Search Results - "Cazzadore, C."

Mutations in dynein genes in patients affected by isolated non-syndromic asthenozoospermia by Zuccarello, D., Ferlin, A., Cazzadore, C., Pepe, A., Garolla, A., Moretti, A., Cordeschi, G., Francavilla, S., Foresta, C.

“…BACKGROUND Asthenozoospermia (AZS) is a common cause of male infertility characterized by reduced forward motility (WHO grade A+B sperm motility <50% or A <…”
Get full text

Lack of the T54A polymorphism of the DAZL gene in infertile Italian patients by Bartoloni, L., Cazzadore, C., Ferlin, A., Garolla, A., Foresta, C.

“…The Thr54Ala polymorphism of the deleted-in-azoospermia-like (DAZL) protein has been associated with susceptibility to spermatogenic failure in the Taiwanese…”
Get full text

A possible association of a human tektin-t gene mutation (A229V) with isolated non-syndromic asthenozoospermia: Case Report by Zuccarello, Daniela, Ferlin, Alberto, Garolla, Andrea, Pati, Mauro A., Moretti, Afra, Cazzadore, Carla, Francavilla, Sandro, Foresta, Carlo

“…Asthenozoospermia (AZS), characterized by grade A + B sperm motility (as in World Health Organization Guidelines) ≤50% or A <25% in fresh ejaculate, may exist…”
Get full text

Deficiency 10p. Report of a case and exclusion mapping of the hexokinase 1 locus to band 10p11.2 by Danesino, C, Lo Curto, F, Bonfant, G, Cazzadore, C, Voltolin, G, Bersi, S

“…A patient deficient for most of the short arm of one chromosome 10 is described. The clinical picture is similar to those of other published cases but includes…”
Get more information