121 related articles for article (PubMed ID: 18846434)
1. Hereditary haemochromatosis gene (HFE) H63D mutation shows an association with abnormal sperm motility.
Gunel-Ozcan A; Basar MM; Kisa U; Ankarali HC
Mol Biol Rep; 2009 Sep; 36(7):1709-14. PubMed ID: 18846434
[TBL] [Abstract][Full Text] [Related]
2. The impact of hemochromatosis mutations and transferrin genotype on gonadotropin serum levels in infertile men.
Buretić-Tomljanović A; Vlastelić I; Radojcić Badovinac A; Starcević-Cizmarević N; Nadalin S; Ristić S
Fertil Steril; 2009 May; 91(5):1793-800. PubMed ID: 18395717
[TBL] [Abstract][Full Text] [Related]
3. Analysis of the hemochromatosis mutations C282Y and H63D in infertile men.
Peterlin B; Kunej T; Hruskovicová H; Ferk P; Gersak K; Zorn B
Fertil Steril; 2006 Dec; 86(6):1796-8. PubMed ID: 17067586
[TBL] [Abstract][Full Text] [Related]
4. An association study of HFE gene mutation with idiopathic male infertility in the Chinese Han population.
Yu XY; Wang BB; Xin ZC; Liu T; Ma K; Jiang J; Fang X; Yu LH; Peng YF; Ma X
Asian J Androl; 2012 Jul; 14(4):599-603. PubMed ID: 22504868
[TBL] [Abstract][Full Text] [Related]
5. Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal).
Spínola C; Brehm A; Spínola H
Ann Hematol; 2011 Jan; 90(1):29-32. PubMed ID: 20714725
[TBL] [Abstract][Full Text] [Related]
6. Frequency of the C282Y and H63D mutations of the hemochromatosis gene (HFE) in 2501 ethnic Danes.
Milman N; Pedersen P; Ovesen L; Melsen GV; Fenger K
Ann Hematol; 2004 Oct; 83(10):654-7. PubMed ID: 15141324
[TBL] [Abstract][Full Text] [Related]
7. The prognostic role of hemochromatosis H63D allele in allogeneic hematopoietic stem cell transplantation.
Sucak GT; Yaşar DG; Yegin ZA; Ergün MA; Ozkurt ZN; Aki ŞZ; Güntekin S
Ann Hematol; 2012 Aug; 91(8):1281-7. PubMed ID: 22362121
[TBL] [Abstract][Full Text] [Related]
8. Mutations of the HFE gene among Turkish hereditary hemochromatosis patients.
Simsek H; Balaban YH; Yilmaz E; Sumer H; Buyukasik Y; Cengiz C; Ozcebe O; Hascelik G; Tatar G
Ann Hematol; 2005 Oct; 84(10):646-9. PubMed ID: 15871018
[TBL] [Abstract][Full Text] [Related]
9. [Study on HFE gene mutations in patients with myelodysplastic syndromes and aplastic anemia].
Nie L; Ai XF; Zheng YZ; Li QH; Yang L; Xiao ZJ
Zhonghua Xue Ye Xue Za Zhi; 2009 Apr; 30(4):223-8. PubMed ID: 19731820
[TBL] [Abstract][Full Text] [Related]
10. [Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland].
Himmelmann A; Bortoluzzi L; Jansen S; Fehr J
Schweiz Med Wochenschr; 2000 Aug; 130(31-32):1112-9. PubMed ID: 11008304
[TBL] [Abstract][Full Text] [Related]
11. High prevalence of non-HFE gene-associated haemochromatosis in patients from southern Italy.
De Marco F; Liguori R; Giardina MG; D'Armiento M; Angelucci E; Lucariello A; Morante R; Cimino L; Galeota-Lanza A; Tarantino G; Ascione A; Budillon G; Vecchione R; Martinelli R; Matarazzo M; De Simone V
Clin Chem Lab Med; 2004 Jan; 42(1):17-24. PubMed ID: 15061375
[TBL] [Abstract][Full Text] [Related]
12. HFE gene mutations in patients with acute leukemia.
Viola A; Pagano L; Laudati D; D'Elia R; D'Amico MR; Ammirabile M; Palmieri S; Prossomariti L; Ferrara F
Leuk Lymphoma; 2006 Nov; 47(11):2331-4. PubMed ID: 17107905
[TBL] [Abstract][Full Text] [Related]
13. Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population.
Kucinskas L; Juzenas S; Sventoraityte J; Cedaviciute R; Vitkauskiene A; Kalibatas V; Kondrackiene J; Kupcinskas L
Ann Hematol; 2012 Apr; 91(4):491-5. PubMed ID: 21947086
[TBL] [Abstract][Full Text] [Related]
14. The association between H63D mutations in HFE and amyotrophic lateral sclerosis in a Dutch population.
Sutedja NA; Sinke RJ; Van Vught PW; Van der Linden MW; Wokke JH; Van Duijn CM; Njajou OT; Van der Schouw YT; Veldink JH; Van den Berg LH
Arch Neurol; 2007 Jan; 64(1):63-7. PubMed ID: 17210810
[TBL] [Abstract][Full Text] [Related]
15. An open population screening study for HFE gene major mutations proves the low prevalence of C282Y mutation in Central Italy.
Floreani A; Rosa Rizzotto E; Basso D; Navaglia F; Zaninotto M; Petridis I; DI Andrea O; Testa R; Marra M; Baldo V; Chiaramonte M
Aliment Pharmacol Ther; 2007 Aug; 26(4):577-86. PubMed ID: 17661761
[TBL] [Abstract][Full Text] [Related]
16. HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.
Trifa AP; Popp RA; Militaru MS; Farcaş MF; Crişan TO; Gana I; Cucuianu A; Pop IV
J Gastrointestin Liver Dis; 2012 Jun; 21(2):177-80. PubMed ID: 22720307
[TBL] [Abstract][Full Text] [Related]
17. A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism.
Njajou OT; Houwing-Duistermaat JJ; Osborne RH; Vaessen N; Vergeer J; Heeringa J; Pols HA; Hofman A; van Duijn CM
Eur J Hum Genet; 2003 Mar; 11(3):225-31. PubMed ID: 12673276
[TBL] [Abstract][Full Text] [Related]
18. HFE mutation H63D predicts risk of iron over load in thalassemia intermedia irrespective of blood transfusions.
Sharma V; Panigrahi I; Dutta P; Tyagi S; Choudhry VP; Saxena R
Indian J Pathol Microbiol; 2007 Jan; 50(1):82-5. PubMed ID: 17474269
[TBL] [Abstract][Full Text] [Related]
19. Genetics of hemochromatosis.
Cullen LM; Anderson GJ; Ramm GA; Jazwinska EC; Powell LW
Annu Rev Med; 1999; 50():87-98. PubMed ID: 10073265
[TBL] [Abstract][Full Text] [Related]
20. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
Zlocha J; Kovács L; Pozgayová S; Kupcová V; Durínová S
Vnitr Lek; 2006 Jun; 52(6):602-8. PubMed ID: 16871764
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]