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P Samperi

Showing results (11-20 of 18) with videos related to

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Clinical and Laboratory Haematology|January 1, 1991
High performance liquid chromatography (HPLC): a simple method to quantify Hb C, O-Arab, Agenogi and FP Samperi, G R Mancuso, S P Dibenedetto, et al.
American Journal of Hematology|December 1, 1992
Clinical, hematological, and molecular features in Sicilians with Hb S-beta-thalassemiaG Schiliro, P Samperi, R Testa, et al.
Hemoglobin|January 1, 1992
Clinical, hematological, and molecular features in Sicilians with sickle cell diseaseG Schilirò, P Samperi, C Consalvo, et al.
Pediatric Hematology and Oncology|July 1, 1991
Diabetes insipidus 9 years after cessation of therapy for acute lymphoblastic leukemiaS P Dibenedetto, G R Mancuso, P Samperi, et al.
Pharmacological Research|July 1, 1991
Antioxidant enzymatic systems and oxidative stress in erythrocytes with G6PD deficiency: effect of deferoxamineA Vanella, A Campisi, C Castorina, et al.
American Journal of Hematology|January 1, 1995
Genetic heterogeneity of beta-thalassemia in southeast SicilyG Schilirò, F Di Gregorio, P Samperi, et al.
American Journal of Hematology|December 12, 1997
Dissection of the association status of two polymorphisms in the beta-globin gene cluster with variations in F-cell number in non-anemic individualsT Merghoub, B Perichon, M Maier-Redelsperger, et al.
British Journal of Haematology|September 6, 2023
Acute chest syndrome in children with sickle cell disease: Data from a national AIEOP cohort identify priority areas of intervention in a hub-and-spoke systemV Munaretto, P Corti, E Bertoni, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Clinical and Laboratory Haematology|January 1, 1991
High performance liquid chromatography (HPLC): a simple method to quantify Hb C, O-Arab, Agenogi and FP Samperi, G R Mancuso, S P Dibenedetto, et al.
American Journal of Hematology|December 1, 1992
Clinical, hematological, and molecular features in Sicilians with Hb S-beta-thalassemiaG Schiliro, P Samperi, R Testa, et al.
Hemoglobin|January 1, 1992
Clinical, hematological, and molecular features in Sicilians with sickle cell diseaseG Schilirò, P Samperi, C Consalvo, et al.
Pediatric Hematology and Oncology|July 1, 1991
Diabetes insipidus 9 years after cessation of therapy for acute lymphoblastic leukemiaS P Dibenedetto, G R Mancuso, P Samperi, et al.
Pharmacological Research|July 1, 1991
Antioxidant enzymatic systems and oxidative stress in erythrocytes with G6PD deficiency: effect of deferoxamineA Vanella, A Campisi, C Castorina, et al.
American Journal of Hematology|January 1, 1995
Genetic heterogeneity of beta-thalassemia in southeast SicilyG Schilirò, F Di Gregorio, P Samperi, et al.
American Journal of Hematology|December 12, 1997
Dissection of the association status of two polymorphisms in the beta-globin gene cluster with variations in F-cell number in non-anemic individualsT Merghoub, B Perichon, M Maier-Redelsperger, et al.
British Journal of Haematology|September 6, 2023
Acute chest syndrome in children with sickle cell disease: Data from a national AIEOP cohort identify priority areas of intervention in a hub-and-spoke systemV Munaretto, P Corti, E Bertoni, et al.
Pageof 2