365 related articles for article (PubMed ID: 17289614)
1. [Importance of hereditary haemochromatosis in the care of diabetes mellitus].
Wittmann I; Wagner L; Markó L; Tamaskó M; Laczy B; Márton M; Cseh J; Melegh B
Orv Hetil; 2007 Jan; 148(3):111-5. PubMed ID: 17289614
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. Hereditary haemochromatosis.
Janssen MC; Swinkels DW
Best Pract Res Clin Gastroenterol; 2009; 23(2):171-83. PubMed ID: 19414144
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. Hereditary haemochromatosis: diagnosis and management in the gene era.
Olynyk JK
Liver; 1999 Apr; 19(2):73-80. PubMed ID: 10220735
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?
Cadet E; Capron D; Gallet M; Omanga-Léké ML; Boutignon H; Julier C; Robson KJ; Rochette J
J Med Genet; 2005 May; 42(5):390-5. PubMed ID: 15863667
[TBL] [Abstract][Full Text] [Related]
8. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
Sham RL; Ou CY; Cappuccio J; Braggins C; Dunnigan K; Phatak PD
Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
[TBL] [Abstract][Full Text] [Related]
9. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000).
Martinelli AL; Filho R; Cruz S; Franco R; Tavella M; Secaf M; Ramalho L; Zucoloto S; Rodrigues S; Zago M
Genet Mol Res; 2005 Mar; 4(1):31-8. PubMed ID: 15841433
[TBL] [Abstract][Full Text] [Related]
10. Defective release of Hepcidin not defective synthesis is the primary pathogenic mechanism in HFE-Haemochromatosis.
Arnold J; Sangwaiya A; Bhatkal B; Arnold A
Med Hypotheses; 2008; 70(6):1197-200. PubMed ID: 18054440
[TBL] [Abstract][Full Text] [Related]
11. Hereditary haemochromatosis: only 1% of adult HFEC282Y homozygotes in South Wales have a clinical diagnosis of iron overload.
McCune CA; Al-Jader LN; May A; Hayes SL; Jackson HA; Worwood M
Hum Genet; 2002 Dec; 111(6):538-43. PubMed ID: 12436244
[TBL] [Abstract][Full Text] [Related]
12. Homozygous G320V mutation in the HJV gene causing juvenile hereditary haemochromatosis type A. A case report.
Militaru MS; Popp RA; Trifa AP
J Gastrointestin Liver Dis; 2010 Jun; 19(2):191-3. PubMed ID: 20593054
[TBL] [Abstract][Full Text] [Related]
13. [Hereditary haemochromatosis: novel genes, novel diseases and hepcidin].
Bergmans JP; Kemna EH; Janssen MC; Jacobs EM; Stalenhoef AF; Marx JJ; Swinkels DW
Ned Tijdschr Geneeskd; 2007 May; 151(20):1121-7. PubMed ID: 17557668
[TBL] [Abstract][Full Text] [Related]
14. [Prevalence of hemochromatosis-associated mutations in the hemochromatosis gene in the Danish population].
Larsen LE; Ellervik C; Appleyard M; Nordestgaard BG; Birgens H; Tybjaerg-Hansen A
Ugeskr Laeger; 2002 Sep; 164(39):4545-7. PubMed ID: 12380399
[TBL] [Abstract][Full Text] [Related]
15. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.
Aguilar-Martinez P; Esculié-Coste C; Bismuth M; Giansily-Blaizot M; Larrey D; Schved JF
Blood Cells Mol Dis; 2001; 27(1):290-3. PubMed ID: 11358390
[TBL] [Abstract][Full Text] [Related]
16. Prevalence of C282Y and H63D mutations in the haemochromatosis (HFE) gene in Tunisian population.
Sassi R; Hmida S; Kaabi H; Hajjej A; Abid A; Abdelkefi S; Yacoub S; Maamar M; Mojaat N; Ben Hamed L; Bellali H; Dridi A; Jridi A; Midouni B; Boukef MK
Ann Genet; 2004; 47(4):325-30. PubMed ID: 15581829
[TBL] [Abstract][Full Text] [Related]
17. Synopsis of the Dutch multidisciplinary guideline for the diagnosis and treatment of hereditary haemochromatosis.
Swinkels DW; Jorna AT; Raymakers RA
Neth J Med; 2007 Dec; 65(11):452-5. PubMed ID: 18079569
[TBL] [Abstract][Full Text] [Related]
18. Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis.
Bridle KR; Frazer DM; Wilkins SJ; Dixon JL; Purdie DM; Crawford DH; Subramaniam VN; Powell LW; Anderson GJ; Ramm GA
Lancet; 2003 Feb; 361(9358):669-73. PubMed ID: 12606179
[TBL] [Abstract][Full Text] [Related]
19. [Diagnosis and treatment of genetic haemochromatosis].
Milman NT
Ugeskr Laeger; 2013 Apr; 175(16):1109-12. PubMed ID: 23651749
[TBL] [Abstract][Full Text] [Related]
20. Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
Merryweather-Clarke AT; Cadet E; Bomford A; Capron D; Viprakasit V; Miller A; McHugh PJ; Chapman RW; Pointon JJ; Wimhurst VL; Livesey KJ; Tanphaichitr V; Rochette J; Robson KJ
Hum Mol Genet; 2003 Sep; 12(17):2241-7. PubMed ID: 12915468
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
