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American Journal of Hematology|November 13, 2007
Association between myeloid malignancies and acquired deficit in protein 4.1R: a retrospective analysis of six patientsCécile Alanio-Bréchot, Pierre-Olivier Schischmanoff, Madeleine Fénéant-Thibault, et al.The Hematology Journal : the Official Journal of the European Haematology Association|May 17, 2003
Ten novel Diamond-Blackfan anemia mutations and three polymorphisms within the rps19 geneAlexis Proust, Lydie Da Costa, Patricia Rince, et al.Pediatric Research|May 9, 2003
Abnormal glycosylation of red cell membrane band 3 in the congenital disorder of glycosylation IgEwa Zdebska, Brigitte Bader-Meunier, Pierre-Olivier Schischmanoff, et al.British Journal of Haematology|June 26, 2003
Therapy-related myelodysplasia and/or acute myeloid leukaemia after autologous haematopoietic progenitor cell transplantation in a prospective single centre cohort of 221 patientsAnne Beauchamp-Nicoud, Danielle Feneux, Chantal Bayle, et al.Blood|October 24, 2002
Ribosomal protein S19 expression during erythroid differentiationLydie Da Costa, Goutham Narla, Thiebaut-Noel Willig, et al.Journal of Pediatric Hematology/Oncology|September 10, 2002
Congenital dyserythropoietic anemia, type 1, in a polynesian patient: response to interferon alpha2bLaurent Roda, Jérôme Pasche, Alain Fournier, et al.British Journal of Haematology|January 23, 2010
Role of the interaction between Lu/BCAM and the spectrin-based membrane skeleton in the increased adhesion of hereditary spherocytosis red cells to lamininEmilie Gauthier, Wassim El Nemer, Marie P Wautier, et al.Blood|February 15, 2003
Nucleolar localization of RPS19 protein in normal cells and mislocalization due to mutations in the nucleolar localization signals in 2 Diamond-Blackfan anemia patients: potential insights into pathophysiologyLydie Da Costa, Gil Tchernia, Philippe Gascard, et al.Blood|December 4, 2004
Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporterIvan Martinez-Duncker, Thierry Dupré, Véronique Piller, et al.Prenatal Diagnosis|May 16, 2003
Sub-lethal hydrops as a manifestation of dehydrated hereditary stomatocytosis in two consecutive pregnanciesSabine Grootenboer-Mignot, Aurore Crétien, Ingrid Laurendeau, et al.Pageof 4