C. Féo

发表

Discocyte‐Echinocyte Reversibility in Blood Stored in CPD over a Period of 56 Days

J. Laczkó, C. Féo, W. Phillips, 1979, Transfusion.

Automated ektacytometry: a new method of measuring red cell deformability and red cell indices.

C. Féo, N. Mohandas, M. Bessis, 1980, Blood cells.

A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.

G. Abou-Alfa, P. Gallagher, C. Féo, 1996, The Journal of clinical investigation.

Bepridil as an antisickling agent: Membrane internalization and cell rigidity

Robert M. Johnson, S. Sarnaik, C. Féo, 1994, American journal of hematology.

The discocyte-echinocyte transformation: comparison of normal and ATP-enriched human erythrocytes.

P. Leblond, C. Féo, Claude J F#{233}o, 1974, Blood.

Separate mechanisms of deformability loss in ATP-depleted and Ca-loaded erythrocytes.

N. Mohandas, S. Shohet, M. R. Clark, 1981, The Journal of clinical investigation.

Echinocytic sensitivity and deformability of human newborn red cells.

N. Mohandas, L. Coulombel, C. Féo, 1982, Biology of the neonate.

Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypes.

F. Galibert, B. Grandchamp, I. Devaux, 1989, Blood.

Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain.

F. Galibert, I. Devaux, C. Féo, 1990, Blood.

[Quantitative study of changes of the shape of erythrocytes produced by cationic and anionic derivatives of phenothiazine].

N. Mohandas, C. Féo, 1974, Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles.

Reduction of membrane band 7 and activation of volume stimulated (K+, Cl−)‐cotransport in a case of congenital stomatocytosis

J. Delaunay, C. Féo, L. Morlé, 1989, British journal of haematology.

Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis.

C. Féo, P. Boivin, M. Lecomte, 1986, Blood.

Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis

C. Féo, P. Boivin, M. Lecomte, 1986 .

Evaluation of covalent antisickling compounds by PO2 scan ektacytometry.

I. Dobo, R. Johnson, C. Féo, 1985, Blood.

A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosis.

O. Bertrand, C. Féo, P. Boivin, 1984, Blood.

Adaptation of the ektacytometer to automated continuous pO2 changes: determination of erythrocyte deformability in sickling disorders.

C. Féo, M. Bessis, M. Nossal, 1983, Cytometry.

Behavior of elliptocytes under shear stress in the rheoscope and ektacytometer.

B. Bull, C. Féo, M. Bessis, 1983, Cytometry.

Herpesvirus-like DNA sequences in non-AIDS Kaposi's sarcoma.

P. Monini, C. Féo, M. Fabris, 1995, The Journal of infectious diseases.

Clarification of role of ATP in red-cell morphology and function

N. Mohandas, C. Féo, 1977, Nature.

Evidence for imbalanced furosemide-sensitive Na+, K+ cotransport in hereditary stomatocytosis.

B. Chailley, C. Féo, J. Delaunay, 2009, Scandinavian journal of haematology.

AUTOIMMUNE HAEMOLYTIC ANAEMIA REVEALED BY HUMAN PARVOVIRUS LINKED ERYTHROBLASTOPENIA

G. Leverger, Y. Bertrand, Y. Bertrand, 1985, The Lancet.

Observation of Echinocytosis in Eight Patients: a Phase Contrast and SEM Study

P. Leblond, C. Féo, G. Tchernia, 1978, British journal of haematology.

La déformabilité des globules rouges. Sa mesure par ektacytométrie. Applications possibles en pharmacologie.

C. Féo, M. Bessis, 1981 .

Role of ATP Depletion on Red Cell Shape and Deformability

N. Mohandas, C. Féo, 1978 .

[1st instance of the absence of an erythrocyte membrane protein (band 4(1)) in a case of familial elliptocytic anemia].

Stefan Fischer, C. Féo, G. Tchernia, 1980, Nouvelle revue francaise d'hematologie.

Severe recessive poikilocytic anaemia with a new spectrin α chain variant

C. Féo, P. Boivin, M. Lecomte, 1990 .

Molecular Defect of Spectrin in the Family of a Child with Congenital Hemolytic Poikilocytic Anemia

F. Gretillat, A. Herrera, C. Féo, 1984, Pediatric Research.

Spectrin beta-chain variant associated with hereditary elliptocytosis.

