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M D Cappellini

Showing results (71-80 of 179) with videos related to

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Human Genetics|January 19, 2007
Gene symbol: HMBS. Disease: porphyria, acute intermittentE Di Pierro, V Besana, S Ausenda, et al.
Human Genetics|June 29, 2007
Gene symbol: CPOXSabrina Ausenda, E Di Pierro, V Besana, et al.
Human Genetics|April 4, 2008
Gene symbol: PPOX. Disease: Porphyria, variegateSabrina Ausenda, E Di Pierro, V Besana, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutaneousValentina Brancaleoni, E Di Pierro, V Besana, et al.
Acta Haematologica|January 1, 1982
The iron status of Italian subjects with beta-thalassemia traitS Fargion, M T Taddei, M D Cappellini, et al.
La Radiologia Medica|November 1, 1992
[Thoracic localizations of extramedullary erythropoiesis]G Nastri, M Cappelletti, M D Cappellini, et al.
Cardiovascular & Hematological Disorders Drug Targets|September 28, 2007
Heparin induced thrombocytopenia: pathogenetic, clinical, diagnostic and therapeutic aspectsR Castelli, E Cassinerio, M D Cappellini, et al.
Acta Haematologica|July 1, 2006
Lung function in beta-thalassemia patients: a longitudinal studyG Piatti, L Allegra, V Fasano, et al.
Human Genetics|April 1, 1995
Molecular characterisation of the glucose-6-phosphate dehydrogenase (G6PD) Ferrara II variantM D Cappellini, F Martinez di Montemuros, C Dotti, et al.
American Journal of Clinical Pathology|November 1, 1986
Association of hereditary spherocytosis and idiopathic hemochromatosis. A synergistic effect in determining iron overloadS Fargion, M D Cappellini, A Piperno, et al.
Pageof 18

Showing results (71-80 of 179) with videos related to

Sort By:
Pageof 18
Human Genetics|January 19, 2007
Gene symbol: HMBS. Disease: porphyria, acute intermittentE Di Pierro, V Besana, S Ausenda, et al.
Human Genetics|June 29, 2007
Gene symbol: CPOXSabrina Ausenda, E Di Pierro, V Besana, et al.
Human Genetics|April 4, 2008
Gene symbol: PPOX. Disease: Porphyria, variegateSabrina Ausenda, E Di Pierro, V Besana, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutaneousValentina Brancaleoni, E Di Pierro, V Besana, et al.
Acta Haematologica|January 1, 1982
The iron status of Italian subjects with beta-thalassemia traitS Fargion, M T Taddei, M D Cappellini, et al.
La Radiologia Medica|November 1, 1992
[Thoracic localizations of extramedullary erythropoiesis]G Nastri, M Cappelletti, M D Cappellini, et al.
Cardiovascular & Hematological Disorders Drug Targets|September 28, 2007
Heparin induced thrombocytopenia: pathogenetic, clinical, diagnostic and therapeutic aspectsR Castelli, E Cassinerio, M D Cappellini, et al.
Acta Haematologica|July 1, 2006
Lung function in beta-thalassemia patients: a longitudinal studyG Piatti, L Allegra, V Fasano, et al.
Human Genetics|April 1, 1995
Molecular characterisation of the glucose-6-phosphate dehydrogenase (G6PD) Ferrara II variantM D Cappellini, F Martinez di Montemuros, C Dotti, et al.
American Journal of Clinical Pathology|November 1, 1986
Association of hereditary spherocytosis and idiopathic hemochromatosis. A synergistic effect in determining iron overloadS Fargion, M D Cappellini, A Piperno, et al.
Pageof 18