Search Results

Does Oxidative Stress Modulate Left Ventricular Diastolic Function in Asymptomatic Subjects with Hereditary Hemochromatosis?

Authors: Shizukuda, Yukitaka; Bolan, Charles D.; Tripodi, Dorothy J.; Sachdev, Vandana; Nguyen, Tammy T.; Botello, Gilberto; Yau, Yu-Ying; Sidenko, Stanislav; Inez, Ernst; Ali, Mir I.; Waclawiw, Myron A.; Leitman, Susan F.; Rosing, Douglas R.

Source: Echocardiography - Jnl Cardiovascular Ultrasound & Allied Techniques, Volume 26, Number 10, November 2009 , pp. 1153-1158(6)

Publisher: Blackwell Publishing

The global burden of iron overload

Authors: Wood, Marnie; Skoien, Richard; Powell, Lawrie

Source: Hepatology International, Volume 3, Number 3, September 2009 , pp. 434-444(11)

Publisher: Springer

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

Iron deficiency and frequency of HFE C282Y gene mutation in Brazilian blood donors

Authors: Terada, C. T.; Santos, P. C. J. L.; Cançado, R. D.; Rostelato, S.; Lopreato, F. R.; Chiattone, C. S.; Guerra-Shinohara, E. M.

Source: Transfusion Medicine, Volume 19, Number 5, October 2009 , pp. 245-251(7)

Publisher: Blackwell Publishing

A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis

Authors: Constantine, Clare C.; Anderson, Greg J.; Vulpe, Chris D.; McLaren, Christine E.; Bahlo, Melanie; Yeap, Heng Lin; Gertig, Dorota M.; Osborne, Nicholas J.; Bertalli, Nadine A.; Beckman, Kenneth B.; Chen, Victoria; Matak, Pavel; McKie, Andrew T.; Delatycki, Martin B.; Olynyk, John K.; English, Dallas R.; Southey, Melissa C.; Giles, Graham G.; Hopper, John L.; Allen, Katrina J.; Gurrin, Lyle C.

Source: British Journal of Haematology, Volume 147, Number 1, October 2009 , pp. 140-149(10)

Publisher: Blackwell Publishing

Outcome of liver transplantation in hereditary hemochromatosis

Authors: Dar, Faisal S; Faraj, Walid; Zaman, Muhammad B; Bartlett, Adam; Bomford, Adrian; O'Sullivan, Adrian; O'Grady, John; Heneghan, Michael; Rela, Mohamed; Heaton, Nigel D

Source: Transplant International, Volume 22, Number 7, July 2009 , pp. 717-724(8)

Publisher: Blackwell Publishing

Elevated mean corpuscular volume in patients with hereditary hemochromatosis

Authors: Mikhail, Sameh; Phatak, Pradyumna

Source: Comparative Clinical Pathology, Volume 18, Number 2, May 2009 , pp. 145-148(4)

Publisher: Springer

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

Serum Transferrin Saturation Increase Is Associated With Decrease of Antibacterial Activity of Serum in Patients With HFE-Related Genetic Hemochromatosis

Authors: Jolivet-Gougeon, Anne; Loréal, Olivier; Ingels, Anne; Danic, Bruno; Ropert, Martine; Bardou-Jacquet, Edouard; Aqodad, Nourdin; Aussant-Bertel, Françoise; Ferec, Claude; Brissot, Pierre

Source: The American Journal of Gastroenterology, Volume 103, Number 10, October 2008 , pp. 2502-2508(7)

Publisher: Blackwell Publishing

Patient-focused outcomes following detection in a hospital-based screening programme for C282Y haemochromatosis

Authors: McCullen; Fletcher; Dimeski; Pink; Powell; Crawford; Hickman

Source: Internal Medicine Journal, Volume 38, Number 8, August 2008 , pp. 651-656(6)

Publisher: Blackwell Publishing

Serum hepcidin levels are innately low in HFE-related haemochromatosis but differ between C282Y-homozygotes with elevated and normal ferritin levels

Authors: van Dijk, Boukje A. C.; Laarakkers, Coby M. M.; Klaver, Siem M.; Jacobs, Esther M. G.; van Tits, Lambertus J. H.; Janssen, Mirian C. H.; Swinkels, Dorine W.

Source: British Journal of Haematology, Volume 142, Number 6, September 2008 , pp. 979-985(7)

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

Modifying factors of the HFE hemochromatosis phenotype

Authors: Deugnier, Yves; Mosser, Jean

Source: Expert Review of Gastroenterology and Hepatology, Volume 2, Number 4, August 2008 , pp. 531-540(10)

Publisher: Expert Reviews

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

HLA haplotype map of river valley populations with hemochromatosis traced through five centuries in Central Sweden

Authors: Olsson, K. Sigvard; Ritter, Bernd; Hansson, Norbeth; Chowdhury, Ruma R.

Source: European Journal of Haematology, Volume 81, Number 1, July 2008 , pp. 36-46(11)

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

The unfolded protein response in hereditary haemochromatosis

Authors: de Almeida, S.F.; de Sousa, M.

Source: Journal of Cellular and Molecular Medicine, Volume 12, Number 2, April 2008 , pp. 421-434(14)

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