Search Results

Hemochromatosis gene mutations and treatment of anemia in patients on hemodialysis

Authors: BROWN, Michaela C.; GAFFNEY, Dairena; GEMMELL, Clare; OAKES, Eleanor; MORRIS, Scott; SPOONER, Richard; JARDINE, Alan G.; GEDDES, Colin C.

Source: Hemodialysis International, Volume 13, Number 4, October 2009 , pp. 460-466(7)

Publisher: Blackwell Publishing

Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes

Authors: Mendes, Ana; Ferro, Ana; Martins, Rute; Picanço, Isabel; Gomes, Susana; Cerqueira, Rute; Correia, Manuel; Nunes, António; Esteves, Jorge; Fleming, Rita; Faustino, Paula

Source: Annals of Hematology, Volume 88, Number 3, March 2009 , pp. 229-234(6)

Publisher: Springer

Behavioral, biochemical, and genetic analysis of iron metabolism in high-intensity blood donors

Authors: Mast, Alan E.; Foster, Tisha M.; Pinder, Holly L.; Beczkiewicz, Craig A.; Bellissimo, Daniel B.; Murphy, Anthony T.; Kovacevic, Steve; Wroblewski, Victor J.; Witcher, Derrick R.

Source: Transfusion, Volume 48, Number 10, October 2008 , pp. 2197-2204(8)

Publisher: Blackwell Publishing

High prevalence of HFE gene mutations in patients with porphyria cutanea tarda in the Czech Republic

Authors: Kratka, K.; Dostalikova-Cimburova, M.; Michalikova, H.; Stransky, J.; Vranova, J.; Horak, J.

Source: British Journal of Dermatology, Volume 159, Number 3, September 2008 , pp. 585-590(6)

Publisher: Blackwell Publishing

Serial serum ferritin measurements in untreated HFE C282Y homozygotes in the Hemochromatosis and Iron Overload Screening Study

Authors: ADAMS, P. C.; REBOUSSIN, D. M.; BARTON, J. C.; ACTON, R. T.; SPEECHLEY, M.; LEIENDECKER-FOSTER, C.; MEENAN, R.; PASSMORE, L.; MCLAREN, C. E.; MCLAREN, G. D.; GORDEUK, V.; DAWKINS, F.; ECKFELDT, J. H.

Source: International Journal of Laboratory Hematology, Volume 30, Number 4, August 2008 , pp. 300-305(6)

Publisher: Blackwell Publishing

Early age-of-onset iron overload and homozygosity for the novel hemojuvelin mutation HJV R54X (exon 3; c.160A→T) in an African American male of West Indies descent

Authors: Murugan; Lee; Kalavar; Barton

Source: Clinical Genetics, Volume 74, Number 1, July 2008 , pp. 88-92(5)

Publisher: Blackwell Publishing

Assessment of the psychological effects of genetic screening for hereditary hemochromatosis

Authors: Elsass, Peter; Pedersen, Palle; Husum, Kristian; Milman, Nils

Source: Annals of Hematology, Volume 87, Number 5, May 2008 , pp. 397-404(8)

Publisher: Springer

The HFE gene heterozygosis H63D: a cofactor for liver damage in patients with steatohepatitis? Epidemiological and clinical considerations

Authors: Neri; Pulvirenti; Signorelli; Ignaccolo; Tsami; Mauceri; Misseri; Interlandi; Cutuli; Castellino

Source: Internal Medicine Journal, Volume 38, Number 4, April 2008 , pp. 254-258(5)

Publisher: Blackwell Publishing

Haplotype analysis of the H63D, IVS2+4t/c, and C282Y polymorphisms of the HFE gene reveals rare events of intragenic recombination

Authors: Curcio, Michele; Fornaciari, Silvia; Mariotti, Maria Luciana; Chelazzi, Silvia; Scatena, Fabrizio; Presciuttini, Silvano

Source: European Journal of Haematology, Volume 80, Number 4, April 2008 , pp. 341-345(5)

