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Results: 1-10 |
Results: 10
Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia
Authors: Da Costa, L Mohandas, N Sorette, M Grange, MJ Tchernia, G Cynober, T
Citation: L. Da Costa et al., Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia, BLOOD, 98(10), 2001, pp. 2894-2899
Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis
Authors: Bader-Meunier, B Gauthier, F Archambaud, F Cynober, T Mielot, F Dommergues, JP Warszawski, J Mohandas, N Tchernia, G
Citation: B. Bader-meunier et al., Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis, BLOOD, 97(2), 2001, pp. 399-403
Heavy transfusions and presence of an anti-protein 4.2 antibody in 4.2(-) hereditary spherocytosis (949delG)
Authors: Beauchamp-Nicoud, A Morle, L Lutz, HU Stammler, P Agulles, O Petermann-Khder, R Iolascon, A Perrotta, S Cynober, T Tchernia, G Delaunay, J Baudin-Creuza, V
Citation: A. Beauchamp-nicoud et al., Heavy transfusions and presence of an anti-protein 4.2 antibody in 4.2(-) hereditary spherocytosis (949delG), HAEMATOLOG, 85(1), 2000, pp. 19-24
Coinheritance of two alpha-spectrin gene defects in a recessive spherocytosis family
Authors: Dhermy, D Steen-Johnsen, J Bournier, O Hetet, G Cynober, T Tchernia, G Grandchamp, B
Citation: D. Dhermy et al., Coinheritance of two alpha-spectrin gene defects in a recessive spherocytosis family, CLIN LAB H, 22(6), 2000, pp. 329-336
Oral magnesium pidolate: effects of long-term administration in patients with sickle cell disease
Authors: De Franceschi, L Bachir, D Galacteros, F Tchernia, G Cynober, T Neuberg, D Beuzard, Y Brugnara, C
Citation: L. De Franceschi et al., Oral magnesium pidolate: effects of long-term administration in patients with sickle cell disease, BR J HAEM, 108(2), 2000, pp. 284-289
Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24
Authors: Grootenboer, S Schischmanoff, PO Laurendeau, I Cynober, T Tchernia, G Dommergues, JP Dhermy, D Bost, M Varet, B Snyder, M Ballas, SK Ducot, B Babron, MC Stewart, GW Gasparini, P Iolascon, A Delaunay, J
Citation: S. Grootenboer et al., Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24, BLOOD, 96(7), 2000, pp. 2599-2605
Elliptocytosis in patients with C-terminal domain mutations of protein 4.1correlates with encoded messenger RNA levels rather than with alterations in primary protein structure
Authors: Moriniere, M Ribeiro, L Dalla Venezia, N Deguillien, M Maillet, P Cynober, T Delhommeau, F Almeida, H Tamagnini, G Delaunay, J Baklouti, F
Citation: M. Moriniere et al., Elliptocytosis in patients with C-terminal domain mutations of protein 4.1correlates with encoded messenger RNA levels rather than with alterations in primary protein structure, BLOOD, 95(5), 2000, pp. 1834-1841
Natural history of hereditary spherocytosis during the first year of life
Authors: Delhommeau, F Cynober, T Schischmanoff, PO Rohrlich, P Delaunay, J Mohandas, N Tchernia, G
Citation: F. Delhommeau et al., Natural history of hereditary spherocytosis during the first year of life, BLOOD, 95(2), 2000, pp. 393-397
The GEN.S: a fortuitous finding of a routine screening test for hereditaryspherocytosis
Authors: Chiron, M Cynober, T Mielot, F Tchernia, G Croisille, L
Citation: M. Chiron et al., The GEN.S: a fortuitous finding of a routine screening test for hereditaryspherocytosis, HEM CELL TH, 41(3), 1999, pp. 113-116
Southeast Asian ovalocytosis in white persons
Authors: Schischmanoff, PO Cynober, T Mielot, F Leclerc, L Vasseur-Godbillon, C Baudin-Creuza, V Magowan, C Yeung, J Mohandas, N Tchernia, G Delaunay, J
Citation: Po. Schischmanoff et al., Southeast Asian ovalocytosis in white persons, HEMOGLOBIN, 23(1), 1999, pp. 47-56
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