Nosocomial infections due to enterococci in patients with acute leukemia.

نویسندگان

  • R Fanci
  • P Pecile
  • A Fabbri
  • C Paci
  • R L Martinez
  • G Longo
چکیده

1. Cohen CM, Dotimas E, Korsgren C. Human erythrocyte membrane protein band 4.2 (Pallidin). Semin Hematol 1993; 30: 119-37. 2. Rybicki AC, Schwartz RS, Hustedt EJ, Cobb CE. Increased rotational mobility and extractability of band 3 from protein 4.2-deficient erythrocyte membranes: evidence of a role for protein 4.2 in strengthening the band 3-cytoskeleton linkage. Blood 1996; 88:2745-53. 3. Iolascon A, Miraglia del Giudice E, Perrotta S, Alloisio N, Morlé L, Delaunay J. Hereditary spherocytosis: from clinic to molecular defects. Haematologica 1998; 83:240-57. 4. Bouhassira EE, Schwartz RS, Yawata Y, et al. An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON). Blood 1992; 79:1846-54. 5. Yawata Y. Red cell membrane protein 4.2: phenotypic, genetic and electron microscopic aspects. Biochim Biophys Acta 1994; 1204: 131-48. 6. Miraglia del Giudice E, Iolascon A, Pinto L, Nobili B, Perrotta S. Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis. Br J Haematol 1994; 88:52-5. 7. Jenkins PB, Gallagher PG, Forget BG. Analysis of a PstI polymorphism of the human erythrocyte band 3 gene (EPB3). Br J Haematol 1993; 85: 816-8. 8. Miraglia del Giudice E, Francese M, Nobili B, et al. High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis. J Pediatr 1998; 132:117-20. 9. Takaoka Y, Ideguchi H, Matsuda M, Sakamoto N, Takeucki T, Fukumaki Y. A novel mutation in the erythrocyte protein 4.2 gene of Japanese patients with hereditary spherocytosis (protein 4.2FUKUOKA). Br J Haematol 1994; 88:527-33. 10. Youssoufian H, Kazazian HH, Phillips DG, et al. Recurrent mutations in haemophilia A give evidence for CpG mutation hotspots. Nature 1986; 324: 380-3.

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عنوان ژورنال:
  • Haematologica

دوره 84 7  شماره 

صفحات  -

تاریخ انتشار 1999