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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.
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.
Haematologica|August 24, 2011
Alterations of red blood cell metabolome in overhydrated hereditary stomatocytosisDhouha Darghouth, Bérengère Koehl, Jean François Heilier, et al.
Cell|March 25, 2008
Erythrocyte Glut1 triggers dehydroascorbic acid uptake in mammals unable to synthesize vitamin CAmélie Montel-Hagen, Sandrina Kinet, Nicolas Manel, et al.
Haematologica|December 18, 2009
Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationshipAchille Iolascon, Roberta Russo, Maria Rosaria Esposito, et al.
European Journal of Haematology|June 30, 2011
The c.273+11dup genetic change in the WAS gene is a functionally neutral polymorphismLaurence Jeanson-Leh, Sabine Charrier, Alexis Proust, et al.
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.
Comptes Rendus Biologies|February 18, 2005
Protein 4.1R expression in normal and dystrophic skeletal muscleFrançois Delhommeau, Nicole Dalla Venezia, Madeleine Morinière, 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.
American Journal of Hematology|October 14, 2010
Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B geneRoberta Russo, Maria Rosaria Esposito, Roberta Asci, et al.
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