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23. A new test for the laboratory diagnosis of spherocytosis. Vettore L; Zanella A; Molaro GL; De Matteis MC; Pavesi M; Mariani M Acta Haematol; 1984; 72(4):258-63. PubMed ID: 6438993 [TBL] [Abstract][Full Text] [Related]
24. Comparison of acidified glycerol lysis test, Pink test and osmotic fragility test in hereditary spherocytosis: effect of incubation. Bucx MJ; Breed WP; Hoffmann JJ Eur J Haematol; 1988 Mar; 40(3):227-31. PubMed ID: 3356239 [TBL] [Abstract][Full Text] [Related]
25. [Evaluation of the "pink test." Comparison of 2 procedures for the diagnosis of hereditary spherocytosis]. Grotto HZ; Sonati MF; Kimura EM; Erbetta A Sangre (Barc); 1993 Oct; 38(5):414-5. PubMed ID: 8140509 [No Abstract] [Full Text] [Related]
26. Modified end-point glycerol hemolysis assay as a screening test for hereditary spherocytosis that requires no venipuncture. Judkiewicz L; Szczepanek A; Bugała I; Bartosz G Am J Hematol; 1987 Sep; 26(1):89-91. PubMed ID: 3631064 [TBL] [Abstract][Full Text] [Related]
27. 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 Haematologica; 2008 Sep; 93(9):1310-7. PubMed ID: 18641031 [TBL] [Abstract][Full Text] [Related]
28. 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. Girodon F; Garçon L; Bergoin E; Largier M; Delaunay J; Fénéant-Thibault M; Maynadié M; Couillaud G; Moreira S; Cynober T Br J Haematol; 2008 Feb; 140(4):468-70. PubMed ID: 18162119 [No Abstract] [Full Text] [Related]
29. The Pink test in the diagnosis of hereditary spherocytosis. Zerhouni F Eur J Haematol; 1988 Nov; 41(5):510-1. PubMed ID: 3208875 [No Abstract] [Full Text] [Related]
30. Evaluation of the cryohemolysis test for hereditary spherocytosis. Piedras J; López Karpovitch X; Avilés G Arch Med Res; 1998; 29(1):89-90. PubMed ID: 9556928 [No Abstract] [Full Text] [Related]
34. [Attempt at diagnosis of hereditary spherocytosis using the ionophore valinomycin]. Sens P; Nahrendorf C; Mittler U; Szibor R Folia Haematol Int Mag Klin Morphol Blutforsch; 1989; 116(5):757-9. PubMed ID: 2481622 [TBL] [Abstract][Full Text] [Related]
35. Prenatal diagnosis of hereditary spherocytosis with osmotic fragility test. Celkan T; Alhaj S Indian Pediatr; 2008 Jan; 45(1):63-4. PubMed ID: 18250512 [No Abstract] [Full Text] [Related]