85 related articles for article (PubMed ID: 8766513)
1. Compound heterozygous mutations in CFTR causing congenital bilateral absence of the vas deferens in a Chinese pedigree.
Li L; Qu X; Cui C; Feng K; Xia Y; Wan F; Ge H; Fang Y; Zhang C; Guo H
Mol Genet Genomic Med; 2024 Jan; 12(1):e2364. PubMed ID: 38284450
[TBL] [Abstract][Full Text] [Related]
2. Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling.
de Souza DAS; Faucz FR; Pereira-Ferrari L; Sotomaior VS; Raskin S
Andrology; 2018 Jan; 6(1):127-135. PubMed ID: 29216686
[TBL] [Abstract][Full Text] [Related]
3. Whole Exome Sequencing Identifies a Rare CFTR Mutation in Brothers With Anomalies of the Vas Deferens: A Case Study.
Campbell K; Dullea A; Schuppe K; Ghomeshi A; Ramsoomair C; Griswold AJ; Khodamoradi K; Ramasamy R
Urology; 2023 May; 175():74-76. PubMed ID: 36858322
[TBL] [Abstract][Full Text] [Related]
4. Prevalence of Low Testosterone in Men With Cystic Fibrosis and Congenital Bilateral Absence of the Vas Deferens: A Cross-sectional Study Using a Large, Multi-institutional Database.
Campbell K; Deebel N; Kohn T; Passarelli R; Velez D; Ramasamy R
Urology; 2023 Dec; 182():143-148. PubMed ID: 37716455
[TBL] [Abstract][Full Text] [Related]
5. Intragenic CFTR Duplication and 5T/12TG Variant in a Patient with Non-Classic Cystic Fibrosis.
Celestino-Soper PB; Simpson E; Tumbleson Brink D; Lynnes TC; Dlouhy S; Vatta M; Yeley J; Brown C; Bai S
Sci Rep; 2016 Dec; 6():38776. PubMed ID: 27996019
[TBL] [Abstract][Full Text] [Related]
6. Swine models of cystic fibrosis reveal male reproductive tract phenotype at birth.
Pierucci-Alves F; Akoyev V; Stewart JC; Wang LH; Janardhan KS; Schultz BD
Biol Reprod; 2011 Sep; 85(3):442-51. PubMed ID: 21593481
[TBL] [Abstract][Full Text] [Related]
7. Are p.I148T, p.R74W and p.D1270N cystic fibrosis causing mutations?
Claustres M; Altiéri JP; Guittard C; Templin C; Chevalier-Porst F; Des Georges M
BMC Med Genet; 2004 Aug; 5():19. PubMed ID: 15287992
[TBL] [Abstract][Full Text] [Related]
8. The CFTR Met 470 allele is associated with lower birth rates in fertile men from a population isolate.
Kosova G; Pickrell JK; Kelley JL; McArdle PF; Shuldiner AR; Abney M; Ober C
PLoS Genet; 2010 Jun; 6(6):e1000974. PubMed ID: 20532200
[TBL] [Abstract][Full Text] [Related]
9. Embryology of the Absent Vas Supported by 2 Cases of Congenital Unilateral Absence of Vas With Varied Associations.
Shepherd G; Rajimwale A
Urol Case Rep; 2014 Mar; 2(2):49-50. PubMed ID: 26952869
[TBL] [Abstract][Full Text] [Related]
10. ECFS standards of care on CFTR-related disorders: Identification and care of the disorders.
Simmonds NJ; Southern KW; De Wachter E; De Boeck K; Bodewes F; Mainz JG; Middleton PG; Schwarz C; Vloeberghs V; Wilschanski M; Bourrat E; Chalmers JD; Ooi CY; Debray D; Downey DG; Eschenhagen P; Girodon E; Hickman G; Koitschev A; Nazareth D; Nick JA; Peckham D; VanDevanter D; Raynal C; Scheers I; Waller MD; Sermet-Gaudelus I; Castellani C;
J Cyst Fibros; 2024 Mar; ():. PubMed ID: 38508949
[TBL] [Abstract][Full Text] [Related]
11. Clinical outcomes of two infants with cystic fibrosis, including presence of the vas deferens, born to a woman with cystic fibrosis taking CFTR modulators during both pregnancies.
Kowalik A; Roberts E; Harris AH; Sund M; Wird S; Kvist O; Hjelte L
J Cyst Fibros; 2024 Jun; ():. PubMed ID: 38876833
[No Abstract] [Full Text] [Related]
12. Molecular analysis of the IVS8-T splice variant 5T and M470V exon 10 missense polymorphism in Iranian males with congenital bilateral absence of the vas deferens.
Radpour R; Gilani MA; Gourabi H; Dizaj AV; Mollamohamadi S
Mol Hum Reprod; 2006 Jul; 12(7):469-73. PubMed ID: 16714368
[TBL] [Abstract][Full Text] [Related]
13. Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France.
Claustres M; Guittard C; Bozon D; Chevalier F; Verlingue C; Ferec C; Girodon E; Cazeneuve C; Bienvenu T; Lalau G; Dumur V; Feldmann D; Bieth E; Blayau M; Clavel C; Creveaux I; Malinge MC; Monnier N; Malzac P; Mittre H; Chomel JC; Bonnefont JP; Iron A; Chery M; Georges MD
Hum Mutat; 2000; 16(2):143-56. PubMed ID: 10923036
[TBL] [Abstract][Full Text] [Related]
14. CFTR mutations and polymorphisms in male infertility.
Cuppens H; Cassiman JJ
Int J Androl; 2004 Oct; 27(5):251-6. PubMed ID: 15379964
[TBL] [Abstract][Full Text] [Related]
15. [Cystic fibrosis transmembrane conductance regulator (CFTR) gene: mutations and clinical phenotypes].
Schwartz M
Ugeskr Laeger; 2003 Feb; 165(9):912-6. PubMed ID: 12661515
[TBL] [Abstract][Full Text] [Related]
16. [Molecular basis of cystic fibrosis and congenital bilateral agenesis of vas deferens].
Bienvenu T; Claustres M
Contracept Fertil Sex; 1996 Jun; 24(6):495-500. PubMed ID: 8766513
[TBL] [Abstract][Full Text] [Related]
17. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens.
Chillón M; Casals T; Mercier B; Bassas L; Lissens W; Silber S; Romey MC; Ruiz-Romero J; Verlingue C; Claustres M
N Engl J Med; 1995 Jun; 332(22):1475-80. PubMed ID: 7739684
[TBL] [Abstract][Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]