The Characterization of Protein 4.1 Presles, a Shortened Variant of RBC Membrane Protein 4.1
Morle, L., Garbarz, M., Alloisio, N., Girot, R., Chaveroche, I., Boivin, P., Delaunay, J.
Published in Blood (01.06.1985)
Published in Blood (01.06.1985)
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Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis
Garbarz, M, Lecomte, MC, Dhermy, D, Feo, C, Chaveroche, I, Gautero, H, Bournier, O, Picat, C, Goepp, A, Boivin, P
Published in Blood (01.06.1986)
Published in Blood (01.06.1986)
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Journal Article
A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosis
Garbarz, M, Dhermy, D, Lecomte, MC, Feo, C, Chaveroche, I, Galand, C, Bournier, O, Bertrand, O, Boivin, P
Published in Blood (01.11.1984)
Published in Blood (01.11.1984)
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Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family. Transmission of the same molecular defect in spectrin through three generations with different clinical expression
Lecomte, M C, Dhermy, D, Garbarz, M, Feo, C, Gautero, H, Bournier, O, Picat, C, Chaveroche, I, Galand, C, Boivin, P
Published in Human genetics (01.12.1987)
Published in Human genetics (01.12.1987)
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Prenatal diagnosis of hereditary elliptocytosis with molecular defect of spectrin
Dhermy, D, Feo, C, Garbarz, M, Lecomte, M C, Bournier, O, Chaveroche, I, Gautero, H, Boivin, P, Daffos, F, Forestier, F
Published in Prenatal diagnosis (01.09.1987)
Published in Prenatal diagnosis (01.09.1987)
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Spectrin nice (β220/216): a shortened β-chain variant associated with an increase of the αI/74 fragment in a case of elliptocytosis
POTHIER, B, MORLE, L, BOIVIN, P, DELAUNAY, J, ALLOISIO, N, DUCLUZEAU, M. T, CALDANI, C, FEO, C, GARBARZ, M, CHAVEROCHE, I, DHERMY, D, LECOMTE, M. C
Published in Blood (01.06.1987)
Published in Blood (01.06.1987)
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Journal Article
Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis
GARBARZ, M, LECOMTE, M. C, DHERMY, D, FEO, C, CHAVEROCHE, I, GAUTERO, H, BOURNIER, O, PICAT, C, GOEPP, A, BOIVIN, P
Published in Blood (01.06.1986)
Published in Blood (01.06.1986)
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Journal Article
Spectrin Nice (β220/216): A Shortened /8-Chain Variant Associated With an Increase of the ax,1AFragment in a Case of Elliptocytosis
Pothier, B., Morle, L., Alloisio, N., Ducluzeau, M.T., Caldani, C., Feo, C., Garbarz, M., Chaveroche, I., Dhermy, D., Lecomte, M.C., Boivin, P., Delaunay, J.
Published in Blood (01.06.1987)
Published in Blood (01.06.1987)
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Journal Article
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
Pothier, B, Morle, L, Alloisio, N, Ducluzeau, MT, Caldani, C, Feo, C, Garbarz, M, Chaveroche, I, Dhermy, D, Lecomte, MC
Published in Blood (01.06.1987)
Published in Blood (01.06.1987)
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Journal Article
A Variant of Erythrocyte Membrane Skeletal Protein Band 4.1 Associated With Hereditary Elliptocytosis
Garbarz, Michel, Dhermy, Didier, Lecomte, Marie-Christine, Féo, Claude, Chaveroche, Isabelle, Galand, Colette, Bournier, Odile, Bertrand, Olivier, Boivin, Pierre
Published in Blood (01.11.1984)
Published in Blood (01.11.1984)
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Journal Article
Abnormal electrophoretic mobility of spectrin tetramers in hereditary elliptocytosis
Dhermy, D, Garbarz, M, Lecomte, M C, Chaveroche, I, Bournier, O, Gautero, H, Blot, I, Boivin, P
Published in Human genetics (01.12.1986)
Published in Human genetics (01.12.1986)
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Aberrant pattern of red cell membrane and cytosolic proteins in a case of congenital dyserythropoietic anaemia
Pothier, B, Morlé, L, Alloisio, N, Ducluzeau, M T, Féo, C, Blanchard, D, Cartron, J P, Garbarz, M, Chaveroche, I, Boivin, P
Published in British journal of haematology (01.07.1987)
Published in British journal of haematology (01.07.1987)
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Pathologic and nonpathologic variants of the spectrin molecule in two black families with hereditary elliptocytosis
Lecomte, M C, Dhermy, D, Garbarz, M, Feo, C, Gautero, H, Bournier, O, Picat, C, Chaveroche, I, Ester, A, Galand, C
Published in Human genetics (01.12.1985)
Published in Human genetics (01.12.1985)
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Red cell membrane alteration involving protein 4.1 and protein 3 in a case of recessively inherited haemolytic anaemia
Morlé, L, Pothier, B, Alloisio, N, Ducluzeau, M T, Marques, S, Olim, G, Martins e Silva, J, Féo, C, Garbarz, M, Chaveroche, I
Published in European journal of haematology (01.05.1987)
Published in European journal of haematology (01.05.1987)
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