Similar articles for PMID: 26547814

Year	Number of Results
1998	2
1999	2
2000	3
2001	6
2002	4
2003	5
2004	3
2005	9
2006	6
2007	5
2008	5
2009	5
2010	2
2011	4
2012	2
2013	3
2014	5
2015	7
2016	11
2017	12
2018	9
2019	9
2020	4
2021	4
2022	5
2023	2
2024	0

1

Analysis of HFE mutations and non-HFE gene mutations (TFR2 and SLC40A1) in patients with phenotypic hemochromatosis from the Basque Country.

Castiella A, Zapata E, De Juan MD, Zubiaurre L, Iribarren A, Otazua P, Fernandez J, Aragón L, Zuriarrain O, Gorostidi A. Castiella A, et al. Int J Lab Hematol. 2016 Feb;38(1):e5-7. doi: 10.1111/ijlh.12444. Epub 2015 Nov 7. Int J Lab Hematol. 2016. PMID: 26547814 No abstract available.

2

Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis.

Del-Castillo-Rueda A, Moreno-Carralero MI, Cuadrado-Grande N, Alvarez-Sala-Walther LA, Enríquez-de-Salamanca R, Méndez M, Morán-Jiménez MJ. Del-Castillo-Rueda A, et al. Gene. 2012 Oct 15;508(1):15-20. doi: 10.1016/j.gene.2012.07.069. Epub 2012 Aug 4. Gene. 2012. PMID: 22890139

3

Identification of novel mutations in HFE, HFE2, TfR2, and SLC40A1 genes in Chinese patients affected by hereditary hemochromatosis.

Wang Y, Du Y, Liu G, Guo S, Hou B, Jiang X, Han B, Chang Y, Nie G. Wang Y, et al. Int J Hematol. 2017 Apr;105(4):521-525. doi: 10.1007/s12185-016-2150-8. Epub 2016 Nov 28. Int J Hematol. 2017. PMID: 27896572

4

The mechanisms of systemic iron homeostasis and etiology, diagnosis, and treatment of hereditary hemochromatosis.

Kawabata H. Kawabata H. Int J Hematol. 2018 Jan;107(1):31-43. doi: 10.1007/s12185-017-2365-3. Epub 2017 Nov 13. Int J Hematol. 2018. PMID: 29134618 Review.

5

The global prevalence of HFE and non-HFE hemochromatosis estimated from analysis of next-generation sequencing data.

Wallace DF, Subramaniam VN. Wallace DF, et al. Genet Med. 2016 Jun;18(6):618-26. doi: 10.1038/gim.2015.140. Epub 2015 Dec 3. Genet Med. 2016. PMID: 26633544 Free article.

6

Non-HFE hemochromatosis.

Pietrangelo A. Pietrangelo A. Semin Liver Dis. 2005 Nov;25(4):450-60. doi: 10.1055/s-2005-923316. Semin Liver Dis. 2005. PMID: 16315138 Review.

7

Molecular pathogenesis of hereditary hemochromatosis.

Liu J, Pu C, Lang L, Qiao L, Abdullahi MA, Jiang C. Liu J, et al. Histol Histopathol. 2016 Aug;31(8):833-40. doi: 10.14670/HH-11-762. Epub 2016 Mar 31. Histol Histopathol. 2016. PMID: 27031690 Review.

8

Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genes.

Radio FC, Majore S, Aurizi C, Sorge F, Biolcati G, Bernabini S, Giotti I, Torricelli F, Giannarelli D, De Bernardo C, Grammatico P. Radio FC, et al. Blood Cells Mol Dis. 2015 Jun;55(1):71-5. doi: 10.1016/j.bcmd.2015.04.001. Epub 2015 Apr 16. Blood Cells Mol Dis. 2015. PMID: 25976471

9

HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants.

Barton JC, Lafreniere SA, Leiendecker-Foster C, Li H, Acton RT, Press RD, Eckfeldt JH. Barton JC, et al. Am J Hematol. 2009 Nov;84(11):710-4. doi: 10.1002/ajh.21524. Am J Hematol. 2009. PMID: 19787796 Free article.

10

The use of a reverse hybridization strip assay for the study of hemochromatosis-associated gene mutations in Lebanon.

Daher RT, Khalik RN, Hoteit RM, Sarieddine DS, Charafeddine KM, Cortas NK, Mahfouz RA. Daher RT, et al. Genet Test Mol Biomarkers. 2011 Dec;15(12):909-11. doi: 10.1089/gtmb.2011.0046. Epub 2011 Jun 20. Genet Test Mol Biomarkers. 2011. PMID: 21689013

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