A Qaseem, M Aronson, N Fitterman, V Snow, … - Annals of internal medicine, 2005 - Am Coll Physicians Hereditary hemochromatosis is a genetic disorder of iron metabolism. Diagnosis
of hereditary hemochromatosis is usually based on a combination of various
genetic or phenotypic criteria. Decisions regarding screening are difficult ... Cited by 41 - Related articles - BL Direct - All 9 versions
- ►annals.org [PDF] B Schmitt, RM Golub, R Green - Annals of internal medicine, 2005 - Am Coll Physicians Background: Therapeutic phlebotomy for hereditary hemochro- matosis is
relatively safe and presumably efficacious when offered before cirrhosis
develops, so screening primary care patients is of substantial interest. ... Cited by 38 - Related articles - BL Direct - All 5 versions
- ►annals.org [PDF] EP Whitlock, BA Garlitz, EL Harris, TL Beil, … - Annals of internal medicine, 2006 - Am Coll Physicians Purpose: To conduct a focused systematic review of heredita- ry hemochromatosis
screening relating to 2 USPSTF criteria, the burden of suffering and the
potential effectiveness of a preven- tive intervention, to determine ... Cited by 55 - Related articles - All 6 versions
[CITATION] Hemochromatosis: from phenotype to genotype
A Qaseem, M Aronson, N Fitterman, V Snow, … - meiga.info Hereditary hemochromatosis is a genetic disorder of iron metabolism. Diagnosis
of hereditary hemochromatosis is usually based on a combination of various
genetic or phenotypic criteria. Decisions regarding screening are difficult ... Related articles - View as HTML
- ►hematologylibrary.org J Waalen, VJ Felitti, T Gelbart, E Beutler - Blood, 2008 - bloodjournal.hematologylibrary.org Because the penetrance of HFE hemochromatosis is low, traditional population
screening measuring the transferrin saturation is unlikely to be cost-effective
because the majority of subjects detected neither have clinical disease nor ... Cited by 20 - Related articles - BL Direct - All 5 versions
LW Powell, JL Dixon, GA Ramm, DM Purdie, … - Archives of Internal Medicine, 2006 - Am Med Assoc Background Hemochromatosis in white subjects is mostly due to homozygosity for
the common C282Y substitution in HFE. Although clinical symptoms are preventable
by early detection of the genetic predisposition and prophylactic ... Cited by 72 - Related articles - All 4 versions
EL Harris, CE McLaren, DM Reboussin, VR … - Archives of Internal Medicine, 2007 - Am Med Assoc Results Compared with their white counterparts, Asian men had a 69-ng/mL
(155-pmol/L) higher adjusted mean SF level and a 3% higher TS level (P<.001);
Asian women had 23-ng/mL (52-pmol/L) higher adjusted mean SF level and a 3% ... Cited by 10 - Related articles - BL Direct - All 5 versions
A Del Castillo Rueda, JA López-Herce Cid, J … - Anales de medicina interna(Madrid. 1983), 2002 - cat.inist.fr Hemocromatosis hereditaria. DiagnÓstico clínico: manifestaciones precoces,
procesos relacionados y formas atípicas. A DEL CASTILLO ... Cited by 13 - Related articles
PC Adams, DM Reboussin, JC Barton, RT … - International Journal of Laboratory Hematology, 2008 - interscience.wiley.com Hemochromatosis has often been associated with progressive iron overload, but
the natural history of iron accumulation in untreated C282Y homozygotes has been
reported infrequently. The Hemochromatosis and Iron Overload Screening ... Cited by 1 - Related articles - All 3 versions
