"Hemochromatosis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed)
Descriptor ID |
D006432
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MeSH Number(s) |
C16.320.565.618.337 C18.452.565.500.480 C18.452.648.618.337
|
Concept/Terms |
Hemochromatosis- Hemochromatosis
- Bronzed Cirrhosis
- Bronzed Cirrhoses
- Cirrhoses, Bronzed
- Cirrhosis, Bronzed
- Diabetes, Bronze
- Haemochromatosis
- Haemochromatoses
- Von Recklenhausen-Applebaum Disease
- Disease, Von Recklenhausen-Applebaum
- Diseases, Von Recklenhausen-Applebaum
- Recklenhausen-Applebaum Disease, Von
- Recklenhausen-Applebaum Diseases, Von
- Von Recklenhausen Applebaum Disease
- Von Recklenhausen-Applebaum Diseases
- Bronze Diabetes
- Iron Storage Disorder
- Disorder, Iron Storage
- Disorders, Iron Storage
- Iron Storage Disorders
- Storage Disorder, Iron
- Storage Disorders, Iron
- Pigmentary Cirrhosis
- Cirrhoses, Pigmentary
- Cirrhosis, Pigmentary
- Pigmentary Cirrhoses
- Troisier-Hanot-Chauffard Syndrome
- Syndrome, Troisier-Hanot-Chauffard
- Syndromes, Troisier-Hanot-Chauffard
- Troisier Hanot Chauffard Syndrome
- Troisier-Hanot-Chauffard Syndromes
- Hemochromatoses
- Hemochromatose
Familial Hemochromatosis- Familial Hemochromatosis
- Familial Hemochromatoses
- Hemochromatoses, Familial
- Hemochromatosis, Familial
- Primary Hemochromatosis
- Genetic Hemochromatosis
- Genetic Hemochromatoses
- Hemochromatoses, Genetic
- Hemochromatosis, Genetic
|
Below are MeSH descriptors whose meaning is more general than "Hemochromatosis".
Below are MeSH descriptors whose meaning is more specific than "Hemochromatosis".
This graph shows the total number of publications written about "Hemochromatosis" by people in this website by year, and whether "Hemochromatosis" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1996 | 1 | 0 | 1 |
2002 | 5 | 0 | 5 |
2004 | 3 | 0 | 3 |
2005 | 4 | 1 | 5 |
2006 | 2 | 0 | 2 |
2010 | 2 | 0 | 2 |
2011 | 1 | 2 | 3 |
2012 | 1 | 0 | 1 |
2014 | 0 | 1 | 1 |
2016 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Hemochromatosis" by people in Profiles.
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Anastasio HB, Grundy M, Birsner ML, Blakemore KJ. Gestational Alloimmune Liver Disease: A Devastating Condition Preventable With Maternal Intravenous Immunoglobulin. Obstet Gynecol. 2016 Nov; 128(5):1092-1094.
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Parrow NL, Fleming RE. Bone morphogenetic proteins as regulators of iron metabolism. Annu Rev Nutr. 2014; 34:77-94.
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Vujic Spasic M, Sparla R, Mleczko-Sanecka K, Migas MC, Breitkopf-Heinlein K, Dooley S, Vaulont S, Fleming RE, Muckenthaler MU. Smad6 and Smad7 are co-regulated with hepcidin in mouse models of iron overload. Biochim Biophys Acta. 2013 Jan; 1832(1):76-84.
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Fleming RE, Feng Q, Britton RS. Knockout mouse models of iron homeostasis. Annu Rev Nutr. 2011 Aug 21; 31:117-37.
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Swinkels DW, Fleming RE. Novel observations in hereditary hemochromatosis: potential implications for clinical strategies. Haematologica. 2011 Apr; 96(4):485-8.
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Tjalsma H, Laarakkers CM, van Swelm RP, Theurl M, Theurl I, Kemna EH, van der Burgt YE, Venselaar H, Dutilh BE, Russel FG, Weiss G, Masereeuw R, Fleming RE, Swinkels DW. Mass spectrometry analysis of hepcidin peptides in experimental mouse models. PLoS One. 2011 Mar 08; 6(3):e16762.
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Chua AC, Delima RD, Morgan EH, Herbison CE, Tirnitz-Parker JE, Graham RM, Fleming RE, Britton RS, Bacon BR, Olynyk JK, Trinder D. Iron uptake from plasma transferrin by a transferrin receptor 2 mutant mouse model of haemochromatosis. J Hepatol. 2010 Mar; 52(3):425-31.
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Moinuddin MJ, Figueredo V, Amanullah AM. Infiltrative diseases of the heart. Rev Cardiovasc Med. 2010; 11(4):218-27.
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Gouya L, Muzeau F, Robreau AM, Letteron P, Couchi E, Lyoumi S, Deybach JC, Puy H, Fleming R, Demant P, Beaumont C, Grandchamp B. Genetic study of variation in normal mouse iron homeostasis reveals ceruloplasmin as an HFE-hemochromatosis modifier gene. Gastroenterology. 2007 Feb; 132(2):679-86.
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Ezquer F, N??ez MT, Rojas A, Asenjo J, Israel Y. Hereditary hemochromatosis: an opportunity for gene therapy. Biol Res. 2006; 39(1):113-24.