Hemochromatosis type 4 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hemochromatosis type 4" in English language version.

refsWebsite

Global rank English rank

21nih.gov

4^th place

15doi.org

2^nd place

1semanticscholar.org

11^th place

8^th place

1harvard.edu

18^th place

17^th place

1rcsb.org

8,838^th place

8,783^rd place

1rarediseases.org

5,181^st place

3,260^th place

doi.org

Roetto, A.; Camaschella, C. (2005). "New insights into iron homeostasis through the study of non-HFE hereditary haemochromatosis". Best Practice & Research Clinical Haematology. 18 (2): 235–250. doi:10.1016/j.beha.2004.09.004. PMID 15737887.
Pietrangelo, A. (2004). "Non-HFE hemochromatosis". Hepatology. 39 (1): 21–29. doi:10.1002/hep.20007. PMID 14752817.
Wallace, D.F.; Subramaniam, V.N. (2007). "Non-HFE haemochromatosis". World Journal of Gastroenterology. 13 (35): 4690–4698. doi:10.3748/wjg.v13.i35.4690. PMC 4611190. PMID 17729390.
Gozzelino, R.; Arosio, P. (2016). "Iron homeostasis in health and disease". International Journal of Molecular Sciences. 17 (1): 130. doi:10.3390/ijms17010130. PMC 4730371. PMID 26805813.
Porto, G.; Brissot, P.; Swinkels, D.W.; Zoller, H.; Kamarainen, O.; Patton, S.; Alonso, I.; Morris, M.; Keeney, S. (2016). "EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)". European Journal of Human Genetics. 24 (4): 479–495. doi:10.1038/ejhg.2015.128. PMC 4929861. PMID 26153218.
MacKenzie, E.L.; Iwasaki, K.; Tsuji, Y. (2008). "Intracellular iron transport and storage: from molecular mechanisms to health implications". Antioxid. Redox Signal. 10 (6): 997–1030. doi:10.1089/ars.2007.1893. PMC 2932529. PMID 18327971.
Chen, S.R.; Yang, L.Q.; Chong, Y.T.; Jie, Y.S.; Wu, Y.K.; Yang, J.; Lin, G.L.; Li, X.H. (2015). "Novel gain of function mutation in the SLC40A1 gene associated with hereditary haemochromatosis type 4". Internal Medicine Journal. 45 (6): 672–676. doi:10.1111/imj.12764. PMID 26059880. S2CID 2426509.
Domenico, I.; Ward, D.M.; Nemeth, E.; Vaughan, M.B.; Musci, G.; Ganz, T.; Kaplan, J.; Kornfeld, S.A. (2005). "The molecular basis of ferroportin-linked hemochromatosis". Proceedings of the National Academy of Sciences of the United States of America. 102 (25): 8955–8960. Bibcode:2005PNAS..102.8955D. doi:10.1073/pnas.0503804102. PMC 1157058. PMID 15956209.
Callebaut, I.; Joubrel, R.; Pissard, S.; Kannengiesser, C.; Gerolami, V.; Ged, C.; Cadet, E.; Cartault, F.; Ka, C.; Gourlaouen, I.; Gourhant, L.; Oudin, C.; Goossens, M.; Grandchamp, B.; De Verneuil, H.; Rochette, J.; Ferec, C.; LeGac, G. (2014). "Comprehensive functional annotationof 18 missense mutations found in suspected hemochromatosis type 4 patients". Human Molecular Genetics. 23 (17): 4479–4490. doi:10.1093/hmg/ddu160. PMID 24714983.
Goodsell, D.S. (2002). "Ferritin and transferrin". RCSB Protein Data Bank. doi:10.2210/rcsb_pdb/mom_2002_11. Retrieved 9 November 2016.
Franchini, M. (2006). "Hereditary iron overload: update on pathophysiology, diagnosis, and treatment". Am. J. Hematol. 81 (3): 202–209. doi:10.1002/ajh.20493. PMID 16493621.
Eaton, J.W.; Qian, M. (2002). "Molecular bases of cellular iron toxicity". Free Radical Biology and Medicine. 32 (9): 833–840. doi:10.1016/s0891-5849(02)00772-4. PMID 11978485.
Kasvosve, I. (2013). "Effect of ferroportin polymorphism on iron homeostasis and infection". Clinica Chimica Acta. 416: 20–25. doi:10.1016/j.cca.2012.11.013. PMID 23178444.
Santos, P.C.J.L.; Dinardo, C.L.; Cancado, R.D.; Schettert, I.T.; Krieger, J.E.; Periera, A.C. (2012). "Non-HFE hemochromatosis". Revista Brasileira de Hematologia e Hemoterapia. 34 (4): 311–6. doi:10.5581/1516-8484.20120079. PMC 3460409. PMID 23049448.
Palmer, WC; Vishnu, P; Sanchez, W; Aqel, B; Riegert-Johnson, D; Seaman, LAK; Bowman, AW; Rivera, CE (December 2018). "Diagnosis and Management of Genetic Iron Overload Disorders". Journal of General Internal Medicine. 33 (12): 2230–2236. doi:10.1007/s11606-018-4669-2. PMC 6258594. PMID 30225768.

