Wednesday, August 20, 2008 - 3:31AM EST

General Interest Articles

1. Reduced exercise capacity in genetic haemochromatosis.

Author
Davidsen ES; Liseth K; Omvik P; Hervig T; Gerdts E;
Institution
Department of Heart Disease, Haukeland University Hospital, University of Bergen, Norway. einar.davidsen@helse-bergen.no
Journal
Eur J Cardiovasc Prev Rehabil. 2007 Jun;14(3):470-5.
Abstract URL
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2. Iron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patients.

Author
McCune CA; Ravine D; Carter K; Jackson HA; Hutton D; Hedderich J; Krawczak M; Worwood M;
Institution
Bristol Royal Infirmary, Malborough St, Bristol BS2 8HW, UK. anne.mccune@ubht.swest.nhs.uk
Journal
Gut. 2006 Apr;55(4):554-62. Epub 2005 Sep 20.
Abstract URL
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3. Screening for hemochromatosis: recommendation statement.

Author
Institution
Journal
Ann Intern Med. 2006 Aug 1;145(3):204-8.
Abstract URL
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4. Reversibility of hepatic fibrosis in treated genetic hemochromatosis: a study of 36 cases.

Author
Falize L; Guillygomarc'h A; Perrin M; Laine F; Guyader D; Brissot P; Turlin B; Deugnier Y;
Institution
Service des Maladies du Foie, CHU Pontchaillou, Rennes, France. ludivine.falize@chu-rennes.fr
Journal
Hepatology. 2006 Aug;44(2):472-7.
Abstract URL
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5. Hemochromatosis and severe iron overload associated with compound heterozygosity for TFR2 R455Q and two novel mutations TFR2 R396X and G792R.

Author
Lee PL; Barton JC;
Institution
Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California, USA.
Journal
Acta Haematol. 2006;115(1-2):102-5.
Abstract URL
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6. Screening for hemochromatosis in asymptomatic subjects with or without a family history.

Author
Powell LW; Dixon JL; Ramm GA; Purdie DM; Lincoln DJ; Anderson GJ; Subramaniam VN; Hewett DG; Searle JW; Fletcher LM; Crawford DH; Rodgers H; Allen KJ; Cavanaugh JA; Bassett ML; Powell LW; Dixon JL; Ramm GA; Purdie DM; Lincoln DJ; Anderson GJ; Subramaniam VN; Hewett DG; Searle JW; Fletcher LM; Crawford DH; Rodgers H; Allen KJ; Cavanaugh JA; Bassett ML;
Institution
Centre for the Advancement of Clinical Research, Royal Brisbane & Women's Hospital, Brisbane, Queensland 4029, Australia. Lawrie.Powell@qimr.edu.au
Journal
Arch Intern Med. 2006 Feb 13;166(3):294-301.
Abstract URL
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7. Neonatal hemochromatosis: long-term experience with favorable outcome.

Author
Grabhorn E; Richter A; Burdelski M; Rogiers X; Ganschow R; Grabhorn E; Richter A; Burdelski M; Rogiers X; Ganschow R;
Institution
Department of Pediatrics, Pediatric Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany. e.grabhorn@uke.uni-hamburg.de
Journal
Pediatrics. 2006 Nov;118(5):2060-5.
Abstract URL
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8. The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis.

Author
Walsh A; Dixon JL; Ramm GA; Hewett DG; Lincoln DJ; Anderson GJ; Subramaniam VN; Dodemaide J; Cavanaugh JA; Bassett ML; Powell LW; Walsh A; Dixon JL; Ramm GA; Hewett DG; Lincoln DJ; Anderson GJ; Subramaniam VN; Dodemaide J; Cavanaugh JA; Bassett ML; Powell LW;
Institution
The Department of Gastroenterology & Hepatology, Royal Brisbane & Women's Hospital, Brisbane, Australia.
Journal
Clin Gastroenterol Hepatol. 2006 Nov;4(11):1403-10. Epub 2006 Sep 18.
Abstract URL
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9. Prevalence of HFE mutations in California newborns.

Author
Hoppe C; Watson RM; Long CM; Lorey F; Robles L; Klitz W; Styles L; Vichinsky E;
Institution
Department of Hematology/Oncology, Children's Hospital and Research Center at Oakland, Oakland, California 94609, USA. CHoppe@mail.cho.org
Journal
Pediatr Hematol Oncol. 2006 Sep;23(6):507-16.
Abstract URL
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10. Screening for hereditary hemochromatosis: a clinical practice guideline from the American College of Physicians.

Author
Qaseem A; Aronson M; Fitterman N; Snow V; Weiss KB; Owens DK;
Institution
American College of Physicians, Philadelphia, Pennsylvania 19106, USA. aqaseem@acponline.org
Journal
Ann Intern Med. 2005 Oct 4;143(7):517-21.
Abstract URL
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