4 - Bibliothèques de l'Université de Lorraine

45. Streichman S. ; Gesheidt Y.
Cryohemolysis for the detection of hereditary spherocytosis
correlation studies with osmotic fragility and autohemolysis
Am J Hematol1998, 206-212
46. Fairbanks G. ; Steck T.I. ; Wallack D.H.F.
Electrophoretic analysis of the major polypeptides of the
human erythrocyte membrane
Biochemistry 1971, 10, 2606-2617
47. Laemli U.K.
Clivage of structural proteins during the assembly of the head
of bacteriophage T4
Nature Vol 227, August 15, 1970,680-685
48. Savvides P. ; Shalev O. ; John K.M. ; Lux S.E.
Combined spectrin and ankyrin deficiency is common in
autosomal dominant hereditary spherocytosis
Blood 1993,82,2953-2960
49. Pelissero G. ; Zappa M. ; Vercellati L. ; Bianchi P. ; Bredi E. ;
Baronciani L. ; Zanella A.
Diagnosis efficiency of red cell membrane analysis by SDS­
PAGE in hereditary spherocytosis
Blood 1997, 90, 271 a
50. Johnson R.M.
Ektacytometry of red cells.
Subcellular biochemistry 1994, Vol 23,161-203
51. Bessis M. ; Mohandas N.
Mesure continue de la déformabilité cellulaire par une méthode
diffractométrique
CR Acad Sci.Ser D, 1974, 278, 3263-3265