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2. Cellular expression and regulation of iron transport and storage proteins in genetic haemochromatosis. Basclain KA; Shilkin KB; Withers G; Reed WD; Jeffrey GP J Gastroenterol Hepatol; 1998 Jun; 13(6):624-34. PubMed ID: 9715407 [TBL] [Abstract][Full Text] [Related]
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4. Alterations in sympathetic nerve traffic in genetic haemochromatosis before and after iron depletion therapy: a microneurographic study. Seravalle G; Piperno A; Mariani R; Pelloni I; Facchetti R; Dell'Oro R; Cuspidi C; Mancia G; Grassi G Eur Heart J; 2016 Mar; 37(12):988-95. PubMed ID: 26715163 [TBL] [Abstract][Full Text] [Related]
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12. Review article: the modern diagnosis and management of haemochromatosis. Adams PC Aliment Pharmacol Ther; 2006 Jun; 23(12):1681-91. PubMed ID: 16817911 [TBL] [Abstract][Full Text] [Related]
13. Differential expression of transferrin receptor in duodenal mucosa in iron overload. Evidence for a site-specific defect in genetic hemochromatosis. Lombard M; Bomford AB; Polson RJ; Bellingham AJ; Williams R Gastroenterology; 1990 Apr; 98(4):976-84. PubMed ID: 2179037 [TBL] [Abstract][Full Text] [Related]
14. Inborn errors of metabolism: iron. Worwood M Br Med Bull; 1999; 55(3):556-67. PubMed ID: 10746346 [TBL] [Abstract][Full Text] [Related]
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19. 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 Isr Med Assoc J; 2004 Jan; 6(1):30-3. PubMed ID: 14740507 [TBL] [Abstract][Full Text] [Related]