harvard.edu

ui.adsabs.harvard.edu

Domenico, I.; Ward, D.M.; Nemeth, E.; Vaughan, M.B.; Musci, G.; Ganz, T.; Kaplan, J.; Kornfeld, S.A. (2005). "The molecular basis of ferroportin-linked hemochromatosis". Proceedings of the National Academy of Sciences of the United States of America. 102 (25): 8955–8960. Bibcode:2005PNAS..102.8955D. doi:10.1073/pnas.0503804102. PMC 1157058. PMID 15956209.

nih.gov

pubmed.ncbi.nlm.nih.gov

Roetto, A.; Camaschella, C. (2005). "New insights into iron homeostasis through the study of non-HFE hereditary haemochromatosis". Best Practice & Research Clinical Haematology. 18 (2): 235–250. doi:10.1016/j.beha.2004.09.004. PMID 15737887.
Pietrangelo, A. (2004). "Non-HFE hemochromatosis". Hepatology. 39 (1): 21–29. doi:10.1002/hep.20007. PMID 14752817.
Wallace, D.F.; Subramaniam, V.N. (2007). "Non-HFE haemochromatosis". World Journal of Gastroenterology. 13 (35): 4690–4698. doi:10.3748/wjg.v13.i35.4690. PMC 4611190. PMID 17729390.
Gozzelino, R.; Arosio, P. (2016). "Iron homeostasis in health and disease". International Journal of Molecular Sciences. 17 (1): 130. doi:10.3390/ijms17010130. PMC 4730371. PMID 26805813.
Porto, G.; Brissot, P.; Swinkels, D.W.; Zoller, H.; Kamarainen, O.; Patton, S.; Alonso, I.; Morris, M.; Keeney, S. (2016). "EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)". European Journal of Human Genetics. 24 (4): 479–495. doi:10.1038/ejhg.2015.128. PMC 4929861. PMID 26153218.
MacKenzie, E.L.; Iwasaki, K.; Tsuji, Y. (2008). "Intracellular iron transport and storage: from molecular mechanisms to health implications". Antioxid. Redox Signal. 10 (6): 997–1030. doi:10.1089/ars.2007.1893. PMC 2932529. PMID 18327971.
Chen, S.R.; Yang, L.Q.; Chong, Y.T.; Jie, Y.S.; Wu, Y.K.; Yang, J.; Lin, G.L.; Li, X.H. (2015). "Novel gain of function mutation in the SLC40A1 gene associated with hereditary haemochromatosis type 4". Internal Medicine Journal. 45 (6): 672–676. doi:10.1111/imj.12764. PMID 26059880. S2CID 2426509.
Domenico, I.; Ward, D.M.; Nemeth, E.; Vaughan, M.B.; Musci, G.; Ganz, T.; Kaplan, J.; Kornfeld, S.A. (2005). "The molecular basis of ferroportin-linked hemochromatosis". Proceedings of the National Academy of Sciences of the United States of America. 102 (25): 8955–8960. Bibcode:2005PNAS..102.8955D. doi:10.1073/pnas.0503804102. PMC 1157058. PMID 15956209.
Callebaut, I.; Joubrel, R.; Pissard, S.; Kannengiesser, C.; Gerolami, V.; Ged, C.; Cadet, E.; Cartault, F.; Ka, C.; Gourlaouen, I.; Gourhant, L.; Oudin, C.; Goossens, M.; Grandchamp, B.; De Verneuil, H.; Rochette, J.; Ferec, C.; LeGac, G. (2014). "Comprehensive functional annotationof 18 missense mutations found in suspected hemochromatosis type 4 patients". Human Molecular Genetics. 23 (17): 4479–4490. doi:10.1093/hmg/ddu160. PMID 24714983.
Franchini, M. (2006). "Hereditary iron overload: update on pathophysiology, diagnosis, and treatment". Am. J. Hematol. 81 (3): 202–209. doi:10.1002/ajh.20493. PMID 16493621.
Eaton, J.W.; Qian, M. (2002). "Molecular bases of cellular iron toxicity". Free Radical Biology and Medicine. 32 (9): 833–840. doi:10.1016/s0891-5849(02)00772-4. PMID 11978485.
Kasvosve, I. (2013). "Effect of ferroportin polymorphism on iron homeostasis and infection". Clinica Chimica Acta. 416: 20–25. doi:10.1016/j.cca.2012.11.013. PMID 23178444.
Santos, P.C.J.L.; Dinardo, C.L.; Cancado, R.D.; Schettert, I.T.; Krieger, J.E.; Periera, A.C. (2012). "Non-HFE hemochromatosis". Revista Brasileira de Hematologia e Hemoterapia. 34 (4): 311–6. doi:10.5581/1516-8484.20120079. PMC 3460409. PMID 23049448.
Palmer, WC; Vishnu, P; Sanchez, W; Aqel, B; Riegert-Johnson, D; Seaman, LAK; Bowman, AW; Rivera, CE (December 2018). "Diagnosis and Management of Genetic Iron Overload Disorders". Journal of General Internal Medicine. 33 (12): 2230–2236. doi:10.1007/s11606-018-4669-2. PMC 6258594. PMID 30225768.

