Citation of this article
Corresponding Author of This Article
Article-Type of This Article
Open-Access Policy of This Article
Times Cited Counts in Google of This Article
Number of Hits and Downloads for This Article
- Total Article Views (5422)
All Articles published online
|
Sep 21, 2007 (publication date) through Apr 25, 2024
Times Cited of This Article
Journal Information of This Article
Publication Name
World Journal of Gastroenterology
ISSN
1007-9327
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Wallace DF, Subramaniam VN. Non-HFE haemochromatosis. World J Gastroenterol 2007; 13(35): 4690-4698 [PMID: 17729390 DOI: 10.3748/wjg.v13.i35.4690] |
|---|---|
| URL: | https://www.wjgnet.com/1007-9327/full/v13/i35/4690.htm |
| Number | Citing Articles |
| 1 |
Gregory Jon Anderson, Christopher D. Vulpe. Mammalian iron transport. Cellular and Molecular Life Sciences 2009; 66(20): 3241 doi: 10.1007/s00018-009-0051-1
|
| 2 |
Gladys O. Latunde‐Dada. Iron metabolism: microbes, mouse, and man. BioEssays 2009; 31(12): 1309 doi: 10.1002/bies.200900101
|
| 3 |
|
| 4 |
Miriam Sandnes, Rune J. Ulvik, Marta Vorland, Håkon Reikvam. Hyperferritinemia—A Clinical Overview. Journal of Clinical Medicine 2021; 10(9): 2008 doi: 10.3390/jcm10092008
|
| 5 |
Caglar Doguer, Jung‐Heun Ha, James F. Collins. Comprehensive Physiology. 2018; : 1433 doi: 10.1002/cphy.c170045
|
| 6 |
Mary K. Allen. Hereditary Hemochromatosis: A Literature Review and Case Report. Physiotherapy Canada 2010; 62(3): 276 doi: 10.3138/physio.62.3.276
|
| 7 |
Cameron J. McDonald, Gautam Rishi, Eriza S. Secondes, Lesa Ostini, Daniel F. Wallace, Darrell H. G. Crawford, Hanlon Sia, Paul Clark, V. Nathan Subramaniam. Evaluation of a bone morphogenetic protein 6 variant as a cause of iron loading. Human Genomics 2018; 12(1) doi: 10.1186/s40246-018-0155-5
|
| 8 |
Kam Sandhu, Kaledas Flintoff, Mark D. Chatfield, Jeannette L. Dixon, Louise E. Ramm, Grant A. Ramm, Lawrie W. Powell, V. Nathan Subramaniam, Daniel F. Wallace. Phenotypic analysis of hemochromatosis subtypes reveals variations in severity of iron overload and clinical disease. Blood 2018; 132(1): 101 doi: 10.1182/blood-2018-02-830562
|
| 9 |
Cameron J. McDonald, Daniel F. Wallace, Lesa Ostini, Sally J. Bell, Barbara Demediuk, V. Nathan Subramaniam. G80S-linked ferroportin disease: Classical ferroportin disease in an Asian family and reclassification of the mutant as iron transport defective. Journal of Hepatology 2011; 54(3): 538 doi: 10.1016/j.jhep.2010.07.048
|
| 10 |
Daniel F. Wallace, Cameron J. McDonald, Lesa Ostini, David Iser, Annabel Tuckfield, V. Nathan Subramaniam. The dynamics of hepcidin‐ferroportin internalization and consequences of a novel ferroportin disease mutation. American Journal of Hematology 2017; 92(10): 1052 doi: 10.1002/ajh.24844
|
| 11 |
Janet L. Kwiatkowski. Oral Iron Chelators. Pediatric Clinics of North America 2008; 55(2): 461 doi: 10.1016/j.pcl.2008.01.005
|
| 12 |
Farhad Zamani, Zohreh Bagheri, Maryam Bayat, Seyed-Mohammad Fereshtehnejad, Ali Basi, Hossein Najmabadi, Hossein Ajdarkosh. Iranian hereditary hemochromatosis patients: Baseline characteristics, laboratory data and gene mutations. Medical Science Monitor 2012; 18(10): CR622 doi: 10.12659/MSM.883489
|
| 13 |
