Human Genome Epidemiology Literature Finder
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Records 1 - 25 (of 25 Records) |
| Query Trace: Porphyria Cutanea Tarda and HFE[original query] |
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| C282Y and H63D mutation of the hemochromatosis gene in German porphyria cutanea tarda patients. Virchows Archiv : an international journal of pathology 2001 Jul 439 (1): 1-5. Tannapfel A, Stölzel U, Köstler E, Melz S, Richter M, Keim V, Schuppan D, Wittekind |
| HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: a prospective study of 36 cases from southern France. The British journal of dermatology 2001 Mar 144 (3): 533-9. Dereure O, Aguilar-Martinez P, Bessis D, Perney P, Vallat C, Guillot B, Blanc F, Guilhou J |
| Porphyria cutanea tarda in Brazilian patients: association with hemochromatosis C282Y mutation and hepatitis C virus infection. The American journal of gastroenterology 2000 Dec 95 (12): 3516-21. Martinelli A L, Zago M A, Roselino A M, Filho A B, Villanova M G, Secaf M, Tavella M H, Ramalho L N, Zucoloto S, Franco R |
| Hemochromatosis (HFE) and transferrin receptor-1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT). Cellular and molecular biology (Noisy-le-Grand, France) 2002 Feb 48 (1): 33-41. Lamoril Jér?me, Andant Christophe, Gouya Laurent, Malonova Eva, Grandchamp Bernard, Martásek Pavel, Deybac Jean-Charles, Puy Her |
| Porphyria cutanea tarda: multiplicity of risk factors including HFE mutations, hepatitis C, and inherited uroporphyrinogen decarboxylase deficiency. Digestive diseases and sciences 2002 Feb 47 (2): 419-26. Egger Norman G, Goeger Douglas E, Payne Deborah A, Miskovsky Emil P, Weinman Steven A, Anderson Karl |
| Porphyria cutanea tarda, C282Y, H63D and S65C HFE gene mutations and hepatitis C infection: a study from southern France. Dermatology (Basel, Switzerland) 2003 206 (3): 212-6. Chiavérini Christine, Halimi Gilles, Ouzan Denis, Halfon Philippe, Ortonne Jean-Paul, Lacour Jean-Philip |
| Porphyria cutanea tarda: the etiological importance of mutations in the HFE gene and viral infection is population-dependent. Cellular and molecular biology (Noisy-le-Grand, France) 2002 Dec 48 (8): 853-9. Hift R J, Corrigall A V, Hancock V, Kannemeyer J, Kirsch R E, Meissner P |
| Hemochromatosis (HFE) gene mutations and response to chloroquine in porphyria cutanea tarda. Archives of dermatology 2003 Mar 139 (3): 309-13. Stölzel Ulrich, Köstler Erich, Schuppan Detlef, Richter Matthias, Wollina Uwe, Doss Manfred O, Wittekind Christian, Tannapfel Andr |
| Clinical relevance of hemochromatosis-related HFE C282Y/H63D gene mutations in patients on chronic dialysis. Clinical nephrology 2002 Dec 58 (6): 438-44. Canavese C, Bergamo D, Barbieri S, Timbaldi M, Thea A, Martina G, Damiani D, Fenoglio R, Donati-Marella B, Priolo |
| Hemochromatosis (HFE) gene mutations and hepatitis C virus infection as risk factors for porphyria cutanea tarda in Hungarian patients. Liver international : official journal of the International Association for the Study of the Liver 2004 Feb 24 (1): 16-20. Nagy Z, Kószó F, Pár A, Emri G, Horkay I, Horányi M, Karádi O, Rumi G, Morvay M, Varga V, Dobozy A, Mózsik G |
| Human leukocyte antigen haplotypes and HFE mutations in Spanish hereditary hemochromatosis and sporadic porphyria cutanea tarda. Journal of gastroenterology and hepatology 2005 Mar 20 (3): 456-62. Gonzalez-Hevilla Mario, de Salamanca Rafael E, Morales Pablo, Martínez-Laso Jorge, Fontanellas Antonio, Castro Maria José, Rojo Ricardo, Moscoso Juan, Zamora Jorge, Serrano-Vela Juan Ignacio, Arnaiz-Villena Anton |
| [Mutations of hemochromatosis gene in volunteer blood donors and Chilean porphyria cutanea tarda patients]. Medicina 2006 66 (5): 421-6. Wolff Carlos F, Armas Rodolfo M, Frank Jorge, Poblete Pamela |
