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69 results

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Page 1
Phenotypic continuum and poor intracytoplasmic sperm injection intracytoplasmic sperm injection prognosis in patients harboring HENMT1 variants.
Wehbe Z, Barbotin AL, Boursier A, Cazin C, Hograindleur JP, Bidart M, Fontaine E, Plouvier P, Puch F, Satre V, Arnoult C, Mustapha SFB, Zouari R, Thierry-Mieg N, Ray PF, Kherraf ZE, Coutton C, Martinez G. Wehbe Z, et al. Among authors: satre v. Andrology. 2024 Aug 9. doi: 10.1111/andr.13730. Online ahead of print. Andrology. 2024. PMID: 39120570 Free article.
End-stage renal failure in Lowe syndrome.
Tricot L, Yahiaoui Y, Teixeira L, Benabdallah L, Rothschild E, Juquel JP, Satre V, Grünfeld JP, Chauveau D. Tricot L, et al. Among authors: satre v. Nephrol Dial Transplant. 2003 Sep;18(9):1923-5. doi: 10.1093/ndt/gfg294. Nephrol Dial Transplant. 2003. PMID: 12937245 No abstract available.
A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation.
Harbuz R, Zouari R, Pierre V, Ben Khelifa M, Kharouf M, Coutton C, Merdassi G, Abada F, Escoffier J, Nikas Y, Vialard F, Koscinski I, Triki C, Sermondade N, Schweitzer T, Zhioua A, Zhioua F, Latrous H, Halouani L, Ouafi M, Makni M, Jouk PS, Sèle B, Hennebicq S, Satre V, Viville S, Arnoult C, Lunardi J, Ray PF. Harbuz R, et al. Among authors: satre v. Am J Hum Genet. 2011 Mar 11;88(3):351-61. doi: 10.1016/j.ajhg.2011.02.007. Am J Hum Genet. 2011. PMID: 21397064 Free PMC article.
MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia.
Coutton C, Zouari R, Abada F, Ben Khelifa M, Merdassi G, Triki C, Escalier D, Hesters L, Mitchell V, Levy R, Sermondade N, Boitrelle F, Vialard F, Satre V, Hennebicq S, Jouk PS, Arnoult C, Lunardi J, Ray PF. Coutton C, et al. Among authors: satre v. Hum Reprod. 2012 Aug;27(8):2549-58. doi: 10.1093/humrep/des160. Epub 2012 May 24. Hum Reprod. 2012. PMID: 22627659
[Genetics of male infertility: the new players].
Coutton C, Satre V, Arnoult C, Ray P. Coutton C, et al. Among authors: satre v. Med Sci (Paris). 2012 May;28(5):497-502. doi: 10.1051/medsci/2012285014. Epub 2012 May 30. Med Sci (Paris). 2012. PMID: 22643003 Free article. Review. French.
Identification of a new recurrent aurora kinase C mutation in both European and African men with macrozoospermia.
Ben Khelifa M, Coutton C, Blum MG, Abada F, Harbuz R, Zouari R, Guichet A, May-Panloup P, Mitchell V, Rollet J, Triki C, Merdassi G, Vialard F, Koscinski I, Viville S, Keskes L, Soulie JP, Rives N, Dorphin B, Lestrade F, Hesters L, Poirot C, Benzacken B, Jouk PS, Satre V, Hennebicq S, Arnoult C, Lunardi J, Ray PF. Ben Khelifa M, et al. Among authors: satre v. Hum Reprod. 2012 Nov;27(11):3337-46. doi: 10.1093/humrep/des296. Epub 2012 Aug 11. Hum Reprod. 2012. PMID: 22888167
69 results