Fikret Aydemir, Supak Jenkitkasemwong, Sukru Gulec, Mitchell D. Knutson. Iron Loading Increases Ferroportin Heterogeneous Nuclear RNA and mRNA Levels in Murine J774 Macrophages. The Journal of Nutrition 2009; 139(3): 434 doi: 10.3945/jn.108.094052
|
| 14 |
Gregory J Anderson, Fudi Wang. Essential but toxic: Controlling the flux of iron in the body. Clinical and Experimental Pharmacology and Physiology 2012; 39(8): 719 doi: 10.1111/j.1440-1681.2011.05661.x
|
| 15 |
|
| 16 |
Pierre Brissot, Edouard Bardou-Jacquet, Marie-Bérengère Troadec, Annick Mosser, Marie-Laure Island, Lénaïck Detivaud, Olivier Loréal, Anne-Marie Jouanolle. Molecular diagnosis of genetic iron-overload disorders. Expert Review of Molecular Diagnostics 2010; 10(6): 755 doi: 10.1586/erm.10.55
|
| 17 |
James F. Collins, Gregory J. Anderson. Physiology of the Gastrointestinal Tract. 2012; : 1921 doi: 10.1016/B978-0-12-382026-6.00071-3
|
| 18 |
James C. Barton, Corwin Q. Edwards, Pradyumna D. Phatak, Robert S. Britton, Bruce R. Bacon. Handbook of Iron Overload Disorders. 2010; : 171 doi: 10.1017/CBO9780511777035.014
|
| 19 |
James C. Barton, Pauline L. Lee, Corwin Q. Edwards. Iron Physiology and Pathophysiology in Humans. 2012; : 529 doi: 10.1007/978-1-60327-485-2_26
|
| 20 |
Yutaka Kohgo. 2. Iron Metabolism and Iron Overload.. Nihon Naika Gakkai Zasshi 2011; 100(9): 2412 doi: 10.2169/naika.100.2412
|
| 21 |
J. Zwerina, T. Dallos. Arthrosen bei hereditären Stoffwechselerkrankungen. Zeitschrift für Rheumatologie 2010; 69(3): 227 doi: 10.1007/s00393-009-0590-8
|
| 22 |
Pierre Brissot, Edouard Bardou-Jacquet, Anne-Marie Jouanolle, Olivier Loréal. Iron disorders of genetic origin: a changing world. Trends in Molecular Medicine 2011; 17(12): 707 doi: 10.1016/j.molmed.2011.07.004
|
| 23 |
C. Callens. Fer et cancers : l’exemple du cancer du sein. Bulletin de l'Académie Nationale de Médecine 2019; 203(6): 424 doi: 10.1016/j.banm.2019.04.018
|
| 24 |
Sowrav Barua, Stefano Ciannella, Lukman Tijani, Jenifer Gomez‐Pastora. Iron in blood cells: Function, relation to disease, and potential for magnetic separation. Biotechnology and Bioengineering 2023; 120(7): 1707 doi: 10.1002/bit.28388
|
| 25 |
Dennis J. Dietzen, Yaser Diab. Biochemical and Molecular Basis of Pediatric Disease. 2021; : 477 doi: 10.1016/B978-0-12-817962-8.00026-3
|
| 26 |
James C. Barton, Corwin Q. Edwards, Pradyumna D. Phatak, Robert S. Britton, Bruce R. Bacon, James C. Barton, Corwin Q. Edwards, Pradyumna D. Phatak, Robert S. Britton, Bruce R. Bacon. Handbook of Iron Overload Disorders. 2010; : 193 doi: 10.1017/CBO9780511777035.017
|
| 27 |
Giada Sebastiani, Kostas Pantopoulos. Disorders associated with systemic or local iron overload: from pathophysiology to clinical practice. Metallomics 2011; 3(10): 971 doi: 10.1039/c1mt00082a
|
| 28 |
Sule Unal, Alberto Piperno, Fatma Gumruk. Iron chelation with deferasirox in a patient with de-novo ferroportin mutation. Journal of Trace Elements in Medicine and Biology 2015; 30: 1 doi: 10.1016/j.jtemb.2015.01.002
|
| 29 |
Ronald L. Sham, Pradyumna D. Phatak, Elizabeta Nemeth, Tomas Ganz. Hereditary hemochromatosis due to resistance to hepcidin: high hepcidin concentrations in a family with C326S ferroportin mutation. Blood 2009; 114(2): 493 doi: 10.1182/blood-2009-04-216226
|
| 30 |
Janet L. Kwiatkowski. Oral Iron Chelators. Hematology/Oncology Clinics of North America 2010; 24(1): 229 doi: 10.1016/j.hoc.2009.11.001
|
| 31 |