| The prevalence of HFE C282Y gene mutation is increased in Spanish patients with porphyria cutanea tarda without hepatitis C virus infection. Journal of the European Academy of Dermatology and Venereology : JEADV 2006 Nov 20 (10): 1201-6. Toll A, Celis R, Ozalla M D, Bruguera M, Herrero C, Ercilla M |
| Hemochromatosis gene sequence deviations in German patients with porphyria cutanea tarda. Physiological research / Academia Scientiarum Bohemoslovaca 2006 55 Suppl 2 (): S75-83. Frank J, Poblete-Gutiérrez P, Weiskirchen R, Gressner O, Merk H F, Lammert |
| The HLA-A1-B8 haplotype hitchhiking with the hemochromatosis mutation: does it affect the phenotype? European journal of haematology 2007 Nov 79 (5): 429-34. Olsson K Sigvard, Ritter Bernd, Hansson Norbe |
| Down-regulation of hepcidin in porphyria cutanea tarda. Blood 2008 Dec 112 (12): 4723-8. Ajioka Richard S, Phillips John D, Weiss Robert B, Dunn Diane M, Smit Maria W, Proll Sean C, Katze Michael G, Kushner James |
| High prevalence of HFE gene mutations in patients with porphyria cutanea tarda in the Czech Republic. The British journal of dermatology 2008 Sep 159 (3): 585-90. Kratka K, Dostalikova-Cimburova M, Michalikova H, Stransky J, Vranova J, Horak |
| Porphyria cutanea tarda, hepatitis C, uroporphyrinogen decarboxylase and mutations of HFE gene. A case-control study. Dermatology (Basel, Switzerland) 2009 218 (1): 15-21. Cribier Bernard, Chiaverini Christine, Dali-Youcef Nassim, Schmitt Michèle, Grima Michèle, Hirth Christine, Lacour Jean-Philippe, Chosidow Olivi |
| [Porphyria cutanea tarda. An analysis of HFE gene mutations, hepatitis viruses, alcohol intake, and other risk factors in 54 patients from Guipúzcoa, Basque Country, Spain]. Revista española de enfermedades digestivas : organo oficial de la Sociedad Española de Patología Digestiva 2008 Dec 100 (12): 774-8. Castiella A, Zapata E, de Juan M D, Múgica F, Barrio J, Otazua P, Arriola J A, Cosme A, Elosegui E, Fernández J, Zubiaurre L, Alzate L F, Utrilla E, |
| Associations among behavior-related susceptibility factors in porphyria cutanea tarda. Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 2010 Mar 8 (3): 297-302, 302.e1. Jalil Sajid, Grady James J, Lee Chul, Anderson Karl |
| Significance of H63D homozygosity in a Basque population with hemochromatosis. Journal of gastroenterology and hepatology 2010 Jul 25 (7): 1295-8. Castiella Agustin, Zapata Eva, de Juan Maria Dolores, Otazua Pedro, Fernandez Javier, Zubiaurre Leire, Arriola Jose A, |
| CYP1A2*1F and GSTM1 alleles are associated with susceptibility to porphyria cutanea tarda. Molecular medicine (Cambridge, Mass.) 0 17 (3-4): 241-7. Wickliffe Jeffrey K, Abdel-Rahman Sherif Z, Lee Chul, Kormos-Hallberg Csilla, Sood Gagan, Rondelli Catherine M, Grady James J, Desnick Robert J, Anderson Karl |
| Precipitating factors of porphyria cutanea tarda in Brazil with emphasis on hemochromatosis gene (HFE) mutations. Study of 60 patients. Anais brasileiros de dermatologia 0 88 (4): 530-40. Vieira Fatima Mendonça Jorge, Nakhle Maria Cristina, Abrantes-Lemos Clarice Pires, Cançado Eduardo Luiz Rachid, Reis Vitor Manoel Silva d |
| The D519G Polymorphism of Glyceronephosphate O-Acyltransferase Is a Risk Factor for Familial Porphyria Cutanea Tarda. PloS one 0 11 (9): e0163322. Farrell Colin P, Overbey Jessica R, Naik Hetanshi, Nance Danielle, McLaren Gordon D, McLaren Christine E, Zhou Luming, Desnick Robert J, Parker Charles J, Phillips John |
| SLC40A1 and CP single nucleotide polymorphisms in porphyria cutanea tarda patients of mixed ancestry. Annals of human genetics 2018 May . Succi Isabella Brasil, Pôrto Luís Cristóvão, Silva Dayse, Nascimento Adriana, Neto Ronald Costa, Fonseca João Carl |
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