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There are 7767 results for: content related to: Porphyria cutanea tarda in the B asque C ountry: significance of HFE gene mutations and of external factors

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

    Internal Medicine Journal

    Volume 38, Issue 4, April 2008, Pages: 254–258, S. Neri, 1 D. Pulvirenti, 1 S. Signorelli, 1 L. Ignaccolo, 1 A. Tsami, 1 B. Mauceri, 1 M. Misseri, 1 D. Interlandi, 1 N. Cutuli and 2 P. Castellino 1

    Version of Record online : 3 OCT 2007, DOI: 10.1111/j.1445-5994.2007.01474.x

  2. Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant conditions and the calculation of recurrence risks for their offspring. I. Autosomal dominant genes.

    American Journal of Medical Genetics

    Volume 95, Issue 1, 6 November 2000, Pages: 43–48, P.A. Otto and Sylvia R.P. Maestrelli

    Version of Record online : 7 NOV 2000, DOI: 10.1002/1096-8628(20001106)95:1<43::AID-AJMG9>3.0.CO;2-5

  3. Two novel mutations in the SLC40A1 and HFE genes implicated in iron overload in a Spanish man

    European Journal of Haematology

    Volume 86, Issue 3, March 2011, Pages: 260–264, Alejandro del-Castillo-Rueda, María-Isabel Moreno-Carralero, Luis-Antonio Álvarez-Sala-Walther, Nuria Cuadrado-Grande, Rafael Enríquez-de-Salamanca, Manuel Méndez and María-Josefa Morán-Jiménez

    Version of Record online : 11 JAN 2011, DOI: 10.1111/j.1600-0609.2010.01565.x

  4. HFE gene mutation is a risk factor for tissue iron accumulation in hemodialysis patients

    Hemodialysis International

    Volume 21, Issue 3, July 2017, Pages: 359–366, Ercan Turkmen, Tolga Yildirim, Rahmi Yilmaz, Tuncay Hazirolan, Gonca Eldem, Engin Yilmaz, Aysun Aybal Kutlugun, Mahmut Altindal and Bulent Altun

    Version of Record online : 23 JAN 2017, DOI: 10.1111/hdi.12537

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    Variation in breast cancer risk of heterozygotes for ataxia-telangiectasia according to environmental factors

    International Journal of Cancer

    Volume 99, Issue 4, 1 June 2002, Pages: 619–623, Béatrice Geoffroy-Perez, Nicolas Janin, Katia Ossian, Anthony Laugé, Dominique Stoppa-Lyonnet and Nadine Andrieu

    Version of Record online : 29 MAR 2002, DOI: 10.1002/ijc.10367

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    2009 International BioIron Society Meeting

    American Journal of Hematology

    Volume 84, Issue 8, August 2009, Pages: E236–E375,

    Version of Record online : 17 JUN 2009, DOI: 10.1002/ajh.21464

  7. Significance of H63D homozygosity in a Basque population with hemochromatosis

    Journal of Gastroenterology and Hepatology

    Volume 25, Issue 7, July 2010, Pages: 1295–1298, Agustin Castiella, Eva Zapata, Maria Dolores De Juan, Pedro Otazua, Javier Fernandez, Leire Zubiaurre and Jose A. Arriola

    Version of Record online : 23 JUN 2010, DOI: 10.1111/j.1440-1746.2010.06247.x

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    Hepatic iron overload in patients with chronic viral hepatitis: Role of HFE gene mutations


    Volume 28, Issue 4, October 1998, Pages: 1105–1109, Dr. Alberto Piperno, Anna Vergani, Ida Malosio, Laura Parma, Laura Fossati, Alessandra Ricci, Giorgio Bovo, Giuseppe Boari and Giuseppe Mancia

    Version of Record online : 30 DEC 2003, DOI: 10.1002/hep.510280427

  9. Hereditary hyperferritinemia cataract syndrome in four patients with mutations in the IRE of the FTL gene

    Clinical Genetics

    Volume 83, Issue 5, May 2013, Pages: 491–493, J Muñoz-Muñoz, N Cuadrado-Grande, M-I Moreno-Carralero, B Hoyos-Sanabria, A Manubes-Guarch, A-F González, P Tejada-Palacios, A del-Castillo-Rueda and M-J Morán-Jiménez

    Version of Record online : 13 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01934.x

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    Lower serum hepcidin and greater parenchymal iron in nonalcoholic fatty liver disease patients with C282Y HFE mutations


    Volume 56, Issue 5, November 2012, Pages: 1730–1740, James E. Nelson, Elizabeth M. Brunt, Kris V. Kowdley and for the Nonalcoholic Steatohepatitis Clinical Research Network

