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M D Cappellini

Showing results (121-130 of 179) with videos related to

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British Journal of Haematology|January 1, 1992
Hereditary spherocytosis characterized by increased spectrin/band 3 ratioE Miraglia del Giudice, S Perrotta, L Pinto, et al.
Blood Cells, Molecules & Diseases|May 22, 2014
Combination of deferasirox and deferoxamine in clinical practice: an alternative scheme of chelation in thalassemia major patientsE Cassinerio, N Orofino, A Roghi, et al.
American Journal of Hematology|April 1, 1992
Binding and suppressive activity of human recombinant ferritins on erythroid cellsS Fargion, M D Cappellini, A L Fracanzani, et al.
Lancet (London, England)|July 2, 1983
Aplastic crisis due to parvovirus infection in pyruvate kinase deficiencyJ R Duncan, C B Potter, M D Cappellini, et al.
Annals of Hematology|March 22, 2017
Bone quality in beta-thalassemia intermedia: relationships with bone quantity and endocrine and hematologic variablesMarina Baldini, A Marcon, F M Ulivieri, et al.
British Journal of Haematology|March 1, 1993
Iron status in red cell pyruvate kinase deficiency: study of Italian casesA Zanella, A Berzuini, M B Colombo, et al.
Journal of Inherited Metabolic Disease|May 26, 2004
Pro-oxidant and antioxidant factors in acute intermittent porphyria: family studiesE Rocchi, P Ventura, A Ronzoni, et al.
Clinical Genetics|November 1, 1994
Molecular characterisation of an Italian G6PD variant responsible for chronic non-spherocytic haemolytic anaemiaF Martinez di Montemuros, M D Cappellini, C Dotti, et al.
Blood Cells, Molecules & Diseases|October 5, 2013
Thalassemic osteopathy: a new marker of bone depositionM Baldini, S Forti, A Orsatti, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Non-transferrin-bound iron in myelodysplastic syndromes: a marker of ineffective erythropoiesis?A Cortelezzi, C Cattaneo, S Cristiani, et al.
Pageof 18

Showing results (121-130 of 179) with videos related to

Sort By:
Pageof 18
British Journal of Haematology|January 1, 1992
Hereditary spherocytosis characterized by increased spectrin/band 3 ratioE Miraglia del Giudice, S Perrotta, L Pinto, et al.
Blood Cells, Molecules & Diseases|May 22, 2014
Combination of deferasirox and deferoxamine in clinical practice: an alternative scheme of chelation in thalassemia major patientsE Cassinerio, N Orofino, A Roghi, et al.
American Journal of Hematology|April 1, 1992
Binding and suppressive activity of human recombinant ferritins on erythroid cellsS Fargion, M D Cappellini, A L Fracanzani, et al.
Lancet (London, England)|July 2, 1983
Aplastic crisis due to parvovirus infection in pyruvate kinase deficiencyJ R Duncan, C B Potter, M D Cappellini, et al.
Annals of Hematology|March 22, 2017
Bone quality in beta-thalassemia intermedia: relationships with bone quantity and endocrine and hematologic variablesMarina Baldini, A Marcon, F M Ulivieri, et al.
British Journal of Haematology|March 1, 1993
Iron status in red cell pyruvate kinase deficiency: study of Italian casesA Zanella, A Berzuini, M B Colombo, et al.
Journal of Inherited Metabolic Disease|May 26, 2004
Pro-oxidant and antioxidant factors in acute intermittent porphyria: family studiesE Rocchi, P Ventura, A Ronzoni, et al.
Clinical Genetics|November 1, 1994
Molecular characterisation of an Italian G6PD variant responsible for chronic non-spherocytic haemolytic anaemiaF Martinez di Montemuros, M D Cappellini, C Dotti, et al.
Blood Cells, Molecules & Diseases|October 5, 2013
Thalassemic osteopathy: a new marker of bone depositionM Baldini, S Forti, A Orsatti, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Non-transferrin-bound iron in myelodysplastic syndromes: a marker of ineffective erythropoiesis?A Cortelezzi, C Cattaneo, S Cristiani, et al.
Pageof 18