Similar articles for PMID: 31522215

Year	Number of Results
1992	1
1997	1
1998	2
1999	6
2000	5
2001	9
2002	7
2003	6
2004	6
2005	7
2006	5
2007	10
2008	3
2009	5
2010	5
2011	7
2012	4
2013	6
2014	5
2015	2
2016	8
2017	13
2018	6
2019	11
2020	26
2021	28
2022	20
2023	11
2024	10
2025	0

1

Association of frequency of hereditary hemochromatosis (HFE) gene mutations (H63D and C282Y) with iron overload in beta-thalassemia major patients in Pakistan.

Sharif Y, Irshad S, Tariq A, Rasheed S, Tariq MH. Sharif Y, et al. Saudi Med J. 2019 Sep;40(9):887-892. doi: 10.15537/smj.2019.9.24482. Saudi Med J. 2019. PMID: 31522215 Free PMC article.

2

Investigation of correlation between H63D and C282Y mutations in HFE gene and serum Ferritin level in beta-thalassemia major patients.

Rahmani R, Naseri P, Safaroghli-Azar A, Tarighi S, Hosseini T, Hojjati MT. Rahmani R, et al. Transfus Clin Biol. 2019 Nov;26(4):249-252. doi: 10.1016/j.tracli.2019.05.003. Epub 2019 May 29. Transfus Clin Biol. 2019. PMID: 31679808

3

Association of HFE Gene Mutations With Serum Ferritin Level and Heart and Liver Iron Overload in Patients With Transfusion-dependent Beta-Thalassemia.

Zekavat OR, Zareian Jahromi M, Haghpanah S, Kargar Jahromi Z, Cohan N. Zekavat OR, et al. J Pediatr Hematol Oncol. 2021 Jan;43(1):e26-e28. doi: 10.1097/MPH.0000000000001944. J Pediatr Hematol Oncol. 2021. PMID: 32925401

4

[HFE gene mutations in Tunisian major beta-Thalassemia and iron overload].

Mellouli F, El Borgi W, Kaabi H, Ben Hassen E, Sassi R, Hmida H, Cherif G, Maamar M, Zouari B, Boukef K, Bejaoui M, Hmida S. Mellouli F, et al. Transfus Clin Biol. 2006 Dec;13(6):353-7. doi: 10.1016/j.tracli.2006.12.002. Epub 2007 Feb 15. Transfus Clin Biol. 2006. PMID: 17303462 French.

5

Frequency of HFE gene mutations in Iranian beta-thalassaemia minor patients.

Jazayeri M, Bakayev V, Adibi P, Haghighi Rad F, Zakeri H, Kalantar E, Zali MR. Jazayeri M, et al. Eur J Haematol. 2003 Dec;71(6):408-11. doi: 10.1046/j.0902-4441.2003.00159.x. Eur J Haematol. 2003. PMID: 14703689

6

H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers.

Melis MA, Cau M, Deidda F, Barella S, Cao A, Galanello R. Melis MA, et al. Haematologica. 2002 Mar;87(3):242-5. Haematologica. 2002. PMID: 11869934

7

The influence of hemochromatosis mutations on iron overload of thalassemia major.

Longo F, Zecchina G, Sbaiz L, Fischer R, Piga A, Camaschella C. Longo F, et al. Haematologica. 1999 Sep;84(9):799-803. Haematologica. 1999. PMID: 10477452

8

Transient elevation of serum ferritin in a Sri Lankan with homozygosity for H63D mutation in the HFE gene: a case report.

Wickramasinghe W, Karunathilaka C, Jayasinghe S, Gooneratne L. Wickramasinghe W, et al. J Med Case Rep. 2020 Jul 9;14(1):93. doi: 10.1186/s13256-020-02428-3. J Med Case Rep. 2020. PMID: 32641120 Free PMC article.

9

Prevalence of the H63D mutation of the HFE in north India: its presence does not cause iron overload in beta thalassemia trait.

Garewal G, Das R, Ahluwalia J, Marwaha RK. Garewal G, et al. Eur J Haematol. 2005 Apr;74(4):333-6. doi: 10.1111/j.1600-0609.2004.00390.x. Eur J Haematol. 2005. PMID: 15777346

10

Effect of the Hemochromatosis Mutations on Iron Overload among the Indian β Thalassemia Carriers.

Nadkarni AH, Singh AA, Colaco S, Hariharan P, Colah RB, Ghosh K. Nadkarni AH, et al. J Clin Lab Anal. 2017 May;31(3):e22054. doi: 10.1002/jcla.22054. Epub 2016 Aug 26. J Clin Lab Anal. 2017. PMID: 27561698 Free PMC article.

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