PMC Links for Books (Select 1475938) - PMC

Select item 101483831.

Non-alcoholic fatty liver disease in hemochromatosis probands with iron overload and HFE p.C282Y/p.C282Y

James C. Barton, J. Clayborn Barton, Ronald T. Acton

BMC Gastroenterol. 2023; 23: 137. Published online 2023 Apr 28. doi: 10.1186/s12876-023-02763-x

PMCID:: PMC10148383

Article PDF–932K

Select item 94986542.

Twenty-Five Years of Contemplating Genotype-Based Hereditary Hemochromatosis Population Screening

Jörg Schmidtke

Genes (Basel) 2022 Sep; 13(9): 1622. Published online 2022 Sep 9. doi: 10.3390/genes13091622

PMCID:: PMC9498654

Article PDF–262K

Select item 93285713.

Iron overload phenotypes and HFE genotypes in white hemochromatosis and iron overload screening study participants without HFE p.C282Y/p.C282Y

James C. Barton, J. Clayborn Barton, Ronald T. Acton

PLoS One. 2022; 17(7): e0271973. Published online 2022 Jul 27. doi: 10.1371/journal.pone.0271973

PMCID:: PMC9328571

Article PDF–820K

Select item 75317704.

Long-term Outcome of Orthotopic Liver Transplantation in Patients With Hemochromatosis: A Summary of a 30-year Transplant Program

Eva Maria Dobrindt, Eriselda Keshi, Julian Neulichedl, Wenzel Schöning, Robert Öllinger, Johann Pratschke, Dennis Eurich

Transplant Direct. 2020 Jun; 6(6): e560. Published online 2020 May 28. doi: 10.1097/TXD.0000000000001007

PMCID:: PMC7531770

Article PDF–835K

Select item 66601365.

HFE gene: structure, function, mutations, and associated iron abnormalities

James C. Barton, Corwin Q. Edwards, Ronald T. Acton

Gene. Author manuscript; available in PMC 2019 Jul 26.

Published in final edited form as: Gene. 2015 Dec 15; 574(2): 179–192. Published online 2015 Oct 9. doi: 10.1016/j.gene.2015.10.009

PMCID:: PMC6660136

Article PDF–635K

Select item 63688586.

Cirrhosis in Hemochromatosis: Independent Risk Factors in 368 HFE p.C282Y Homozygotes

James C. Barton, Christine E. McLaren, Wen-pin Chen, Grant A. Ramm, Gregory J. Anderson, Lawrie W Powell, V. Nathan Subramaniam, Paul C. Adams, Pradyumna D. Phatak, Lyle C. Gurrin, John D. Phillips, Charles J. Parker, Mary J. Emond, Gordon D. McLaren

Ann Hepatol. Author manuscript; available in PMC 2019 Feb 9.

Published in final edited form as: Ann Hepatol. 2018 Aug 24; 17(5): 871–879. doi: 10.5604/01.3001.0012.3169

PMCID:: PMC6368858

Article PDF–461K

Select item 59042347.

Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotype

Paul Adams, Albert Altes, Pierre Brissot, Barbara Butzeck, Ioav Cabantchik, Rodolfo Cançado, Sonia Distante, Patricia Evans, Robert Evans, Tomas Ganz, Domenico Girelli, Rolf Hultcrantz, Gordon McLaren, Ben Marris, Nils Milman, Elizabeta Nemeth, Peter Nielsen, Brigitte Pineau, Alberto Piperno, Graça Porto, Dianne Prince, John Ryan, Mayka Sanchez, Paulo Santos, Dorine Swinkels, Emerência Teixeira, Ketil Toska, Annick Vanclooster, Desley White, Contributors and Hemochromatosis International Taskforce

Hepatol Int. 2018 Mar; 12(2): 83–86. Published online 2018 Mar 27. doi: 10.1007/s12072-018-9855-0

PMCID:: PMC5904234

Article PDF–333K

Select item 39402108.

Neonatal Hemochromatosis

Amy G. Feldman, Peter F. Whitington

J Clin Exp Hepatol. 2013 Dec; 3(4): 313–320. Published online 2013 Nov 27. doi: 10.1016/j.jceh.2013.10.004

PMCID:: PMC3940210

Article PDF–1.1M

Select item 39342699.

Erythrocytapheresis compared with whole blood phlebotomy for the treatment of hereditary haemochromatosis

Tatjana Sundic, Tor Hervig, Signe Hannisdal, Jörg Assmus, Rune J. Ulvik, Richard W. Olaussen, Sigbjørn Berentsen

Blood Transfus. 2014 Jan; 12(Suppl 1): s84–s89. doi: 10.2450/2013.0128-13

PMCID:: PMC3934269

Article PDF–861K

Select item 314912510.

Diagnosis and Management of Hemochromatosis: 2011 Practice Guideline by the American Association for the Study of Liver Diseases

Bruce R Bacon, Paul C Adams, Kris V Kowdley, Lawrie W Powell, Anthony S Tavill

Hepatology. 2011 Jul; 54(1): 328–343. doi: 10.1002/hep.24330

PMCID:: PMC3149125

Article PDF–374K

Select item 303404411.

A Phase 1/2, Dose-Escalation Trial of Deferasirox for the Treatment of Iron Overload in HFE-Related Hereditary Hemochromatosis

Pradyumna Phatak, Pierre Brissot, Mark Wurster, Paul C Adams, Herbert L Bonkovsky, John Gross, Peter Malfertheiner, Gordon D McLaren, Claus Niederau, Alberto Piperno, Lawrie W Powell, Mark W Russo, Ulrich Stoelzel, Wolfgang Stremmel, Louis Griffel, Nicola Lynch, Yiyun Zhang, Antonello Pietrangelo

Hepatology. 2010 Nov; 52(5): 1671–1679. doi: 10.1002/hep.23879

PMCID:: PMC3034044

Article PDF–391K

Select item 285720312.

Homozygous deletion of HFE is the common cause of hemochromatosis in Sardinia

Gérald Le Gac, Rita Congiu, Isabelle Gourlaouen, Milena Cau, Claude Férec, Maria Antonietta Melis

Haematologica. 2010 Apr; 95(4): 685–687. Published online 2009 Dec 8. doi: 10.3324/haematol.2009.016816

PMCID:: PMC2857203

Article PDF–365K

Select item 195496413.

Proton pump inhibitors suppress absorption of dietary non‐haem iron in hereditary haemochromatosis

Carol Hutchinson, Catherine A Geissler, Jonathan J Powell, Adrian Bomford

Gut. 2007 Sep; 56(9): 1291–1295. Published online 2007 Apr 30. doi: 10.1136/gut.2006.108613

PMCID:: PMC1954964

Article PDF–189K

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