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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

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

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

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

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ASH Publications

American Society of Hematology

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

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

Email alerts

ASH Publications

American Society of Hematology

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