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S P Dibenedetto

Showing results (1-10 of 19) with videos related to

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Haematologica|September 1, 1991
Non inherited hemoglobin anomaliesS P Dibenedetto, G Russo Mancuso, A Di Cataldo, et al.
Leukemia & Lymphoma|February 26, 1999
Detection of minimal residual disease: methods and relationship to outcome in T-lineage acute lymphoblastic leukemiaS P Dibenedetto, L Lo Nigro, A Di Cataldo, et al.
American Journal of Medical Genetics|March 17, 1997
Presence of hemoglobinopathies in Sicily: a historic perspectiveG Schilirò, E Mirabile, R Testa, et al.
American Journal of Hematology|February 1, 1993
A mild type of Hb S-beta(+)-thalassemia [-92(C-->T)] in a Sicilian familyV Divoky, E Baysal, G Schiliro, et al.
Haematologica|September 1, 1990
Unusual sickle cell disease observed for the first time in Italy: Hb S-Hb D Los AngelesP Samperi, S P Dibenedetto, A di Cataldo, et al.
Minerva Pediatrica|May 1, 1990
[Hemoglobin Shepherds Bush in a Sicilian family]S P Dibenedetto, P Samperi, G Tumminelli, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 1, 1995
Levels of L-asparagine in CSF after intramuscular administration of asparaginase from Erwinia in children with acute lymphoblastic leukemiaS P Dibenedetto, A Di Cataldo, R Ragusa, et al.
Blood|August 1, 1997
Detectable molecular residual disease at the beginning of maintenance therapy indicates poor outcome in children with T-cell acute lymphoblastic leukemiaS P Dibenedetto, L Lo Nigro, S P Mayer, et al.
European Journal of Pediatrics|September 1, 1993
Growth and growth hormone in children during and after therapy for acute lymphoblastic leukaemiaM Caruso-Nicoletti, M Mancuso, G Spadaro, et al.
Haematologica|March 1, 1990
Hematological findings in 375 Sicilians with Hb S traitG Schilirò, F F Comisi, R Testa, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Haematologica|September 1, 1991
Non inherited hemoglobin anomaliesS P Dibenedetto, G Russo Mancuso, A Di Cataldo, et al.
Leukemia & Lymphoma|February 26, 1999
Detection of minimal residual disease: methods and relationship to outcome in T-lineage acute lymphoblastic leukemiaS P Dibenedetto, L Lo Nigro, A Di Cataldo, et al.
American Journal of Medical Genetics|March 17, 1997
Presence of hemoglobinopathies in Sicily: a historic perspectiveG Schilirò, E Mirabile, R Testa, et al.
American Journal of Hematology|February 1, 1993
A mild type of Hb S-beta(+)-thalassemia [-92(C-->T)] in a Sicilian familyV Divoky, E Baysal, G Schiliro, et al.
Haematologica|September 1, 1990
Unusual sickle cell disease observed for the first time in Italy: Hb S-Hb D Los AngelesP Samperi, S P Dibenedetto, A di Cataldo, et al.
Minerva Pediatrica|May 1, 1990
[Hemoglobin Shepherds Bush in a Sicilian family]S P Dibenedetto, P Samperi, G Tumminelli, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 1, 1995
Levels of L-asparagine in CSF after intramuscular administration of asparaginase from Erwinia in children with acute lymphoblastic leukemiaS P Dibenedetto, A Di Cataldo, R Ragusa, et al.
Blood|August 1, 1997
Detectable molecular residual disease at the beginning of maintenance therapy indicates poor outcome in children with T-cell acute lymphoblastic leukemiaS P Dibenedetto, L Lo Nigro, S P Mayer, et al.
European Journal of Pediatrics|September 1, 1993
Growth and growth hormone in children during and after therapy for acute lymphoblastic leukaemiaM Caruso-Nicoletti, M Mancuso, G Spadaro, et al.
Haematologica|March 1, 1990
Hematological findings in 375 Sicilians with Hb S traitG Schilirò, F F Comisi, R Testa, et al.
Pageof 2