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Maria Lombardi

Showing results (21-30 of 108) with videos related to

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Cancer Causes & Control : CCC|April 15, 2016
Meat intake and non-Hodgkin lymphoma: a meta-analysis of observational studiesAngelo G Solimini, Anna Maria Lombardi, Caterina Palazzo, et al.
Hematology (Amsterdam, Netherlands)|August 2, 2017
Congenital prothrombin defects: they are not only associated with bleeding but also with thrombosis: a new classification is neededAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|May 31, 2007
The M flax rust resistance pre-mRNA is alternatively spliced and contains a complex upstream untranslated regionSimon Schmidt, Maria Lombardi, Donald M Gardiner, et al.
Scientific Reports|June 21, 2023
The impact of facial expression and communicative gaze of a humanoid robot on individual Sense of AgencyMaria Lombardi, Cecilia Roselli, Kyveli Kompatsiari, et al.
Frontiers in Bioscience (Landmark Edition)|January 7, 2022
Role of misfolding in rare enzymatic deficits and use of pharmacological chaperones as therapeutic approachGioena Pampalone, Silvia Grottelli, Leonardo Gatticchi, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 2, 2016
Pulmonary embolism in congenital bleeding disorders: intriguing discrepancies among different clotting factors deficienciesAntonio Girolami, Elisabetta Cosi, Valentina Tasinato, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|July 1, 2017
Bleeding manifestations in heterozygotes with prothrombin deficiency or abnormalities vs. unaffected family members as observed during a long follow-up studyAntonio Girolami, Claudia Santarossa, Elisabetta Cosi, et al.
European Journal of Haematology|April 29, 2016
Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years)Antonio Girolami, Elisabetta Cosi, Claudia Santarossa, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 4, 2008
Genetic study in patients with factor XII deficiency: a report of three new mutations exon 13 (Q501STOP), exon 14 (P547L) and -13C>T promoter region in three compound heterozygotesAnna Maria Lombardi, Elisabetta Bortoletto, Pamela Scarparo, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|December 30, 2016
Factor X Friuli Coagulation Disorder: Almost 50 Years LaterAntonio Girolami, Elisabetta Cosi, Claudia Santarossa, et al.
Pageof 11

Showing results (21-30 of 108) with videos related to

Sort By:
Pageof 11
Cancer Causes & Control : CCC|April 15, 2016
Meat intake and non-Hodgkin lymphoma: a meta-analysis of observational studiesAngelo G Solimini, Anna Maria Lombardi, Caterina Palazzo, et al.
Hematology (Amsterdam, Netherlands)|August 2, 2017
Congenital prothrombin defects: they are not only associated with bleeding but also with thrombosis: a new classification is neededAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|May 31, 2007
The M flax rust resistance pre-mRNA is alternatively spliced and contains a complex upstream untranslated regionSimon Schmidt, Maria Lombardi, Donald M Gardiner, et al.
Scientific Reports|June 21, 2023
The impact of facial expression and communicative gaze of a humanoid robot on individual Sense of AgencyMaria Lombardi, Cecilia Roselli, Kyveli Kompatsiari, et al.
Frontiers in Bioscience (Landmark Edition)|January 7, 2022
Role of misfolding in rare enzymatic deficits and use of pharmacological chaperones as therapeutic approachGioena Pampalone, Silvia Grottelli, Leonardo Gatticchi, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 2, 2016
Pulmonary embolism in congenital bleeding disorders: intriguing discrepancies among different clotting factors deficienciesAntonio Girolami, Elisabetta Cosi, Valentina Tasinato, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|July 1, 2017
Bleeding manifestations in heterozygotes with prothrombin deficiency or abnormalities vs. unaffected family members as observed during a long follow-up studyAntonio Girolami, Claudia Santarossa, Elisabetta Cosi, et al.
European Journal of Haematology|April 29, 2016
Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years)Antonio Girolami, Elisabetta Cosi, Claudia Santarossa, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 4, 2008
Genetic study in patients with factor XII deficiency: a report of three new mutations exon 13 (Q501STOP), exon 14 (P547L) and -13C>T promoter region in three compound heterozygotesAnna Maria Lombardi, Elisabetta Bortoletto, Pamela Scarparo, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|December 30, 2016
Factor X Friuli Coagulation Disorder: Almost 50 Years LaterAntonio Girolami, Elisabetta Cosi, Claudia Santarossa, et al.
Pageof 11