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Hemoglobin|December 5, 2009
Southeast Asian ovalocytosis and a sickle cell trait in a young patient with sudden retinal stroke: a fortuitous association?Fabrizia Favale, Martine Gardembas, Olivier Pajot, et al.
European Journal of Haematology|January 27, 2007
Dehydrated hereditary stomatocytosis mimicking familial hyperkalaemic hypertension: clinical and genetic investigationGeneviève Beaurain, Flavie Mathieu, Sabine Grootenboer, et al.
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.
Pediatric Hematology and Oncology|May 27, 2006
Incidence of hereditary spherocytosis in a population of jaundiced neonatesVéronique Saada, Thérèse Cynober, Yves Brossard, 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.
American Journal of Physiology. Cell Physiology|October 21, 2011
Human RhAG ammonia channel is impaired by the Phe65Ser mutation in overhydrated stomatocytic red cellsSandrine Genetet, Pierre Ripoche, Julien Picot, et al.
Blood Cells, Molecules & Diseases|August 16, 2011
Homozygous deletion of EPB41 genuine AUG-containing exons results in mRNA splicing defects, NMD activation and protein 4.1R complete deficiency in hereditary elliptocytosisFaouzi Baklouti, Madeleine Morinière, Amel Haj-Khélil, et al.
Hemoglobin|November 17, 2010
A dyserythropoietic anemia associated with homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), a variant with an unstable α chainLoïc Garçon, Achille Iolascon, Serge Pissard, 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.
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