204 related articles for article (PubMed ID: 11552248)
1. [Genetic background and DNA diagnostics of hemochromatosis].
Heliö T; Färkkilä M; Halme L; Karlsson M; Palotie A; Kontula K
Duodecim; 1998; 114(14):1404-9. PubMed ID: 11552248
[No Abstract] [Full Text] [Related]
2. [Clinical usefulness of the detection of mutations of the HFE gene in hemochromatosis].
Oliva R; Sánchez M; Bruguera M; Rodés J
Gastroenterol Hepatol; 2000 Nov; 23(9):433-5. PubMed ID: 11126040
[No Abstract] [Full Text] [Related]
3. Rapid diagnosis of hemochromatosis gene Cys282Tyr mutation by SSCP analysis.
Hertzberg MS; McDonald D; Mirochnik O
Am J Hematol; 1998 Mar; 57(3):260-1. PubMed ID: 9495384
[No Abstract] [Full Text] [Related]
4. [Hereditary hemochromatosis].
Parkkila S
Duodecim; 2000; 116(8):829-36. PubMed ID: 11787126
[No Abstract] [Full Text] [Related]
5. Population screening for hemochromatosis.
Adams PC
Hepatology; 1999 Apr; 29(4):1324-7. PubMed ID: 10094982
[No Abstract] [Full Text] [Related]
6. Haemochromatosis and HLA-H.
Jazwinska EC; Cullen LM; Busfield F; Pyper WR; Webb SI; Powell LW; Morris CP; Walsh TP
Nat Genet; 1996 Nov; 14(3):249-51. PubMed ID: 8896549
[No Abstract] [Full Text] [Related]
7. HFE mutation analysis in patients with hepatitis C virus with positive screening for iron overload.
Remacha AF; Carrasco M; Sardá MP; Barceló MJ; Baiget M
Haematologica; 1999 Mar; 84(3):284-5. PubMed ID: 10189401
[No Abstract] [Full Text] [Related]
8. Haemochromatosis and HLA-H.
Jouanolle AM; Gandon G; Jézéquel P; Blayau M; Campion ML; Yaouanq J; Mosser J; Fergelot P; Chauvel B; Bouric P; Carn G; Andrieux N; Gicquel I; Le Gall JY; David V
Nat Genet; 1996 Nov; 14(3):251-2. PubMed ID: 8896550
[No Abstract] [Full Text] [Related]
9. Genetic hemochromatosis: why is discovery of the HLA-H gene of interest to rheumatologists?
Puéchal X
Rev Rhum Engl Ed; 1997 Oct; 64(10):527-9. PubMed ID: 9385688
[No Abstract] [Full Text] [Related]
10. Haemochromatosis, HFE and genetic complexity.
Risch N
Nat Genet; 1997 Dec; 17(4):375-6. PubMed ID: 9398831
[No Abstract] [Full Text] [Related]
11. Genetic irony beyond haemochromatosis: clinical effects of HLA-H mutations.
Beutler E
Lancet; 1997 Feb; 349(9048):296-7. PubMed ID: 9024367
[No Abstract] [Full Text] [Related]
12. Overestimation of HFE C282Y homozygous hemochromatosis prevalence as the result of a common primer-binding site polymorphism.
Press RD
Mol Diagn; 1999 Dec; 4(4):391-2. PubMed ID: 10671650
[No Abstract] [Full Text] [Related]
13. Haemochromatosis... definite maybe!
Nat Genet; 1996 Aug; 13(4):375-6. PubMed ID: 8696321
[No Abstract] [Full Text] [Related]
14. Hemochromatosis after the gene discovery: revisiting the diagnostic strategy.
Brissot P; Moirand R; Guyader D; Loréal O; Turlin B; Deugnier Y
J Hepatol; 1998; 28 Suppl 1():14-8. PubMed ID: 9575443
[No Abstract] [Full Text] [Related]
15. [Molecular genetic diagnosis in hemochromatosis].
Gehrke SG; Stremmel W
Dtsch Med Wochenschr; 1999 Apr; 124(14):431-4. PubMed ID: 10230385
[No Abstract] [Full Text] [Related]
16. Traffic jam for hemochromatosis mutant protein.
Adams PC
Hepatology; 1997 Dec; 26(6):1684-5. PubMed ID: 9398018
[No Abstract] [Full Text] [Related]
17. Mutations of the hereditary hemochromatosis candidate gene HLA-H in porphyria cutanea tarda.
Santos M; Clevers HC; Marx JJ
N Engl J Med; 1997 May; 336(18):1327-8. PubMed ID: 9132598
[No Abstract] [Full Text] [Related]
18. Putting a hold on 'HLA-H'.
Mercier B; Mura C; Ferec C
Nat Genet; 1997 Mar; 15(3):234. PubMed ID: 9054932
[No Abstract] [Full Text] [Related]
19. Screening for iron overload and HFE mutations in a university hospital.
Remacha AF; Carrasco M; Sardà MP; Barceló MJ; Blesa I; Baiget M
Haematologica; 2000 Aug; 85(8):873-4. PubMed ID: 10942939
[No Abstract] [Full Text] [Related]
20. Iron beware: a common HFE gene polymorphism may prevent the accurate molecular diagnosis of homozygous hemochromatosis in low-risk, but not high-risk groups.
Press RD
Hepatology; 2000 Feb; 31(2):540-2. PubMed ID: 10655286
[No Abstract] [Full Text] [Related]
[Next] [New Search]
