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2001 1
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2005 1
2011 1
2012 1
2013 1
2024 0

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Page 1
Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update.
Bolton-Maggs PH, Langer JC, Iolascon A, Tittensor P, King MJ; General Haematology Task Force of the British Committee for Standards in Haematology. Bolton-Maggs PH, et al. Br J Haematol. 2012 Jan;156(1):37-49. doi: 10.1111/j.1365-2141.2011.08921.x. Epub 2011 Nov 5. Br J Haematol. 2012. PMID: 22055020 Free article.
Guideline: the laboratory diagnosis of malaria. General Haematology Task Force of the British Committee for Standards in Haematology.
Bailey JW, Williams J, Bain BJ, Parker-Williams J, Chiodini PL; General Haematology Task Force of the British Committee for Standards in Haematology. Bailey JW, et al. Br J Haematol. 2013 Dec;163(5):573-80. doi: 10.1111/bjh.12572. Epub 2013 Oct 8. Br J Haematol. 2013. PMID: 24219330 Free article.
UK National External Quality Assessment Service surveys indicate continuing problems in malaria diagnosis: inaccurate calculation of parasitaemia or failure to estimate it altogether, difficulty distinguishing Plasmodium vivax from P. ovale, reporting malaria parasites when none …
UK National External Quality Assessment Service surveys indicate continuing problems in malaria diagnosis: inaccurate calculation of parasit …
Guidelines for the diagnosis and management of hereditary spherocytosis.
Bolton-Maggs PH, Stevens RF, Dodd NJ, Lamont G, Tittensor P, King MJ; General Haematology Task Force of the British Committee for Standards in Haematology. Bolton-Maggs PH, et al. Br J Haematol. 2004 Aug;126(4):455-74. doi: 10.1111/j.1365-2141.2004.05052.x. Br J Haematol. 2004. PMID: 15287938 Free article. Review.
It is relatively common in Caucasian populations; most affected individuals have mild or only moderate haemolysis. There is usually a family history, and a typical clinical and laboratory picture so that the diagnosis is often easily made without additional laboratory test …
It is relatively common in Caucasian populations; most affected individuals have mild or only moderate haemolysis. There is usually a fam
Guidelines for the diagnosis, investigation and management of polycythaemia/erythrocytosis.
McMullin MF, Bareford D, Campbell P, Green AR, Harrison C, Hunt B, Oscier D, Polkey MI, Reilly JT, Rosenthal E, Ryan K, Pearson TC, Wilkins B; General Haematology Task Force of the British Committee for Standards in Haematology. McMullin MF, et al. Br J Haematol. 2005 Jul;130(2):174-95. doi: 10.1111/j.1365-2141.2005.05535.x. Br J Haematol. 2005. PMID: 16029446 Free article. No abstract available.
Antenatal testing for haemoglobinopathies.
Bain BJ, Amos RJ, Bareford D, Chapman C, Davies SC, Old JM, Wild BJ; General Haematology Task Force of the British Committee for Standards in Haematology. Bain BJ, et al. Br J Haematol. 2001 Jun;113(4):1083-4. doi: 10.1046/j.1365-2141.2001.02821-8.x. Br J Haematol. 2001. PMID: 11442512 Free article. No abstract available.