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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1963 1
1964 5
1965 4
1966 6
1967 4
1968 6
1969 7
1970 9
1971 6
1972 8
1973 8
1974 9
1975 7
1976 11
1977 9
1978 7
1979 15
1980 14
1981 6
1982 17
1983 13
1984 15
1985 10
1986 9
1987 16
1988 29
1989 20
1990 22
1991 26
1992 21
1993 20
1994 33
1995 36
1996 42
1997 31
1998 71
1999 62
2000 73
2001 57
2002 96
2003 64
2004 63
2005 68
2006 65
2007 76
2008 56
2009 65
2010 52
2011 56
2012 39
2013 48
2014 41
2015 35
2016 37
2017 48
2018 41
2019 41
2020 34
2021 28
2022 23
2023 25
2024 5

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1,776 results

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Page 1
ACG Clinical Guideline: Hereditary Hemochromatosis.
Kowdley KV, Brown KE, Ahn J, Sundaram V. Kowdley KV, et al. Am J Gastroenterol. 2019 Aug;114(8):1202-1218. doi: 10.14309/ajg.0000000000000315. Am J Gastroenterol. 2019. PMID: 31335359 Review.
Hereditary hemochromatosis (HH) is one of the most common genetic disorders among persons of northern European descent. ...
Hereditary hemochromatosis (HH) is one of the most common genetic disorders among persons of northern European descent. ...
Diagnosis and management of hereditary haemochromatosis.
Murphree CR, Nguyen NN, Raghunathan V, Olson SR, DeLoughery T, Shatzel JJ. Murphree CR, et al. Vox Sang. 2020 May;115(4):255-262. doi: 10.1111/vox.12896. Epub 2020 Feb 20. Vox Sang. 2020. PMID: 32080859 Review.
Haemochromatosis.
Adams PC, Jeffrey G, Ryan J. Adams PC, et al. Lancet. 2023 May 27;401(10390):1811-1821. doi: 10.1016/S0140-6736(23)00287-8. Epub 2023 Apr 27. Lancet. 2023. PMID: 37121243 Review.
Hemochromatosis.
Olynyk JK, Ramm GA. Olynyk JK, et al. N Engl J Med. 2022 Dec 8;387(23):2159-2170. doi: 10.1056/NEJMra2119758. N Engl J Med. 2022. PMID: 36477033 Review. No abstract available.
Hereditary hemochromatosis: pathogenesis, diagnosis, and treatment.
Pietrangelo A. Pietrangelo A. Gastroenterology. 2010 Aug;139(2):393-408, 408.e1-2. doi: 10.1053/j.gastro.2010.06.013. Epub 2010 Jun 11. Gastroenterology. 2010. PMID: 20542038 Review.
In humans, loss of TfR2, HJV, and hepcidin itself or FPN mutations result in full-blown hemochromatosis. Unlike these rare instances, in white people, homozygotes for C282Y polymorphism in HFE are numerous, but they are only predisposed to hemochromatosis; complete …
In humans, loss of TfR2, HJV, and hepcidin itself or FPN mutations result in full-blown hemochromatosis. Unlike these rare instances, …
Hereditary Hemochromatosis: Rapid Evidence Review.
Kane SF, Roberts C, Paulus R. Kane SF, et al. Am Fam Physician. 2021 Sep 1;104(3):263-270. Am Fam Physician. 2021. PMID: 34523883 Free article. Review.
Hereditary hemochromatosis is an autosomal recessive disorder that disrupts iron homeostasis, resulting in systemic iron overload. ...Genetic testing for the hereditary hemochromatosis genes should be offered after 18 years of age to first-degree relatives of patien …
Hereditary hemochromatosis is an autosomal recessive disorder that disrupts iron homeostasis, resulting in systemic iron overload. .. …
Gestational alloimmune liver disease and neonatal hemochromatosis.
Whitington PF. Whitington PF. Semin Liver Dis. 2012 Nov;32(4):325-32. doi: 10.1055/s-0032-1329901. Epub 2013 Feb 8. Semin Liver Dis. 2012. PMID: 23397533 Review.
Neonatal hemochromatosis (NH) is a clinical syndrome consisting of liver disease and pathologic siderosis of various extrahepatic tissues. NH is a form of secondary hemochromatosis in which severe fetal liver injury causes iron overload due to poor regulation of mat …
Neonatal hemochromatosis (NH) is a clinical syndrome consisting of liver disease and pathologic siderosis of various extrahepatic tis …
Hereditary hemochromatosis.
Pietrangelo A. Pietrangelo A. Biochim Biophys Acta. 2006 Jul;1763(7):700-10. doi: 10.1016/j.bbamcr.2006.05.013. Epub 2006 May 27. Biochim Biophys Acta. 2006. PMID: 16891003 Free article. Review.
The advent of the genetics era has profoundly changed the way we look at iron related diseases, particularly hemochromatosis. New discoveries have challenged historical concepts about the disease, such as its monogenic nature, intestinal origin or complete phenotypic penet …
The advent of the genetics era has profoundly changed the way we look at iron related diseases, particularly hemochromatosis. New dis …
Hemochromatosis: Hereditary hemochromatosis and HFE gene.
Katsarou MS, Papasavva M, Latsi R, Drakoulis N. Katsarou MS, et al. Vitam Horm. 2019;110:201-222. doi: 10.1016/bs.vh.2019.01.010. Epub 2019 Feb 8. Vitam Horm. 2019. PMID: 30798813 Review.
Hereditary Hemochromatosis (HH) is an autosomal recessive genetic disease, characterized by an excessively increased absorption of dietary iron. ...Therefore, genotypic check is vital in order to prevent the development of this type of hemochromatosis....
Hereditary Hemochromatosis (HH) is an autosomal recessive genetic disease, characterized by an excessively increased absorption of di …
Juvenile haemochromatosis.
Griffiths WJH, Besser M, Bowden DJ, Kelly DA. Griffiths WJH, et al. Lancet Child Adolesc Health. 2021 Jul;5(7):524-530. doi: 10.1016/S2352-4642(20)30392-8. Epub 2021 Apr 15. Lancet Child Adolesc Health. 2021. PMID: 33861982 Review.
Typical manifestations include heart failure, endocrine failure (including diabetes and hypogonadism), cirrhosis, and arthropathy. Compared with HFE haemochromatosis, juvenile haemochromatosis affects female and male individuals similarly, presents at a younger age, and ca …
Typical manifestations include heart failure, endocrine failure (including diabetes and hypogonadism), cirrhosis, and arthropathy. Co …
1,776 results