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T Saad

Showing results (51-60 of 127) with videos related to

Pageof 13
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Neoplasma|July 8, 2009
Variation of bone marrow CD34+ cell subsets in myelodysplastic syndromes according to who typesS C Reis, F Traina, K Metze, et al.
American Journal of Hematology|March 8, 2000
beta-thalassemia trait might increase the severity of hemochromatosis in subjects with the C282Y mutation in the HFE geneV R Arruda, M F Agostinho, R Cançado, et al.
Hemoglobin|April 13, 2001
Hydroxyurea promotes the reduction of spontaneous BFU-e to normal levels in SS and S/beta thalassemic patientsC Bincoletto, R C Perlingeiro, S T Saad, et al.
British Journal of Haematology|November 13, 2001
beta-Spectrin S(ta) Bárbara: a novel frameshift mutation in hereditary spherocytosis associated with detectable levels of mRNA and a germ cell line mosaicismD S Bassères, A S Duarte, H Hassoun, et al.
Biochemistry and Molecular Biology International|June 1, 1997
cDNA-derived amino-acid sequence of a land turtle (Geochelone carbonaria) beta-chain hemoglobinS Bordin, A N Meza, S T Saad, et al.
Blood|February 7, 1998
Beta-spectrin Promiss-ao: a translation initiation codon mutation of the beta-spectrin gene (ATG --> GTG) associated with hereditary spherocytosis and spectrin deficiency in a Brazilian familyD S Bassères, D L Vicentim, F F Costa, et al.
Acta Haematologica|August 6, 1998
Expression of spectrin alphaI/50 hereditary elliptocytosis and its association with the alphaLELY alleleD S Bassères, P H Pranke, D Vicentim, et al.
Neoplasma|September 18, 2010
The impact of several phenotypic features at diagnosis on survival of patients with myelodysplastic syndromesS C Reis-Alves, F Traina, S T Saad, et al.
American Journal of Hematology|May 9, 2001
p53, Mdm2, and c-Myc overexpression is associated with a poor prognosis in aggressive non-Hodgkin's lymphomasK B Pagnano, J Vassallo, I Lorand-Metze, et al.
Postgraduate Medical Journal|December 1, 1990
Acute myocardial infarction in sickle cell anaemia associated with severe hypoxiaS T Saad, V R Arruda, O O Junqueira, et al.
Pageof 13

Showing results (51-60 of 127) with videos related to

Sort By:
Pageof 13
Neoplasma|July 8, 2009
Variation of bone marrow CD34+ cell subsets in myelodysplastic syndromes according to who typesS C Reis, F Traina, K Metze, et al.
American Journal of Hematology|March 8, 2000
beta-thalassemia trait might increase the severity of hemochromatosis in subjects with the C282Y mutation in the HFE geneV R Arruda, M F Agostinho, R Cançado, et al.
Hemoglobin|April 13, 2001
Hydroxyurea promotes the reduction of spontaneous BFU-e to normal levels in SS and S/beta thalassemic patientsC Bincoletto, R C Perlingeiro, S T Saad, et al.
British Journal of Haematology|November 13, 2001
beta-Spectrin S(ta) Bárbara: a novel frameshift mutation in hereditary spherocytosis associated with detectable levels of mRNA and a germ cell line mosaicismD S Bassères, A S Duarte, H Hassoun, et al.
Biochemistry and Molecular Biology International|June 1, 1997
cDNA-derived amino-acid sequence of a land turtle (Geochelone carbonaria) beta-chain hemoglobinS Bordin, A N Meza, S T Saad, et al.
Blood|February 7, 1998
Beta-spectrin Promiss-ao: a translation initiation codon mutation of the beta-spectrin gene (ATG --> GTG) associated with hereditary spherocytosis and spectrin deficiency in a Brazilian familyD S Bassères, D L Vicentim, F F Costa, et al.
Acta Haematologica|August 6, 1998
Expression of spectrin alphaI/50 hereditary elliptocytosis and its association with the alphaLELY alleleD S Bassères, P H Pranke, D Vicentim, et al.
Neoplasma|September 18, 2010
The impact of several phenotypic features at diagnosis on survival of patients with myelodysplastic syndromesS C Reis-Alves, F Traina, S T Saad, et al.
American Journal of Hematology|May 9, 2001
p53, Mdm2, and c-Myc overexpression is associated with a poor prognosis in aggressive non-Hodgkin's lymphomasK B Pagnano, J Vassallo, I Lorand-Metze, et al.
Postgraduate Medical Journal|December 1, 1990
Acute myocardial infarction in sickle cell anaemia associated with severe hypoxiaS T Saad, V R Arruda, O O Junqueira, et al.
Pageof 13