    Version of Record online : 20 SEP 2012, DOI: 10.1002/hep.25856

  11. Analysis of HFE mutations and non-HFE gene mutations (TFR2 and SLC40A1) in patients with phenotypic hemochromatosis from the basque country

    International Journal of Laboratory Hematology

    Volume 38, Issue 1, February 2016, Pages: e5–e7, A. Castiella, E. Zapata, M. D. De Juan, L. Zubiaurre, A. Iribarren, P. Otazua, J. Fernandez, L. Aragón, O. Zuriarrain and A. Gorostidi

    Version of Record online : 7 NOV 2015, DOI: 10.1111/ijlh.12444

  12. Non conventional mutations associated with myeloproliferative disorders are absent in splanchnic venous thrombosis cases

    Liver International

    Volume 32, Issue 10, November 2012, Pages: 1596–1597, Anshul Jadli, Bipin Kulkarni, Kanjaksha Ghosh and Shrimati Shetty

    Version of Record online : 23 JUL 2012, DOI: 10.1111/j.1478-3231.2012.02851.x

  13. The molecular basis of low activity levels of coagulation factor VII: a Brazilian cohort


    Volume 21, Issue 5, September 2015, Pages: 670–680, F.Y. Rabelo, L. L. Jardim, M. B. Landau, T. Gadelha, M. F. B. Corrêa, I.F.M. Pereira and S. M. Rezende

    Version of Record online : 31 MAR 2015, DOI: 10.1111/hae.12645

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    Risk of obstetric and thromboembolic complications in family members of women with previous adverse obstetric outcomes carrying common inherited thombophilias

    Journal of Thrombosis and Haemostasis

    Volume 10, Issue 2, February 2012, Pages: 223–228, M. VILLANI, G. L. TISCIA, M. MARGAGLIONE, D. COLAIZZO, L. FISCHETTI, P. VERGURA and E. GRANDONE

    Version of Record online : 2 FEB 2012, DOI: 10.1111/j.1538-7836.2011.04583.x

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    Vol. 10, Issue 6, 1203–1204, Version of Record online: 31 MAY 2012

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    Heterozygous Hfe gene deletion leads to impaired glucose homeostasis, but not liver injury in mice fed a high-calorie diet

    Physiological Reports

    Volume 4, Issue 12, June 2016, Laurence Britton, Lesley Jaskowski, Kim Bridle, Nishreen Santrampurwala, Janske Reiling, Nick Musgrave, V. Nathan Subramaniam and Darrell Crawford

    Version of Record online : 28 JUN 2016, DOI: 10.14814/phy2.12837

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

    British Journal of Dermatology

    Volume 159, Issue 3, September 2008, Pages: 585–590, K. Kratka, M. Dostalikova-Cimburova, H. Michalikova, J. Stransky, J. Vranova and J. Horak

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1365-2133.2008.08693.x

  17. HFE codon 63/282 (H63D/C282Y) dimorphism in German patients with genetic hemochromatosis

    Tissue Antigens

    Volume 51, Issue 3, March 1998, Pages: 270–275, R. Gottschalk, C. Seidl, T. Löffler, E. Seifried, D. Hoelzer and J.P. Kaltwasser

    Version of Record online : 30 SEP 2008, DOI: 10.1111/j.1399-0039.1998.tb03101.x

  18. Effects of HFE gene mutations and alcohol on iron status, liver biochemistry and morbidity

    Journal of Gastroenterology and Hepatology


    Version of Record online : 16 JUN 2005, DOI: 10.1111/j.1440-1746.2005.03967.x

  19. Single strand conformational polymorphism analysis of human CD1 genes in different ethnic groups

    Tissue Antigens

    Volume 53, Issue 6, June 1999, Pages: 545–550, M. Oteo, J.F. Parra, I. Mirones, L.I. Giménez, F. Setién and E. Martínez-Naves

    Version of Record online : 5 JAN 2002, DOI: 10.1034/j.1399-0039.1999.530604.x

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    Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age

    International Journal of Cancer

    Volume 125, Issue 1, 1 July 2009, Pages: 78–83, Zumin Shi, Daniel Johnstone, Bente A. Talseth-Palmer, Tiffany-Jane Evans, Allan D. Spigelman, Claire Groombridge, Elizabeth A. Milward, John K. Olynyk, Janina Suchy, Grzegorz Kurzawski, Jan Lubinski and Rodney J. Scott

    Version of Record online : 3 FEB 2009, DOI: 10.1002/ijc.24304