Azoospermia y fertilización asistida: rol de la histología testicular en el éxito de icsi

Vinay, José Ignacio; Valdevenito, Raúl; Palma, Cristián; Lecaros, Nicolás; Gallegos, Iván; Vantman, David; Castro, Andrea; Flórez, Martha; Piottante, Antonio; Vantman, Dorón; Veis, Hugo.
Rev. chil. urol ; 78(2): 71-75, ago. 2013. graf
Artículo en Español | LILACS | ID: lil-774060

Documentos relacionados

  1. A bi-allelic REC114 loss-of-function variant causes meiotic arrest and nonobstructive azoospermia.
  2. Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia.
  3. Genetic profiling of azoospermic men to identify the etiology and predict reproductive potential.
  4. A novel splicing mutation in helicase for meiosis 1 leads to non-obstructive azoospermia.
  5. Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia.
  6. Sertoli cell-only syndrome: advances, challenges, and perspectives in genetics and mechanisms.
  7. A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest.
  8. Identification of two hidden clinical subgroups among men with idiopathic cryptozoospermia.
  9. Bi-allelic MEI1 variants cause meiosis arrest and non-obstructive azoospermia.
  10. Biallelic mutations in <i>CFAP54</i> cause male infertility with severe MMAF and NOA.