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Lucia Perseu

Showing results (1-10 of 23) with videos related to

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Blood Cells, Molecules & Diseases|November 19, 2011
Delayed fetal hemoglobin switching in subjects with KLF1 gene mutationStefania Satta, Lucia Perseu, Liliana Maccioni, et al.
Hemoglobin|January 6, 2012
A new β chain hemoglobin variant with increased oxygen affinity: Hb Santa Giusta Sardegna [β93(F9)Cys→Trp; HBB c.282T>G]Antonella Fais, Maria Carla Sollaino, Susanna Barella, et al.
Haematologica|October 2, 2009
Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermediaMaria Carla Sollaino, Maria Elisabetta Paglietti, Lucia Perseu, et al.
Hemoglobin|October 16, 2004
Hb Belfast [beta15(A12)Trp-->Arg]: definition of the clinical and hematological phenotypeRenzo Galanello, Lucia Perseu, Susanna Barella, et al.
British Journal of Haematology|November 30, 2004
Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patientsRenzo Galanello, Lucia Perseu, Chiara Perra, et al.
Haematologica|January 25, 2012
Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusionFabrice Danjou, Franco Anni, Lucia Perseu, et al.
Bioelectrochemistry (Amsterdam, Netherlands)|May 20, 2008
New analytical tools and epidemiological data for the identification of HbA2 borderline subjects in the screening for beta-thalassemiaAndrea Mosca, Renata Paleari, Renzo Galanello, et al.
Blood|August 9, 2011
KLF1 gene mutations cause borderline HbA(2)Lucia Perseu, Stefania Satta, Paolo Moi, et al.
Haematologica|January 29, 2011
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrinStefania Satta, Lucia Perseu, Paolo Moi, et al.
Cell Death and Differentiation|December 13, 2017
Deficiency in interferon type 1 receptor improves definitive erythropoiesis in Klf1 null miceMaria Francesca Manchinu, Carla Brancia, Cristian Antonio Caria, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Blood Cells, Molecules & Diseases|November 19, 2011
Delayed fetal hemoglobin switching in subjects with KLF1 gene mutationStefania Satta, Lucia Perseu, Liliana Maccioni, et al.
Hemoglobin|January 6, 2012
A new β chain hemoglobin variant with increased oxygen affinity: Hb Santa Giusta Sardegna [β93(F9)Cys→Trp; HBB c.282T>G]Antonella Fais, Maria Carla Sollaino, Susanna Barella, et al.
Haematologica|October 2, 2009
Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermediaMaria Carla Sollaino, Maria Elisabetta Paglietti, Lucia Perseu, et al.
Hemoglobin|October 16, 2004
Hb Belfast [beta15(A12)Trp-->Arg]: definition of the clinical and hematological phenotypeRenzo Galanello, Lucia Perseu, Susanna Barella, et al.
British Journal of Haematology|November 30, 2004
Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patientsRenzo Galanello, Lucia Perseu, Chiara Perra, et al.
Haematologica|January 25, 2012
Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusionFabrice Danjou, Franco Anni, Lucia Perseu, et al.
Bioelectrochemistry (Amsterdam, Netherlands)|May 20, 2008
New analytical tools and epidemiological data for the identification of HbA2 borderline subjects in the screening for beta-thalassemiaAndrea Mosca, Renata Paleari, Renzo Galanello, et al.
Blood|August 9, 2011
KLF1 gene mutations cause borderline HbA(2)Lucia Perseu, Stefania Satta, Paolo Moi, et al.
Haematologica|January 29, 2011
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrinStefania Satta, Lucia Perseu, Paolo Moi, et al.
Cell Death and Differentiation|December 13, 2017
Deficiency in interferon type 1 receptor improves definitive erythropoiesis in Klf1 null miceMaria Francesca Manchinu, Carla Brancia, Cristian Antonio Caria, et al.
Pageof 3