Results 91 to 100 of about 15,574 (181)

Clinical features and microsurgical reconstruction of congenital unilateral absence of the vas deferens with obstructive azoospermia: a tertiary care center experience. [PDF]

Asian J Androl, 2023
Zhou YH, Dong JJ, Zhi EL, Yao CC, Huang YH, Tian RH, Chen HX, Dai YB, Tang YX, Liu NC, Chen HR, Zhao FJ, Li Z, Li P.   +13 more
europepmc   +1 more source

A Case of Cystic Fibrosis in a Japanese Man With Congenital Bilateral Absence of the Vas Deferens and Recurrent Pancreatitis Caused by a Homozygous c.1210-11 T > G Variant of the Cystic Fibrosis Transmembrane Conductance Regulator Gene. [PDF]

Reprod Med Biol
Saito T, Kuroda S, Takeshima T, Kawahara T, Teranishi J, Karibe J, Anzai F, Tanoshima M, Makiyama K, Yumura Y.   +9 more
europepmc   +1 more source

Duplication of the Vas Deferens: A Rare Anomaly. [PDF]

Ochsner J, 2021
Osama M, Khan AA, Mohiuddin O, Saad CM, Naseer S, Zaheer F.   +5 more
europepmc   +1 more source

Vas Deferens [PDF]

, 2020
openaire   +1 more source

A Case of Ectopic Vas Deferens With Contralateral Vesicoureteral Reflux Causing Recurrent Pyelonephritis and Epididymitis. [PDF]

Cureus
Kobayashi K, Johnin K, Wada A, Yamanaka K, Kageyama S.   +4 more
europepmc   +1 more source

Development of assays for the characterization of sperm motility parameters, viability, and membrane integrity in the epididymis and vas deferens of the greater rhea (Rhea americana). [PDF]

Anim Reprod, 2023
Bezerra LGP, Silva AM, Dantas MRT, Dos Santos RP, Moreira SSJ, Pereira AG, de Oliveira MF, Comizzoli P, Silva AR.   +8 more
europepmc   +1 more source

Incidental finding of duplication of vas deferens in inguinal hernia: a case report of rare anomaly. [PDF]

J Surg Case Rep
Shrestha B, Yadav K, Kandel G, Yadav P, Subedi S.   +4 more
europepmc   +1 more source

Loss-of-function CFTR p.G970D missense mutation might cause congenital bilateral absence of the vas deferens and be associated with impaired spermatogenesis. [PDF]

Asian J Androl, 2023
Hou JW, Li XL, Wang L, Dai CL, Li N, Jiang XH, Tan YQ, Tian EP, Li QT, Xu WM.   +9 more
europepmc   +1 more source

Cystic fibrosis-causing variants in Chinese patients with congenital absence of the vas deferens: a cohort and meta-analysis. [PDF]

Asian J Androl
Lu Y, Wang J, Cai ZL, Li TY, Li HJ, Wang BB.   +5 more
europepmc   +1 more source

CFTR mutations causing congenital unilateral absence of the vas deferens (CUAVD) and congenital absence of the uterus (CAU) in a consanguineous family. [PDF]

Asian J Androl, 2022
Ghouchanatigh MD, Khan R, Mojarrad M, Hameed U, Zubair M, Waqas A, Jalali M, Kalantari M, Shamsa A, Zhang H, Shi QH.   +10 more
europepmc   +1 more source