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Volumn 125, Issue 3, 2011, Pages 136-140

Reliability of EMA binding test in the diagnosis of hereditary spherocytosis in Italian patients

Author keywords

[No Author keywords available]

Indexed keywords

ANAZOLENE SODIUM; EOSIN 5' MALEIMIDE; MALEIMIDE; SPECTRIN; UNCLASSIFIED DRUG;

EID: 78649776046     PISSN: 00015792     EISSN: None     Source Type: Journal    
DOI: 10.1159/000322253     Document Type: Article
Times cited : (13)

References (16)
  • 3
    • 0016121645 scopus 로고
    • Glicerol lysis time of incubated erytrocytes in the diagnosis of hereditary spherocytosis
    • Gottfried EL, Robertson NA: Glicerol lysis time of incubated erytrocytes in the diagnosis of hereditary spherocytosis. J Lab Clin Med 1974; 84: 746-751.
    • (1974) J. Lab. Clin. Med. , vol.84 , pp. 746-751
    • Gottfried, E.L.1    Robertson, N.A.2
  • 4
    • 0018934120 scopus 로고
    • Acidified glycerol lysis test: A screening test for spherocytosis
    • Zanella A, Izzo C, Rebulla P, Zanuso F, Perroni L, Sirchia G: Acidified glycerol lysis test: a screening test for spherocytosis. Brit J Haematol 1980; 45: 481-486. (Pubitemid 10034100)
    • (1980) British Journal of Haematology , vol.45 , Issue.3 , pp. 481-486
    • Zanella, A.1    Izzo, C.2    Rebulla, P.3
  • 5
    • 0023917618 scopus 로고
    • Comparison of acidified glycerol lysis test pink test and osmotic fragility test in hereditary spherocytosis: Effect of incubation
    • Bucx MJL, Breed WPM, Hoffmann JJML: Comparison of acidified glycerol lysis test. Pink test and osmotic fragility test in hereditary spherocytosis: effect of incubation. Eur J Haematol 1988; 40: 227-231.
    • (1988) Eur. J. Haematol. , vol.40 , pp. 227-231
    • Bucx, M.J.L.1    Breed, W.P.M.2    Hoffmann, J.J.M.L.3
  • 6
    • 0024511224 scopus 로고
    • Normal erythrocyte osmotic fragility in hereditary spherocytosis
    • DOI 10.1016/S0022-3476(89)80794-2
    • Kornes D, Pearson HA: Normal erytrocyte osmotic fragility in the hereditary spherocytosis. J Pediatr 1989; 114: 264-266. (Pubitemid 19059122)
    • (1989) Journal of Pediatrics , vol.114 , Issue.2 , pp. 264-266
    • Korones, D.1    Pearson, H.A.2
  • 8
    • 0015236352 scopus 로고
    • Electrophoretic analysis of the major polypeptide of the human erythrocyte membrane
    • Fairbank G, Steck TL, Wallach DFH: Electrophoretic analysis of the major polypeptide of the human erythrocyte membrane. Biochemistry 1971; 10: 2606-2617.
    • (1971) Biochemistry , vol.10 , pp. 2606-2617
    • Fairbank, G.1    Steck, T.L.2    Wallach, D.F.H.3
  • 9
    • 0034494630 scopus 로고    scopus 로고
    • Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia
    • DOI 10.1046/j.1365-2141.2000.02416.x
    • King MJ, Behrens J, Rogers C, Flynn C, Greenwood D, Chambers K: Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anemia. Brit J Haematol 2000; 111: 924-933. (Pubitemid 32098933)
    • (2000) British Journal of Haematology , vol.111 , Issue.3 , pp. 924-933
    • King, M.-J.1    Behrens, J.2    Rogers, C.3    Flynn, C.4    Greenwood, D.5    Chambers, K.6
  • 10
    • 50849126820 scopus 로고    scopus 로고
    • Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect
