Page 1 | Search Results | Blood | American Society of Hematology

Skip Nav Destination

1-18 of 18

Sort by

Sort Order Select

Journal Articles

Modulation of Clinical Expression and Band 3 Deficiency in Hereditary Spherocytosis

N. Alloisio, P. Texier, A. Vallier, M.L. Ribeiro, L. Morlé, M. Bozon, E. Bursaux, P. Maillet, P. Gonçalves, M.J.A. Tanner, G. Tamagnini, J. Delaunay

Blood (1997) 90 (1): 414–420.

https://doi.org/10.1182/blood.V90.1.414

Published: 1997

Journal Articles

Hereditary spherocytosis with band 3 deficiency. Association with a nonsense mutation of the band 3 gene (allele Lyon), and aggravation by a low-expression allele occurring in trans (allele Genas)

N Alloisio, P Maillet, G Carre, P Texier, A Vallier, F Baklouti, N Philippe, J Delaunay

Blood (1996) 88 (3): 1062–1069.

https://doi.org/10.1182/blood.V88.3.1062.1062

Published: 1996

Journal Articles

The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulum

N Alloisio, P Texier, L Denoroy, C Berger, E Miraglia del Giudice, S Perrotta, A Iolascon, F Gilsanz, G Berger, J Guichard

Blood (1996) 87 (10): 4433–4439.

https://doi.org/10.1182/blood.V87.10.4433.bloodjournal87104433

Published: 1996

Journal Articles

A deletional frameshift mutation in protein 4.2 gene (allele 4.2 Lisboa) associated with hereditary hemolytic anemia

S Hayette, D Dhermy, ME dos Santos, M Bozon, D Drenckhahn, N Alloisio, P Texier, J Delaunay, L Morle

Blood (1995) 85 (1): 250–256.

https://doi.org/10.1182/blood.V85.1.250.bloodjournal851250

Published: 1995

Journal Articles

Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74)

S Perrotta, E Miraglia del Giudice, N Alloisio, G Sciarratta, L Pinto, J Delaunay, S Cutillo, A Iolascon

Blood (1994) 83 (11): 3346–3349.

https://doi.org/10.1182/blood.V83.11.3346.3346

Published: 1994

Journal Articles

Elliptopoikilocytosis associated with the alpha 469 His-->Pro mutation in spectrin Barcelona (alpha I/50-46b)

N Dalla Venezia, N Alloisio, A Forissier, L Denoroy, M Aymerich, JL Vives- Corrons, J Besalduch, I Besson, J Delaunay

Blood (1993) 82 (5): 1661–1665.

https://doi.org/10.1182/blood.V82.5.1661.1661

Published: 1993

Journal Articles

Evidence that red blood cell protein p55 may participate in the skeleton-membrane linkage that involves protein 4.1 and glycophorin C

N Alloisio, N Dalla Venezia, A Rana, K Andrabi, P Texier, F Gilsanz, JP Cartron, J Delaunay, AH Chishti

Blood (1993) 82 (4): 1323–1327.

https://doi.org/10.1182/blood.V82.4.1323.1323

Published: 1993

Journal Articles

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

N Alloisio, R Wilmotte, J Marechal, P Texier, L Denoroy, C Feo, Z Benhadji- Zouaoui, J Delaunay

Blood (1993) 81 (10): 2791–2798.

https://doi.org/10.1182/blood.V81.10.2791.2791

Published: 1993

Journal Articles

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

N Alloisio, R Wilmotte, L Morlé, F Baklouti, J Maréchal, MT Ducluzeau, L Denoroy, C Féo, BG Forget, R Kastally, J Delaunay

Blood (1992) 80 (3): 809–815.

https://doi.org/10.1182/blood.V80.3.809.809

Published: 1992

Journal Articles

Elliptocytogenic alpha I/36 spectrin Sfax lacks nine amino acids in helix 3 of repeat 4. Evidence for the activation of a cryptic 5'-splice site in exon 8 of spectrin alpha-gene

F Baklouti, J Maréchal, R Wilmotte, N Alloisio, L Morlé, MT Ducluzeau, L Denoroy, A Mrad, MH Ben Aribia, R Kastally, J Delaunay

Blood (1992) 79 (9): 2464–2470.

https://doi.org/10.1182/blood.V79.9.2464.2464

Published: 1992

Journal Articles

Molecular analysis of hereditary elliptocytosis with reduced protein 4.1 in the French Northern Alps

