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G Saglio

Showing results (141-150 of 286) with videos related to

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Tumori|August 1, 1982
Chemotherapy of advanced non-Hodgkin lymphomas: a report of 35 casesG Büchi, U Mazza, C Camaschella, et al.
Minerva Medica|January 31, 1979
[Drepanocytic homozygosis with exceptionally long survival. Clinical case]M A Ciocca Vasino, C Furlani, P D Bertello, et al.
European Journal of Haematology|March 1, 1994
Repeated PCR in CML during IFN-alpha therapyA M Liberati, E Donti, C Rosso, et al.
Progress in Clinical and Biological Research|January 1, 1985
Heterogeneity of molecular defects underlying hereditary persistence of fetal hemoglobin in Mediterranean areaS Ottolenghi, B Giglioni, C Casini, et al.
Human Genetics|May 1, 1988
A frequent A gamma-hereditary persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with beta-thalassemiaS Ottolenghi, C Camaschella, P Comi, et al.
Leukemia|January 1, 1989
Acute lymphoblastic leukemia with the 4;11 translocation exhibiting early T cell featuresF Lo Coco, P Francia di Celle, G Alimena, et al.
Leukemia|August 1, 1993
Molecular evidence of minimal residual disease after treatment for leukaemia and lymphoma: an updated meeting report and reviewM N Potter, N C Cross, J J van Dongen, et al.
Medical and Pediatric Oncology|January 1, 1991
Analysis of N-ras gene mutations in medulloblastomas by polymerase chain reaction and oligonucleotide probes in formalin-fixed, paraffin-embedded tissuesA Iolascon, A Lania, M Badiali, et al.
Annals of Hematology|February 1, 1996
Analysis of microsatellite instability in chronic lymphoproliferative disordersG Volpe, B Gamberi, C Pastore, et al.
Blood|October 1, 1996
Neutrophilic-chronic myeloid leukemia: a distinct disease with a specific molecular marker (BCR/ABL with C3/A2 junction)F Pane, F Frigeri, M Sindona, et al.
Pageof 29

Showing results (141-150 of 286) with videos related to

Sort By:
Pageof 29
Tumori|August 1, 1982
Chemotherapy of advanced non-Hodgkin lymphomas: a report of 35 casesG Büchi, U Mazza, C Camaschella, et al.
Minerva Medica|January 31, 1979
[Drepanocytic homozygosis with exceptionally long survival. Clinical case]M A Ciocca Vasino, C Furlani, P D Bertello, et al.
European Journal of Haematology|March 1, 1994
Repeated PCR in CML during IFN-alpha therapyA M Liberati, E Donti, C Rosso, et al.
Progress in Clinical and Biological Research|January 1, 1985
Heterogeneity of molecular defects underlying hereditary persistence of fetal hemoglobin in Mediterranean areaS Ottolenghi, B Giglioni, C Casini, et al.
Human Genetics|May 1, 1988
A frequent A gamma-hereditary persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with beta-thalassemiaS Ottolenghi, C Camaschella, P Comi, et al.
Leukemia|January 1, 1989
Acute lymphoblastic leukemia with the 4;11 translocation exhibiting early T cell featuresF Lo Coco, P Francia di Celle, G Alimena, et al.
Leukemia|August 1, 1993
Molecular evidence of minimal residual disease after treatment for leukaemia and lymphoma: an updated meeting report and reviewM N Potter, N C Cross, J J van Dongen, et al.
Medical and Pediatric Oncology|January 1, 1991
Analysis of N-ras gene mutations in medulloblastomas by polymerase chain reaction and oligonucleotide probes in formalin-fixed, paraffin-embedded tissuesA Iolascon, A Lania, M Badiali, et al.
Annals of Hematology|February 1, 1996
Analysis of microsatellite instability in chronic lymphoproliferative disordersG Volpe, B Gamberi, C Pastore, et al.
Blood|October 1, 1996
Neutrophilic-chronic myeloid leukemia: a distinct disease with a specific molecular marker (BCR/ABL with C3/A2 junction)F Pane, F Frigeri, M Sindona, et al.
Pageof 29