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Massimo Cugno

Showing results (101-110 of 147) with videos related to

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Medicina (Kaunas, Lithuania)|March 14, 2020
Hereditary Deficiency of the Second Component of Complement: Early Diagnosis and 21-Year Follow-Up of a FamilyRosa Maria Dellepiane, Lucia Augusta Baselli, Marco Cazzaniga, et al.
Pediatric Nephrology (Berlin, Germany)|January 22, 2025
Efficacy of complement inhibition with pegcetacoplan in children with C3 glomerulopathyMaria Cristina Mancuso, Massimo Cugno, Samantha Griffini, et al.
Internal and Emergency Medicine|January 21, 2011
Inflammatory and prothrombotic parameters in normotensive non-diabetic obese women: effect of weight loss obtained by gastric bandingMassimo Cugno, Roberto Castelli, Daniela Mari, et al.
Journal of Clinical Medicine|January 8, 2023
IgG and IgE Autoantibodies to IgE Receptors in Chronic Spontaneous Urticaria and Their Role in the Response to OmalizumabCarlo Alberto Maronese, Silvia Mariel Ferrucci, Chiara Moltrasio, et al.
Orphanet Journal of Rare Diseases|May 18, 2016
Invasive meningococcal disease in three siblings with hereditary deficiency of the 8(th) component of complement: evidence for the importance of an early diagnosisRosa Maria Dellepiane, Laura Dell'Era, Paola Pavesi, et al.
The Journal of Allergy and Clinical Immunology|January 6, 2007
Activation of the tissue factor pathway of blood coagulation in patients with chronic urticariaRiccardo Asero, Alberto Tedeschi, Raffaella Coppola, et al.
The Journal of Allergy and Clinical Immunology. in Practice|April 6, 2021
The Pathogenesis of Chronic Spontaneous Urticaria: The Role of Infiltrating CellsAna M Giménez-Arnau, Laurence DeMontojoye, Riccardo Asero, et al.
International Journal of Laboratory Hematology|January 12, 2021
Relationship between thrombin generation parameters and prothrombin fragment 1 + 2 plasma levelsMarco Capecchi, Erica Scalambrino, Samantha Griffini, et al.
Thrombosis Research|September 5, 2020
Genetic and molecular evidence for complement dysregulation in patients with HELLP syndromeMario Bazzan, Tullia Todros, Silvana Tedeschi, et al.
The American Journal of Gastroenterology|August 23, 2002
Kallikrein-kinin system activation in Crohn's disease: differences in intestinal and systemic markersMassimo Devani, Massimo Cugno, Maurizio Vecchi, et al.
Pageof 15

Showing results (101-110 of 147) with videos related to

Sort By:
Pageof 15
Medicina (Kaunas, Lithuania)|March 14, 2020
Hereditary Deficiency of the Second Component of Complement: Early Diagnosis and 21-Year Follow-Up of a FamilyRosa Maria Dellepiane, Lucia Augusta Baselli, Marco Cazzaniga, et al.
Pediatric Nephrology (Berlin, Germany)|January 22, 2025
Efficacy of complement inhibition with pegcetacoplan in children with C3 glomerulopathyMaria Cristina Mancuso, Massimo Cugno, Samantha Griffini, et al.
Internal and Emergency Medicine|January 21, 2011
Inflammatory and prothrombotic parameters in normotensive non-diabetic obese women: effect of weight loss obtained by gastric bandingMassimo Cugno, Roberto Castelli, Daniela Mari, et al.
Journal of Clinical Medicine|January 8, 2023
IgG and IgE Autoantibodies to IgE Receptors in Chronic Spontaneous Urticaria and Their Role in the Response to OmalizumabCarlo Alberto Maronese, Silvia Mariel Ferrucci, Chiara Moltrasio, et al.
Orphanet Journal of Rare Diseases|May 18, 2016
Invasive meningococcal disease in three siblings with hereditary deficiency of the 8(th) component of complement: evidence for the importance of an early diagnosisRosa Maria Dellepiane, Laura Dell'Era, Paola Pavesi, et al.
The Journal of Allergy and Clinical Immunology|January 6, 2007
Activation of the tissue factor pathway of blood coagulation in patients with chronic urticariaRiccardo Asero, Alberto Tedeschi, Raffaella Coppola, et al.
The Journal of Allergy and Clinical Immunology. in Practice|April 6, 2021
The Pathogenesis of Chronic Spontaneous Urticaria: The Role of Infiltrating CellsAna M Giménez-Arnau, Laurence DeMontojoye, Riccardo Asero, et al.
International Journal of Laboratory Hematology|January 12, 2021
Relationship between thrombin generation parameters and prothrombin fragment 1 + 2 plasma levelsMarco Capecchi, Erica Scalambrino, Samantha Griffini, et al.
Thrombosis Research|September 5, 2020
Genetic and molecular evidence for complement dysregulation in patients with HELLP syndromeMario Bazzan, Tullia Todros, Silvana Tedeschi, et al.
The American Journal of Gastroenterology|August 23, 2002
Kallikrein-kinin system activation in Crohn's disease: differences in intestinal and systemic markersMassimo Devani, Massimo Cugno, Maurizio Vecchi, et al.
Pageof 15