Houda Hamdi-Rozé, Zeineb Ben Ali, Martine Ropert, Lénaïck Detivaud, Samira Aggoune, Dominique Simon, Gilles Pelletier, Yves Deugnier, Véronique David, Edouard Bardou-Jacquet. Variable expressivity of HJV related hemochromatosis: “Juvenile” hemochromatosis?. Blood Cells, Molecules, and Diseases 2019; 74: 30 doi: 10.1016/j.bcmd.2018.10.006
|
| 32 |
Paulo Caleb Júnior de Lima Santos, Alexandre C. Pereira, Rodolfo D. Cançado, Isolmar T. Schettert, Rosario D.C. Hirata, Mario H. Hirata, Maria Stella Figueiredo, Carlos S. Chiattone, Jose E. Krieger, Elvira M. Guerra-Shinohara. Hemojuvelin and Hepcidin Genes Sequencing in Brazilian Patients with Primary Iron Overload. Genetic Testing and Molecular Biomarkers 2010; 14(6): 803 doi: 10.1089/gtmb.2010.0056
|
| 33 |
Richard S. Ajioka, John D. Phillips, Robert B. Weiss, Diane M. Dunn, Maria W. Smit, Sean C. Proll, Michael G. Katze, James P. Kushner. Down-regulation of hepcidin in porphyria cutanea tarda. Blood 2008; 112(12): 4723 doi: 10.1182/blood-2008-02-138222
|
| 34 |
Jaya P. Gnana-Prakasam, Muthusamy Thangaraju, Kebin Liu, Yonju Ha, Pamela M. Martin, Sylvia B. Smith, Vadivel Ganapathy. Absence of iron-regulatory protein Hfe results in hyperproliferation of retinal pigment epithelium: role of cystine/glutamate exchanger. Biochemical Journal 2009; 424(2): 243 doi: 10.1042/BJ20090424
|
| 35 |
J. Zwerina, T. Dallos. Arthrosen bei hereditären Stoffwechselerkrankungen. Der Orthopäde 2010; 39(6): 637 doi: 10.1007/s00132-010-1646-9
|
| 36 |
Yasuhiro Nagayoshi, Masafumi Nakayama, Satoru Suzuki, Jun Hokamaki, Hideki Shimomura, Kenichi Tsujita, Masaya Fukuda, Takuro Yamashita, Yoshinori Nakamura, Seigo Sugiyama, Hisao Ogawa. A Q312X mutation in the hemojuvelin gene is associated with cardiomyopathy due to juvenile haemochromatosis☆. European Journal of Heart Failure 2008; 10(10): 1001 doi: 10.1016/j.ejheart.2008.07.012
|
| 37 |
Daniel F. Wallace, V. Nathan Subramaniam. Iron Physiology and Pathophysiology in Humans. 2012; : 399 doi: 10.1007/978-1-60327-485-2_20
|
| 38 |
M. Ruivard. Surcharges en fer d’origine génétique et hépatosidérose dysmétabolique. La Revue de Médecine Interne 2009; 30(1): 35 doi: 10.1016/j.revmed.2008.05.004
|
| 39 |
Daniel F. Wallace, Jonathan M. Harris, V. Nathan Subramaniam. Functional analysis and theoretical modeling of ferroportin reveals clustering of mutations according to phenotype. American Journal of Physiology-Cell Physiology 2010; 298(1): C75 doi: 10.1152/ajpcell.00621.2008
|
| 40 |
Clare C. Constantine, Greg J. Anderson, Chris D. Vulpe, Christine E. McLaren, Melanie Bahlo, Heng Lin Yeap, Dorota M. Gertig, Nicholas J. Osborne, Nadine A. Bertalli, Kenneth B. Beckman, Victoria Chen, Pavel Matak, Andrew T. McKie, Martin B. Delatycki, John K. Olynyk, Dallas R. English, Melissa C. Southey, Graham G. Giles, John L. Hopper, Katrina J. Allen, Lyle C. Gurrin. A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis. British Journal of Haematology 2009; 147(1): 140 doi: 10.1111/j.1365-2141.2009.07843.x
|
| 41 |
Burkhard Rodeck, René Santer, Nicole Muschol, Martin Burdelski, Michael Melter, Rainer Ganschow, Ulrich Baumann. Pädiatrische Gastroenterologie, Hepatologie und Ernährung. 2013; : 443 doi: 10.1007/978-3-642-24710-1_17
|
| 42 |
