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

Year Number of Results
1899 2
1901 1
1909 1
1911 1
1912 5
1917 1
1918 3
1921 1
1922 2
1925 1
1928 1
1930 4
1931 2
1933 2
1934 1
1936 2
1938 2
1939 1
1940 1
1941 1
1942 2
1945 4
1946 10
1947 11
1948 15
1949 19
1950 33
1951 39
1952 55
1953 72
1954 71
1955 66
1956 59
1957 53
1958 58
1959 33
1960 56
1961 58
1962 52
1963 93
1964 143
1965 104
1966 83
1967 92
1968 90
1969 95
1970 81
1971 77
1972 74
1973 76
1974 71
1975 69
1976 69
1977 89
1978 96
1979 91
1980 86
1981 76
1982 82
1983 107
1984 113
1985 90
1986 84
1987 116
1988 127
1989 123
1990 123
1991 140
1992 119
1993 120
1994 155
1995 147
1996 176
1997 227
1998 277
1999 302
2000 345
2001 322
2002 343
2003 335
2004 334
2005 382
2006 351
2007 364
2008 317
2009 333
2010 332
2011 340
2012 282
2013 278
2014 265
2015 280
2016 273
2017 255
2018 246
2019 241
2020 165
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10,840 results
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Page 1
Haemochromatosis.
Brissot P, Pietrangelo A, Adams PC, de Graaff B, McLaren CE, Loréal O. Brissot P, et al. Nat Rev Dis Primers. 2018 Apr 5;4:18016. doi: 10.1038/nrdp.2018.16. Nat Rev Dis Primers. 2018. PMID: 29620054 Review.
The most common form of haemochromatosis is due to homozygous mutations (specifically, the C282Y mutation) in HFE, which encodes hereditary haemochromatosis protein. Non-HFE forms of haemochromatosis due to mutations in HAMP, HJV or TFR2 are much rarer. Mutat …
The most common form of haemochromatosis is due to homozygous mutations (specifically, the C282Y mutation) in HFE, which encodes here …
Hemochromatosis - modern condition of the problem.
Voloshinа NB, Osipenko MF, Litvinova NV, Voloshin AN. Voloshinа NB, et al. Ter Arkh. 2018 Apr 19;90(3):107-112. doi: 10.26442/terarkh2018903107-112. Ter Arkh. 2018. PMID: 30701865 Review.
Hereditary hemochromatosis is the most common genetic disorder. Without therapeutic intervention the disease can lead to the development of life-threatening complications such as cirrhosis, hepatocellular carcinoma. The article presents data on pathogenesis, diagnosis and …
Hereditary hemochromatosis is the most common genetic disorder. Without therapeutic intervention the disease can lead to the developm …
Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotype.
Adams P, Altes A, Brissot P, Butzeck B, Cabantchik I, Cançado R, Distante S, Evans P, Evans R, Ganz T, Girelli D, Hultcrantz R, McLaren G, Marris B, Milman N, Nemeth E, Nielsen P, Pineau B, Piperno A, Porto G, Prince D, Ryan J, Sanchez M, Santos P, Swinkels D, Teixeira E, Toska K, Vanclooster A, White D; Contributors and Hemochromatosis International Taskforce. Adams P, et al. Hepatol Int. 2018 Mar;12(2):83-86. doi: 10.1007/s12072-018-9855-0. Epub 2018 Mar 27. Hepatol Int. 2018. PMID: 29589198 Free PMC article.
Although guidelines are available for hereditary hemochromatosis, a high percentage of the recommendations within them are not shared between the different guidelines. ...This final version was approved at the Hemochromatosis International meeting on 12th May 2017 i …
Although guidelines are available for hereditary hemochromatosis, a high percentage of the recommendations within them are not shared …
Haemochromatosis: a clinical update for the practising physician.
Radford-Smith DE, Powell EE, Powell LW. Radford-Smith DE, et al. Intern Med J. 2018 May;48(5):509-516. doi: 10.1111/imj.13784. Intern Med J. 2018. PMID: 29722188 Review.
Haemochromatosis is most commonly due to the autosomal recessive inheritance of a C282Y substitution in the HFE protein, whereby both alleles of the corresponding gene are affected. ...Enigmatically, the penetrance of both raised iron indices and clinically significant dis
Haemochromatosis is most commonly due to the autosomal recessive inheritance of a C282Y substitution in the HFE protein, whereby both
Diagnosis and therapy of genetic haemochromatosis (review and 2017 update).
Fitzsimons EJ, Cullis JO, Thomas DW, Tsochatzis E, Griffiths WJH; British Society for Haematology. Fitzsimons EJ, et al. Br J Haematol. 2018 May;181(3):293-303. doi: 10.1111/bjh.15164. Epub 2018 Apr 16. Br J Haematol. 2018. PMID: 29663319 No abstract available.
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.
This review presents a new concept of hemochromatosis which stems from the idea that, beyond their genetic diversities, all known hemochromatoses have in common the same metabolic abnormality: the genetically determined failure to prevent unneeded iron from entering …
This review presents a new concept of hemochromatosis which stems from the idea that, beyond their genetic diversities, all known …
Haemochromatosis.
[No authors listed] [No authors listed] Nat Rev Dis Primers. 2018 Apr 5;4:18019. doi: 10.1038/nrdp.2018.19. Nat Rev Dis Primers. 2018. PMID: 29620056 Review. No abstract available.
[Haemochromatosis and Arthropathies].
Braner A. Braner A. Dtsch Med Wochenschr. 2018 Aug;143(16):1167-1173. doi: 10.1055/a-0505-9244. Epub 2018 Aug 7. Dtsch Med Wochenschr. 2018. PMID: 30086562 Review. German.
Arthropathy is the most common and often the earliest clinical manifestation of hereditary hemochromatosis (HH). It is difficult to treat and there is a high risk for early endoprosthetic joint replacement. ...To promote further research into hemochromatosis arthrop …
Arthropathy is the most common and often the earliest clinical manifestation of hereditary hemochromatosis (HH). It is difficult to t …
Haemochromatosis arthropathy - a conundrum of the Celtic curse.
Kiely PD. Kiely PD. J R Coll Physicians Edinb. 2018 Sep;48(3):233-238. doi: 10.4997/JRCPE.2018.307. J R Coll Physicians Edinb. 2018. PMID: 30191911 Review.
Genetic haemochromatosis is an autosomal recessive disorder, mostly due to HFE gene mutation, leading to loss of hepcidin and unregulated iron loading. ...
Genetic haemochromatosis is an autosomal recessive disorder, mostly due to HFE gene mutation, leading to loss of hepcidin and unregul …
Neuromuscular manifestations in hereditary haemochromatosis.
Wouthuis SF, van Deursen CT, te Lintelo MP, Rozeman CA, Beekman R. Wouthuis SF, et al. J Neurol. 2010 Sep;257(9):1465-72. doi: 10.1007/s00415-010-5548-x. Epub 2010 Apr 1. J Neurol. 2010. PMID: 20358215
Involvement of peripheral nerves and skeletal muscles has been reported in the course of hereditary haemochromatosis (HH) but a systematic study is lacking. ...
Involvement of peripheral nerves and skeletal muscles has been reported in the course of hereditary haemochromatosis (HH) but a syste …
10,840 results
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