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V Gabutti

Showing results (31-40 of 51) with videos related to

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Blood|December 1, 1994
Natural protection against severe Plasmodium falciparum malaria due to impaired rosette formationJ Carlson, G B Nash, V Gabutti, et al.
Minerva Medica|May 19, 1970
[Physiopathological and cytogenetic findings in 2 cases of plasma cell leukemia]P Masera, G Benzio, G L Pagliardi, et al.
Audiology : Official Organ of the International Society of Audiology|January 1, 1988
Hearing loss and desferrioxamine in homozygous beta-thalassemiaR Albera, F Pia, B Morra, et al.
Progress in Clinical and Biological Research|January 1, 1989
Quality of life and life expectancy in thalassemic patients with complicationsV Gabutti, A Piga, L Sacchetti, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1986
[Bone marrow aplasia]G Fiandino, V Gabutti, M Messina, et al.
Stem Cells (Dayton, Ohio)|July 1, 1993
Expansion of cord blood progenitors and use for hemopoietic reconstitutionV Gabutti, F Timeus, U Ramenghi, et al.
Bone Marrow Transplantation|January 1, 1993
Human cord blood progenitors: kinetics, regulation and their use for hemopoietic reconstitutionV Gabutti, F Timeus, U Ramenghi, et al.
Archives of Disease in Childhood|December 1, 1982
Early iron overload in beta-thalassaemia major: when to start chelation therapy?S Fargion, M T Taddei, V Gabutti, et al.
British Journal of Haematology|August 1, 1991
A newly-characterized alpha-thalassaemia-1 deletion removes the entire alpha-like globin gene cluster in an Italian familyP Fortina, I Dianzani, A Serra, et al.
Bone Marrow Transplantation|August 26, 1998
Cell adhesion molecules in cord blood hematopoietic progenitorsF Timeus, N Crescenzio, D Marranca, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Blood|December 1, 1994
Natural protection against severe Plasmodium falciparum malaria due to impaired rosette formationJ Carlson, G B Nash, V Gabutti, et al.
Minerva Medica|May 19, 1970
[Physiopathological and cytogenetic findings in 2 cases of plasma cell leukemia]P Masera, G Benzio, G L Pagliardi, et al.
Audiology : Official Organ of the International Society of Audiology|January 1, 1988
Hearing loss and desferrioxamine in homozygous beta-thalassemiaR Albera, F Pia, B Morra, et al.
Progress in Clinical and Biological Research|January 1, 1989
Quality of life and life expectancy in thalassemic patients with complicationsV Gabutti, A Piga, L Sacchetti, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1986
[Bone marrow aplasia]G Fiandino, V Gabutti, M Messina, et al.
Stem Cells (Dayton, Ohio)|July 1, 1993
Expansion of cord blood progenitors and use for hemopoietic reconstitutionV Gabutti, F Timeus, U Ramenghi, et al.
Bone Marrow Transplantation|January 1, 1993
Human cord blood progenitors: kinetics, regulation and their use for hemopoietic reconstitutionV Gabutti, F Timeus, U Ramenghi, et al.
Archives of Disease in Childhood|December 1, 1982
Early iron overload in beta-thalassaemia major: when to start chelation therapy?S Fargion, M T Taddei, V Gabutti, et al.
British Journal of Haematology|August 1, 1991
A newly-characterized alpha-thalassaemia-1 deletion removes the entire alpha-like globin gene cluster in an Italian familyP Fortina, I Dianzani, A Serra, et al.
Bone Marrow Transplantation|August 26, 1998
Cell adhesion molecules in cord blood hematopoietic progenitorsF Timeus, N Crescenzio, D Marranca, et al.
Pageof 6