These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. A novel SLC40A1 p.Y333H mutation with gain of function of ferroportin: A recurrent cause of haemochromatosis in China. Zhang W; Xu A; Li Y; Zhao S; Zhou D; Wu L; Zhang B; Zhao X; Wang Y; Wang X; Duan W; Wang Q; Nan Y; You H; Jia J; Ou X; Huang J; Liver Int; 2019 Jun; 39(6):1120-1127. PubMed ID: 30500107 [TBL] [Abstract][Full Text] [Related]
4. The mechanisms of systemic iron homeostasis and etiology, diagnosis, and treatment of hereditary hemochromatosis. Kawabata H Int J Hematol; 2018 Jan; 107(1):31-43. PubMed ID: 29134618 [TBL] [Abstract][Full Text] [Related]
5. HFE, hepcidin and ferroportin gene mutations are not present in Indian patients with primary haemochromatosis. Shukla P; Julka S; Bhatia E; Shah S; Nagral A; Aggarwal R Natl Med J India; 2006; 19(1):20-3. PubMed ID: 16570681 [TBL] [Abstract][Full Text] [Related]
6. Long-term phlebotomy successfully alleviated hepatic iron accumulation in a ferroportin disease patient with a mutation in SLC40A1: a case report. Nishina S; Tomiyama Y; Ikuta K; Tatsumi Y; Toki Y; Kato A; Kato K; Yoshioka N; Sasaki K; Hara Y; Hino K BMC Gastroenterol; 2021 Mar; 21(1):111. PubMed ID: 33673803 [TBL] [Abstract][Full Text] [Related]
8. New insights into the regulation of iron homeostasis. Deicher R; Hörl WH Eur J Clin Invest; 2006 May; 36(5):301-9. PubMed ID: 16634833 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Inherited Disorders of Iron Overload. Pantopoulos K Front Nutr; 2018; 5():103. PubMed ID: 30420953 [TBL] [Abstract][Full Text] [Related]
16. Non- Lv T; Zhang W; Xu A; Li Y; Zhou D; Zhang B; Li X; Zhao X; Wang Y; Wang X; Duan W; Wang Q; Xu H; Zheng J; Zhao R; Zhu L; Dong Y; Lu L; Chen Y; Long J; Zheng S; Wang W; You H; Jia J; Ou X; Huang J J Med Genet; 2018 Oct; 55(10):650-660. PubMed ID: 30166352 [TBL] [Abstract][Full Text] [Related]
17. 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]