Paul C Adams, Lucie Richard, Matthew Weir & Mark Speechley. (2021) Survival and development of health conditions after iron depletion therapy in C282Y-linked hemochromatosis patients. Canadian Liver Journal 4:4, pages 381-390.
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K. Sigvard Olsson, Olof Wålinder, Ulf Jansson, Maria Wilbe, Marie-Louise Bondeson, Eva-Lena Stattin, Ruma Raha-Chowdhury & Roger Williams. (2017) Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes. Hereditas 154:1.
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James C. Barton & Ronald T. Acton. (2017)
Diabetes in
HFE
Hemochromatosis
. Journal of Diabetes Research 2017, pages 1-16.
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Lawrie W Powell, Rebecca C Seckington & Yves Deugnier. (2016) Haemochromatosis. The Lancet 388:10045, pages 706-716.
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Paul C. Adams. 2015. Yamada' s Textbook of Gastroenterology. Yamada' s Textbook of Gastroenterology
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James C. Barton & J. Clayborn Barton. (2015)
Autoimmune Conditions in 235 Hemochromatosis Probands with
HFE
C282Y Homozygosity and Their First-Degree Relatives
. Journal of Immunology Research 2015, pages 1-11.
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Mónica Costa, Eugénia Cruz, James C. Barton, Ketil Thorstensen, Sandra Morais, Berta M. da Silva, Jorge P. Pinto, Cristina P. Vieira, Jorge Vieira, Ronald T. Acton & Graça Porto. (2013) Effects of Highly Conserved Major Histocompatibility Complex (MHC) Extended Haplotypes on Iron and Low CD8+ T Lymphocyte Phenotypes in HFE C282Y Homozygous Hemochromatosis Patients from Three Geographically Distant Areas. PLoS ONE 8:11, pages e79990.
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James C. BartonJ. Clayborn Barton. (2012)
Dupuytren's Contracture in Alabama
HFE
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Trefor Higgins, John H. Eckfeldt, James C. Barton & Basil T. Doumas. 2012. Tietz Textbook of Clinical Chemistry and Molecular Diagnostics. Tietz Textbook of Clinical Chemistry and Molecular Diagnostics
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Catherine Geissler & Mamta Singh. (2011) Iron, Meat and Health. Nutrients 3:3, pages 283-316.
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Paul C. Adams & James C. Barton. (2010) How I treat hemochromatosis. Blood 116:3, pages 317-325.
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James C. Barton, Corwin Q. Edwards, Pradyumna D. Phatak, Robert S. Britton & Bruce R. BaconJames C. Barton, Corwin Q. Edwards, Pradyumna D. Phatak, Robert S. Britton & Bruce R. Bacon. 2011. Handbook of Iron Overload Disorders. Handbook of Iron Overload Disorders
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Tor-Arne Hagve, Arne Åsberg, Rune Ulvik, Berit Borch-Iohnsen & Ketil Thorstensen. (2009) Hemokromatose – fra underdiagnostisert kuriositet til folkesykdom. Tidsskrift for Den norske legeforening 129:9, pages 863-866.
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Gordon D. McLaren & Victor R. Gordeuk. (2009) Hereditary hemochromatosis: insights from the Hemochromatosis and Iron Overload Screening (HEIRS) Study. Hematology 2009:1, pages 195-206.
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C. J. CROOKS, J. WEST, M. SOLAYMANI-DODARAN & T. R. CARD. (2009) The epidemiology of haemochromatosis: a population-based study. Alimentary Pharmacology & Therapeutics 29:2, pages 183-192.
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James C. BartonCatherine Leiendecker-FosterDavid M. ReboussinPaul C. AdamsRonald T. ActonJohn H. Eckfeldt. (2008)
Thyroid-Stimulating Hormone and Free Thyroxine Levels in Persons with
HFE
C282Y Homozygosity, a Common Hemochromatosis Genotype: The HEIRS Study
. Thyroid 18:8, pages 831-838.
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. (2008)
Iron-Overload–Related Disease in
HFE
Hereditary Hemochromatosis
. New England Journal of Medicine 358:21, pages 2293-2295.
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Arne Åsberg, Ketil Thorstensen, Wenche Irgens & Kristian Hveem. (2008) Screening for hemochromatosis. Blood 111:7, pages 3896-3896.
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Jill Waalen, Vincent J. Felitti, Terri Gelbart & Ernest Beutler. (2008) Screening for hemochromatosis by measuring ferritin levels: a more effective approach. Blood 111:7, pages 3373-3376.
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Paul C Adams & James C Barton. (2007) Haemochromatosis. The Lancet 370:9602, pages 1855-1860.
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Ernest Beutler & Terri Gelbart. (2006) Helicobacter pylori infection and HFE hemochromatosis. Blood Cells, Molecules, and Diseases 37:3, pages 188-191.
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Bruce Newman. (2006) Iron depletion by whole-blood donation harms menstruating females: The current whole-blood-collection paradigm needs to be changed. Transfusion 46:10, pages 1667-1681.
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P. C. ADAMS. (2006) Review article: the modern diagnosis and management of haemochromatosis. Alimentary Pharmacology and Therapeutics 23:12, pages 1681-1691.
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Paul C Adams. (2006) Hemochromatosis case definition: out of focus?. Nature Clinical Practice Gastroenterology & Hepatology 3:4, pages 178-179.
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Ernest Beutler. (2006) Hemochromatosis: Genetics and Pathophysiology. Annual Review of Medicine 57:1, pages 331-347.
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Paul C. Adams. 2006. Zakim and Boyer's Hepatology. Zakim and Boyer's Hepatology
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Karen F. Murray & Robert L. Carithers. (2005) AASLD practice guidelines: Evaluation of the patient for liver transplantation. Hepatology 41:6, pages 1407-1432.
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Mark Worwood. (2005) Inherited iron loading: genetic testing in diagnosis and management. Blood Reviews 19:2, pages 69-88.
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Gary Jeffrey & Paul C Adams. 2004. Evidence‐based Gastroenterology and Hepatology. Evidence‐based Gastroenterology and Hepatology
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Ernest Beutler. (2004) Natural History of Hemochromatosis. Mayo Clinic Proceedings 79:3, pages 305-306.
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M. Lucasa, F. Solanoa, M. Lucas-Ramosb & F. Fabianic. (2004) Análisis de la asociación entre riesgo de isquemia cardíaca, mutaciones de la hemocromatosis (HFE), metabolismo férrico y lipídico. Clínica e Investigación en Arteriosclerosis 16:3, pages 85-89.
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Ernest Beutler. (2003) Rebuttal to Ajioka and Kushner. Blood 101:9, pages 3354-3357.
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Ernest Beutler, Jill Waalen & Vincent Felitti. (2003) Screening strategies in c282y‐linked haemochromatosis. British Journal of Haematology 120:6, pages 1089-1090.
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Ernest Beutler, A. Victor Hoffbrand & James D. Cook. (2003) Iron Deficiency and Overload. Hematology 2003:1, pages 40-61.
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Anne McCune & Mark Worwood. (2003) Headache as a presenting symptom in hereditary. Annals of Neurology 53:1, pages 145-145.
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Pauline Lee, Terri Gelbart, Carol West, Carol Halloran & Ernest Beutler. (2002) Seeking Candidate Mutations That Affect Iron Homeostasis. Blood Cells, Molecules, and Diseases 29:3, pages 471-487.
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