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Frontiers in Pharmacology|January 27, 2022
Treating Rare Diseases in Africa: The Drugs Exist but the Need Is UnmetLucio Luzzatto, Julie MakaniInternational Journal of Hematology|August 24, 2006
Recent advances in biological and clinical aspects of paroxysmal nocturnal hemoglobinuriaLucio Luzzatto, Giacomo GianfaldoniBritish Journal of Haematology|November 15, 2020
Paroxysmal nocturnal haemoglobinuria (PNH): novel therapies for an ancient diseaseLucio Luzzatto, Anastasios KaradimitrisBritish Journal of Haematology|December 31, 2013
G6PD deficiency: a classic example of pharmacogenetics with on-going clinical implicationsLucio Luzzatto, Elisa SenecaCell|April 6, 2022
Of mice and men: From hematopoiesis in mouse models to curative gene therapy for sickle cell diseaseJulie Makani, Lucio LuzzattoBlood|March 18, 2006
The mutation rate in PIG-A is normal in patients with paroxysmal nocturnal hemoglobinuria (PNH)David J Araten, Lucio LuzzattoBritish Journal of Haematology|July 6, 2018
Advances in understanding the pathogenesis of acquired aplastic anaemiaLucio Luzzatto, Antonio M RisitanoHematology/Oncology Clinics of North America|April 5, 2016
Glucose-6-Phosphate Dehydrogenase DeficiencyLucio Luzzatto, Caterina Nannelli, Rosario NotaroBlood|July 24, 2020
Glucose-6-phosphate dehydrogenase deficiencyLucio Luzzatto, Mwashungi Ally, Rosario NotaroPageof 20