMed] [Google Scholar]
  3. Tuttelmann F, Simoni M, Kliesch S, et al. Copy number variants in patients with severe oligozoospermia, Sertoli-cell-only syndrome. PLoS One 2011 ; 6 : e19426. [CrossRef] [PubMed] [Google Scholar]
  4. Ravel C, Berthaut I, Bresson JL, Siffroi JP. Prevalence of chromosomal abnormalities in phenotypically normal and fertile adult males: large-scale survey of over 10, 000 sperm donor karyotypes. Hum Reprod 2006 ; 21 : 1484–1489. [CrossRef] [PubMed] [Google Scholar]
  5. Gekas J, Thepot F, Turleau C, et al. Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and men. Hum Reprod 2001 ; 16 : 82–90. [CrossRef] [PubMed] [Google Scholar]
  6. Reijo R, Lee TY, Salo P, et al. Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene. Nat Genet 1995 ; 10 : 383–393. [CrossRef] [PubMed] [Google Scholar]
  7. Vogt PH. Azoospermia factor (AZF) in Yq11: towards a molecular understanding of its function for human male fertility and spermatogenesis. Reprod Biomed Online 2005 ; 10 : 81–93. [CrossRef] [PubMed] [Google Scholar]
  8. Foresta C, Moro E, Ferlin A. Prognostic value of Y deletion analysis. The role of current methods. Hum Reprod 2001 ; 16 : 1543–1547. [CrossRef] [PubMed] [Google Scholar]
  9. Dumur V, Gervais R, Rigot JM, et al. Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype. Hum Genet 1996 ; 97 : 7–10. [PubMed] [Google Scholar]
  10. Stuppia L, Antonucci I, Binni F, et al. Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs. Eur J Hum Genet 2005 ; 13 : 959–964. [CrossRef] [PubMed] [Google Scholar]
  11. Tuttelmann F, Werny F, Cooper TG, et al. Clinical experience with azoospermia: aetiology and chances for spermatozoa detection upon biopsy. Int J Androl 2011 ; 34 : 291–298. [CrossRef] [PubMed] [Google Scholar]
  12. Matzuk MM, Lamb DJ. The biology of infertility: research advances and clinical challenges. Nat Med 2008 ; 14 : 1197–1213. [CrossRef] [PubMed] [Google Scholar]
  13. Papaioannou MD, Nef S. MicroRNAs in the testis: building up male fertility. J Androl 2010 ; 31 : 26–33. [CrossRef] [PubMed] [Google Scholar]
  14. Tuttelmann F, Rajpert-De Meyts E, Nieschlag E, Simoni M. Gene polymorphisms and male infertility-a meta-analysis and literature review. Reprod Biomed Online 2007 ; 15 : 643–658. [CrossRef] [PubMed] [Google Scholar]
  15. Dam AH, Koscinski I, Kremer JA, et al. Homozygous mutation in SPATA16 is associated with male infertility in human globozoospermia. Am J Hum Genet 2007 ; 81 : 813–820. [CrossRef] [PubMed] [Google Scholar]
  16. Dieterich K, Soto Rifo R, Faure AK, et al. Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility. Nat Genet 2007 ; 39 : 661–665. [CrossRef] [PubMed] [Google Scholar]
  17. Harbuz R, Zouari R, Pierre V, et al. A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation. Am J Hum Genet 2011 ; 88 : 351–361. [CrossRef] [PubMed] [Google Scholar]
  18. Koscinski I, Elinati E, Fossard C, et al. DPY19L2 deletion as a major cause of globozoospermia. Am J Hum Genet 2011 ; 88 : 344–350. [CrossRef] [PubMed] [Google Scholar]
  19. Ben Khelifa M, Zouari R, Harbuz R, et al. A new AURKC mutation causing macrozoospermia: implications for human spermatogenesis and clinical diagnosis. Mol Hum Reprod 2011 ; 17 : 762–768. [CrossRef] [PubMed] [Google Scholar]
  20. Dieterich K, Zouari R, Harbuz R, et al. The Aurora kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population. Hum Mol Genet 2009 ; 18 : 1301–1309. [CrossRef] [PubMed] [Google Scholar]
  21. Nistal M, Paniagua R, Herruzo A. Multi-tailed spermatozoa in a case with asthenospermia and teratospermia. Virchows Arch B Cell Pathol 1977 ; 26 : 111–118. [PubMed] [Google Scholar]
  22. Harbuz R, Zouari R, Dieterich K, et al. Function of aurora kinase C (AURKC) in human reproduction. Gynecol Obstet Fertil 2009 ; 37 : 546–551. [CrossRef] [PubMed] [Google Scholar]
  23. Devillard F, Metzler-Guillemain C, Pelletier R, et al. Polyploidy in large-headed sperm: FISH study of three cases. Hum Reprod 2002 ; 17 : 1292–1298. [CrossRef] [PubMed] [Google Scholar]
  24. Guthauser B, Albert M, Ferfouri F, et al. Inverse correlation between chromatin condensation and sperm head size in a case of enlarged sperm heads. Reprod Biomed Online 2011 ; 23 : 711–716. [CrossRef] [PubMed] [Google Scholar]
  25. Ray PF. Predictable male causes of in vitro fertilization (IVF) with intra cytoplasmic sperm injection (ICSI) failure. Gynecol Obstet Fertil 2010 ; 38 : 114–118. [CrossRef] [PubMed] [Google Scholar]
  26. Dam AH, Feenstra I, Westphal JR, et al. Globozoospermia revisited. Hum Reprod Update 2007 ; 13 : 63–75. [CrossRef] [PubMed] [Google Scholar]
  27. Liu G, Shi QW, Lu GX. A newly discovered mutation in PICK1 in a human with globozoospermia. Asian J Androl 2010 ; 12 : 556–560. [CrossRef] [PubMed] [Google Scholar]
  28. Stankiewicz P, Lupski JR. Structural variation in the human genome and its role in disease. Annu Rev Med 2010 ; 61 : 437–455. [CrossRef] [PubMed] [Google Scholar]
  29. Honigberg L, Kenyon C. Establishment of left/right asymmetry in neuroblast migration by UNC-40/DCC, UNC-73/Trio and DPY-19 proteins in C. elegans. Development 2000 ; 127 : 4655–4668. [PubMed] [Google Scholar]
  30. Ray PF, Arnoult C. La délétion homozygote du gène DPY19L2 est responsable de la majorité des cas de globozoospermie. Med Sci (Paris) 2011 ; 27 : 692–693. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  31. Arnoult C, Escoffier J, Munch L, et al. Les phospholipases, enzymes clés de la physiologie spermatique : quels enjeux thérapeutiques ? Med Sci (Paris) 2012 ; 28 : 512–518. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  32. Ray PF. Deciphering the genetics of male infertility: progress and challenges. J Urol 2011 ; 186 : 1183–1184. [CrossRef] [PubMed] [Google Scholar]

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