- ►chello.nl [PDF] E Beutler, VJ Felitti, JA Koziol, NJ Ho, T … - The Lancet, 2002 - Elsevier The most common symptoms of haemo-chromatosis, including poor general health,
diabetes, arthropathies, arrhythmias, impotence, and skin pigmentation were no
more prevalent among the 152 identified homozygotes than among the ... Cited by 567 - Related articles - BL Direct - All 13 versions
- ►biost.at [PDF] MJ Khoury, LL McCabe, ERB McCabe - The New England journal of medicine, 2003 - nejm.highwire.org In 1999, the American Academy of Pediatrics and the Health Resources and
Services Administration convened the Newborn Screening Task Force to address the
lack of consistency in the disorders included in screening programs and the ... Cited by 235 - Related articles - BL Direct - All 22 versions
- ►annals.org LW Powell, DK George, SM McDonnell, KV … - Annals of internal medicine, 1998 - Am Coll Physicians If untreated, hemochromatosis can cause serious illness and early death, but the
disease is still substantially under-diagnosed. The cornerstone of screening and
case detection is the measurement of serum transferrin saturation and the ... Cited by 182 - Related articles - BL Direct - All 5 versions
WR Kim, RS Brown Jr, NA Terrault, H El- … - Heart disease - safesecureweb.com Accurate knowledge of the burden of liver disease is essential in formulating
health care policies to prioritize health interventions and research and to
allocate resources accordingly. Liver disease is thought to be relatively ... Cited by 181 - Related articles - View as HTML - BL Direct - All 8 versions
HA Jackson, K Carter, C Darke, MG Guttridge … - British journal of haematology, 2001 - pt.wkhealth.com People with genetic haemochromatosis (GH) accumulate iron from excessive dietary
absorption. In populations of northern European origin, over 90% of patients are
homozygous for the C282Y mutation of the HFE gene. While about 1 in 200 ... Cited by 153 - Related articles - BL Direct - All 7 versions
- ►bmj.com SD Ryder - British Medical Journal, 2003 - gut.bmj.com Cancer care has been the subject of increased scrutiny, with the development of
care guidelines forming a major part of the strategy to reduce cancer related
mortality in the UK. There is a strong suggestion that HCC is a disease ... Cited by 133 - Related articles - All 26 versions
- ►annals.org ME Cogswell, SM McDonnell, MJ Khoury, AL … - Annals of internal medicine, 1998 - Am Coll Physicians Published clinical research offers little evidence to suggest that population
screening for hemochromatosis done by using genetic testing improves clinical
outcomes.Although one recently discovered mutation, C282Y, accounts for 60% ... Cited by 116 - Related articles - BL Direct - All 4 versions
- ►nih.gov [PDF] A Bomford - The Lancet, 2002 - Elsevier After identification of the hereditary haemochromatosis gene HFE, and receipt of
confirmation that most patients with the condition were homozygous for a single,
founder mutation (C282Y), most assumed that C282Y would be a prevalent, ... Cited by 113 - Related articles - All 18 versions
