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Maria Elisabetta Paglietti

Showing results (1-10 of 8) with videos related to

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Acta Haematologica|September 24, 2014
Investigating the alpha1(NcoI) mutationMaria Franca Desogus, Maria Elisabetta Paglietti, Maria Carla Sollaino, et al.
Blood|September 25, 2010
Homozygous deletion of the major alpha-globin regulatory element (MCS-R2) responsible for a severe case of hemoglobin H diseaseMaria Carla Sollaino, Maria Elisabetta Paglietti, Daniela Loi, 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.
Haematologica|July 14, 2011
Two atypical forms of HbH disease in SardiniaMaria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, et al.
Hemoglobin|March 21, 2012
First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian childMaria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, et al.
Acta Haematologica|January 23, 2016
The Problem of Borderline Hemoglobin A2 Levels in the Screening for β-Thalassemia Carriers in SardiniaMaria Elisabetta Paglietti, Stefania Satta, Maria Carla Sollaino, et al.
Blood Cells, Molecules & Diseases|March 27, 2017
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutationStefania Satta, Maria Elisabetta Paglietti, Maria Carla Sollaino, et al.
Blood Cells, Molecules & Diseases|November 23, 2017
Hematological phenotypes in children according to the α-globin genotypesRaffaella Origa, Susanna Barella, Maria Elisabetta Paglietti, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Acta Haematologica|September 24, 2014
Investigating the alpha1(NcoI) mutationMaria Franca Desogus, Maria Elisabetta Paglietti, Maria Carla Sollaino, et al.
Blood|September 25, 2010
Homozygous deletion of the major alpha-globin regulatory element (MCS-R2) responsible for a severe case of hemoglobin H diseaseMaria Carla Sollaino, Maria Elisabetta Paglietti, Daniela Loi, 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.
Haematologica|July 14, 2011
Two atypical forms of HbH disease in SardiniaMaria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, et al.
Hemoglobin|March 21, 2012
First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian childMaria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, et al.
Acta Haematologica|January 23, 2016
The Problem of Borderline Hemoglobin A2 Levels in the Screening for β-Thalassemia Carriers in SardiniaMaria Elisabetta Paglietti, Stefania Satta, Maria Carla Sollaino, et al.
Blood Cells, Molecules & Diseases|March 27, 2017
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutationStefania Satta, Maria Elisabetta Paglietti, Maria Carla Sollaino, et al.
Blood Cells, Molecules & Diseases|November 23, 2017
Hematological phenotypes in children according to the α-globin genotypesRaffaella Origa, Susanna Barella, Maria Elisabetta Paglietti, et al.
Pageof 1