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M D Cappellini

Showing results (41-50 of 179) with videos related to

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Human Genetics|September 17, 2003
Gene symbol: UROD. Disease: Porphyria, cutanea tardaF Martinez di Montemuros, D Tavazzi, E Patti, et al.
Birth Defects Original Article Series|January 1, 1987
Clinical features of thalassemia intermedia in ItalyG Fiorelli, M Sampietro, M Romano, et al.
Haematologica|September 1, 1990
Iron metabolism in thalassemia intermediaG Fiorelli, S Fargion, A Piperno, et al.
Scandinavian Journal of Haematology|April 1, 1982
Foetal type acetylcholinesterase in an anaemic patient with high HbFC Garrè, R Ravazzolo, P Strada, et al.
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutaneousValentina Brancaleoni, E Dipierro, S Ausenda, et al.
Hemoglobin|December 22, 1998
Indices of membrane alterations in beta-thalassemic erythrocytesD Tavazzi, A Comino, F Turrini, et al.
Annals of the New York Academy of Sciences|December 13, 2005
Coagulation and splenectomy: an overviewM D Cappellini, E Grespi, E Cassinerio, et al.
Blood|June 25, 1998
An erythroid-specific transcript generates the soluble form of NADH-cytochrome b5 reductase in humansA Bulbarelli, A Valentini, M DeSilvestris, et al.
Hemoglobin|December 22, 1998
Cross evaluation of three flow cytometric F cell counting methods performed by different laboratoriesG S Paterakis, S L Thein, E Fibach, et al.
Annals of Hematology|September 13, 2022
Cardiopulmonary testing in adult patients with β-thalassemia major in comparison to healthy subjectsG Piatti, M Giuditta, D Consonni, et al.
Pageof 18

Showing results (41-50 of 179) with videos related to

Sort By:
Pageof 18
Human Genetics|September 17, 2003
Gene symbol: UROD. Disease: Porphyria, cutanea tardaF Martinez di Montemuros, D Tavazzi, E Patti, et al.
Birth Defects Original Article Series|January 1, 1987
Clinical features of thalassemia intermedia in ItalyG Fiorelli, M Sampietro, M Romano, et al.
Haematologica|September 1, 1990
Iron metabolism in thalassemia intermediaG Fiorelli, S Fargion, A Piperno, et al.
Scandinavian Journal of Haematology|April 1, 1982
Foetal type acetylcholinesterase in an anaemic patient with high HbFC Garrè, R Ravazzolo, P Strada, et al.
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutaneousValentina Brancaleoni, E Dipierro, S Ausenda, et al.
Hemoglobin|December 22, 1998
Indices of membrane alterations in beta-thalassemic erythrocytesD Tavazzi, A Comino, F Turrini, et al.
Annals of the New York Academy of Sciences|December 13, 2005
Coagulation and splenectomy: an overviewM D Cappellini, E Grespi, E Cassinerio, et al.
Blood|June 25, 1998
An erythroid-specific transcript generates the soluble form of NADH-cytochrome b5 reductase in humansA Bulbarelli, A Valentini, M DeSilvestris, et al.
Hemoglobin|December 22, 1998
Cross evaluation of three flow cytometric F cell counting methods performed by different laboratoriesG S Paterakis, S L Thein, E Fibach, et al.
Annals of Hematology|September 13, 2022
Cardiopulmonary testing in adult patients with β-thalassemia major in comparison to healthy subjectsG Piatti, M Giuditta, D Consonni, et al.
Pageof 18