HFE遺傳性血色病 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "HFE遺傳性血色病" in Chinese language version.

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18nih.gov

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11doi.org

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archive.org

Jones H, Hedley-Whyte E. Idiopathic hemochromatosis (IHC): dementia and ataxia as presenting signs. Neurology. 1983, 33 (11): 1479–83. PMID 6685241.
Nielsen J, Jensen L, Krabbe K. Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome. J Neurol Neurosurg Psychiatry. 1995, 59 (3): 318–21. PMID 7673967.
Dadone MM, Kushner JP, Edwards CQ, Bishop DT, Skolnick MH. Hereditary hemochromatosis. Analysis of laboratory expression of the disease by genotype in 18 pedigrees. American Journal of Clinical Pathology. August 1982, 78 (2): 196–207. PMID 7102818.

cdc.gov

Centers for Disease Control and Prevention. Iron Overload and Hemochromatosis. [2009-05-23]. （原始内容存档于2009-06-05）.

doi.org

Allen KJ, Gurrin LC, Constantine CC; et al. Iron-overload-related disease in HFE hereditary hemochromatosis. N. Engl. J. Med. January 2008, 358 (3): 221–30. PMID 18199861. doi:10.1056/NEJMoa073286.
Franchini M. Hereditary iron overload: update on pathophysiology, diagnosis, and treatment. Am. J. Hematol. March 2006, 81 (3): 202–9. PMID 16493621. doi:10.1002/ajh.20493.
Pietrangelo A. Hereditary hemochromatosis - a new look at an old disease. N. Engl. J. Med. June 2004, 350 (23): 2383–97. PMID 15175440. doi:10.1056/NEJMra031573.
Costello D, Walsh S, Harrington H, Walsh C. Concurrent hereditary haemochromatosis and idiopathic Parkinson's disease: a case report series. J Neurol Neurosurg Psychiatry. 2004, 75 (4): 631–3. PMID 15026513. doi:10.1136/jnnp.2003.027441.
Mendes AI, Ferro A, Martins R; et al. Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes. Ann. Hematol. March 2009, 88 (3): 229–34. PMID 18762941. doi:10.1007/s00277-008-0572-y.
Olynyk J, Cullen D, Aquilia S, Rossi E, Summerville L, Powell L. A population-based study of the clinical expression of the hemochromatosis gene. N Engl J Med. 1999, 341 (10): 718–24. PMID 10471457. doi:10.1056/NEJM199909023411002.
Olynyk JK, Trinder D, Ramm GA, Britton RS, Bacon BR. Hereditary hemochromatosis in the post-HFE era. Hepatology. September 2008, 48 (3): 991–1001. PMID 18752323. doi:10.1002/hep.22507.
Vujić Spasić M, Kiss J, Herrmann T; et al. Hfe acts in hepatocytes to prevent hemochromatosis. Cell Metab. 2008, 7 (2): 173–8. PMID 18249176. doi:10.1016/j.cmet.2007.11.014.
Shizukuda Y, Bolan C, Nguyen T, Botello G, Tripodi D, Yau Y, Waclawiw M, Leitman S, Rosing D. Oxidative stress in asymptomatic subjects with hereditary hemochromatosis. Am J Hematol. 2007, 82 (3): 249–50. PMID 16955456. doi:10.1002/ajh.20743.

dx.doi.org

Mendes AI, Ferro A, Martins R; et al. Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes. Ann. Hematol. March 2009, 88 (3): 229–34. PMID 18762941. doi:10.1007/s00277-008-0572-y.
Olynyk JK, Trinder D, Ramm GA, Britton RS, Bacon BR. Hereditary hemochromatosis in the post-HFE era. Hepatology. September 2008, 48 (3): 991–1001. PMID 18752323. doi:10.1002/hep.22507.

ebscohost.com

dynaweb.ebscohost.com

http://dynaweb.ebscohost.com/Detail.aspx?id=116469&sid=14aa79e5-a881-407c-94e7-339b81c4cd18@sessionmgr3^{[永久失效連結]} accessed 2008-10-15

harvard.edu

sickle.bwh.harvard.edu

The interaction of iron and erythropoietin. （原始内容存档于2009-04-01）.
Transferrin and Iron Transport Physiology. [2009-05-23]. （原始内容存档于2007-03-07）.