ncbi.nlm.nih.gov

Wallace, D.F.; Subramaniam, V.N. (2007). "Non-HFE haemochromatosis". World Journal of Gastroenterology. 13 (35): 4690–4698. doi:10.3748/wjg.v13.i35.4690. PMC 4611190. PMID 17729390.
Gozzelino, R.; Arosio, P. (2016). "Iron homeostasis in health and disease". International Journal of Molecular Sciences. 17 (1): 130. doi:10.3390/ijms17010130. PMC 4730371. PMID 26805813.
Porto, G.; Brissot, P.; Swinkels, D.W.; Zoller, H.; Kamarainen, O.; Patton, S.; Alonso, I.; Morris, M.; Keeney, S. (2016). "EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)". European Journal of Human Genetics. 24 (4): 479–495. doi:10.1038/ejhg.2015.128. PMC 4929861. PMID 26153218.
MacKenzie, E.L.; Iwasaki, K.; Tsuji, Y. (2008). "Intracellular iron transport and storage: from molecular mechanisms to health implications". Antioxid. Redox Signal. 10 (6): 997–1030. doi:10.1089/ars.2007.1893. PMC 2932529. PMID 18327971.
Domenico, I.; Ward, D.M.; Nemeth, E.; Vaughan, M.B.; Musci, G.; Ganz, T.; Kaplan, J.; Kornfeld, S.A. (2005). "The molecular basis of ferroportin-linked hemochromatosis". Proceedings of the National Academy of Sciences of the United States of America. 102 (25): 8955–8960. Bibcode:2005PNAS..102.8955D. doi:10.1073/pnas.0503804102. PMC 1157058. PMID 15956209.
Santos, P.C.J.L.; Dinardo, C.L.; Cancado, R.D.; Schettert, I.T.; Krieger, J.E.; Periera, A.C. (2012). "Non-HFE hemochromatosis". Revista Brasileira de Hematologia e Hemoterapia. 34 (4): 311–6. doi:10.5581/1516-8484.20120079. PMC 3460409. PMID 23049448.
Palmer, WC; Vishnu, P; Sanchez, W; Aqel, B; Riegert-Johnson, D; Seaman, LAK; Bowman, AW; Rivera, CE (December 2018). "Diagnosis and Management of Genetic Iron Overload Disorders". Journal of General Internal Medicine. 33 (12): 2230–2236. doi:10.1007/s11606-018-4669-2. PMC 6258594. PMID 30225768.

rarediseases.org

"Ferroportin Disease". National Organization for Rare Disorders. Retrieved 9 November 2016.

rcsb.org

pdb101.rcsb.org

Goodsell, D.S. (2002). "Ferritin and transferrin". RCSB Protein Data Bank. doi:10.2210/rcsb_pdb/mom_2002_11. Retrieved 9 November 2016.

semanticscholar.org

api.semanticscholar.org

Chen, S.R.; Yang, L.Q.; Chong, Y.T.; Jie, Y.S.; Wu, Y.K.; Yang, J.; Lin, G.L.; Li, X.H. (2015). "Novel gain of function mutation in the SLC40A1 gene associated with hereditary haemochromatosis type 4". Internal Medicine Journal. 45 (6): 672–676. doi:10.1111/imj.12764. PMID 26059880. S2CID 2426509.