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Stefania Satta

Showing results (11-20 of 17) with videos related to

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Annals of Hepatology|April 13, 2015
IFNL3 polymorphisms and HCV infection in patients with beta thalassemiaRaffaella Origa, Giuseppe Marceddu, Fabrice Danjou, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 8, 2024
Wilson's disease in Sardinian population: The experience of a pediatric referral centerGeorgios Loudianos, Stefania Satta, Maria B Lepori, et al.
Blood|August 22, 2009
Amelioration of Sardinian beta0 thalassemia by genetic modifiersRenzo Galanello, Serena Sanna, Lucia Perseu, et al.
Journal of Translational Medicine|September 4, 2016
A validated cellular biobank for β-thalassemiaLucia Carmela Cosenza, Laura Breda, Giulia Breveglieri, et al.
Haematologica|December 7, 2014
A genetic score for the prediction of beta-thalassemia severityFabrice Danjou, Marcella Francavilla, Franco Anni, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 5, 2008
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemiaManuela Uda, Renzo Galanello, Serena Sanna, et al.
Nature Genetics|March 23, 2011
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approachBelinda Giardine, Joseph Borg, Douglas R Higgs, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Annals of Hepatology|April 13, 2015
IFNL3 polymorphisms and HCV infection in patients with beta thalassemiaRaffaella Origa, Giuseppe Marceddu, Fabrice Danjou, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 8, 2024
Wilson's disease in Sardinian population: The experience of a pediatric referral centerGeorgios Loudianos, Stefania Satta, Maria B Lepori, et al.
Blood|August 22, 2009
Amelioration of Sardinian beta0 thalassemia by genetic modifiersRenzo Galanello, Serena Sanna, Lucia Perseu, et al.
Journal of Translational Medicine|September 4, 2016
A validated cellular biobank for β-thalassemiaLucia Carmela Cosenza, Laura Breda, Giulia Breveglieri, et al.
Haematologica|December 7, 2014
A genetic score for the prediction of beta-thalassemia severityFabrice Danjou, Marcella Francavilla, Franco Anni, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 5, 2008
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemiaManuela Uda, Renzo Galanello, Serena Sanna, et al.
Nature Genetics|March 23, 2011
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approachBelinda Giardine, Joseph Borg, Douglas R Higgs, et al.
Pageof 2