J. Delaunay, C. Féo, P. Boivin, 1982, The Journal of clinical investigation.

Spectrin Nice (beta 220/216): a shortened beta-chain variant associated with an increase of the alpha I/74 fragment in a case of elliptocytosis.

C. Féo, M. Lecomte, D. Dhermy, 1987, Blood.

Vitamin E deficiency is responsible for neurologic abnormalities in cholestatic children.

F. Alvarez, P. Landrieu, C. Féo, 1985, The Journal of pediatrics.

elliptocytosis A new abnormal variant of spectrin in black patients with hereditary

C. Féo, P. Boivin, M. Lecomte, 2011 .

homozygous elliptocytosis Double inheritance of an alpha I/65 spectrin variant in a child with

C. Féo, P. Boivin, M. Lecomte, 2011 .

Pathologic and nonpathologic variants of the spectrin molecule in two black families with hereditary elliptocytosis

C. Féo, P. Boivin, M. Lecomte, 2004, Human Genetics.

The role of lysolecithin formed in plasma on the discocyte-echinocyte transformation. A commentary.

C. Féo, 1972, Nouvelle revue francaise d'hematologie.

Enrichment of blood units with young red cells (neocytes) with the IBM 2991 cell washer

M. Maier‐Redelsperger, R. Girot, C. Féo, 1987, European journal of haematology.

The effect of cell hydration on the deformability of normal and sickle erythrocytes

D W Ross, M. Gulley, E. Orringer, 1982, American journal of hematology.

Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.

F. Costa, B. Forget, C. Féo, 1990, The Journal of clinical investigation.

Prenatal diagnosis of hereditary elliptocytosis with molecular defect of spectrin

C. Féo, F. Daffos, F. Forestier, 1987, Prenatal diagnosis.

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

C. Féo, P. Boivin, J. Delaunay, 1987, European journal of haematology.

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

H. Wajcman, J. Delobel, C. Féo, 1988, British journal of haematology.

A new abnormal variant of spectrin in black patients with hereditary elliptocytosis.

C. Féo, P. Boivin, M. Lecomte, 1985, Blood.

Spectrin f-Chain Variant Associated with Hereditary

J., C. Féo, M. Lecomte, 2022 .

A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblings

C. Féo, J. Delaunay, N. Alloisio, 1990, British journal of haematology.

Abnormal rheological response of erythrocytes caused by nitroimidazoles and hyperthermia.

M. Marden, M. Rybczyńska, C. Féo, 1993, International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group.

Hereditary Pyropoikilocytosis and Elliptocytosis in a White French Family (Arg to His) at Position 22 of the Spectrin a1 Domain With the Spectrin Variant Related to a CGT to CAT Codon Change

F. Galibert, B. Forget, I. Devaux, 2016 .

Familial isolated vitamin E deficiency. Extensive study of a large family with a 5-year therapeutic follow-up

P. Landrieu, J. Amiel, J. Mazière, 1995, Journal of Inherited Metabolic Disease.

Spectrin Jendouba: an alpha II/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self-association site.

L. Denoroy, B. Forget, C. Féo, 1992, Blood.

domain codon change (Arg to His) at position 22 of the spectrin alpha I family with the spectrin alpha I/74 variant related to a CGT to CAT Hereditary pyropoikilocytosis and elliptocytosis in a white French

F. Galibert, I. Devaux, C. Féo, 2013 .

Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family

C. Féo, P. Boivin, M. Lecomte, 1987, Human Genetics.

The influence of suspension osmolarity and erythrocyte volume on cell deformability.

C. Féo, W. M. Phillips, 1982, Nouvelle revue francaise d'hematologie.

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

C. Féo, P. Boivin, M. Lecomte, 1986, Nouvelle revue francaise d'hematologie.

A splice site mutation of alpha-spectrin gene causing skipping of exon 18 in hereditary elliptocytosis.

L. Denoroy, C. Féo, J. Delaunay, 1993, Blood.

with HE and HPP phenotypes Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred

F. Galibert, B. Grandchamp, I. Devaux, 2011 .

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

M. Marden, C. Dodé, H. Wajcman, 1988 .

Commentary of papers

W. Groner, N. Mohandas, S. Shohet, 1981 .