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Journal Articles

Lenalidomide (LEN) in INT 2 and High Risk MDS with DEL 5q. Interim Results of a Phase II Trial by the GFM.

S. Burcheri, MD, T. Prebet, MD, O. Beyne-Rauzy, MD, R.M. Mbida, MD, N. Hoarau, MD, L. Legros, MD, C. Ravoet, MD, F. Dreyfus, MD, A. Stamatoullas, MD, M.P. Chaury, MD, J. Delaunay, MD, G. Laurent, MD, N. Vey, MD, L. Ades, MD, C. Gardin, MD, Pierre Fenaux, MD

Blood (2007) 110 (11): 820.

https://doi.org/10.1182/blood.V110.11.820.820

Published: 2007

Journal Articles

Allogeneic Stem Cell Transplantation (SCT) with Non Myeloablative Conditioning Regimen (NST) Following Intensive Consolidation May Be Equivalent to Conventional alloSCT and Superior to autoSCT for Patients over 50 with Acute Myeloid Leukemia (AML) in 1 st CR: First Results of the AML 2001 Trial.

B. Lioure, J. Delaunay, D. Blaise, N. Milpied, P. Guardiola, J.Y. Cahn, B. Witz, E. Jourdan, L. Legros, E. Randriamalala, M. Ojeda, C. Himberlin, Michel Attal

Blood (2006) 108 (11): 319.

https://doi.org/10.1182/blood.V108.11.319.319

Published: 2006

Journal Articles

Natural history of hereditary spherocytosis during the first year of life

F. Delhommeau, T. Cynober, P. O. Schischmanoff, P. Rohrlich, J. Delaunay, N. Mohandas, G. Tchernia

Blood (2000) 95 (2): 393–397.

https://doi.org/10.1182/blood.V95.2.393

Published: 2000

Journal Articles

Familial Pseudohyperkalemia Maps to the Same Locus as Dehydrated Hereditary Stomatocytosis (Hereditary Xerocytosis)

A. Iolascon, G.W. Stewart, J.F. Ajetunmobi, S. Perrotta, J. Delaunay, M. Carella, L. Zelante, P. Gasparini

Blood (1999) 93 (9): 3120–3123.

https://doi.org/10.1182/blood.V93.9.3120

Published: 1999

Journal Articles

A Large Deletion Within the Protein 4.1 Gene Associated With a Stable Truncated mRNA and an Unaltered Tissue-Specific Alternative Splicing

N. Dalla Venezia, P. Maillet, L. Morlé, L. Roda, J. Delaunay, F. Baklouti

Blood (1998) 91 (11): 4361–4367.

https://doi.org/10.1182/blood.V91.11.4361

Published: 1998

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

Asynchronous regulation of splicing events within protein 4.1 pre-mRNA during erythroid differentiation

F Baklouti, SC Huang, TK Tang, J Delaunay, VT Marchesi, EJ Jr Benz

Blood (1996) 87 (9): 3934–3941.

https://doi.org/10.1182/blood.V87.9.3934.bloodjournal8793934

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

A second allele of spectrin alpha-gene associated with the alpha I/65 phenotype (allele alpha Ponte de Sor) [letter]

L Boulanger, D Dhermy, M Garbarz, C Silva, J Randon, R Wilmotte, J Delaunay

Blood (1994) 84 (6): 2056.

https://doi.org/10.1182/blood.V84.6.2056.2056

Published: 1994

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

Prevalent skipping of an individual exon accounts for shortened protein 4.1 Presles

S Feddal, S Hayette, F Baklouti, R Rimokh, R Wilmotte, JP Magaud, J Maréchal, EJ Benz, Jr, R Girot, J Delaunay, L Morlé

Blood (1992) 80 (11): 2925–2930.

https://doi.org/10.1182/blood.V80.11.2925.2925

Published: 1992

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

Human erythrocyte band 3 polymorphism (band 3 Memphis): characterization of the structural modification (Lys 56----Glu) by protein chemistry methods

D Yannoukakos, C Vasseur, C Driancourt, Y Blouquit, J Delaunay, H Wajcman, E Bursaux

Blood (1991) 78 (4): 1117–1120.

https://doi.org/10.1182/blood.V78.4.1117.1117

Published: 1991

Journal Articles

An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216)

WT Tse, PG Gallagher, B Pothier, FF Costa, A Scarpa, J Delaunay, BG Forget

Blood (1991) 78 (2): 517–523.

https://doi.org/10.1182/blood.V78.2.517.517

Published: 1991

NARROW

Lenalidomide (LEN) in INT 2 and High Risk MDS with DEL 5q. Interim Results of a Phase II Trial by the GFM.

Allogeneic Stem Cell Transplantation (SCT) with Non Myeloablative Conditioning Regimen (NST) Following Intensive Consolidation May Be Equivalent to Conventional alloSCT and Superior to autoSCT for Patients over 50 with Acute Myeloid Leukemia (AML) in 1 st CR: First Results of the AML 2001 Trial.

Natural history of hereditary spherocytosis during the first year of life

Familial Pseudohyperkalemia Maps to the Same Locus as Dehydrated Hereditary Stomatocytosis (Hereditary Xerocytosis)

A Large Deletion Within the Protein 4.1 Gene Associated With a Stable Truncated mRNA and an Unaltered Tissue-Specific Alternative Splicing

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)

Asynchronous regulation of splicing events within protein 4.1 pre-mRNA during erythroid differentiation

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

A second allele of spectrin alpha-gene associated with the alpha I/65 phenotype (allele alpha Ponte de Sor) [letter]

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

Prevalent skipping of an individual exon accounts for shortened protein 4.1 Presles

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

Human erythrocyte band 3 polymorphism (band 3 Memphis): characterization of the structural modification (Lys 56----Glu) by protein chemistry methods

An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216)

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