Similar articles for PMID: 22674401

Year	Number of Results
1997	1
1998	4
1999	7
2000	6
2001	6
2002	5
2003	6
2004	6
2005	10
2006	3
2007	4
2008	7
2009	5
2010	4
2011	4
2012	6
2013	4
2014	3
2015	3
2018	1
2019	1
2021	1
2022	1
2024	0

1

Diagnosis of hereditary hemochromatosis in the era of genetic testing.

Trieß C, von Figura G, Stuhrmann M, Butzeck B, Krayenbuehl PA, Strnad P, Kulaksiz H. Trieß C, et al. Dig Dis Sci. 2012 Nov;57(11):2988-94. doi: 10.1007/s10620-012-2243-z. Epub 2012 Jun 7. Dig Dis Sci. 2012. PMID: 22674401

2

[Molecular genetic diagnostics and screening of hereditary hemochromatosis].

Zlocha J, Kovács L, Pozgayová S, Kupcová V, Durínová S. Zlocha J, et al. Vnitr Lek. 2006 Jun;52(6):602-8. Vnitr Lek. 2006. PMID: 16871764 Slovak.

3

Clinical manifestations of hemochromatosis in HFE C282Y homozygotes identified by screening.

McLaren GD, McLaren CE, Adams PC, Barton JC, Reboussin DM, Gordeuk VR, Acton RT, Harris EL, Speechley MR, Sholinsky P, Dawkins FW, Snively BM, Vogt TM, Eckfeldt JH; Hemochromatosis and Iron Overload Screen (HEIRS) Study Research Investigators. McLaren GD, et al. Can J Gastroenterol. 2008 Nov;22(11):923-30. doi: 10.1155/2008/907356. Can J Gastroenterol. 2008. PMID: 19018338 Free PMC article.

4

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. Aguilar-Martinez P, et al. Blood Cells Mol Dis. 2001 Jan-Feb;27(1):290-3. doi: 10.1006/bcmd.2001.0382. Blood Cells Mol Dis. 2001. PMID: 11358390

5

[Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland].

Himmelmann A, Bortoluzzi L, Jansen S, Fehr J. Himmelmann A, et al. Schweiz Med Wochenschr. 2000 Aug 8;130(31-32):1112-9. Schweiz Med Wochenschr. 2000. PMID: 11008304 German.

6

[Molecular genetic analysis and clinical aspects of patients with hereditary hemochromatosis].

Lange U, Teichmann J, Dischereit G. Lange U, et al. Orthopade. 2014 Aug;43(8):772-9. doi: 10.1007/s00132-014-2318-y. Orthopade. 2014. PMID: 24906241 German.

7

Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis.

Bittencourt PL, Palácios SA, Couto CA, Cançado EL, Carrilho FJ, Laudanna AA, Kalil J, Gayotto LC, Goldberg AC. Bittencourt PL, et al. Braz J Med Biol Res. 2002 Mar;35(3):329-35. doi: 10.1590/s0100-879x2002000300007. Braz J Med Biol Res. 2002. PMID: 11887210 Free article.

8

Underdiagnosis of hereditary haemochromatosis: lack of presentation or penetration?

Ryan E, Byrnes V, Coughlan B, Flanagan AM, Barrett S, O'Keane JC, Crowe J. Ryan E, et al. Gut. 2002 Jul;51(1):108-12. doi: 10.1136/gut.51.1.108. Gut. 2002. PMID: 12077102 Free PMC article.

9

Hereditary hemochromatosis in north-eastern Romania.

Voicu PM, Cojocariu C, Petrescu-Dănilă E, Stanciu C, Covic M, Rusu M, Trifan A. Voicu PM, et al. Rev Med Chir Soc Med Nat Iasi. 2010 Oct-Dec;114(4):982-7. Rev Med Chir Soc Med Nat Iasi. 2010. PMID: 21495455

10

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. Cadet E, et al. J Med Genet. 2005 May;42(5):390-5. doi: 10.1136/jmg.2004.027284. J Med Genet. 2005. PMID: 15863667 Free PMC article.

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