mayoclinic.com

Hemochromatosis: Symptoms. Mayo Foundation for Medical Education and Research (MFMER). （原始内容存档于2008-04-30）.
Hemochromatosis: Tests and diagnosis. Mayo Foundation for Medical Education and Research (MFMER). [2009-04-20]. （原始内容存档于2013-05-31）.
Hemochromatosis: Complications. Mayo Foundation for Medical Education and Research (MFMER). （原始内容存档于2008-03-07）.
Hemochromatosis: Treatments and drugs. Mayo Foundation for Medical Education and Research (MFMER). [2009-05-25]. （原始内容存档于2008-03-07）.
Hemochromatosis: Causes. Mayo Foundation for Medical Education and Research (MFMER). （原始内容存档于2008-03-07）.

nejm.org

content.nejm.org

Allen KJ, Gurrin LC, Constantine CC; et al. Iron-overload-related disease in HFE hereditary hemochromatosis. N. Engl. J. Med. January 2008, 358 (3): 221–30. PMID 18199861. doi:10.1056/NEJMoa073286.

nih.gov

ncbi.nlm.nih.gov

Allen KJ, Gurrin LC, Constantine CC; et al. Iron-overload-related disease in HFE hereditary hemochromatosis. N. Engl. J. Med. January 2008, 358 (3): 221–30. PMID 18199861. doi:10.1056/NEJMoa073286.
Franchini M. Hereditary iron overload: update on pathophysiology, diagnosis, and treatment. Am. J. Hematol. March 2006, 81 (3): 202–9. PMID 16493621. doi:10.1002/ajh.20493.
Jacobs EM, Verbeek AL, Kreeftenberg HG; et al. Changing aspects of HFE-related hereditary haemochromatosis and endeavours to early diagnosis. Neth J Med. December 2007, 65 (11): 419–24 [2009-05-23]. PMID 18079564. （原始内容存档于2021-05-06）.
Pietrangelo A. Hereditary hemochromatosis - a new look at an old disease. N. Engl. J. Med. June 2004, 350 (23): 2383–97. PMID 15175440. doi:10.1056/NEJMra031573.
Jones H, Hedley-Whyte E. Idiopathic hemochromatosis (IHC): dementia and ataxia as presenting signs. Neurology. 1983, 33 (11): 1479–83. PMID 6685241.
Costello D, Walsh S, Harrington H, Walsh C. Concurrent hereditary haemochromatosis and idiopathic Parkinson's disease: a case report series. J Neurol Neurosurg Psychiatry. 2004, 75 (4): 631–3. PMID 15026513. doi:10.1136/jnnp.2003.027441.
Nielsen J, Jensen L, Krabbe K. Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome. J Neurol Neurosurg Psychiatry. 1995, 59 (3): 318–21. PMID 7673967.
Dadone MM, Kushner JP, Edwards CQ, Bishop DT, Skolnick MH. Hereditary hemochromatosis. Analysis of laboratory expression of the disease by genotype in 18 pedigrees. American Journal of Clinical Pathology. August 1982, 78 (2): 196–207. PMID 7102818.
Tanner MA, He T, Westwood MA, Firmin DN, Pennell DJ. Multi-center validation of the transferability of the magnetic resonance T2* technique for the quantification of tissue iron. Haematologica. 2006, 91 (10): 1388–91. PMID 17018390.
Pedrup A, Poulsen H. Hemochromatosis and Vitiligo. Archives of Dermatology. 1964, 90 (1): 34–37. PMID 14149720.
Mendes AI, Ferro A, Martins R; et al. Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes. Ann. Hematol. March 2009, 88 (3): 229–34. PMID 18762941. doi:10.1007/s00277-008-0572-y.
Olynyk J, Cullen D, Aquilia S, Rossi E, Summerville L, Powell L. A population-based study of the clinical expression of the hemochromatosis gene. N Engl J Med. 1999, 341 (10): 718–24. PMID 10471457. doi:10.1056/NEJM199909023411002.
Olynyk JK, Trinder D, Ramm GA, Britton RS, Bacon BR. Hereditary hemochromatosis in the post-HFE era. Hepatology. September 2008, 48 (3): 991–1001. PMID 18752323. doi:10.1002/hep.22507.
Vujić Spasić M, Kiss J, Herrmann T; et al. Hfe acts in hepatocytes to prevent hemochromatosis. Cell Metab. 2008, 7 (2): 173–8. PMID 18249176. doi:10.1016/j.cmet.2007.11.014.
Shizukuda Y, Bolan C, Nguyen T, Botello G, Tripodi D, Yau Y, Waclawiw M, Leitman S, Rosing D. Oxidative stress in asymptomatic subjects with hereditary hemochromatosis. Am J Hematol. 2007, 82 (3): 249–50. PMID 16955456. doi:10.1002/ajh.20743.

