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Blood
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August 1, 1996
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 Carré, et al.
Pediatrie
|
January 1, 1992
[Cerebrovascular accidents and sickle cell disease]
P Castell, R Capdeville, Y Bertrand, et al.
Leukemia
|
January 21, 2006
Cooperation of activating Ras/rtk signal transduction pathway mutations and inactivating myeloid differentiation gene mutations in M0 AML: a study of 45 patients
C Roumier, S Lejeune-Dumoulin, A Renneville, et al.
Leukemia
|
January 25, 2008
BCR-ABL mutants spread resistance to non-mutated cells through a paracrine mechanism
J Liu, S Joha, T Idziorek, et al.
Human Heredity
|
January 1, 1980
beta+ -Thalassemia intermedia. Genetic and biochemical study of a family including 3 cases
T Philip, G Souillet, N Philippe, et al.
British Journal of Haematology
|
November 1, 1995
A new alpha chain variant Hb Sallanches [alpha 2 104(G11) Cys-->Tyr] associated with HbH disease in one homozygous patient
F Morlé, A Francina, R Ducrocq, et al.
Archives Francaises De Pediatrie
|
August 1, 1977
[Generalized BCG infection in mixed and severe immunologic deficiency. Unfavorable outcome in spite of an attempted bone marrow transplant]
C Genin, J L Touraine, F Berger, et al.
Archives Francaises De Pediatrie
|
February 1, 1983
[Varicella-zoster virus infections in the immunosuppressed child. Treatment with Acyclovir and controls]
D Peyramond, G A Denoyel, T Philip, et al.
The Journal of Pediatrics
|
December 1, 1994
Partial albinism with immunodeficiency (Griscelli syndrome)
C Klein, N Philippe, F Le Deist, et al.
Blood
|
May 15, 1990
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 Maréchal, et al.
Page
of 11
Search research articles
Search
Showing results (41-50 of 107) with videos related to
Sort By:
Page
of 11
Blood
|
August 1, 1996
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 Carré, et al.
Pediatrie
|
January 1, 1992
[Cerebrovascular accidents and sickle cell disease]
P Castell, R Capdeville, Y Bertrand, et al.
Leukemia
|
January 21, 2006
Cooperation of activating Ras/rtk signal transduction pathway mutations and inactivating myeloid differentiation gene mutations in M0 AML: a study of 45 patients
C Roumier, S Lejeune-Dumoulin, A Renneville, et al.
Leukemia
|
January 25, 2008
BCR-ABL mutants spread resistance to non-mutated cells through a paracrine mechanism
J Liu, S Joha, T Idziorek, et al.
Human Heredity
|
January 1, 1980
beta+ -Thalassemia intermedia. Genetic and biochemical study of a family including 3 cases
T Philip, G Souillet, N Philippe, et al.
British Journal of Haematology
|
November 1, 1995
A new alpha chain variant Hb Sallanches [alpha 2 104(G11) Cys-->Tyr] associated with HbH disease in one homozygous patient
F Morlé, A Francina, R Ducrocq, et al.
Archives Francaises De Pediatrie
|
August 1, 1977
[Generalized BCG infection in mixed and severe immunologic deficiency. Unfavorable outcome in spite of an attempted bone marrow transplant]
C Genin, J L Touraine, F Berger, et al.
Archives Francaises De Pediatrie
|
February 1, 1983
[Varicella-zoster virus infections in the immunosuppressed child. Treatment with Acyclovir and controls]
D Peyramond, G A Denoyel, T Philip, et al.
The Journal of Pediatrics
|
December 1, 1994
Partial albinism with immunodeficiency (Griscelli syndrome)
C Klein, N Philippe, F Le Deist, et al.
Blood
|
May 15, 1990
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 Maréchal, et al.
Page
of 11