Takumu Hasebe, Hiroki Tanaka, Koji Sawada, Shunsuke Nakajima, Takaaki Ohtake, Mikihiro Fujiya, Yutaka Kohgo. Bone morphogenetic protein-binding endothelial regulator of liver sinusoidal endothelial cells induces iron overload in a fatty liver mouse model. Journal of Gastroenterology 2017; 52(3): 341 doi: 10.1007/s00535-016-1237-6
|
| 43 |
Ruben Pauwels, Els Vandecasteele, Daniel Devos, Walter Pauwels, Michel De Pauw. An unexpected cause of liver cirrhosis and cardiomyopathy in a young man. Acta Clinica Belgica 2017; : 1 doi: 10.1080/17843286.2017.1409474
|
| 44 |
Jaya P. Gnana-Prakasam, Amany Tawfik, Michelle Romej, Sudha Ananth, Pamela M. Martin, Sylvia B. Smith, Vadivel Ganapathy. Iron-mediated retinal degeneration in haemojuvelin-knockout mice. Biochemical Journal 2012; 441(2): 599 doi: 10.1042/BJ20111148
|
| 45 |
D.R. Richardson, D.S. Kalinowski, S. Lau, P.J. Jansson, D.B. Lovejoy. Cancer cell iron metabolism and the development of potent iron chelators as anti-tumour agents. Biochimica et Biophysica Acta (BBA) - General Subjects 2009; 1790(7): 702 doi: 10.1016/j.bbagen.2008.04.003
|
| 46 |
V. Nathan Subramaniam, Cameron J. McDonald, Lesa Ostini, Patricia E. Lusby, Leesa F. Wockner, Grant A. Ramm, Daniel F. Wallace. Hepatic Iron Deposition Does Not Predict Extrahepatic Iron Loading in Mouse Models of Hereditary Hemochromatosis. The American Journal of Pathology 2012; 181(4): 1173 doi: 10.1016/j.ajpath.2012.06.025
|
| 47 |
Arch G. Mainous, Robert U. Wright, Mary M. Hulihan, Waleed O. Twal, Christine E. McLaren, Vanessa A. Diaz, Gordon D. McLaren, W. Scott Argraves, Althea M. Grant. Telomere length and elevated iron: The influence of phenotype and HFE genotype. American Journal of Hematology 2013; 88(6): 492 doi: 10.1002/ajh.23438
|
| 48 |
Christine E. McLaren, Chad P. Garner, Clare C. Constantine, Stela McLachlan, Chris D. Vulpe, Beverly M. Snively, Victor R. Gordeuk, Debbie A. Nickerson, James D. Cook, Catherine Leiendecker-Foster, Kenneth B. Beckman, John H. Eckfeldt, Lisa F. Barcellos, Joseph A. Murray, Paul C. Adams, Ronald T. Acton, Anthony A. Killeen, Gordon D. McLaren, Marc Tjwa. Genome-Wide Association Study Identifies Genetic Loci Associated with Iron Deficiency. PLoS ONE 2011; 6(3): e17390 doi: 10.1371/journal.pone.0017390
|
| 49 |
Taija S. Koskenkorva-Frank, Günter Weiss, Willem H. Koppenol, Susanna Burckhardt. The complex interplay of iron metabolism, reactive oxygen species, and reactive nitrogen species: Insights into the potential of various iron therapies to induce oxidative and nitrosative stress. Free Radical Biology and Medicine 2013; 65: 1174 doi: 10.1016/j.freeradbiomed.2013.09.001
|
| 50 |
James F. Collins, Shireen R.L. Flores, Xiaoyu Wang, Gregory J. Anderson. Physiology of the Gastrointestinal Tract. 2018; : 1451 doi: 10.1016/B978-0-12-809954-4.00060-8
|
| 51 |
Fernando Oliveira, Sara Rocha, Rúben Fernandes. Iron Metabolism: From Health to Disease. Journal of Clinical Laboratory Analysis 2014; 28(3): 210 doi: 10.1002/jcla.21668
|
| 52 |
I. Muoz Rojas, F.L. Reinoso Prez, A. Lpez de la Gua, F. Hernndez Navarro. Trastornos del metabolismo del hierro. Medicine - Programa de Formaci?n M?dica Continuada Acreditado 2008; 10(20): 1318 doi: 10.1016/S0211-3449(08)75386-4
|
| 53 |
Cameron J McDonald, Daniel F Wallace, Darrell H G Crawford, V Nathan Subramaniam. Iron storage disease in Asia‐Pacific populations: The importance of non‐HFE mutations. Journal of Gastroenterology and Hepatology 2013; 28(7): 1087 doi: 10.1111/jgh.12222
|
| 54 |
