Variant Haemoglobins: A Guide to Identification

Variant Haemoglobins: A Guide to Identification

Volumn , Issue , 2010, Pages

  Bain, Barbara J ^a   Wild, Barbara J ^b   Stephens, Adrian D ^b   Phelan, Lorraine A ^c  

^a ST MARY S HOSPITAL   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON HOSPITALS   (United Kingdom)

^c IMPERIAL COLLEGE HEALTHCARE NHS TRUST   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 80051668479     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9781444328318     Document Type: Book

References (43)

1. Kunkel HG and Wallenius G (1955) New haemoglobin in normal adult blood. Science, 122,288.
2. Lehmann H (1957) News and views: International Society of Hematology, the haemoglobinopathies. Blood, 12,90-92.
3. Kunkel HG and Bearn AG (1957) Minor hemoglobin components of normal human blood. Fed Proc, 16,760-762.
4. Allen DW, Schroeder WA and Balog J (1958) Observations on the chromatographic heterogeneity of normal adult and fetal hemoglobin: a study of the effect of crystallization and chromatography on the heterogeneity and isoleucine content. J Amer Chem Soc, 80,1628-1634.
5. Clegg MD and Schroeder WA (1959) The chromatographic study of normal adult human hemoglobin including a comparison of hemoglobin from normal and phenylketonuric individuals. J Amer Chem Soc, 81,6065-6069.
6. Huisman THJ and Horton BF (1965) Studies of the heterogeneity of hemoglobin VII: chromatographic and electrophoretic investigations of minor hemo globin fractions present in normal and in vitro modified red blood cell hemolysates. J Chromat, 18,116-123.
7. Schnek AG and Schroeder WA (1960) The relation between the minor components of whole normal human adult hemoglobin as isolated by chromatography and starch block electrophoresis. J Amer Chem Soc, 83,1472-1478.
8. Bain BJ (2006) Haemoglobinopathy Diagnosis, 2nd edn. Blackwell Publishing, Oxford.
9. Globin Gene Server. http://globin.cse.psu.edu/. Electronic database hosted by Pennsylvania State University, USA and McMaster University, Canada (accessed 1 January 2010).
10. Steinberg MH, Forget BG, Higgs DR and Weatherall DJ (2009) Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management, 2nd edn. Cambridge University Press, Cambridge.
11. Weatherall DJ and Clegg JB (2001) The Thalassaemia Syndromes, 4th edn. Blackwell Science, Oxford.
12. Wild BJ and Bain BJ (2006) Investigation of abnormal haemoglobins and thalassaemia. In Dacie and Lewis Practical Haematology, Lewis SM, Bain BJ and Bates I (eds). Churchill Livingstone, Philadelphia, pp. 217-310.
13. Bain BJ (2006) Haemoglobinopathy Diagnosis, 2nd edn. Blackwell Publishing, Oxford.
14. Steinberg MH, Forget BG, Nagel RL, Weatherall DJ and Higgs DR (2009) Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management. Cambridge University Press, Cambridge.
15. Weatherall DJ and Clegg JB (2001) The Thalassaemia Syndromes, 4th edn. Blackwell Science, Oxford.
16. Globin Gene Server. http://globin.cse.psu.edu/. Electronic database hosted by Pennsylvania State University, USA and McMaster University, Canada (accessed 1 January 2010).
17. Lafferty JD, McFarlane AG and Chui DHK (2002) Evaluation of a dual haemoglobin A 2 /A 1c quantitation kit on the Bio-Rad Variant II automated hemoglobin analyzer. Arch Pathol Lab Med, 126,1494-1500.
18. Millar CM, Phelan L and Bain BJ (2002) Diabetes mellitus diagnosed following request for haemoglobin electrophoresis. Br J Haematol, 117,778.
19. Grey V, Wilkinson M, Phelan L, Hughes C and Bain BJ (2007) Inaccuracy of high-performance liquid chromatography estimation of haemoglobin F in the presence of increased haemoglobin A 1c. Clin Lab Haematol, 29,42-44.
20. Chen D, Crimmins DL, Hsu FF, Lindberg FP and Scott MG (1998) Hemoglobin Raleigh as the cause of a falsely increased hemoglobin A 1C in an automated ion-exchange HPLC method. Clin Chem, 44,1296-1301.
21. Robinson AR, Robson M, Harrison AP and Zuelzer WW (1957) A new technique for differentiation of hemoglobin. J Lab Clin Med, 50,745-752.
