30 related articles for article (PubMed ID: 9550327)
1. Quantification of liver iron overload disease with laser ablation inductively coupled plasma mass spectrometry.
Kim P; Weiskirchen S; Uerlings R; Kueppers A; Stellmacher F; Viveiros A; Zoller H; Weiskirchen R
BMC Med Imaging; 2018 Dec; 18(1):51. PubMed ID: 30514216
[TBL] [Abstract][Full Text] [Related]
2. Frequencies of HFE gene mutations associated with haemochromatosis in the population of Libya living in Benghazi.
Elmrghni S; Dixon RA; Williams DR
Int J Clin Exp Med; 2011; 4(3):200-4. PubMed ID: 21977233
[TBL] [Abstract][Full Text] [Related]
3. Prevalence of 845G>A HFE mutation in Slavic populations: an east-west linear gradient in South Slavs.
Adler G; Clark JS; Łoniewska B; Ciechanowicz A
Croat Med J; 2011 Jun; 52(3):351-7. PubMed ID: 21674831
[TBL] [Abstract][Full Text] [Related]
4. HLA-A and -B alleles and haplotypes in hemochromatosis probands with HFE C282Y homozygosity in central Alabama.
Barton JC; Acton RT
BMC Med Genet; 2002 Oct; 3():9. PubMed ID: 12370085
[TBL] [Abstract][Full Text] [Related]
5. C282Y and H63D mutations in the HFE gene have no effect on iron overload disorders in Japan.
Shiono Y; Ikeda R; Hayashi H; Wakusawa S; Sanae F; Takikawa T; Imaizumi Y; Yano M; Yoshioka K; Kawanaka M; Yamada G
Intern Med; 2001 Sep; 40(9):852-6. PubMed ID: 11579943
[TBL] [Abstract][Full Text] [Related]
6. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.
Gottschalk R; Seidl C; Schilling S; Braner A; Seifried E; Hoelzer D; Kaltwasser JP
Eur J Immunogenet; 2000 Jun; 27(3):129-34. PubMed ID: 10940080
[TBL] [Abstract][Full Text] [Related]
7. HFE mutations, iron deficiency and overload in 10,500 blood donors.
Jackson HA; Carter K; Darke C; Guttridge MG; Ravine D; Hutton RD; Napier JA; Worwood M
Br J Haematol; 2001 Aug; 114(2):474-84. PubMed ID: 11529872
[TBL] [Abstract][Full Text] [Related]
8. Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls.
Sánchez M; Bruguera M; Bosch J; Rodés J; Ballesta F; Oliva R
J Hepatol; 1998 Nov; 29(5):725-8. PubMed ID: 9833909
[TBL] [Abstract][Full Text] [Related]
9. HFE codon 63/282 (H63D/C282Y) dimorphism in German patients with genetic hemochromatosis.
Gottschalk R; Seidl C; Löffler T; Seifried E; Hoelzer D; Kaltwasser JP
Tissue Antigens; 1998 Mar; 51(3):270-5. PubMed ID: 9550327
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [Genetic hemochromatosis and the HFE gene].
Moirand R
Bull Acad Natl Med; 2000; 184(2):325-35; discussion 335-6. PubMed ID: 10989541
[TBL] [Abstract][Full Text] [Related]
12.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
13.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No 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]