Haemochromatosis

Brissot, Pierre, Pietrangelo, Antonello, Adams, Paul C., de Graaff, Barbara, McLaren, Christine E., Loréal, Olivier·2018·Nature Reviews Disease Primers

Cites (223)

Items 201–226 of 226

  1. Novel missense mutation in the TMPRSS6 gene in a Japanese female with iron-refractory iron deficiency anemia
    Tsutomu Sato, Satoshi Iyama, Kazuyuki Murase, Yusuke Kamihara, Kaoru Ono, Shohei Kikuchi, Kohichi Takada, Koji Miyanishi, Yasushi Sato, Rishu Takimoto et al. · 2011 · International Journal of Hematology
  2. Hepcidin Expression Does Not Rescue the Iron-Poor Phenotype of Kupffer Cells in Hfe-Null Mice After Liver Transplantation
    Cinzia Garuti, Yinghua Tian, Giuliana Montosi, Manuela Sabelli, Elena Corradini, Rolf Graf, Paolo Ventura, Alberto Vegetti, Pierre‐Alain Clavien, Antonello Pietrangelo · 2010 · Gastroenterology
  3. The Natural History of Untreated HFE-Related Hemochromatosis
    Paul C. Adams · 2009 · Acta Haematologica
  4. HFE Genotype Modifies the Influence of Heme Iron Intake on Iron Status
    Darren Charles Greenwood, Janet Elizabeth Cade, Jennifer A. Moreton, B O Hara, Victoria Jane Burley, Juliette A. Randerson‐Moor, Kairen Kukalizch, D Thompson, Mark Worwood, David Timothy Bishop · 2005 · Epidemiology
  5. Psychological Adjustment and Knowledge About Hereditary Hemochromatosis in a Clinic‐Based Sample: A Prospective Study
    Bettina Meiser, Stewart M. Dunn, Jeannette L. Dixon, Lawrie W. Powell · 2005 · Journal of Genetic Counseling
  6. GNPAT Variant associated with severe iron overload in HFE hemochromatosis
    Edouard Bardou‐Jacquet, Marie de Tayrac, Jean Mosser, Yves Deugnier · 2015 · Hepatology
  7. Intestinal absorption and enterohepatic cycling of biliary iron originating from plasma non-transferrin-bound iron in rats
    Pierre Brissot, Ulrich Bolder, C D Schteingart, Josiane Arnaud, Alan F. Hofmann · 1997 · Hepatology
  8. Natural History of Hemochromatosis
    Ernest Beutler · 2004 · Mayo Clinic Proceedings
  9. Rare HFE variants are the most frequent cause of hemochromatosis in non‐c282y homozygous patients with hemochromatosis
    Houda Hamdi‐Rozé, M.-P. Beaumont-Epinette, Zeineb Ben Ali, Caroline Le Lan, Véronique Loustaud-Ratti, Xavier Causse, Olivier Loréal, Yves Deugnier, Pierre Brissot, Anne‐Marie Jouanolle et al. · 2016 · American Journal of Hematology
  10. Cost-Effectiveness of Different Population Screening Strategies for Hereditary Haemochromatosis in Australia
    Barbara de Graaff, Amanda L. Neil, Lei Si, Kwang Chien Yee, Kristy A. Sanderson, Lyle C. Gurrin, Andrew John Palmer · 2016 · Applied Health Economics and Health Policy
  11. Eligibility and Exclusion of Hemochromatosis Patients as Voluntary Blood Donors
    Mark A. Levstik, PC Adams · 1998 · Canadian Journal of Gastroenterology
  12. Elevated transferrin saturation, health-related quality of life and telomere length
    Arch G. Mainous, Robert U. Wright, Mary Hulihan, Waleed O. Twal, Christine E. McLaren, Vanessa A. Díaz, Gordon D. McLaren, W. Scott Argraves, Althea M. Grant · 2013 · BioMetals
  13. High prevalence of thrombocytopenia in SLE patients with a high level of anticardiolipin antibodies combined with lupus anticoagulant
