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Pathologie-Biologie
|
October 1, 1988
[Interaction between various alkylxanthines and the proteins of the erythrocyte skeleton]
J Delaunay, B Pothier, F Baklouti, et al.
Human Mutation
|
January 1, 1996
Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosis
P Maillet, N Alloisio, L Morlé, et al.
American Journal of Hematology
|
April 1, 1984
Thalassemia-like abnormalities of the red cell membrane in hemoglobin E trait and disease
E Dorléac, L Morlé, O Gentilhomme, et al.
Biochimica Et Biophysica Acta
|
June 11, 1985
Red cell membrane sialoglycoprotein beta in homozygous and heterozygous 4.1(-) hereditary elliptocytosis
N Alloisio, L Morlé, D Bachir, et al.
Blood
|
May 30, 1998
A large deletion within the protein 4.1 gene associated with a stable truncated mRNA and an unaltered tissue-specific alternative splicing
N D Venezia, P Maillet, L Morlé, et al.
Scandinavian Journal of Haematology
|
September 1, 1984
The Hb F composition in a Moroccan family with beta zero-thalassaemia and Hb O-Arab
F Morlé, L Morlé, F Baklouti, et al.
American Journal of Hematology
|
December 1, 1982
Kinetic alterations of the red cell membrane phosphatase in alpha- and beta-thalassemia
L Morlé, E Dorléac, N Alloisio, et al.
Blood
|
June 1, 1985
The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1
L Morlé, M Garbarz, N Alloisio, et al.
Hemoglobin
|
January 1, 1984
The association of hemoglobin Knossos and hemoglobin Lepore in an Algerian patient
L Morlé, F Morlé, E Dorléac, 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 stomatocytosis
L Morlé, B Pothier, N Alloisio, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 44) with videos related to
Sort By:
Page
of 5
Pathologie-Biologie
|
October 1, 1988
[Interaction between various alkylxanthines and the proteins of the erythrocyte skeleton]
J Delaunay, B Pothier, F Baklouti, et al.
Human Mutation
|
January 1, 1996
Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosis
P Maillet, N Alloisio, L Morlé, et al.
American Journal of Hematology
|
April 1, 1984
Thalassemia-like abnormalities of the red cell membrane in hemoglobin E trait and disease
E Dorléac, L Morlé, O Gentilhomme, et al.
Biochimica Et Biophysica Acta
|
June 11, 1985
Red cell membrane sialoglycoprotein beta in homozygous and heterozygous 4.1(-) hereditary elliptocytosis
N Alloisio, L Morlé, D Bachir, et al.
Blood
|
May 30, 1998
A large deletion within the protein 4.1 gene associated with a stable truncated mRNA and an unaltered tissue-specific alternative splicing
N D Venezia, P Maillet, L Morlé, et al.
Scandinavian Journal of Haematology
|
September 1, 1984
The Hb F composition in a Moroccan family with beta zero-thalassaemia and Hb O-Arab
F Morlé, L Morlé, F Baklouti, et al.
American Journal of Hematology
|
December 1, 1982
Kinetic alterations of the red cell membrane phosphatase in alpha- and beta-thalassemia
L Morlé, E Dorléac, N Alloisio, et al.
Blood
|
June 1, 1985
The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1
L Morlé, M Garbarz, N Alloisio, et al.
Hemoglobin
|
January 1, 1984
The association of hemoglobin Knossos and hemoglobin Lepore in an Algerian patient
L Morlé, F Morlé, E Dorléac, 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 stomatocytosis
L Morlé, B Pothier, N Alloisio, et al.
Page
of 5