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T Saad

Showing results (61-70 of 127) with videos related to

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Gene|May 11, 2019
Potential protective effects of Dapagliflozin in gentamicin induced nephrotoxicity rat model via modulation of apoptosis associated miRNAsDoaa I Mohamed, Eman Khairy, Sherin S T Saad, et al.
American Journal of Hematology|May 20, 1999
Spontaneous erythroid colony formation in Brazilian patients with sickle cell diseaseR C Perlingeiro, F F Costa, S T Saad, et al.
Blood|January 15, 1995
Glucose-6-phosphate dehydrogenase deficiency in sickle cell disease by DNA analysisS T Saad, F F Costa, T S Salles, et al.
Haematologia|September 5, 1998
The relationship of bone marrow histology with the molecular pattern in chronic myeloid leukemiaA C Vigorito, I Lorand-Metze, M L Chauffaile, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|October 1, 1993
Rapid identification of beta-globin structural mutations by sequencing the mRNA from peripheral blood reticulocytesS R Miranda, M S Gonçalves, M F Sonati, et al.
British Journal of Haematology|June 1, 1997
Beta-spectrin Campinas: a novel shortened beta-chain variant associated with skipping of exon 30 and hereditary elliptocytosisD S Basserès, P H Pranke, T S Sales, et al.
Annals of Clinical Microbiology and Antimicrobials|February 15, 2024
Genomic characterization, in vitro, and preclinical evaluation of two microencapsulated lytic phages VB_ST_E15 and VB_ST_SPNIS2 against clinical multidrug-resistant Salmonella serovarsReem A Youssef, Masarra M Sakr, Rania I Shebl, et al.
British Journal of Haematology|February 13, 2001
A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosisP G Gallagher, J D Ferreira, F F Costa, et al.
British Journal of Haematology|October 1, 1994
Red cell membrane protein abnormalities in hereditary spherocytosis in BrazilS T Saad, F F Costa, D L Vicentim, et al.
Sao Paulo Medical Journal = Revista Paulista De Medicina|September 1, 1996
Comparison of red cell distribution width and a red cell discriminant function incorporating volume dispersion for distinguishing iron deficiency from beta thalassemia trait in patients with microcytosisC S Lima, A R Reis, H Z Grotto, et al.
Pageof 13

Showing results (61-70 of 127) with videos related to

Sort By:
Pageof 13
Gene|May 11, 2019
Potential protective effects of Dapagliflozin in gentamicin induced nephrotoxicity rat model via modulation of apoptosis associated miRNAsDoaa I Mohamed, Eman Khairy, Sherin S T Saad, et al.
American Journal of Hematology|May 20, 1999
Spontaneous erythroid colony formation in Brazilian patients with sickle cell diseaseR C Perlingeiro, F F Costa, S T Saad, et al.
Blood|January 15, 1995
Glucose-6-phosphate dehydrogenase deficiency in sickle cell disease by DNA analysisS T Saad, F F Costa, T S Salles, et al.
Haematologia|September 5, 1998
The relationship of bone marrow histology with the molecular pattern in chronic myeloid leukemiaA C Vigorito, I Lorand-Metze, M L Chauffaile, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|October 1, 1993
Rapid identification of beta-globin structural mutations by sequencing the mRNA from peripheral blood reticulocytesS R Miranda, M S Gonçalves, M F Sonati, et al.
British Journal of Haematology|June 1, 1997
Beta-spectrin Campinas: a novel shortened beta-chain variant associated with skipping of exon 30 and hereditary elliptocytosisD S Basserès, P H Pranke, T S Sales, et al.
Annals of Clinical Microbiology and Antimicrobials|February 15, 2024
Genomic characterization, in vitro, and preclinical evaluation of two microencapsulated lytic phages VB_ST_E15 and VB_ST_SPNIS2 against clinical multidrug-resistant Salmonella serovarsReem A Youssef, Masarra M Sakr, Rania I Shebl, et al.
British Journal of Haematology|February 13, 2001
A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosisP G Gallagher, J D Ferreira, F F Costa, et al.
British Journal of Haematology|October 1, 1994
Red cell membrane protein abnormalities in hereditary spherocytosis in BrazilS T Saad, F F Costa, D L Vicentim, et al.
Sao Paulo Medical Journal = Revista Paulista De Medicina|September 1, 1996
Comparison of red cell distribution width and a red cell discriminant function incorporating volume dispersion for distinguishing iron deficiency from beta thalassemia trait in patients with microcytosisC S Lima, A R Reis, H Z Grotto, et al.
Pageof 13