Similar articles for PMID: 11336458

Year	Number of Results
1988	1
1997	2
1998	5
1999	18
2000	13
2001	14
2002	9
2003	7
2004	4
2005	4
2006	8
2007	5
2008	4
2009	4
2010	7
2011	3
2012	4
2013	2
2014	2
2015	2
2016	1
2017	3
2018	1
2022	3
2024	0

1

Diagnosis of hemochromatosis in family members of probands: a comparison of phenotyping and HFE genotyping.

Barton JC, Rothenberg BE, Bertoli LF, Acton RT. Barton JC, et al. Genet Med. 1999 Mar-Apr;1(3):89-93. doi: 10.1097/00125817-199903000-00005. Genet Med. 1999. PMID: 11336458 Free article.

2

Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis.

Porto G, Alves H, Rodrigues P, Cabeda JM, Portal C, Ruivo A, Justiça B, Wolff R, De Sousa M. Porto G, et al. Immunogenetics. 1998 Apr;47(5):404-10. doi: 10.1007/s002510050376. Immunogenetics. 1998. PMID: 9510559

3

A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria.

Brissot P, Moirand R, Jouanolle AM, Guyader D, Le Gall JY, Deugnier Y, David V. Brissot P, et al. J Hepatol. 1999 Apr;30(4):588-93. doi: 10.1016/s0168-8278(99)80188-3. J Hepatol. 1999. PMID: 10207799

4

Correlation between iron status and genetic hemochromatosis (codon C282Y) in a large German population.

Wrede CE, Hutzler S, Bollheimer LC, Buettner R, Hellerbrand C, Schöelmerich J, Palitzsch KD. Wrede CE, et al. Isr Med Assoc J. 2004 Jan;6(1):30-3. Isr Med Assoc J. 2004. PMID: 14740507 Free article.

5

Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands.

Barton JC, Sawada-Hirai R, Rothenberg BE, Acton RT. Barton JC, et al. Blood Cells Mol Dis. 1999 Jun-Aug;25(3-4):147-55. doi: 10.1006/bcmd.1999.0240. Blood Cells Mol Dis. 1999. PMID: 10575540

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. Gottschalk R, et al. Eur J Immunogenet. 2000 Jun;27(3):129-34. doi: 10.1046/j.1365-2370.2000.00215.x. Eur J Immunogenet. 2000. PMID: 10940080

7

Relation between HFE mutations and mild iron-overload expression.

Mura C, Le Gac G, Raguénes O, Mercier AY, Le Guen A, Férec C. Mura C, et al. Mol Genet Metab. 2000 Apr;69(4):295-301. doi: 10.1006/mgme.2000.2981. Mol Genet Metab. 2000. PMID: 10870847

8

Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study.

McLaren CE, Barton JC, Eckfeldt JH, McLaren GD, Acton RT, Adams PC, Henkin LF, Gordeuk VR, Vulpe CD, Harris EL, Harrison BW, Reiss JA, Snively BM. McLaren CE, et al. Am J Hematol. 2010 Feb;85(2):101-5. doi: 10.1002/ajh.21585. Am J Hematol. 2010. PMID: 20095037 Free PMC article.

9

Hemochromatosis and iron-overload screening in a racially diverse population.

Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, Dawkins FW, Acton RT, Harris EL, Gordeuk VR, Leiendecker-Foster C, Speechley M, Snively BM, Holup JL, Thomson E, Sholinsky P; Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators. Adams PC, et al. N Engl J Med. 2005 Apr 28;352(17):1769-78. doi: 10.1056/NEJMoa041534. N Engl J Med. 2005. PMID: 15858186 Free article.

10

HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening.

Barton JC, Acton RT, Leiendecker-Foster C, Lovato L, Adams PC, McLaren GD, Eckfeldt JH, McLaren CE, Reboussin DM, Gordeuk VR, Speechley MR, Reiss JA, Press RD, Dawkins FW; Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators. Barton JC, et al. Genet Test. 2007 Fall;11(3):269-75. doi: 10.1089/gte.2007.0003. Genet Test. 2007. PMID: 17949288

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