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Journal Articles

Prognostic Significance of Early Treatment Response in Pediatric Relapsed Acute Myeloid Leukemia: Results from the International Study Relapsed AML 2001/01.

Gertjan J. Kaspers, M. Zimmermann, D. Reinhardt, R. Tamminga, B. Gibson, H. Armendariz, M. Dworzak, S. Ha, L. Hovi, A. Maschan, N. Philippe, B. Razzouk, C. Rizzari, P. Smisek, O. Smith, B. Stark, A. Will, U. Creutzig

Blood (2007) 110 (11): 1843.

https://doi.org/10.1182/blood.V110.11.1843.1843

Published: 2007

Journal Articles

Relapsed Acute Myeloid Leukemia in Children and Adolescents: Interim Report of the International Randomised Phase III Study Relapsed AML 2001/01.

Gertjan J. Kaspers, M. Zimmermann, G. Fleischhack, R. Tamminga, Brenda Gibson, H. Armendariz, M. Dworzak, S. Ha, L. Hovi, A. Maschan, N. Philippe, Bassem Razzouk, C. Rizzari, P. Smisek, Owen Smith, Batia Stark, A. Will, Ursula Creutzig

Blood (2006) 108 (11): 2013.

https://doi.org/10.1182/blood.V108.11.2013.2013

Published: 2006

Journal Articles

Relapsed Acute Myeloid Leukemia in Children and Adolescents: Interim Results of the International Randomised Phase III Study “Relapsed AML 2001/01”.

Gertjan J. Kaspers, M. Zimmermann, G. Fleischhack, R. Tamminga, B. Gibson, H. Armendariz, M. Dworzak, S. Ha, L. Hovi, A. Maschan, N. Philippe, B. Razzouk, C. Rizzari, P. Smisek, O. Smith, B. Stark, U. Creutzig

Blood (2005) 106 (11): 897.

https://doi.org/10.1182/blood.V106.11.897.897

Published: 2005

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

p16 gene homozygous deletions in acute lymphoblastic leukemia

B Quesnel, C Preudhomme, N Philippe, M Vanrumbeke, I Dervite, JL Lai, F Bauters, E Wattel, P Fenaux

Blood (1995) 85 (3): 657–663.

https://doi.org/10.1182/blood.V85.3.657.bloodjournal853657

Published: 1995

Journal Articles

Increased thrombin generation in a child with a combined factor IX and protein C deficiency

C Negrier, M Berruyer, A Durin, N Philippe, M Dechavanne

Blood (1993) 81 (3): 690–695.

https://doi.org/10.1182/blood.V81.3.690.690

Published: 1993

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

NARROW

Prognostic Significance of Early Treatment Response in Pediatric Relapsed Acute Myeloid Leukemia: Results from the International Study Relapsed AML 2001/01.

Relapsed Acute Myeloid Leukemia in Children and Adolescents: Interim Report of the International Randomised Phase III Study Relapsed AML 2001/01.

Relapsed Acute Myeloid Leukemia in Children and Adolescents: Interim Results of the International Randomised Phase III Study “Relapsed AML 2001/01”.

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)

p16 gene homozygous deletions in acute lymphoblastic leukemia

Increased thrombin generation in a child with a combined factor IX and protein C deficiency

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

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ASH Publications

American Society of Hematology

Prognostic Significance of Early Treatment Response in Pediatric Relapsed Acute Myeloid Leukemia: Results from the International Study Relapsed AML 2001/01.

Relapsed Acute Myeloid Leukemia in Children and Adolescents: Interim Report of the International Randomised Phase III Study Relapsed AML 2001/01.

Relapsed Acute Myeloid Leukemia in Children and Adolescents: Interim Results of the International Randomised Phase III Study “Relapsed AML 2001/01”.

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)

p16 gene homozygous deletions in acute lymphoblastic leukemia

Increased thrombin generation in a child with a combined factor IX and protein C deficiency

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

Email alerts

ASH Publications

American Society of Hematology

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