    • Mariani M, Barcellini W, Vercellati C, Marcello AP, Fermo E, Pedotti P, Boschetti C, Zanella A: Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect. Haematol 2008; 93: 1283-1288.
    • (2008) Haematol. , vol.93 , pp. 1283-1288
    • Mariani, M.1    Barcellini, W.2    Vercellati, C.3    Marcello, A.P.4    Fermo, E.5    Pedotti, P.6    Boschetti, C.7    Zanella, A.8
  • 12
    • 38349154864 scopus 로고    scopus 로고
    • Usefulness of the eosin-5-maleimide cytometric method as a first-line screening test for the diagnosis of hereditary spherocytosis: Comparison with ektacytometry and protein electrophoresis
    • Girordon F, Garçon L, Bergoin E, Largier M, Delaunay J, Fénéant-Thibault M, Maynadié M, Couillaud G, Moreira S, Cynober T: Usefulness of the eosin-5-maleimide cytometric method as a first-line screening test for the diagnosis of hereditary spherocytosis: comparison with ektacytometry and protein electrophoresis. Brit J Haematol 2008; 140: 468-470.
    • (2008) Brit. J. Haematol. , vol.140 , pp. 468-470
    • Girordon, F.1    Garçon, L.2    Bergoin, E.3    Largier, M.4    Delaunay, J.5    Fénéant-Thibault, M.6    Maynadié, M.7    Couillaud, G.8    Moreira, S.9    Cynober, T.10
  • 13
    • 47549102275 scopus 로고    scopus 로고
    • Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis
    • DOI 10.1002/cyto.b.20413
    • King MJ, Telfer P, MacKinnon H, Langabeer L, McMahon C, Darbyshire P, Dhermy D: Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis. Cytometry B Clin Cytom 2008; 74: 244-250. (Pubitemid 352007322)
    • (2008) Cytometry Part B - Clinical Cytometry , vol.74 , Issue.4 , pp. 244-250
    • King, M.-J.1    Telfer, P.2    MacKinnon, H.3    Langabeer, L.4    McMahon, C.5    Darbyshire, P.6    Dhermy, D.7
  • 14
    • 33749573629 scopus 로고    scopus 로고
    • Flow cytometry as a diagnostic tool for hereditary spherocytosis
    • DOI 10.1159/000094679
    • Stoya G, Gruhn B, Vogelsang H, Baumann E, Linss W: Flow cytometry as a diagnostic tool for hereditary spherocytosis. Acta Haematol 2006; 116: 186-191. (Pubitemid 44532963)
    • (2006) Acta Haematologica , vol.116 , Issue.3 , pp. 186-191
    • Stoya, G.1    Gruhn, B.2    Vogelsang, H.3    Baumann, E.4    Linss, W.5
  • 15
    • 0347064082 scopus 로고    scopus 로고
    • Eosin-5- maleimide binding to band 3 and Rh-related proteins forms the basis of a screening test for hereditary spherocytosis
    • King MJ, Smythe JS, Mushens R: Eosin-5- maleimide binding to band 3 and Rh-related proteins forms the basis of a screening test for hereditary spherocytosis. Brit J Haematol 2004; 124: 106-113.
    • (2004) Brit. J. Haematol. , vol.124 , pp. 106-113
    • King, M.J.1    Smythe, J.S.2    Mushens, R.3
  • 16
    • 0031454349 scopus 로고    scopus 로고
    • Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele
    • Miraglia Del Giudice E, Francese M, Polito R, Nobili B, Iolascon A, Perrotta S: Apparently normal Ankirin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele. Haematol 1997; 82: 332-333. (Pubitemid 28023311)
    • (1997) Haematologica , vol.82 , Issue.3 , pp. 332-333
    • Miraglia Del Giudice, E.1    Francese, M.2    Polito, R.3    Nobili, B.4    Iolascon, A.5    Perrotta, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.