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Giovanna D'Andrea

Showing results (1-10 of 49) with videos related to

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International Journal of Environmental Research and Public Health|September 10, 2021
Rare Defects: Looking at the Dark Face of the ThrombosisGiovanna D'Andrea, Maurizio Margaglione
Haematologica|December 23, 2003
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphismGiovanna D'Andrea, Maurizio Margaglione,
Blood Reviews|February 1, 2008
Oral anticoagulants: Pharmacogenetics Relationship between genetic and non-genetic factorsGiovanna D'Andrea, Rosa D'Ambrosio, Maurizio Margaglione
Journal of Clinical Medicine|June 2, 2021
The Genetics of Hereditary Angioedema: A ReviewRosa Santacroce, Giovanna D'Andrea, Angela Bruna Maffione, et al.
Thrombosis and Haemostasis|June 27, 2002
Glanzmann's thrombasthenia: identification of 19 new mutations in 30 patientsGiovanna D'Andrea, Donatella Colaizzo, Gennaro Vecchione, et al.
European Journal of Haematology|December 16, 2011
Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian familyArturo Cafolla, Giovanna D'Andrea, Erminia Baldacci, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 25, 2024
Homozygous MTHFR C677T carriers develop idiopathic portal vein thrombosis 20 years earlier than wild typePaul Rj Ames, Giovanna D'Andrea, Alessia Arcaro, et al.
Ophthalmic Genetics|February 23, 2024
Homozygous MTHFR C667T carriers ≤45 years old develop central retinal vein occlusion five years earlier than wild typePaul Rj Ames, Alessia Arcaro, Giovanna D'Andrea, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 16, 2021
Homozygous methylentetrahydrofolate reductase C667T genotype anticipates age at venous thromboembolism by one decadePaul R J Ames, Giovanna D'Andrea, Vincenzo Marottoli, et al.
Haematologica|March 26, 2003
The factor V (FV) gene ASP79HIS polymorphism modulates FV plasma levels and affects the activated protein C resistance phenotype in presence of the FV Leiden mutationAnna Bossone, Filomena Cappucci, Giovanna D'Andrea, et al.
Pageof 5

Showing results (1-10 of 49) with videos related to

Sort By:
Pageof 5
International Journal of Environmental Research and Public Health|September 10, 2021
Rare Defects: Looking at the Dark Face of the ThrombosisGiovanna D'Andrea, Maurizio Margaglione
Haematologica|December 23, 2003
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphismGiovanna D'Andrea, Maurizio Margaglione,
Blood Reviews|February 1, 2008
Oral anticoagulants: Pharmacogenetics Relationship between genetic and non-genetic factorsGiovanna D'Andrea, Rosa D'Ambrosio, Maurizio Margaglione
Journal of Clinical Medicine|June 2, 2021
The Genetics of Hereditary Angioedema: A ReviewRosa Santacroce, Giovanna D'Andrea, Angela Bruna Maffione, et al.
Thrombosis and Haemostasis|June 27, 2002
Glanzmann's thrombasthenia: identification of 19 new mutations in 30 patientsGiovanna D'Andrea, Donatella Colaizzo, Gennaro Vecchione, et al.
European Journal of Haematology|December 16, 2011
Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian familyArturo Cafolla, Giovanna D'Andrea, Erminia Baldacci, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 25, 2024
Homozygous MTHFR C677T carriers develop idiopathic portal vein thrombosis 20 years earlier than wild typePaul Rj Ames, Giovanna D'Andrea, Alessia Arcaro, et al.
Ophthalmic Genetics|February 23, 2024
Homozygous MTHFR C667T carriers ≤45 years old develop central retinal vein occlusion five years earlier than wild typePaul Rj Ames, Alessia Arcaro, Giovanna D'Andrea, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 16, 2021
Homozygous methylentetrahydrofolate reductase C667T genotype anticipates age at venous thromboembolism by one decadePaul R J Ames, Giovanna D'Andrea, Vincenzo Marottoli, et al.
Haematologica|March 26, 2003
The factor V (FV) gene ASP79HIS polymorphism modulates FV plasma levels and affects the activated protein C resistance phenotype in presence of the FV Leiden mutationAnna Bossone, Filomena Cappucci, Giovanna D'Andrea, et al.
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