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Items: 1 to 20 of 27

1.
Elevated transferrin saturation in individuals with alcohol use disorder: Association with HFE polymorphism and alcohol withdrawal severity
Danielle S. Kroll, Katherine L. McPherson, Peter Manza, Melanie L. Schwandt, Pei-Hong Shen, David Goldman, Nancy Diazgranados, Gene-Jack Wang, Corinde E. Wiers, Nora D. Volkow
Addict Biol. Author manuscript; available in PMC 2023 Mar 1.
Published in final edited form as: Addict Biol. 2022 Mar; 27(2): e13144. doi: 10.1111/adb.13144
PMCID:
PMC9373047
AbstractArticlePDF–549K
2.
Elevated Transferrin Saturation, Health-Related Quality of Life and Telomere Length
Arch G. Mainous, III, Robert U. Wright, Mary M. Hulihan, Waleed O. Twal, Christine E. McLaren, Vanessa A. Diaz, Gordon D. McLaren, W. Scott Argraves, Althea M. Grant
Biometals. Author manuscript; available in PMC 2014 May 27.
Published in final edited form as: Biometals. 2014 Feb; 27(1): 135–141. Published online 2013 Dec 15. doi: 10.1007/s10534-013-9693-4
PMCID:
PMC4034347
AbstractArticlePDF–46K
3.
Total Mortality by Elevated Transferrin Saturation in Patients With Diabetes
Christina Ellervik, Henrik Ullits Andersen, Anne Tybjærg-Hansen, Merete Frandsen, Henrik Birgens, Børge G. Nordestgaard, Thomas Mandrup-Poulsen
Diabetes Care. 2013 Sep; 36(9): 2646–2654. Published online 2013 Aug 13. doi: 10.2337/dc12-2032
PMCID:
PMC3747880
AbstractArticlePDF–216K
4.
Elevated Transferrin Saturation and Risk of Diabetes: Three population-based studies
Christina Ellervik, Thomas Mandrup-Poulsen, Henrik Ullits Andersen, Anne Tybjærg-Hansen, Merete Frandsen, Henrik Birgens, Børge G. Nordestgaard
Diabetes Care. 2011 Oct; 34(10): 2256–2258. Published online 2011 Sep 15. doi: 10.2337/dc11-0416
Correction in:
Diabetes Care. 2012 Aug; 35(8): 1809.
PMCID:
PMC3177722
AbstractArticlePDF–1.2M
5.
Iron overload is rare in patients homozygous for the H63D mutation
Melissa Kelley, Nikhil Joshi, Yagang Xie, Mark Borgaonkar
Can J Gastroenterol Hepatol. 2014 Apr; 28(4): 198–202. doi: 10.1155/2014/468521
PMCID:
PMC4071918
AbstractArticlePDF–752K
6.
Iron Overload and HFE Gene Mutations in Czech Patients with Chronic Liver Diseases
Marketa Dostalikova-Cimburova, Karolina Kratka, Jaroslav Stransky, Ivana Putova, Blanka Cieslarova, Jiri Horak
Dis Markers. 2012; 32(1): 65–72. Published online 2012 Feb 1. doi: 10.3233/DMA-2012-0861
PMCID:
PMC3826488
SummaryPDF–148K
7.
Heritability of Serum Iron Measures in the Hemochromatosis and Iron Overload Screening (HEIRS) Family Study
Christine E. McLaren, James C. Barton, John H. Eckfeldt, Gordon D. McLaren, Ronald T. Acton, Paul C. Adams, Leora F. Henkin, Victor R. Gordeuk, Chris D. Vulpe, Emily L. Harris, Barbara W. Harrison, Jacob A. Reiss, Beverly M. Snively
Am J Hematol. Author manuscript; available in PMC 2013 Nov 4.
Published in final edited form as: Am J Hematol. 2010 Feb; 85(2): 10.1002/ajh.21585. doi: 10.1002/ajh.21585
PMCID:
PMC3816512
AbstractArticlePDF–57K
8.
Iron overload in HFE C282Y heterozygotes at first genetic testing: a strategy for identifying rare HFE variants
Patricia Aguilar-Martinez, Bernard Grandchamp, Séverine Cunat, Estelle Cadet, François Blanc, Marlène Nourrit, Kaiss Lassoued, Jean-François Schved, Jacques Rochette
Haematologica. 2011 Apr; 96(4): 507–514. Published online 2011 Jan 12. doi: 10.3324/haematol.2010.029751
PMCID:
PMC3069226
AbstractArticlePDF–338K
9.
Post mortem identification of deoxyguanosine kinase (DGUOK) gene mutations combined with impaired glucose homeostasis and iron overload features in four infants with severe progressive liver failure
Ewa Pronicka, Anna Węglewska-Jurkiewicz, Joanna Taybert, Maciej Pronicki, Tamara Szymańska-Dębińska, Agnieszka Karkucińska-Więckowska, Joanna Jakóbkiewicz-Banecka, Paweł Kowalski, Dorota Piekutowska-Abramczuk, Magdalena Pajdowska, Piotr Socha, Jolanta Sykut-Cegielska, Grzegorz Węgrzyn
J Appl Genet. 2011; 52(1): 61–66. Published online 2010 Nov 16. doi: 10.1007/s13353-010-0008-y
PMCID:
PMC3026684
AbstractArticlePDF–142K
10.
