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Journal Articles

Low-Dose Dasatinib as Front-Line Therapy for Elderly (> 60 Years) Patients with CML

Raffaele Porrini, Enrico Montefusco, Roberto Latagliata, MD, Massimo Breccia, MD, Paolo Vigneri, MD, PhD, Luigia Luciano, MD, Antonella Gozzini, MD, Fausto Castagnetti, S. Ulisciani, medical, doctor, Francesco Cavazzini, M. Annunziata, F. Sora', Antonella Russo Rossi, Patrizia Pregno, Malgorzata Monika Trawinska, E. Crisa', Pellegrino Musto, MD, Mario Tiribelli, G. Binotto, U. Occhini, C. Feo, Bruno Martino, Paolo Avanzini, E. Spina, Fabrizio Pane, MD, Valeria Santini, MD, Gianantonio Rosti, Giovanna Rege Cambrin, Giuliana Alimena
Journal: Blood
Blood (2010) 116 (21): 2293.
https://doi.org/10.1182/blood.V116.21.2293.2293
Published: 2010
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
Journal: Blood
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
Journal: Blood
Blood (1992) 80 (3): 809–815.
https://doi.org/10.1182/blood.V80.3.809.809
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
Journal: Blood
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
Journal: Blood
Blood (1989) 74 (3): 1126–1133.
https://doi.org/10.1182/blood.V74.3.1126.1126
Published: 1989
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
Journal: Blood
Blood (1987) 69 (6): 1759–1765.
https://doi.org/10.1182/blood.V69.6.1759.1759
Published: 1987
Journal Articles

Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis

M Garbarz, MC Lecomte, D Dhermy, C Feo, I Chaveroche, H Gautero, O Bournier, C Picat, A Goepp, P Boivin
Journal: Blood
Blood (1986) 67 (6): 1661–1667.
https://doi.org/10.1182/blood.V67.6.1661.1661
Published: 1986
Journal Articles

A new abnormal variant of spectrin in black patients with hereditary elliptocytosis

MC Lecomte, D Dhermy, C Solis, A Ester, C Feo, H Gautero, O Bournier, P Boivin
Journal: Blood
Blood (1985) 65 (5): 1208–1217.
https://doi.org/10.1182/blood.V65.5.1208.1208
Published: 1985
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
Journal: Blood
Blood (1984) 64 (5): 1006–1015.
https://doi.org/10.1182/blood.V64.5.1006.1006
Published: 1984