22. Schneider RG and Barwick RC (1978) Measuring relative electrophoretic mobilities of mutant hemoglobins and globin chains. Hemoglobin, 2,417-435.
23. Lehmann H and Huntsman RG (1966) Man ' s Haemoglobins, 2nd edn. North Holland Publishing, Amsterdam, pp. 411-412.
24. National Institute for Biological Standards and Control. www.nibsc.ac.uk/ (accessed 1 January 2010).
25. Worthington D on behalf of the Laborarory Subgroup (2009) Sickle Cell and Thalassaemia Handbook for Laboratories. NHS Screening Programme, London. http://sct.screening.nhs.uk./
26. Wild BJ, Green BN, Cooper EK, Lalloz MR, Erten S, Stephens AD and Layton DM (2001) Rapid identification of hemoglobin variants by electrospray ionization mass spectrometry. Blood Cells Mol Dis, 27,691-704.
27. Wild BJ, Green BN and Stephens AD (2004) The potential of electrospray ionization mass spectrometry for the diagnosis of hemoglobin variants found in newborn screening. Blood Cells Mol Dis, 33,308-317.
28. Daniel YA, Turner C, Haynes RM, Hunt BJ and Dalton RN (2005) Rapid and specific detection of clinically significant haemoglobinopathies using electrospray mass spectrometry-mass spectrometry. Br J Haematol, 130,635-643.
29. Routy JP, Monte M, Beaulieu R, Toma E, St-Pierre L and Dumont M (1993) Increase of hemoglobin A2 in human immunodeficiency virus-1-infected patients treated with zidovudine. Am J Hematol, 43,86-90.
30. Wilkinson MJ, Bain BJ, Phelan L and Benzie A (2007) Increased haemoglobin A 2 percentage in HIV infection: disease or treatment? AIDS, 14,37-42.
31. Bain BJ (2006) Haemoglobinopathy Diagnosis, 2nd edn, Blackwell Publishing, Oxford.
32. Levere RD, Lichtman HC and Levine J (1964) Effect of iron deficiency anaemia on the metabolism of the heterogenic haemoglobins in sickle cell trait, Nature, 202,499-501.
33. Bain BJ (1993) Blood film features of sickle cell-haemoglobin C disease. Brit J Haematol, 83,516-518.
34. Ryan K, Bain BJ, Worthington D, James J, Plews D, Mason A et al.; British Committee for Standards in Haematology (2010) Significant haemoglobinopathies: guidelines for screening and diagnosis. Br J Haematol, 149,35-49. www.bcshguidelines.com/ pdf/significant_final_sept09.pdf (accessed 18 May 2010).
35. Bain BJ, Amos RJ, Bareford D, Chapman C, Davies SC, Old JM and Wild BJ, on behalf of the General Haematology Task Force of the British Committee for Standards in Haematology (2001) Antenatal testing for haemoglobinopathies. Br J Haematol, 113,1083-1084.
36. Worthington D on behalf of the Laborarory Subgroup (2009) Sickle Cell and Thalassaemia Handbook for Laboratories. NHS Screening Programme, London. http://sct.screening.nhs.uk./
37. Galanello R, Ruggeri R, Addis M, Paglietti E and Cao A (1981) Hemoglobin A2 in beta-thalassemia heterozygotes. Hemoglobin, 5,613-618.
38. Abdel-Gadir D, Phelan L and Bain BJ (2007) Haemoglobin A2' and its significance in β thalassaemia diagnosis. Int J Lab Hematol, 31,315-319.
39. Rugless MJ, Fisher CA, Stephens AD, Amos RJ, Mohammed T and Old JM (2006) Hb Bart ' s in cord blood: an accurate indicator of α-thalassemia. Hemoglobin, 30,57-62.
40. Fucharoen S, Winichagoon P, Wisedpanichkij R, Sae-Ngow B, Sriphanich R, Oncoung W et al. (1998) Prenatal and postnatal diagnosis of thalassemias and hemoglobinopathies by HPLC. Clin Chem, 44,740-748.
41. Bowden DK, Hill AV, Higgs DR, Oppenheimer SJ, Weatherall DJ and Clegg JB (1987) Different hematologic phenotypes are associated with the leftward (- α 4.2) and rightward (- α 3.7) α +-thalassemia deletions. J Clin Invest, 79,39-43.
42. Steinberg MH (1991) The interactions of β-thalassaemia with hemoglobinopathies. Hematol/ Oncol Clinics North Amer, 5,453-473.
43. Fucharoen S (2001) Hemoglobin E disorders. In: Steinberg MH, Forget BG, Higgs DR and Nagel RL, eds. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management. Cambridge University Press, Cambridge, pp. 1139-1154.