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Journal Articles

Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact site

N Parquet, I Devaux, L Boulanger, C Galand, P Boivin, MC Lecomte, D Dhermy, M Garbarz

Blood (1994) 84 (1): 303–308.

https://doi.org/10.1182/blood.V84.1.303.303

Published: 1994

Journal Articles

Spectrin beta Tandil, a novel shortened beta-chain variant associated with hereditary elliptocytosis is due to a deletional frameshift mutation in the beta-spectrin gene

M Garbarz, L Boulanger, S Pedroni, MC Lecomte, H Gautero, C Galand, P Boivin, L Feldman, D Dhermy

Blood (1992) 80 (4): 1066–1073.

https://doi.org/10.1182/blood.V80.4.1066.1066

Published: 1992

Journal Articles

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

M Garbarz, MC Lecomte, C Feo, I Devaux, C Picat, C Lefebvre, F Galibert, H Gautero, O Bournier, C Galand

Blood (1990) 75 (8): 1691–1698.

https://doi.org/10.1182/blood.V75.8.1691.1691

Published: 1990

Journal Articles

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

MC Lecomte, M Garbarz, B Grandchamp, C Feo, H Gautero, I Devaux, O Bournier, C Galand, L d'Auriol, F Galibert

Blood (1989) 74 (3): 1126–1133.

https://doi.org/10.1182/blood.V74.3.1126.1126

Published: 1989

Journal Articles

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

M Garbarz, D Dhermy, MC Lecomte, C Feo, I Chaveroche, C Galand, O Bournier, O Bertrand, P Boivin

Blood (1984) 64 (5): 1006–1015.

https://doi.org/10.1182/blood.V64.5.1006.1006

Published: 1984

Journal Articles

A shortened variant of red cell membrane protein 4.1

N Alloisio, E Dorleac, J Delaunay, R Girot, C Galand, P Boivin

Blood (1982) 60 (1): 265–267.

https://doi.org/10.1182/blood.V60.1.265.265

Published: 1982

Journal Articles

Causal mechanisms of multiple acquired red cell enzyme defects in a patient with acquired dyserythropoiesis

A Kahn, D Cottreau, C Boyer, J Marie, C Galand, P Boivin

Blood (1976) 48 (5): 653–662.

https://doi.org/10.1182/blood.V48.5.653.653

Published: 1976

NARROW

Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact site

Spectrin beta Tandil, a novel shortened beta-chain variant associated with hereditary elliptocytosis is due to a deletional frameshift mutation in the beta-spectrin gene

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

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

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

A shortened variant of red cell membrane protein 4.1

Causal mechanisms of multiple acquired red cell enzyme defects in a patient with acquired dyserythropoiesis

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ASH Publications

American Society of Hematology

Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact site

Spectrin beta Tandil, a novel shortened beta-chain variant associated with hereditary elliptocytosis is due to a deletional frameshift mutation in the beta-spectrin gene

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

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

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

A shortened variant of red cell membrane protein 4.1

Causal mechanisms of multiple acquired red cell enzyme defects in a patient with acquired dyserythropoiesis

Email alerts

ASH Publications

American Society of Hematology

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