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47. Erythrocytapheresis compared with whole blood phlebotomy for the treatment of hereditary haemochromatosis. Sundic T; Hervig T; Hannisdal S; Assmus J; Ulvik RJ; Olaussen RW; Berentsen S Blood Transfus; 2014 Jan; 12 Suppl 1(Suppl 1):s84-9. PubMed ID: 24333062 [TBL] [Abstract][Full Text] [Related]
48. Screening and early detection of hemochromatosis. McDonnell S; Grummer-Strawn L; Trowbridge F Am Fam Physician; 1997 Feb; 55(2):440-2. PubMed ID: 9054215 [No Abstract] [Full Text] [Related]
49. [Preclinical hereditary hemochromatosis--is there an indication for preventive screening?]. Grønbaek KE; Milman N; Skødt V Ugeskr Laeger; 1995 Jul; 157(30):4249-50. PubMed ID: 7653009 [TBL] [Abstract][Full Text] [Related]
50. Laboratory screening procedures and their clinical implications. Well-population screening. Whitby LG Proc R Soc Med; 1968 Aug; 61(8):763-6. PubMed ID: 5673396 [No Abstract] [Full Text] [Related]
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