Ferroportin disease: A systematic meta-analysis of clinical and molecular findings
Roman Mayr, Andreas R. Janecke, Melanie Schranz, William J.H. Griffiths, Wolfgang Vogel, Antonello Pietrangelo, Heinz Zoller
J Hepatol. 2010 Nov; 53(5-3): 941–949. doi: 10.1016/j.jhep.2010.05.016
Correction in:
J Hepatol. 2011 Sep; 55(3): 734–736.
PMCID:
PMC2956830
AbstractArticle
11.
Human mutation D157G in ferroportin leads to hepcidin-independent binding of Jak2 and ferroportin down-regulation
Ivana De Domenico, Eric Lo, Diane M. Ward, Jerry Kaplan
Blood. 2010 Apr 8; 115(14): 2956–2959. Prepublished online 2010 Feb 2. doi: 10.1182/blood-2009-10-251306
PMCID:
PMC2854436
AbstractArticle
12.
Mechanism of increased iron absorption in murine model of hereditary hemochromatosis: Increased duodenal expression of the iron transporter DMT1
Robert E. Fleming, Mary C. Migas, XiaoYan Zhou, Jinxing Jiang, Robert S. Britton, Elizabeth M. Brunt, Shunji Tomatsu, Abdul Waheed, Bruce R. Bacon, William S. Sly
Proc Natl Acad Sci U S A. 1999 Mar 16; 96(6): 3143–3148. doi: 10.1073/pnas.96.6.3143
PMCID:
PMC15909
AbstractArticlePDF–169K
13.
Ferroportin inhibitor vamifeport ameliorates ineffective erythropoiesis in a mouse model of b-thalassemia with blood transfusions
Natarajaswamy Kalleda, Anna Flace, Patrick Altermatt, Giada Ingoglia, Cédric Doucerain, Naja Nyffenegger, Franz Dürrenberger, Vania Manolova
Haematologica. 2023 Oct 1; 108(10): 2703–2714. Published online 2023 May 11. doi: 10.3324/haematol.2022.282328
PMCID:
PMC10543196
AbstractArticlePDF–1.5M
14.
Alcoholic Hepatitis Mimicking Iron Overload Disorders With Hyperferritinemia and Severely Elevated Transferrin Saturation: A Case Report
Salina Munankami, Shefali Amin, Manish Shrestha, Rubina Paudel, Arpan Pokhrel
Cureus. 2023 Jul; 15(7): e41727. Published online 2023 Jul 11. doi: 10.7759/cureus.41727
PMCID:
PMC10415023
AbstractArticlePDF–138K
15.
Vascular Aging and Damage in Patients with Iron Metabolism Disorders
Krzysztof Młodziński, Michał Świątczak, Justyna Rohun, Jacek Wolf, Krzysztof Narkiewicz, Marcin Hellmann, Ludmiła Daniłowicz-Szymanowicz
Diagnostics (Basel) 2022 Nov; 12(11): 2817. Published online 2022 Nov 16. doi: 10.3390/diagnostics12112817
PMCID:
PMC9689457
AbstractArticlePDF–582K
16.
Autoimmune Hepatitis in the Setting of Iron Overload Secondary to Heterozygous HFE Gene Mutation
Sukhjinder Chauhan, Rasiq Zackria, Deb K Mukhopadhyay
Cureus. 2022 Aug; 14(8): e27614. Published online 2022 Aug 2. doi: 10.7759/cureus.27614
PMCID:
PMC9436270
AbstractArticlePDF–188K
17.
NTBI levels in C282Y homozygotes after therapeutic phlebotomy
Eleanor Ryan, Keith Mulready, Erwin Wiegerinck, Jennifer Russell, Dorine W. Swinkels, Stephen Stewart
EJHaem. 2022 Aug; 3(3): 644–652. Published online 2022 Jul 27. doi: 10.1002/jha2.507
PMCID:
PMC9422009
AbstractArticlePDF–445K
18.
In the presence of autoantibodies and iron overload, do not judge a book by its cover: A case report
Nur Yazdali Koylu, Bahadir Koylu, Cenk Sokmensuer, Yasemin Balaban
Hepatol Forum. 2021 May; 2(2): 76–79. Published online 2021 May 24. doi: 10.14744/hf.2021.2021.0013
PMCID:
PMC9138916
AbstractArticlePDF–576K
19.
Autoimmune Hepatitis: Diagnostic Dilemma When It Is Disguised as Iron Overload Syndrome
Gyanendra K. Acharya, Hung-I Liao, Simona Frunza-Stefan, Ronakkumar Patel, Moe Khaing
J Clin Exp Hepatol. 2017 Sep; 7(3): 269–273. Published online 2017 Mar 16. doi: 10.1016/j.jceh.2017.03.006
PMCID:
PMC5620361
AbstractArticlePDF–706K
20.
Dysregulation of iron and copper homeostasis in nonalcoholic fatty liver
Elmar Aigner, Günter Weiss, Christian Datz
World J Hepatol. 2015 Feb 27; 7(2): 177–188. Published online 2015 Feb 27. doi: 10.4254/wjh.v7.i2.177
PMCID:
PMC4342600
AbstractArticlePDF–2.2M

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