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Hereditary haemochromatosis: a tale of eight siblings

Authors: Pande, Shrikant D; Ariyaratnam, Rajkumar; Burke, Michael J

Source: Clinical Medicine, Journal of the Royal College of Physicians, Volume 9, Number 6, December 2009 , pp. 624-626(3)

Publisher: Royal College of Physicians

A novel missense mutation in SLC40A1 results in resistance to hepcidin and confirms the existence of two ferroportin-associated iron overload diseases

Authors: Létocart, Emilie; Le Gac, Gérald; Majore, Silvia; Ka, Chandran; Radio, Francesca C.; Gourlaouen, Isabelle; De Bernardo, Carmelilia; Férec, Claude; Grammatico, Paola

Source: British Journal of Haematology, Volume 147, Number 3, November 2009 , pp. 379-385(7)

Publisher: Blackwell Publishing

An update on the epidemiology of calcium pyrophosphate dihydrate crystal deposition disease

Authors: Richette, Pascal; Bardin, Thomas; Doherty, Michael

Source: Rheumatology, Volume 48, Number 7, 4 July 2009 , pp. 711-715(5)

Publisher: Oxford University Press

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

Pathogenesis of chronic pancreatitis: A comprehensive update and a look into the future

Authors: Andersson, Roland; Tingstedt, Bobby; Xia, Jinglin

Source: Scandinavian Journal of Gastroenterology, Volume 44, Number 6, June 2009 , pp. 661-663(3)

Publisher: Informa Healthcare

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

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

Asymptomatic individuals at genetic risk of haemochromatosis take appropriate steps to prevent disease related to iron overload

Authors: Allen, Katrina J.; Nisselle, Amy E.; Collins, Veronica R.; Williamson, Robert; Delatycki, Martin B.

Source: Liver International, Volume 28, Number 3, March 2008 , pp. 363-369(7)

Publisher: Blackwell Publishing

Hereditary iron and copper deposition: Diagnostics, pathogenesis and therapeutics

Authors: Aaseth, Jan; Flaten, Trond Peder; Andersen, Ole

Source: Scandinavian Journal of Gastroenterology, Volume 42, Number 6, 2007 , pp. 673-681(9)

Publisher: Informa Healthcare

Prevalence of hepatic iron overload and association with hepatocellular cancer in end-stage liver disease: results from the National Hemochromatosis Transplant Registry

Authors: Ko, Cynthia; Siddaiah, Narendra; Berger, Jose; Gish, Robert; Brandhagen, David; Sterling, Richard K.; Cotler, Scott J.; Fontana, Robert J.; McCashland, Timothy M.; Han, Steven H. B.; Gordon, Frederic D.; Schilsky, Michael L.; Kowdley, Kris V.

Source: Liver International, Volume 27, Number 10, December 2007 , pp. 1394-1401(8)

Publisher: Blackwell Publishing

All that is hypogonadal in haemochromatosis is not due to iron deposition

Authors: O'Sullivan, E.; McDermott, J.; Walsh, C.

Source: Irish Journal of Medical Science, Volume 176, Number 1, March 2007 , pp. 45-47(3)

Publisher: Springer

Porphyria Cutanea Tarda: Effects and Risk Factors for Hepatotoxicity from High-dose Chloroquine Treatment

Authors: Rossmann-Ringdahl, Ingrid; Olsson, Rolf

Source: Acta Dermato-Venereologica, Volume 87, Number 5, September 2007 , pp. 401-405(5)

Publisher: Medical Journals Limited

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

Dietary iron overload in the African and hepatocellular carcinoma

Authors: Kew, Michael C.; Asare, George A.

Source: Liver International, Volume 27, Number 6, August 2007 , pp. 735-741(7)

Publisher: Blackwell Publishing

Generalized Pruritus Revealing Hereditary Haemochromatosis

Authors: Kluger, Nicolas; Raison-Peyron, Nadia; Rigole, Hélène; Bessis, Didier; Blanc, François; Guillot, Bernard

Source: Acta Dermato-Venereologica, Volume 87, Number 3, May 2007 , pp. 277-277(1)

Publisher: Medical Journals Limited

Hereditary haemochromatosis and blood donation

Author: León de González, G.

Source: ISBT Science Series, Volume 2, Number 1, July 2007 , pp. 12-18(7)

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

Spontaneous bilateral carotid artery dissection and hereditary haemochromatosis: what relationship?

Authors: Gallerini, S.; Morelli, N.; Chiti, A.; Baldacci, F.; Sonnoli, C.; Orlandi, G.; Murri, L.

Source: Neurological Sciences, Volume 27, Number 4, September 2006 , pp. 291-292(2)

Publisher: Springer

Lack of clinical manifestation of hereditary haemochromatosis in South African patients with multiple sclerosis

Authors: Kotze, Maritha; de Villiers, J; Warnich, Louise; Schmidt, Stephen; Carr, Jonathan; Mansvelt, Erna; Fourie, Elba; van Rensburg, Susan

Source: Metabolic Brain Disease, Volume 21, Numbers 2-3, September 2006 , pp. 105-116(12)

Publisher: Springer