Manuel A Lescano, Letícia C Tavares, Paulo C J L Santos. Juvenile hemochromatosis: <i>HAMP</i> mutation and severe iron overload treated with phlebotomies and deferasirox. World Journal of Clinical Cases 2017; 5(10): 381-383 doi: 10.12998/wjcc.v5.i10.381
|
| 55 |
Pierre Brissot, Marie-Bérengère Troadec, Edouard Bardou-Jacquet, Caroline Le Lan, Anne-Marie Jouanolle, Yves Deugnier, Olivier Loréal. Current approach to hemochromatosis. Blood Reviews 2008; 22(4): 195 doi: 10.1016/j.blre.2008.03.001
|
| 56 |
Jaya P. Gnana-Prakasam, Ming Zhang, Pamela M. Martin, Sally S. Atherton, Sylvia B. Smith, Vadivel Ganapathy. Expression of the iron-regulatory protein haemojuvelin in retina and its regulation during cytomegalovirus infection. Biochemical Journal 2009; 419(3): 533 doi: 10.1042/BJ20082240
|
| 57 |
Dilum Ekanayake, Clinton Roddick, Murtaza Khanbhai, Lawrie W. Powell. Homozygosity For The C282Y Substitution In The HFE Gene: The Incomplete Penetrance And Variable Expressivity. EMJ Hepatology 2015; : 79 doi: 10.33590/emjhepatol/10312409
|
| 58 |
Giada Sebastiani, Kostas Pantopoulos. Cellular and Molecular Biology of Metals. 2010; : 351 doi: 10.1201/9781420059984-c13
|
| 59 |
Surjit Kaila Srai, Paul Sharp. Iron Physiology and Pathophysiology in Humans. 2012; : 3 doi: 10.1007/978-1-60327-485-2_1
|
| 60 |
James C. Barton, Corwin Q. Edwards, Pradyumna D. Phatak, Robert S. Britton, Bruce R. Bacon. Handbook of Iron Overload Disorders. 2010; : 181 doi: 10.1017/CBO9780511777035.015
|
| 61 |
T. Herta, J. Fischer, T. Berg. Genetik metabolischer und viraler Lebererkrankungen. Der Gastroenterologe 2017; 12(1): 16 doi: 10.1007/s11377-016-0128-y
|
| 62 |
Sukru Gulec, Gregory J. Anderson, James F. Collins. Mechanistic and regulatory aspects of intestinal iron absorption. American Journal of Physiology-Gastrointestinal and Liver Physiology 2014; 307(4): G397 doi: 10.1152/ajpgi.00348.2013
|
| 63 |
Nicole Soranzo, Tim D Spector, Massimo Mangino, Brigitte Kühnel, Augusto Rendon, Alexander Teumer, Christina Willenborg, Benjamin Wright, Li Chen, Mingyao Li, Perttu Salo, Benjamin F Voight, Philippa Burns, Roman A Laskowski, Yali Xue, Stephan Menzel, David Altshuler, John R Bradley, Suzannah Bumpstead, Mary-Susan Burnett, Joseph Devaney, Angela Döring, Roberto Elosua, Stephen E Epstein, Wendy Erber, Mario Falchi, Stephen F Garner, Mohammed J R Ghori, Alison H Goodall, Rhian Gwilliam, Hakon H Hakonarson, Alistair S Hall, Naomi Hammond, Christian Hengstenberg, Thomas Illig, Inke R König, Christopher W Knouff, Ruth McPherson, Olle Melander, Vincent Mooser, Matthias Nauck, Markku S Nieminen, Christopher J O'Donnell, Leena Peltonen, Simon C Potter, Holger Prokisch, Daniel J Rader, Catherine M Rice, Robert Roberts, Veikko Salomaa, Jennifer Sambrook, Stefan Schreiber, Heribert Schunkert, Stephen M Schwartz, Jovana Serbanovic-Canic, Juha Sinisalo, David S Siscovick, Klaus Stark, Ida Surakka, Jonathan Stephens, John R Thompson, Uwe Völker, Henry Völzke, Nicholas A Watkins, George A Wells, H-Erich Wichmann, David A Van Heel, Chris Tyler-Smith, Swee Lay Thein, Sekar Kathiresan, Markus Perola, Muredach P Reilly, Alexandre F R Stewart, Jeanette Erdmann, Nilesh J Samani, Christa Meisinger, Andreas Greinacher, Panos Deloukas, Willem H Ouwehand, Christian Gieger. A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. Nature Genetics 2009; 41(11): 1182 doi: 10.1038/ng.467
|