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Year Number of Results
1952 1
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1979 3
1981 1
1983 3
1984 2
1985 1
1986 3
1987 5
1989 3
1990 1
1991 7
1992 2
1993 7
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1995 6
1996 2
1997 5
1998 8
1999 9
2000 16
2001 19
2002 32
2003 30
2004 20
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2007 39
2008 37
2009 34
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2024 4

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687 results

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Page 1
Hereditary hemochromatosis.
Ajioka RS, Kushner JP. Ajioka RS, et al. Semin Hematol. 2002 Oct;39(4):235-41. doi: 10.1053/shem.2002.35634. Semin Hematol. 2002. PMID: 12382198 Review.
Hereditary hemochromatosis (hh, type 1 hemochromatosis) is an autosomal recessive trait characterized by hyperabsorption of dietary iron. ...The prevalence of organ damage due to iron overload, however, remains a controversial issue. Published e …
Hereditary hemochromatosis (hh, type 1 hemochromatosis) is an autosomal recessive trait characterized by …
Hereditary hemochromatosis: An update vision of the laboratory diagnosis.
Molina CA, Ros NG, Tarancón RG, Varas LR, Flores VR, Álvarez SI. Molina CA, et al. J Trace Elem Med Biol. 2023 Jul;78:127194. doi: 10.1016/j.jtemb.2023.127194. Epub 2023 May 6. J Trace Elem Med Biol. 2023. PMID: 37163822
Haemochromatosis (HC) is an inherited disorder of iron metabolism. The 85-90% of Hereditary hemochromatosis cases are caused by mutations in HFE gene (HC type 1). ...The presence of C282Y mutation in homozygosis is compatible with the diagnosis of HC …
Haemochromatosis (HC) is an inherited disorder of iron metabolism. The 85-90% of Hereditary hemochromatosis cases are caused b …
Laboratory Evaluation of Hereditary Hemochromatosis.
Sonagra AD, Zubair M. Sonagra AD, et al. 2023 Jul 17. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Jul 17. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 37603641 Free Books & Documents.
In 1977, Simon et al reported the association between an HLA class I-like molecule and the presumed hemochromatosis gene on chromosome 6p, establishing the genetic basis of what is now referred to as hereditary hemochromatosis (HH). Although one of the most c …
In 1977, Simon et al reported the association between an HLA class I-like molecule and the presumed hemochromatosis gene on chromosom …
Identification of Genes for Hereditary Hemochromatosis.
Gerhard GS, Paynton BV, DiStefano JK. Gerhard GS, et al. Methods Mol Biol. 2018;1706:353-365. doi: 10.1007/978-1-4939-7471-9_19. Methods Mol Biol. 2018. PMID: 29423808 Review.
Hereditary hemochromatosis (HH) is one of the most common genetically transmitted conditions in individuals of Northern European ancestry. ...There are four main classes of HH, as well as five individual molecular subtypes, caused by mutations in five genes, and the …
Hereditary hemochromatosis (HH) is one of the most common genetically transmitted conditions in individuals of Northern Europe …
Juvenile Hemochromatosis.
Piperno A, Bertola F, Bentivegna A. Piperno A, et al. 2005 Feb 17 [updated 2020 Jan 9]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2005 Feb 17 [updated 2020 Jan 9]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301349 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Juvenile hemochromatosis is characterized by onset of severe iron overload occurring typically in the first to third decades of life. ...MANAGEMENT: Treatment of manifestations: Phlebotomy for treatment of iron overload as for HFE hemochromatos …
CLINICAL CHARACTERISTICS: Juvenile hemochromatosis is characterized by onset of severe iron overload occurring typically in the first …
[Hereditary hemochromatosis].
Niederau C. Niederau C. Med Klin (Munich). 2009 Dec 15;104(12):931-46. doi: 10.1007/s00063-009-1192-6. Med Klin (Munich). 2009. PMID: 20039160 Review. German.
Genetic hemochromatosis is classified into four subtypes of which only type 1 is of clinical importance in Caucasians. ...Type 4 hemochromatosis follows an autosomal dominant trait; the corresponding mutation affects the basolateral iron carrier …
Genetic hemochromatosis is classified into four subtypes of which only type 1 is of clinical importance in Caucasians. …
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.
HFE-related (type 1) hemochromatosis remains the most frequent form, characterized by C282Y mutation homozygosity. Rare forms of hereditary hemochromatosis include type 2 (A and B, juvenile hemochromatosis caused by HJV and HAMP mu …
HFE-related (type 1) hemochromatosis remains the most frequent form, characterized by C282Y mutation homozygosity. Rare …
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.
Hereditary hemochromatosis is a rare genetic disorder that can have significant clinical consequences. ...Treatment of patients with the clinical phenotype of hereditary hemochromatosis is commonly through phlebotomy for removal of excess iron stores. …
Hereditary hemochromatosis is a rare genetic disorder that can have significant clinical consequences. ...Treatment of patient …
Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genes.
Radio FC, Majore S, Aurizi C, Sorge F, Biolcati G, Bernabini S, Giotti I, Torricelli F, Giannarelli D, De Bernardo C, Grammatico P. Radio FC, et al. Blood Cells Mol Dis. 2015 Jun;55(1):71-5. doi: 10.1016/j.bcmd.2015.04.001. Epub 2015 Apr 16. Blood Cells Mol Dis. 2015. PMID: 25976471
Hereditary hemochromatosis (HH) is a heterogeneous disorder of iron metabolism. The most common form of the disease is Classic or type 1 HH, mainly caused by a biallelic missense p.Cys282Tyr (c.845G>A) mutation in the HFE gene. ...
Hereditary hemochromatosis (HH) is a heterogeneous disorder of iron metabolism. The most common form of the disease is Classic …
Primary Non-HFE Hemochromatosis: A Review.
Turshudzhyan A, Wu DC, Wu GY. Turshudzhyan A, et al. J Clin Transl Hepatol. 2023 Aug 28;11(4):925-931. doi: 10.14218/JCTH.2022.00373. Epub 2023 Feb 2. J Clin Transl Hepatol. 2023. PMID: 37408807 Free PMC article. Review.
However, four types of hemochromatosis do not involve the HFE gene. They are non-HFE hemochromatosis type 2A (HFE2, encoding HJV), type 2B (HAMP, encoding hepcidin), type 3 (TFR2, encoding transferring receptor-2), and types 4A and B (SLC40A1, e …
However, four types of hemochromatosis do not involve the HFE gene. They are non-HFE hemochromatosis type 2A (HFE2, enc …
687 results