Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
My NCBI Filters
Results by year

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

Year Number of Results
1966 1
1982 1
1988 5
1989 1
1994 1
1996 2
1997 4
1998 6
1999 8
2000 9
2001 2
2002 3
2003 2
2004 5
2005 1
2006 5
2007 3
2008 2
2009 2
2011 1
2012 1
2013 6
2014 2
2015 4
2017 1
2018 1
2021 0
Text availability
Article attribute
Article type
Publication date

Similar articles for PMID: 10654968

77 results
Results by year
Filters applied: . Clear all
Page 1
Hereditary hemochromatosis in siblings: diagnosis by genotyping.
Nowicki MJ, Bacon BR. Nowicki MJ, et al. Pediatrics. 2000 Feb;105(2):426-9. doi: 10.1542/peds.105.2.426. Pediatrics. 2000. PMID: 10654968 No abstract available.
Diagnosis and management of hereditary hemochromatosis.
Salgia RJ, Brown K. Salgia RJ, et al. Clin Liver Dis. 2015 Feb;19(1):187-98. doi: 10.1016/j.cld.2014.09.011. Epub 2014 Oct 23. Clin Liver Dis. 2015. PMID: 25454304 Review.
Differential diagnosis of hereditary hemochromatosis from other liver disorders by genetic analysis: gene mutation analysis of patients previously diagnosed with hemochromatosis by liver biopsy.
Bartolo C, McAndrew PE, Sosolik RC, Cawley KA, Balcerzak SP, Brandt JT, Prior TW. Bartolo C, et al. Arch Pathol Lab Med. 1998 Jul;122(7):633-7. Arch Pathol Lab Med. 1998. PMID: 9674544
[Hereditary hemochromatosis: molecular diagnosis and effect of treatment].
Szczeklik W, Dropiński J, Dziedzina S, Szułdrzyński K, Biesiada G, Mach T, Sanak M. Szczeklik W, et al. Pol Arch Med Wewn. 2004 May;111(5):593-6. Pol Arch Med Wewn. 2004. PMID: 15508811 Polish.
An HFE intronic variant promotes misdiagnosis of hereditary hemochromatosis.
Somerville MJ, Sprysak KA, Hicks M, Elyas BG, Vicen-Wyhony L. Somerville MJ, et al. Am J Hum Genet. 1999 Sep;65(3):924-6. doi: 10.1086/302550. Am J Hum Genet. 1999. PMID: 10441599 Free PMC article. No abstract available.
[Molecular biology analysis: hereditary hemochromatosis, Wilson disease, alpha 1-antitrypsin deficiency and Dubin-Johnson syndrome].
Arnold C. Arnold C. Praxis (Bern 1994). 1998 Oct 14;87(42):1390-6. Praxis (Bern 1994). 1998. PMID: 9824945 Review. German.
Hereditary hemochromatosis: missed diagnosis or misdiagnosis?
Cherfane CE, Hollenbeck RD, Go J, Brown KE. Cherfane CE, et al. Am J Med. 2013 Nov;126(11):1010-5. doi: 10.1016/j.amjmed.2013.07.013. Epub 2013 Sep 18. Am J Med. 2013. PMID: 24054178
Identification of hereditary hemochromatosis pedigrees and a novel SLC40A1 mutation in Chinese population.
An P, Jiang L, Guan Y, Wang H, Wang J, Tian Y, Yang W, Shi Y, Xue J, Min J, Wang F. An P, et al. Blood Cells Mol Dis. 2017 Mar;63:34-36. doi: 10.1016/j.bcmd.2017.01.002. Epub 2017 Jan 11. Blood Cells Mol Dis. 2017. PMID: 28110135 No abstract available.
About genetic diagnosis of hereditary hemochromatosis.
Michel H. Michel H. Ann Biol Clin (Paris). 2018 Apr 1;76(2):131. doi: 10.1684/abc.2018.1338. Ann Biol Clin (Paris). 2018. PMID: 29623879 English. No abstract available.
Rapid diagnosis of asymptomatic hereditary haemochromatosis by detection of the Cys282Tyr mutation in the HLA-H gene.
Aslam S, Standen GR. Aslam S, et al. Postgrad Med J. 1997 Sep;73(863):573-4. doi: 10.1136/pgmj.73.863.573. Postgrad Med J. 1997. PMID: 9373599 Free PMC article.
77 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page