Publisher: Blackwell Publishing

Non-prescription supplement-induced hepatitis with hyperferritinemia and mutation (H63D) in the HFE gene

Authors: Fujii, Hideki; Takagaki, Nobumasa; Yoh, Takaharu; Morita, Atsuhiro; Ohkawara, Tohru; Yamaguchi, Kanji; Minami, Masahito; Sawa, Yoshihiko; Okanoue, Takeshi; Ohkawara, Yasuo; Itoh, Yoshito

Source: Hepatology Research, Volume 38, Number 3, March 2008 , pp. 319-323(5)

Publisher: Blackwell Publishing

Analysis of the HFE gene (H63D and C282Y) mutations in patients with iron overload, family members and controls from Antioquia, Northwest Colombia

Source: Clinical Genetics, Volume 73, Number 1, January 2008 , pp. 92-93(2)

Publisher: Blackwell Publishing

Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis

Authors: Lawless; White; Mankan; O'Dwyer; Norris

Source: Tissue Antigens, Volume 70, Number 4, October 2007 , pp. 294-300(7)

Publisher: Blackwell Publishing

Analysis of the HFE gene (C282Y, H63D and S65C) mutations in a general Chinese Han population

Authors: Lin; Yan; Xu; Zhu; Zhou

Source: Tissue Antigens, Volume 70, Number 3, September 2007 , pp. 252-255(4)

Publisher: Blackwell Publishing

An open population screening study for HFE gene major mutations proves the low prevalence of C282Y mutation in Central Italy

Authors: FLOREANI, A.; RIZZOTTO, E. ROSA; BASSO, D.; NAVAGLIA, F.; ZANINOTTO, M.; PETRIDIS, I.; DI ANDREA, O.; TESTA, R.; MARRA, M.; BALDO, V.; CHIARAMONTE, M.

Source: Alimentary Pharmacology & Therapeutics, Volume 26, Number 4, August 2007 , pp. 577-586(10)

Publisher: Blackwell Publishing

HFE C282Y gene variant is a risk factor for the progression to decompensated liver disease in chronic viral hepatitis C subjects in the Czech population

Authors: Pácal, Lukáš; Husa, Petr; Znojil, Vladimír; Kan˘ková, Kater˘ina

Source: Hepatology Research, Volume 37, Number 9, September 2007 , pp. 740-747(8)

Publisher: Blackwell Publishing

Status of HFE mutation in thalassemia syndromes in north India

Authors: Agarwal, Sarita; Tewari, D.; Arya, V.; Moorchung, N.; Tripathi, R.; Chaudhuri, G.; Pradhan, M.

Source: Annals of Hematology, Volume 86, Number 7, July 2007 , pp. 483-485(3)

Publisher: Springer

Hemochromatosis gene mutations, liver function tests and iron status in alcohol-dependent patients admitted for detoxification

Authors: Robinson, Geoffrey; Narasimhan, Seshasayee; Weatherall, Mark; Beasley, Richard

Source: Journal of Gastroenterology and Hepatology, Volume 22, Number 6, June 2007 , pp. 852-854(3)

Publisher: Blackwell Publishing

A novel homozygous frameshift deletion c.471del of HFE associated with hemochromatosis

Authors: Cukjati; Koren; Čurin Šerbec,; Vidan-Jeras; Rupreht

Source: Clinical Genetics, Volume 71, Number 4, April 2007 , pp. 350-353(4)

Publisher: Blackwell Publishing

Prevalence of C282Y, H63D and S65C mutations of the hemochromatosis (HFE) gene in a population from southeastern Spain (Murcia Region)

Source: Clinical Genetics, Volume 71, Number 1, January 2007 , pp. 97-98(2)

Publisher: Blackwell Publishing

H63D homozygotes with hyperferritinaemia: is this genotype, the primary cause of iron overload?

Authors: de Diego, Carles; Opazo, Sonsoles; Murga, Maria J.; Martínez-Castro, Pedro

Source: European Journal of Haematology, Volume 78, Number 1, January 2007 , pp. 66-71(6)

Publisher: Blackwell Publishing