Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1999 2
2000 1
2002 6
2003 1
2004 4
2005 4
2006 3
2007 1
2008 3
2009 5
2010 1
2011 2
2012 2
2013 1
2014 3
2015 1
2017 3
2018 4
2019 4
2020 1
2023 2
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

47 results

Results by year

Filters applied: . Clear all
Page 1
Juvenile hemochromatosis.
Camaschella C, Roetto A, De Gobbi M. Camaschella C, et al. Semin Hematol. 2002 Oct;39(4):242-8. doi: 10.1053/shem.2002.35635. Semin Hematol. 2002. PMID: 12382199 Review.
Juvenile hemochromatosis or type 2 hemochromatosis is a rare inherited recessive disease, which leads to severe iron overload earlier in life than HFE-related hemochromatosis. ...The type 2 hemochromatosis locus maps to chromosome 1q21, but the gene has not yet been …
Juvenile hemochromatosis or type 2 hemochromatosis is a rare inherited recessive disease, which leads to severe iron overload …
Current approach to hemochromatosis.
Brissot P, Troadec MB, Bardou-Jacquet E, Le Lan C, Jouanolle AM, Deugnier Y, Loréal O. Brissot P, et al. Blood Rev. 2008 Jul;22(4):195-210. doi: 10.1016/j.blre.2008.03.001. Epub 2008 Apr 21. Blood Rev. 2008. PMID: 18430498 Review.
Five major categories are now established: HFE-related or type1 hemochromatosis, frequently found in Caucasians, and four rarer diseases which are type 2 (A and B) hemochromatosis (juvenile hemochromatosis), type 3 hemochromatosis (transferrin receptor 2 hemochromat …
Five major categories are now established: HFE-related or type1 hemochromatosis, frequently found in Caucasians, and four rarer diseases whi …
Non-HFE hemochromatosis: pathophysiological and diagnostic aspects.
Bardou-Jacquet E, Ben Ali Z, Beaumont-Epinette MP, Loreal O, Jouanolle AM, Brissot P. Bardou-Jacquet E, et al. Clin Res Hepatol Gastroenterol. 2014 Apr;38(2):143-54. doi: 10.1016/j.clinre.2013.11.003. Epub 2013 Dec 8. Clin Res Hepatol Gastroenterol. 2014. PMID: 24321703 Free article. Review.
To date, four types of hemochromatosis have been identified: HFE-related or type1 hemochromatosis, the most frequent form in Caucasians, and four rare types, named type 2 (A and B) hemochromatosis (juvenile hemochromatosis due to hemojuvelin and hepcidin mutation), …
To date, four types of hemochromatosis have been identified: HFE-related or type1 hemochromatosis, the most frequent form in Caucasians, and …
Diagnostic evaluation of hereditary hemochromatosis (HFE and non-HFE).
Bardou-Jacquet E, Brissot P. Bardou-Jacquet E, et al. Hematol Oncol Clin North Am. 2014 Aug;28(4):625-35, v. doi: 10.1016/j.hoc.2014.04.006. Epub 2014 Jun 2. Hematol Oncol Clin North Am. 2014. PMID: 25064704 Review.
Rare forms of hereditary hemochromatosis include type 2 (A and B, juvenile hemochromatosis caused by HJV and HAMP mutation), type 3 (related to TFR2 mutation), and type 4 (A and B, ferroportin disease). ...
Rare forms of hereditary hemochromatosis include type 2 (A and B, juvenile hemochromatosis caused by HJV and HAMP mutation), t …
Variable expressivity of HJV related hemochromatosis: "Juvenile" hemochromatosis?
Hamdi-Rozé H, Ben Ali Z, Ropert M, Detivaud L, Aggoune S, Simon D, Pelletier G, Deugnier Y, David V, Bardou-Jacquet E. Hamdi-Rozé H, et al. Blood Cells Mol Dis. 2019 Feb;74:30-33. doi: 10.1016/j.bcmd.2018.10.006. Epub 2018 Oct 22. Blood Cells Mol Dis. 2019. PMID: 30389309 Free article.
Juvenile hemochromatosis is a rare autosomal recessive disease due to variants in the Hemojuvelin (HJV) gene. ...Surprisingly, this study revealed a late age of onset in some patients, contrasting with the commonly accepted definition of "juvenile" hemochr …
Juvenile hemochromatosis is a rare autosomal recessive disease due to variants in the Hemojuvelin (HJV) gene. ...Surprisingly, …
Recent developments in liver pathology.
Yan BC, Hart JA. Yan BC, et al. Arch Pathol Lab Med. 2009 Jul;133(7):1078-86. doi: 10.5858/133.7.1078. Arch Pathol Lab Med. 2009. PMID: 19642734 Free article. Review.
Clinical, morphologic, and molecular genetic studies have also established juvenile hemochromatosis and pediatric nonalcoholic steatohepatitis as entities distinct from their adult counterparts. OBJECTIVE: To review the recent molecular genetic characterization of t …
Clinical, morphologic, and molecular genetic studies have also established juvenile hemochromatosis and pediatric nonalcoholic …
Hemochromatosis--neonatal and young subjects.
Cox TM, Halsall DJ. Cox TM, et al. Blood Cells Mol Dis. 2002 Nov-Dec;29(3):411-7. doi: 10.1006/bcmd.2002.0580. Blood Cells Mol Dis. 2002. PMID: 12547231 Review.
Juvenile hemochromatosis (JH) is an autosomal recessive disease causing iron overload before age 30 in both sexes. ...
Juvenile hemochromatosis (JH) is an autosomal recessive disease causing iron overload before age 30 in both sexes. ...
Hemojuvelin: the hepcidin story continues.
Malyszko J. Malyszko J. Kidney Blood Press Res. 2009;32(2):71-6. doi: 10.1159/000208988. Epub 2009 Mar 14. Kidney Blood Press Res. 2009. PMID: 19287179 Free article. Review.
Hemojuvelin (HJV) is a membrane protein that is responsible for the iron overload condition known as juvenile hemochromatosis. HJV, highly expressed in the liver, skeletal muscle and heart, seems to play a role in iron absorption and release from cells and has anti- …
Hemojuvelin (HJV) is a membrane protein that is responsible for the iron overload condition known as juvenile hemochromatosis. …
47 results