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C Féo

Showing results (1-10 of 16) with videos related to

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Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles|December 2, 1974
[Quantitative study of changes of the shape of erythrocytes produced by cationic and anionic derivatives of phenothiazine]N Mohandas, C Féo
American Journal of Hematology|August 1, 1994
Bepridil as an antisickling agent: membrane internalization and cell rigidityR M Johnson, C Acquaye, C Féo, et al.
British Journal of Haematology|January 1, 1989
Reduction of membrane band 7 and activation of volume stimulated (K+, Cl-)-cotransport in a case of congenital stomatocytosisL Morlé, B Pothier, N Alloisio, et al.
Blood|May 1, 1985
A new abnormal variant of spectrin in black patients with hereditary elliptocytosisM C Lecomte, D Dhermy, C Solis, et al.
Blood|May 15, 1993
A splice site mutation of alpha-spectrin gene causing skipping of exon 18 in hereditary elliptocytosisN Alloisio, R Wilmotte, J Maréchal, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1983
[Congenital hemolytic anemia with erythrocyte thermal instability and defect of spectrin tetrameric polymerization. Study of erythrocyte deformability in a new case of hereditary pyropoikilocytosis using diffraction viscosimetry]D Dhermy, C Féo, M Garbarz, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1986
Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 casesD Dhermy, M Garbarz, M C Lecomte, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Familial isolated vitamin E deficiency. Extensive study of a large family with a 5-year therapeutic follow-upJ Amiel, J C Maziere, I Beucler, et al.
Blood|November 1, 1984
A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosisM Garbarz, D Dhermy, M C Lecomte, et al.
Blood|April 15, 1990
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 domainM Garbarz, M C Lecomte, C Féo, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles|December 2, 1974
[Quantitative study of changes of the shape of erythrocytes produced by cationic and anionic derivatives of phenothiazine]N Mohandas, C Féo
American Journal of Hematology|August 1, 1994
Bepridil as an antisickling agent: membrane internalization and cell rigidityR M Johnson, C Acquaye, C Féo, et al.
British Journal of Haematology|January 1, 1989
Reduction of membrane band 7 and activation of volume stimulated (K+, Cl-)-cotransport in a case of congenital stomatocytosisL Morlé, B Pothier, N Alloisio, et al.
Blood|May 1, 1985
A new abnormal variant of spectrin in black patients with hereditary elliptocytosisM C Lecomte, D Dhermy, C Solis, et al.
Blood|May 15, 1993
A splice site mutation of alpha-spectrin gene causing skipping of exon 18 in hereditary elliptocytosisN Alloisio, R Wilmotte, J Maréchal, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1983
[Congenital hemolytic anemia with erythrocyte thermal instability and defect of spectrin tetrameric polymerization. Study of erythrocyte deformability in a new case of hereditary pyropoikilocytosis using diffraction viscosimetry]D Dhermy, C Féo, M Garbarz, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1986
Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 casesD Dhermy, M Garbarz, M C Lecomte, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Familial isolated vitamin E deficiency. Extensive study of a large family with a 5-year therapeutic follow-upJ Amiel, J C Maziere, I Beucler, et al.
Blood|November 1, 1984
A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosisM Garbarz, D Dhermy, M C Lecomte, et al.
Blood|April 15, 1990
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 domainM Garbarz, M C Lecomte, C Féo, et al.
Pageof 2