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Hemoglobin|August 12, 2003
An extreme consequence of splenectomy in dehydrated hereditary stomatocytosis: gradual thrombo-embolic pulmonary hypertension and lung-heart transplantationXavier Jaïs, Stephen J Till, Thérèse Cynober, et al.
European Journal of Haematology|June 11, 2005
Recurrent V75M mutation within the Wiskott-Aldrich syndrome protein: description of a homozygous female patientAlexis Proust, Benoît Guillet, Isabelle Pellier, et al.
Blood Cells, Molecules & Diseases|April 3, 2007
Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCRAlexis Proust, Benoît Guillet, Capucine Picard, et al.
Blood|October 21, 2006
Impaired ribosome biogenesis in Diamond-Blackfan anemiaValérie Choesmel, Daniel Bacqueville, Jacques Rouquette, et al.
Pediatric Nephrology (Berlin, Germany)|April 2, 2010
Disorders of sex development and Diamond-Blackfan anemia: is there an association?Julia Hoefele, Anne-Marie Bertrand, Maximilian Stehr, et al.
Blood|January 5, 2008
Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin AAshley M Toye, Rosalind C Williamson, Moudji Khanfar, et al.
Journal of Pediatric Hematology/Oncology|August 13, 2005
Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in a cohort of French childrenBrigitte Bader-Meunier, Guy Leverger, Gil Tchernia, et al.
British Journal of Haematology|December 11, 2002
Protein A Sepharose immunoadsorption can restore the efficacy of platelet concentrates in patients with Glanzmann's thrombasthenia and anti-glycoprotein IIb-IIIa antibodiesIsabelle Martin, Fayçal Kriaa, Valérie Proulle, et al.
Blood|September 20, 2002
A splicing alteration of 4.1R pre-mRNA generates 2 protein isoforms with distinct assembly to spindle poles in mitotic cellsFrançois Delhommeau, Corinne Vasseur-Godbillon, Philippe Leclerc, et al.
Haematologica|September 5, 2008
Study of the effects of proteasome inhibitors on ribosomal protein S19 (RPS19) mutants, identified in patients with Diamond-Blackfan anemiaAurore Crétien, Corinne Hurtaud, Hélène Moniz, et al.
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