    Junzo Nojima, Etsuji Suehisa, Hirohiko Kuratsune, Takashi Machii, Masayuki Toku, Hisato Tada, Kouzi Yamaguti, Takao Koike, Yuzuru Kanakura, Teruo Kitani et al. · 1998 · American Journal of Hematology
  14. Pathogens, Metabolic Adaptation, and Human Diseases—An Iron-Thrifty Genetic Model
    Antonello Pietrangelo · 2015 · Gastroenterology
  15. Non-HFE Hemochromatosis
    Daniel F. Wallace, V. Nathan Subramaniam · 2011 · Humana Press eBooks
  16. Hereditary hypotransferrinemia can lead to elevated transferrin saturation and, when associated to HFE or HAMP mutations, to iron overload
    M.-P. Beaumont-Epinette, Jean-Bernard Delobel, Martine Ropert, Yves Deugnier, Olivier Loréal, Anne‐Marie Jouanolle, Pierre Brissot, Edouard Bardou‐Jacquet · 2014 · Blood Cells Molecules and Diseases
  17. Quality of life utility values for hereditary haemochromatosis in Australia
    Barbara de Graaff, Amanda L. Neil, Kristy A. Sanderson, Kwang Chien Yee, Andrew John Palmer · 2016 · Health and Quality of Life Outcomes
  18. Course of iron parameters in HFE‐hemochromatosis patients during initial treatment with erythrocytapheresis compared to phlebotomy
    Eva Rombout‐Sestrienkova, Ger H. Koek, Rabin E. J. Neslo, Marian van Kraaij, Paul P.C.A. Menheere, Ad Masclee, Dorine W. Swinkels · 2016 · Journal of Clinical Apheresis
  19. Total and Cause-Specific Mortality by Elevated Transferrin Saturation and Hemochromatosis Genotype in Individuals With Diabetes: Two General Population Studies
    Christina Ellervik, Thomas R Mandrup-Poulsen, Anne Tybjærg‐Hansen, Børge Grønne Nordestgaard · 2013 · Diabetes Care
  20. GNPAT p.D519G is independently associated with markedly increased iron stores in HFE p.C282Y homozygotes
    James C. Barton, Wen‐Pin Chen, Mary Jane Emond, Pradyumna D. Phatak, V. Nathan Subramaniam, Paul C. Adams, Lyle C. Gurrin, Gregory Jon Anderson, Grant A. Ramm, Lawrie W. Powell et al. · 2016 · Blood Cells Molecules and Diseases
  21. Optimizing the management of hereditary haemochromatosis: the value of MRI R2* quantification to predict and monitor body iron stores
    Manuela França, Luis Martí‐Bonmatí, Sara Silva, Carla Oliveíra, Ángel Alberich‐Bayarri, Filipa Vilas Boas, Helena Miranda, Graça Porto · 2017 · British Journal of Haematology
  22. Phenotypic expression of a novel C282Y/R226G compound heterozygous state in HFE hemochromatosis: Molecular dynamics and biochemical studies
    Christine Cézard, Amrathlal Rabbind Singh, Gérald Le Gac, Isabelle Gourlaouen, Claude Férec, Jacques Rochette · 2013 · Blood Cells Molecules and Diseases
  23. Haemochromatosis gene frequency in a control and diabetic Irish population
    L. Kirk, Jeremy Bird, S. Ramadan, A. Samad, Gani I. Adebayo, W. Lourens, J. Williams · 2008 · Irish Journal of Medical Science (1971 -)
  24. Accepting hereditary hemochromatosis blood donors: ask not why, ask why not
    Kamille A. West, Anne F. Eder · 2016 · Transfusion
  25. HFE-Associated Hereditary Hemochromatosis
    Richard Skoien, Lawrie W. Powell · 2011 · Humana Press eBooks
  26. Should we treat individuals homozygous for HFE p.Cys282Tyr with ferritin 300–1000 μg/L?
    James C. Barton · 2017 · The Lancet Haematology