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Translational Neuroscience
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July 15, 2024
Acute ischemic STROKE - from laboratory to the Patient's BED (STROKELABED): A translational approach to reperfusion injury. Study Protocol
Alessandro 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 model
Paolo 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 study
Emilia 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 antagonists
Alessia 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 Stress
Matteo 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 Italy
Betti 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 deficiency
Stefania 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 domains
Monica 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 analysis
Stefania Petrini, Adele D'Amico, Patrizio Sale, et al.
Page
of 17
Search research articles
Search
Showing results (121-130 of 169) with videos related to
Sort By:
Page
of 17
Translational Neuroscience
|
July 15, 2024
Acute ischemic STROKE - from laboratory to the Patient's BED (STROKELABED): A translational approach to reperfusion injury. Study Protocol
Alessandro 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 model
Paolo 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 study
Emilia 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 antagonists
Alessia 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 Stress
Matteo 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 Italy
Betti 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 deficiency
Stefania 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 domains
Monica 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 analysis
Stefania Petrini, Adele D'Amico, Patrizio Sale, et al.
Page
of 17