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Results: 1-10 |
Results: 10
Macrothrombocytopenia with abnormal demarcation membranes in megakaryocytes and neutropenia with a complete lack of sialyl-Lewis-X antigen in leukocytes - a new syndrome?
Authors: Willig, TN Breton-Gorius, J Elbim, C Mignotte, V Kaplan, C Mollicone, R Pasquier, C Filipe, A Mielot, F Cartron, JP Gougerot-Pocidalo, MA Debili, N Guichard, J Deommergues, JP Mohandas, N Tchernia, G
Citation: Tn. Willig et al., Macrothrombocytopenia with abnormal demarcation membranes in megakaryocytes and neutropenia with a complete lack of sialyl-Lewis-X antigen in leukocytes - a new syndrome?, BLOOD, 97(3), 2001, pp. 826-828
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
Hemophagocytic syndrome in primary human herpes virus-6 infection: a rare condition after liver transplantation
Authors: Lecointe, D Fabre, M Habes, D Mielot, F Bernard, O Nordmann, P
Citation: D. Lecointe et al., Hemophagocytic syndrome in primary human herpes virus-6 infection: a rare condition after liver transplantation, GASTRO CL B, 24(12), 2000, pp. 1227-1228
Severe congenital dyserythropoietic anaemia type I: prenatal management, transfusion support and alpha-interferon therapy
Authors: Parez, N Dommergues, M Zupan, V Chambost, ZH Fieschi, JB Delaunay, J Mielot, F Cramer, EM Dommergues, JP Wickramasinghe, SN Tchernia, G
Citation: N. Parez et al., Severe congenital dyserythropoietic anaemia type I: prenatal management, transfusion support and alpha-interferon therapy, BR J HAEM, 110(2), 2000, pp. 420-423
Dyserythropoiesis associated with a Fas-deficient condition in childhood
Authors: Bader-Meunier, B Rieux-Laucat, F Croisille, L Yvart, J Mielot, F Dommergues, JP Ledeist, F Tchernia, G
Citation: B. Bader-meunier et al., Dyserythropoiesis associated with a Fas-deficient condition in childhood, BR J HAEM, 108(2), 2000, pp. 300-304
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
Childhood myelodysplastic syndromes
Authors: Mielot, F
Citation: F. Mielot, Childhood myelodysplastic syndromes, PED HEM ONC, 16(4), 1999, pp. 283-284
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
Hematologic involvement in mitochondrial cytopathies in childhood: A retrospective study of bone marrow smears
Authors: Bader-Meunier, B Mielot, F Breton-Gorius, J Cramer, E Guichard, J Landrieu, P Dommergues, JP Tchernia, G
Citation: B. Bader-meunier et al., Hematologic involvement in mitochondrial cytopathies in childhood: A retrospective study of bone marrow smears, PEDIAT RES, 46(2), 1999, pp. 158-162
Suppression of CDA II expression in a homozygote
Authors: Beauchamp-Nicoud, A Schischmanoff, PO Alloisio, N Boivin, P Parsons, SF Mielot, F Tchernia, G Legrand, A del Giudice, EM Gasparini, P Iolascon, A Wickramasinghe, SN Delaunay, J
Citation: A. Beauchamp-nicoud et al., Suppression of CDA II expression in a homozygote, BR J HAEM, 106(4), 1999, pp. 948-953
Risultati: 1-10 |