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Betti Giusti

Showing results (121-130 of 169) with videos related to

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Translational Neuroscience|July 15, 2024
Acute ischemic STROKE - from laboratory to the Patient's BED (STROKELABED): A translational approach to reperfusion injury. Study ProtocolAlessandro Sodero, Emilia Conti, Benedetta Piccardi, et al.
Archives of Dermatological Research|February 9, 2008
Use of donor bone marrow mesenchymal stem cells for treatment of skin allograft rejection in a preclinical rat modelPaolo Sbano, Aldo Cuccia, Benedetta Mazzanti, et al.
European Journal of Neurology|January 24, 2023
Cognitive phenotypes and factors associated with cognitive decline in a cohort of older patients with atrial fibrillation: The Strat-AF studyEmilia Salvadori, Eleonora Barucci, Carmen Barbato, et al.
Life Sciences|June 9, 2024
The serum metabolomic profiles of atrial fibrillation patients treated with direct oral anticoagulants or vitamin K antagonistsAlessia Vignoli, Anna Maria Gori, Martina Berteotti, et al.
Thrombosis and Haemostasis|December 7, 2017
Erythrocyte Membrane Fluidity Alterations in Sudden Sensorineural Hearing Loss Patients: The Role of Oxidative StressMatteo Becatti, Rossella Marcucci, Amanda Mannucci, et al.
Thrombosis and Haemostasis|May 27, 2020
Sars-CoV-2 Induced Coagulopathy and Prognosis in Hospitalized Patients: A Snapshot from ItalyBetti Giusti, Anna Maria Gori, Manuel Alessi, et al.
Internal and Emergency Medicine|January 30, 2020
Genetic and nutritional factors determining circulating levels of lipoprotein(a): results of the "Montignoso Study"Alice Sereni, Elena Sticchi, Anna Maria Gori, et al.
Molecular and Cellular Neurosciences|September 20, 2005
Altered expression of the MCSP/NG2 chondroitin sulfate proteoglycan in collagen VI deficiencyStefania Petrini, Alessandra Tessa, William B Stallcup, et al.
Blood Advances|July 30, 2020
Noncanonical type 2B von Willebrand disease associated with mutations in the VWF D'D3 and D4 domainsMonica Sacco, Stefano Lancellotti, Mattia Ferrarese, et al.
Neuromuscular Disorders : NMD|June 26, 2007
Ullrich myopathy phenotype with secondary ColVI defect identified by confocal imaging and electron microscopy analysisStefania Petrini, Adele D'Amico, Patrizio Sale, et al.
Pageof 17

Showing results (121-130 of 169) with videos related to

Sort By:
Pageof 17
Translational Neuroscience|July 15, 2024
Acute ischemic STROKE - from laboratory to the Patient's BED (STROKELABED): A translational approach to reperfusion injury. Study ProtocolAlessandro Sodero, Emilia Conti, Benedetta Piccardi, et al.
Archives of Dermatological Research|February 9, 2008
Use of donor bone marrow mesenchymal stem cells for treatment of skin allograft rejection in a preclinical rat modelPaolo Sbano, Aldo Cuccia, Benedetta Mazzanti, et al.
European Journal of Neurology|January 24, 2023
Cognitive phenotypes and factors associated with cognitive decline in a cohort of older patients with atrial fibrillation: The Strat-AF studyEmilia Salvadori, Eleonora Barucci, Carmen Barbato, et al.
Life Sciences|June 9, 2024
The serum metabolomic profiles of atrial fibrillation patients treated with direct oral anticoagulants or vitamin K antagonistsAlessia Vignoli, Anna Maria Gori, Martina Berteotti, et al.
Thrombosis and Haemostasis|December 7, 2017
Erythrocyte Membrane Fluidity Alterations in Sudden Sensorineural Hearing Loss Patients: The Role of Oxidative StressMatteo Becatti, Rossella Marcucci, Amanda Mannucci, et al.
Thrombosis and Haemostasis|May 27, 2020
Sars-CoV-2 Induced Coagulopathy and Prognosis in Hospitalized Patients: A Snapshot from ItalyBetti Giusti, Anna Maria Gori, Manuel Alessi, et al.
Internal and Emergency Medicine|January 30, 2020
Genetic and nutritional factors determining circulating levels of lipoprotein(a): results of the "Montignoso Study"Alice Sereni, Elena Sticchi, Anna Maria Gori, et al.
Molecular and Cellular Neurosciences|September 20, 2005
Altered expression of the MCSP/NG2 chondroitin sulfate proteoglycan in collagen VI deficiencyStefania Petrini, Alessandra Tessa, William B Stallcup, et al.
Blood Advances|July 30, 2020
Noncanonical type 2B von Willebrand disease associated with mutations in the VWF D'D3 and D4 domainsMonica Sacco, Stefano Lancellotti, Mattia Ferrarese, et al.
Neuromuscular Disorders : NMD|June 26, 2007
Ullrich myopathy phenotype with secondary ColVI defect identified by confocal imaging and electron microscopy analysisStefania Petrini, Adele D'Amico, Patrizio Sale, et al.
Pageof 17