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Abbreviation : CUAVD
Long Form : congenital unilateral absence of the vas deferens
No. Year Title Co-occurring Abbreviation
1  2020 Prevalence of CBAVD in azoospermic men carrying pathogenic CFTR mutations - Evaluated in a cohort of 639 non-vasectomized azoospermic men. CBAVD, OA
2  2018 CFTR variants and renal abnormalities in males with congenital unilateral absence of the vas deferens (CUAVD): a systematic review and meta-analysis of observational studies. ORs, RA
3  2015 [Detection of CFTR gene mutations in azoospermia patients with congenital unilateral absence of the vas deferens]. ---
4  2013 Advantages of magnetic resonance imaging (MRI) of the seminal vesicles and intra-abdominal vas deferens in patients with congenital absence of the vas deferens. CAVD, CBAVD, CFTR, MRI, SV, TRUS
5  2007 Correlation between CFTR gene mutations in Iranian men with congenital absence of the vas deferens and anatomical genital phenotype. CBAVD
6  2005 [Clinical features & diagnostic and therapeutic strategies of congenital absence of the vas deferens]. ART, CAVD, CBAVD, ICSI
7  2002 Clinical and genetic features of patients with congenital unilateral absence of the vas deferens. CF
8  2001 Genetic, andrological and clinical characteristics of patients with congenital bilateral absence of the vas deferens. CBAVD, CF, CFTR
9  2000 Clinical findings in congenital absence of the vasa deferentia. CBAVD
10  2000 [Study of CFTR gene mutation in Chinese CUAVD patients]. CFTR, SSCP
11  1999 Proportion of cystic fibrosis gene mutations not detected by routine testing in men with obstructive azoospermia. CBAVD, CFTR
12  1996 Cystic fibrosis and infertility caused by congenital bilateral absence of the vas deferens and related clinical entities. CBAVD, CF, CFTR
13  1995 Congenital unilateral absence of the vas deferens: a heterogeneous disorder with two distinct subpopulations based upon aetiology and mutational status of the cystic fibrosis gene. CBAVD, CF
14  1995 Extensive analysis of 40 infertile patients with congenital absence of the vas deferens: in 50% of cases only one CFTR allele could be detected. CBAVD, CF