Lingue

Sezione Medicina della Sessualitą e Andrologia

Congressi

 21-Dic-2009   Stampa la pagina corrente   Mostra la posizione di questa pagina nella mappa

Elenco Pubblicazioni

Elenco Pubblicazioni

  1. Muratori M, Tamburrino L, Tocci V, Costantino A, Marchiani S, Giachini C, Laface I, Krausz C, Meriggiola MC, Forti G, Baldi E. (2009) Small variations in crucial steps of tunel assay coupled to flow cytometry greatly affect measures of sperm DNA fragmentation. J Androl, accepted.
  2. Giachini C, Nuti F, Turner DJ, Laface I, Xue Y, Daguin F, Forti G, Tyler-Smith C, Krausz C. (2009) TSPY1 copy number variation influences spermatogenesis and shows differences among Y lineages. J Clin Endocrinol Metab. 94:4016-22.
  3. Krausz C, Giachini C, Xue Y, O'Bryan MK, Gromoll J, Rajpert-de Meyts E, Oliva R, Aknin-Seifer I, Erdei E, Jorgensen N, Simoni M, Ballescà JL, Levy R, Balercia G, Piomboni P, Nieschlag E, Forti G, McLachlan R, Tyler-Smith C. (2009) Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background. J Med Genet. 46:21-31.
  4. Giachini C, Laface I, Guarducci E, Balercia G, Forti G, Krausz C. (2008) Partial AZFc deletions and duplications: clinical correlates in the Italian population. Hum Genet. 124:399-410.
  5. Nuti F, Marinari E, Erdei E, El-Hamshari M, Echavarria MG, Ars E, Balercia G, Merksz M, Giachini C, Shaeer KZ, Forti G, Ruiz-Castané E, Krausz C. (2008) The leucine-rich repeat-containing G protein-coupled receptor 8 gene T222P mutation does not cause cryptorchidism. J Clin Endocrinol Metab. 93:1072-6.
  6. Krausz C, Giachini C. (2007) Genetic risk factors in male infertility. Arch Androl. 53:125-33. Review.
  7. Giachini C, Nuti F, Marinari E, Forti G, Krausz C. (2007) Partial AZFc deletions in infertile men with cryptorchidism. Hum Reprod. 22:2398-403.
  8. Giachini C, Guarducci E, Longepied G, Degl'Innocenti S, Becherini L, Forti G, Mitchell MJ, Krausz C. (2005) The gr/gr deletion(s): a new genetic test in male infertility? J Med Genet. 42:497-502.
 

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