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C. Feo

French Institute of Health and Medical Research

18

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310

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Red cell membrane alteration involving protein 4.1 and protein 3 in a case of recessively inherited haemolytic anaemia

2009 European Journal of Haematology
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Citations (2)
Evidence for Imbalanced Furosemide-Sensitive Na+, K+ Cotransport in Hereditary Stomatocytosis

2009 Scandinavian Journal of Haematology
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Abnormal rheological response of erythrocytes caused by nitroimidazoles and hyperthermia

1993 International Journal of Hyperthermia
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A haemolytic syndrome associated with the complete absence of red cell membrane protein 4•2 in two Tunisian siblings

1990 British Journal of Haematology
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Hemoglobin Athens‐Georgia [α2 β2 40(C6)Arg→Lys] in association with β0‐thalassemia in Tunisia

1989 American Journal of Hematology
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Occurrence of hereditary spherocytosis and β thalassaemia in the same family: globin chain synthesis and visco diffractometric studies

1988 British Journal of Haematology
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Hemoglobin J Guantanamo [α2β2 128 (H6) Ala→Asp] in association with hemoglobin C and α‐thalassemia in a family from Benin

1988 American Journal of Hematology
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Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family

1987 Human Genetics
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Prenatal diagnosis of hereditary elliptocytosis with molecular defect of spectrin.

1987 Prenatal Diagnosis
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Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 cases.

1986 Nouvelle revue française d'hématologie
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Citations (29)