digestive.niddk.nih.gov

Hemochromatosis （页面存档备份，存于互联网档案馆） National Digestive Diseases Information Clearinghouse, National Institutes of Health, U.S. Department of Health and Human Services
Hemochromatosis-Diagnosis （页面存档备份，存于互联网档案馆） National Digestive Diseases Information Clearinghouse, National Institutes of Health, U.S. Department of Health and Human Services

nlm.nih.gov

Todd Gersten. Ferritin. Medical Encyclopedia. MedlinePlus. 2009-01-12 [2009-05-26]. （原始内容存档于2016-07-05）.

psu.edu

live.psu.edu

Celtic Curse. [2009-05-23]. （原始内容存档于2009-05-31）.

scripps.edu

Gérard Lucotte. Celtic Origin of the C282Y Mutation of Hemochromatosis (PDF). Blood Cells, Molecules, and Diseases. 1998, 24 (20): 433–438 [2009-05-26]. （原始内容 (PDF)存档于2008-12-02）.

web.archive.org

Jacobs EM, Verbeek AL, Kreeftenberg HG; et al. Changing aspects of HFE-related hereditary haemochromatosis and endeavours to early diagnosis. Neth J Med. December 2007, 65 (11): 419–24 [2009-05-23]. PMID 18079564. （原始内容存档于2021-05-06）.
The interaction of iron and erythropoietin. （原始内容存档于2009-04-01）.
Centers for Disease Control and Prevention. Iron Overload and Hemochromatosis. [2009-05-23]. （原始内容存档于2009-06-05）.
Celtic Curse. [2009-05-23]. （原始内容存档于2009-05-31）.
Biography of Daniel von Recklinghausen. [2009-05-23]. （原始内容存档于2016-03-04）.
Hemochromatosis （页面存档备份，存于互联网档案馆） National Digestive Diseases Information Clearinghouse, National Institutes of Health, U.S. Department of Health and Human Services
Hemochromatosis: Symptoms. Mayo Foundation for Medical Education and Research (MFMER). （原始内容存档于2008-04-30）.
Hemochromatosis-Diagnosis （页面存档备份，存于互联网档案馆） National Digestive Diseases Information Clearinghouse, National Institutes of Health, U.S. Department of Health and Human Services
Hemochromatosis: Tests and diagnosis. Mayo Foundation for Medical Education and Research (MFMER). [2009-04-20]. （原始内容存档于2013-05-31）.
Transferrin and Iron Transport Physiology. [2009-05-23]. （原始内容存档于2007-03-07）.
Todd Gersten. Ferritin. Medical Encyclopedia. MedlinePlus. 2009-01-12 [2009-05-26]. （原始内容存档于2016-07-05）.
Hemochromatosis: Complications. Mayo Foundation for Medical Education and Research (MFMER). （原始内容存档于2008-03-07）.
Hemochromatosis: Treatments and drugs. Mayo Foundation for Medical Education and Research (MFMER). [2009-05-25]. （原始内容存档于2008-03-07）.
Gérard Lucotte. Celtic Origin of the C282Y Mutation of Hemochromatosis (PDF). Blood Cells, Molecules, and Diseases. 1998, 24 (20): 433–438 [2009-05-26]. （原始内容 (PDF)存档于2008-12-02）.
Hemochromatosis: Causes. Mayo Foundation for Medical Education and Research (MFMER). （原始内容存档于2008-03-07）.

whonamedit.com

Biography of Daniel von Recklinghausen. [2009-05-23]. （原始内容存档于2016-03-04）.

zuidencomm.nl

Jacobs EM, Verbeek AL, Kreeftenberg HG; et al. Changing aspects of HFE-related hereditary haemochromatosis and endeavours to early diagnosis. Neth J Med. December 2007, 65 (11): 419–24 [2009-05-23]. PMID 18079564. （原始内容存档于2021-05-06）.