S Feddal, G Brunet, L Roda, S Chabanis, N Alloisio, L Morle, MT Ducluzeau, J Marechal, JM Robert, EJ Benz, Jr, J Delaunay, F Baklouti

Blood (1991) 78 (8): 2113–2119.

https://doi.org/10.1182/blood.V78.8.2113.2113

Published: 1991

Journal Articles

Assignment of Sp alpha I/74 hereditary elliptocytosis to the alpha- or beta-chain of spectrin through in vitro dimer reconstitution

B Pothier, N Alloisio, J Marechal, L Morle, MT Ducluzeau, C Caldani, N Philippe, J Delaunay

Blood (1990) 75 (10): 2061–2069.

https://doi.org/10.1182/blood.V75.10.2061.2061

Published: 1990

Journal Articles

Spectrin Oran (alpha II/21), a new spectrin variant concerning the alpha II domain and causing severe elliptocytosis in the homozygous state

N Alloisio, L Morle, B Pothier, AF Roux, J Marechal, MT Ducluzeau, Z Benhadji- Zouaoui, J Delaunay

Blood (1988) 71 (4): 1039–1047.

https://doi.org/10.1182/blood.V71.4.1039.1039

Published: 1988

Journal Articles

Spectrin Tunis (alpha I/78): a new alpha I variant that causes asymptomatic hereditary elliptocytosis in the heterozygous state

L Morle, N Alloisio, MT Ducluzeau, B Pothier, R Blibech, R Kastally, J Delaunay

Blood (1988) 71 (2): 508–511.

https://doi.org/10.1182/blood.V71.2.508.508

Published: 1988

Journal Articles

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

B Pothier, L Morle, N Alloisio, MT Ducluzeau, C Caldani, C Feo, M Garbarz, I Chaveroche, D Dhermy, MC Lecomte

Blood (1987) 69 (6): 1759–1765.

https://doi.org/10.1182/blood.V69.6.1759.1759

Published: 1987

Journal Articles

The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1

L Morle, M Garbarz, N Alloisio, R Girot, I Chaveroche, P Boivin, J Delaunay

Blood (1985) 65 (6): 1511–1517.

https://doi.org/10.1182/blood.V65.6.1511.bloodjournal6561511

Published: 1985

Journal Articles

The heterozygous form of 4.1(-) hereditary elliptocytosis [the 4.1(-) trait]

N Alloisio, L Morle, E Dorleac, O Gentilhomme, D Bachir, D Guetarni, P Colonna, M Bost, Z Zouaoui, L Roda

Blood (1985) 65 (1): 46–51.

https://doi.org/10.1182/blood.V65.1.46.46

Published: 1985

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

NARROW

Modulation of Clinical Expression and Band 3 Deficiency in Hereditary Spherocytosis

Hereditary spherocytosis with band 3 deficiency. Association with a nonsense mutation of the band 3 gene (allele Lyon), and aggravation by a low-expression allele occurring in trans (allele Genas)

The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulum

A deletional frameshift mutation in protein 4.2 gene (allele 4.2 Lisboa) associated with hereditary hemolytic anemia

Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74)

Elliptopoikilocytosis associated with the alpha 469 His-->Pro mutation in spectrin Barcelona (alpha I/50-46b)

Evidence that red blood cell protein p55 may participate in the skeleton-membrane linkage that involves protein 4.1 and glycophorin C

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

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

Elliptocytogenic alpha I/36 spectrin Sfax lacks nine amino acids in helix 3 of repeat 4. Evidence for the activation of a cryptic 5'-splice site in exon 8 of spectrin alpha-gene

Molecular analysis of hereditary elliptocytosis with reduced protein 4.1 in the French Northern Alps

Assignment of Sp alpha I/74 hereditary elliptocytosis to the alpha- or beta-chain of spectrin through in vitro dimer reconstitution

Spectrin Oran (alpha II/21), a new spectrin variant concerning the alpha II domain and causing severe elliptocytosis in the homozygous state

Spectrin Tunis (alpha I/78): a new alpha I variant that causes asymptomatic hereditary elliptocytosis in the heterozygous state

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

The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1

The heterozygous form of 4.1(-) hereditary elliptocytosis [the 4.1(-) trait]

A shortened variant of red cell membrane protein 4.1

Email alerts

ASH Publications

American Society of Hematology

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only