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Piero C Giordano

Showing results (1-10 of 86) with videos related to

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International Journal of Laboratory Hematology|February 17, 2012
Editorial: measurement of HbA2Piero C Giordano
Clinical Biochemistry|July 14, 2009
Prospective and retrospective primary prevention of hemoglobinopathies in multiethnic societiesPiero C Giordano
Mediterranean Journal of Hematology and Infectious Diseases|March 19, 2011
Screening and genetic diagnosis of hemoglobinopathies in southern and northern europe: two examplesAntonio Amato, Piero C Giordano
Mediterranean Journal of Hematology and Infectious Diseases|March 29, 2014
The Price of Mercy: Comment to the Paper Entitled "Prevention of Beta Thalassemia In Northern Israel - A Cost-Benefit Analysis" by Koren et Al. recently published in Mediterranean Journal of Hematology and Infectious DiseasesPiero C Giordano, Eliezer Rachmilewitz
International Journal of Environmental Research and Public Health|June 13, 2014
Genetic epidemiology and preventive healthcare in multiethnic societies: the hemoglobinopathiesPiero C Giordano, Cornelis L Harteveld, Egbert Bakker
Hemoglobin|January 22, 2005
A confidential inquiry estimating the number of patients affected with sickle cell disease and thalassemia major confirms the need for a prevention strategy in the NetherlandsPiero C Giordano, Marelle J Bouva, Cornelis L Harteveld
Prenatal Diagnosis|August 27, 2005
Estimating the attitude of immigrants toward primary prevention of the hemoglobinopathiesPiero C Giordano, Ashwin A Dihal, Cornelis L Harteveld
Hemoglobin|January 29, 2013
Hb Treviso [α91(FG3)Leu→Phe (α2)]: a new slightly unstable hemoglobin variant with moderately decreased oxygen affinityGiuseppina Barberio, Daniela Leone, Giovanni Ivaldi, et al.
Hemoglobin|April 18, 2009
Frequency of alpha-globin gene triplications and their interaction with beta-thalassemia mutationsPiero C Giordano, Margaretha Bakker-Verwij, Cornelis L Harteveld
Hemoglobin|July 26, 2008
An alpha0-thalassemia-like mutation: Hb Suan-Dok [alpha109(G16)Leu-->Arg] carried by a recombinant -alpha(3.7) geneKamran Moradkhani, Elodie Mazurier, Piero C Giordano, et al.
Pageof 9

Showing results (1-10 of 86) with videos related to

Sort By:
Pageof 9
International Journal of Laboratory Hematology|February 17, 2012
Editorial: measurement of HbA2Piero C Giordano
Clinical Biochemistry|July 14, 2009
Prospective and retrospective primary prevention of hemoglobinopathies in multiethnic societiesPiero C Giordano
Mediterranean Journal of Hematology and Infectious Diseases|March 19, 2011
Screening and genetic diagnosis of hemoglobinopathies in southern and northern europe: two examplesAntonio Amato, Piero C Giordano
Mediterranean Journal of Hematology and Infectious Diseases|March 29, 2014
The Price of Mercy: Comment to the Paper Entitled "Prevention of Beta Thalassemia In Northern Israel - A Cost-Benefit Analysis" by Koren et Al. recently published in Mediterranean Journal of Hematology and Infectious DiseasesPiero C Giordano, Eliezer Rachmilewitz
International Journal of Environmental Research and Public Health|June 13, 2014
Genetic epidemiology and preventive healthcare in multiethnic societies: the hemoglobinopathiesPiero C Giordano, Cornelis L Harteveld, Egbert Bakker
Hemoglobin|January 22, 2005
A confidential inquiry estimating the number of patients affected with sickle cell disease and thalassemia major confirms the need for a prevention strategy in the NetherlandsPiero C Giordano, Marelle J Bouva, Cornelis L Harteveld
Prenatal Diagnosis|August 27, 2005
Estimating the attitude of immigrants toward primary prevention of the hemoglobinopathiesPiero C Giordano, Ashwin A Dihal, Cornelis L Harteveld
Hemoglobin|January 29, 2013
Hb Treviso [α91(FG3)Leu→Phe (α2)]: a new slightly unstable hemoglobin variant with moderately decreased oxygen affinityGiuseppina Barberio, Daniela Leone, Giovanni Ivaldi, et al.
Hemoglobin|April 18, 2009
Frequency of alpha-globin gene triplications and their interaction with beta-thalassemia mutationsPiero C Giordano, Margaretha Bakker-Verwij, Cornelis L Harteveld
Hemoglobin|July 26, 2008
An alpha0-thalassemia-like mutation: Hb Suan-Dok [alpha109(G16)Leu-->Arg] carried by a recombinant -alpha(3.7) geneKamran Moradkhani, Elodie Mazurier, Piero C Giordano, et al.
Pageof 9