- ►annals.org HB El-Serag, JM Inadomi, KV Kowdley - Annals of internal medicine, 2000 - Am Coll Physicians Add to CiteULike Add to Complore Add to Connotea Add to Del.icio.us Add to Digg
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Background: Screening for hereditary hemochromatosis is traditionally done ... Cited by 74 - Related articles - BL Direct - All 5 versions
PC Adams, AE Kertesz, LS Valberg - Hepatology, 1995 - interscience.wiley.com Although hereditary hemochromatosis is an autosomal recessive disease, most
homozygotes are concerned with the genetic implications for their children. The
optimal age for testing children and the cost implications of screening ... Cited by 48 - Related articles - BL Direct - All 3 versions
A Åsberg, S Tretli, K Hveem, KS Bjerve - Scandinavian journal of gastroenterology, 2002 - informahealthcare.com AÊsberg A, Tretli S, Hveem K, Bjerve KS. Benefit of population-base d screening
for phenotypic hemo- chromatosis in young men. Scand J Gastroenterol
2002;37;1212–1219. Background: Hereditary hemochromatosi s (HH) is a ... Cited by 24 - Related articles - BL Direct - All 7 versions
AG Mainous, DE King, WS Pearson, DR Garr - Journal of family practice, 2002 - jfponline.com From the Department of Family Medicine, Medical University of South Carolina,
Charleston, SC. This study was funded in part through grant 1D12HP00023-01 from
the Health Resources and Services Administration. The authors report no ... Cited by 13 - Related articles - Cached - BL Direct - All 5 versions
- ►nih.gov M Krawczak, DN Cooper, J Schmidtke - The American Journal of Human Genetics, 2001 - Elsevier Screening for genetic variants that predispose individuals or their offspring to
disease may be performed at the general population level or may instead be
targeted at the relatives of previously identified carriers. The latter ... Cited by 42 - Related articles - BL Direct - All 7 versions
- ►bmj.com M Bhavnani, D Lloyd, A Bhattacharyya, J … - British Medical Journal, 2000 - gut.bmj.com In clinical studies of patients with GH, abnormal serum aminotransferase
activity has been found in 65-75% of cases. 5 6 George and colleagues 7 found
abnormalities of serum aminotransferase in 48% of patients with GH ... Cited by 36 - Related articles - BL Direct - All 7 versions
M Delatycki, K Allen, R Williamson - The Lancet, 2002 - Elsevier Most cases of haemochromatosis, a genetically inherited iron-overload disease,
are due to homozygosity for one mutation, C282Y, in the HFE gene. 2 People at
high risk of developing the disease (up to one per 200 population in ... Cited by 32 - Related articles - BL Direct - All 5 versions
S Dubois, KV Kowdley - Alimentary Pharmacology and Therapeutics, 2004 - interscience.wiley.com Patients with hereditary haemochromatosis are at risk for significant morbidity
from iron overload as well as reduced life-expectancy once cirrhosis is
established. Although inexpensive, sensitive screening tests and effective ... Cited by 25 - Related articles - BL Direct - All 9 versions
[CITATION] AGA Medical Position Statement: Evaluation of Liver Chemistry Tests
