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Stefania Satta

Showing results (1-10 of 17) with videos related to

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Journal of Human Genetics|March 18, 2026
Allelic variation in the ATP7B gene promoter. Implications for phenotype variability, neurodegeneration and Pt resistance in tumor diseasesSimona Incollu, Isadora Asunis, Stefania Satta, et al.
Blood Cells, Molecules & Diseases|November 19, 2011
Delayed fetal hemoglobin switching in subjects with KLF1 gene mutationStefania Satta, Lucia Perseu, Liliana Maccioni, et al.
Blood|August 15, 2002
Homozygosity for nondeletion delta-beta(0) thalassemia resulting in a silent clinical phenotypeRenzo Galanello, Susanna Barella, Stefania Satta, 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.
Journal of Child Neurology|October 9, 2024
Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case SeriesPaolo Currao, Marta Balzarini, Dario Pruna, 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.
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.
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.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Journal of Human Genetics|March 18, 2026
Allelic variation in the ATP7B gene promoter. Implications for phenotype variability, neurodegeneration and Pt resistance in tumor diseasesSimona Incollu, Isadora Asunis, Stefania Satta, et al.
Blood Cells, Molecules & Diseases|November 19, 2011
Delayed fetal hemoglobin switching in subjects with KLF1 gene mutationStefania Satta, Lucia Perseu, Liliana Maccioni, et al.
Blood|August 15, 2002
Homozygosity for nondeletion delta-beta(0) thalassemia resulting in a silent clinical phenotypeRenzo Galanello, Susanna Barella, Stefania Satta, 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.
Journal of Child Neurology|October 9, 2024
Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case SeriesPaolo Currao, Marta Balzarini, Dario Pruna, 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.
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.
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.
Pageof 2