285 related articles for article (PubMed ID: 9412228)
21. Cystic fibrosis presenting as acute pancreatitis and obstructive azoospermia in a young adult male with a novel mutation in the CFTR gene.
Conway SP; Peckham DG; Chu CE; Ellis LA; Ahmed M; Taylor GR
Pediatr Pulmonol; 2002 Dec; 34(6):491-5. PubMed ID: 12422349
[TBL] [Abstract][Full Text] [Related]
22. [An analysis of the mutations in the gene of the mucoviscidosis transmembrane regulator protein (MTRP) in patients with congenital bilateral aplasia of the vas deferens].
Gusak NM; Gorovenko NG; Gorpinchenko II; Karmeliuk SO
Tsitol Genet; 1996; 30(5):48-53. PubMed ID: 9026991
[TBL] [Abstract][Full Text] [Related]
23. Genetic investigations of CFTR mutations in congenital absence of vas deferens, uterus, and vagina as a cause of infertility.
Radpour R; Gourabi H; Dizaj AV; Holzgreve W; Zhong XY
J Androl; 2008; 29(5):506-13. PubMed ID: 18567645
[TBL] [Abstract][Full Text] [Related]
24. Expression of the cystic fibrosis transmembrane conductance regulator (CFTR) mRNA in normal and pathological adult human epididymis.
Patrizio P; Salameh WA
J Reprod Fertil Suppl; 1998; 53():261-70. PubMed ID: 10645285
[TBL] [Abstract][Full Text] [Related]
25. Significance of CFTR gene mutations in patients with congenital aplasia of vas deferens with special regard to renal aplasia.
Schwarzer JU; Schwarz M
Andrologia; 2012 Oct; 44(5):305-7. PubMed ID: 22340520
[TBL] [Abstract][Full Text] [Related]
26. Improved detection of cystic fibrosis mutations in infertility patients with DNA sequence analysis.
Danziger KL; Black LD; Keiles SB; Kammesheidt A; Turek PJ
Hum Reprod; 2004 Mar; 19(3):540-6. PubMed ID: 14998948
[TBL] [Abstract][Full Text] [Related]
27. Genetics of cystic fibrosis.
Lommatzsch ST; Aris R
Semin Respir Crit Care Med; 2009 Oct; 30(5):531-8. PubMed ID: 19760540
[TBL] [Abstract][Full Text] [Related]
28. [Unilateral partial deferential agenesia and CFTR gene composite heterozygoty (deltaF508/V938G)].
Robin G; Lefèbvre-Khalil V; Dumur V; Lemaître L; Mitchell V; Rigot JM; Marcelli F
Gynecol Obstet Fertil; 2007 Jun; 35(6):561-4. PubMed ID: 17507277
[TBL] [Abstract][Full Text] [Related]
29. Normal vas deferens in fetuses with cystic fibrosis.
Gaillard DA; Carré-Pigeon F; Lallemand A
J Urol; 1997 Oct; 158(4):1549-52. PubMed ID: 9302172
[TBL] [Abstract][Full Text] [Related]
30. The role of the F508C mutation in congenital bilateral absence of the vas deferens.
Havasi V; Keiles S; Hambuch T; Sorscher EJ; Kammesheidt A
Genet Med; 2008 Dec; 10(12):910-4. PubMed ID: 19092444
[TBL] [Abstract][Full Text] [Related]
31. [Role of deep seminal tract imaging in the diagnosis of unilateral agenesis of the vas deferens. Case report of a patient with CFTR gene mutation].
Marcelli F; Robin G; Mitchell V; Dumur V; Puech P; Lemaitre L; Rigot JM
Prog Urol; 2006 Nov; 16(5):617-9. PubMed ID: 17175965
[TBL] [Abstract][Full Text] [Related]
32. Detection of cystic fibrosis transmembrane conductance regulator (CFTR) gene rearrangements enriches the mutation spectrum in congenital bilateral absence of the vas deferens and impacts on genetic counselling.
Ratbi I; Legendre M; Niel F; Martin J; Soufir JC; Izard V; Costes B; Costa C; Goossens M; Girodon E
Hum Reprod; 2007 May; 22(5):1285-91. PubMed ID: 17329263
[TBL] [Abstract][Full Text] [Related]
33. Asymptomatic cystic fibrosis diagnosed in an adult evaluated for hematuria.
Reynolds JC; Tiu AB; Berg BW
Am J Kidney Dis; 2002 Jan; 39(1):E3. PubMed ID: 11774129
[TBL] [Abstract][Full Text] [Related]
34. Clinical, andrological and genetic characteristics of patients with congenital bilateral absence of vas deferens (CBAVD).
Samli H; Samli MM; Yilmaz E; Imirzalioglu N
Arch Androl; 2006; 52(6):471-7. PubMed ID: 17050329
[TBL] [Abstract][Full Text] [Related]
35. Heterogenous spectrum of CFTR gene mutations in Indian patients with congenital absence of vas deferens.
Sharma N; Acharya N; Singh SK; Singh M; Sharma U; Prasad R
Hum Reprod; 2009 May; 24(5):1229-36. PubMed ID: 19181743
[TBL] [Abstract][Full Text] [Related]
36. [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]
37. 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]
38. Vas deferens anomalies in paediatric age.
Campagnola S; Fasoli L; Flessati P; Sulpasso M; Castellani C
Minerva Pediatr; 1999; 51(7-8):265-9. PubMed ID: 10634059
[TBL] [Abstract][Full Text] [Related]
39. p.Leu636Pro mutation is associated with cystic fibrosis transmembrane conductance regulator-related disorders (congenital bilateral absence of vas deferens).
Salvatore D; Dell'Edera D; Colangelo C; Smaldore G
Int J Urol; 2015 Aug; 22(8):803-4. PubMed ID: 25944622
[No Abstract] [Full Text] [Related]
40. [Congenital agenesis of the vas deferens and cystic fibrosis].
Kugler A; Laccone F; Weidner W; Kallerhoff M
Urologe A; 1995 Jul; 34(4):348-50. PubMed ID: 7545847
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
