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Davide Nicoli

Showing results (31-40 of 64) with videos related to

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Rheumatology (Oxford, England)|January 25, 2011
CC chemokine receptor 5 polymorphism in chronic periaortitisLuigi Boiardi, Augusto Vaglio, Davide Nicoli, et al.
Clinical and Experimental Dermatology|August 29, 2025
Clinical, dermoscopic and confocal microscopy features of multiple primary melanomas according to germline variant status: a retrospective, hospital-based studyMarco Spadafora, Beatrice Melli, Jonida Bardhushi, et al.
Rheumatology International|September 8, 2012
IL-23A, IL-23R, IL-17A and IL-17R polymorphisms in different psoriatic arthritis clinical manifestations in the northern Italian populationMaria Grazia Catanoso, Luigi Boiardi, Pierluigi Macchioni, et al.
Arthritis and Rheumatism|October 2, 2007
PlA1/A2 polymorphism of the platelet glycoprotein receptor IIIA and risk of cranial ischemic complications in giant cell arteritisCarlo Salvarani, Bruno Casali, Enrico Farnetti, et al.
Journal of Human Genetics|October 29, 2019
Alazami syndrome: the first case of papillary thyroid carcinomaIvan Ivanovski, Stefano Giuseppe Caraffi, Elisa Magnani, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|April 23, 2015
Polymorphisms in cyclooxygenase-2 gene in endometrial cancer patientsFederica Torricelli, Vincenzo Dario Mandato, Enrico Farnetti, et al.
BMC Cancer|April 18, 2015
HNF1B polymorphism influences the prognosis of endometrial cancer patients: a cohort studyVincenzo Dario Mandato, Enrico Farnetti, Federica Torricelli, et al.
Fetal and Pediatric Pathology|April 24, 2025
Thoracic Giant Venous Malformation in a Stillbirth with <i>Pik3ca</i> Somatic MutationNunzio Cosimo Mario Salfi, Sabrina Gismondi, Anna Martinelli, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|December 19, 2022
Mother-newborn ABO group discrepancy caused by a rare BW.17 variantChiara Marraccini, Barbara Iotti, Petronilla Vanzanelli, et al.
Annals of the Rheumatic Diseases|September 6, 2015
MicroRNA markers of inflammation and remodelling in temporal arteries from patients with giant cell arteritisStefania Croci, Alessandro Zerbini, Luigi Boiardi, et al.
Pageof 7

Showing results (31-40 of 64) with videos related to

Sort By:
Pageof 7
Rheumatology (Oxford, England)|January 25, 2011
CC chemokine receptor 5 polymorphism in chronic periaortitisLuigi Boiardi, Augusto Vaglio, Davide Nicoli, et al.
Clinical and Experimental Dermatology|August 29, 2025
Clinical, dermoscopic and confocal microscopy features of multiple primary melanomas according to germline variant status: a retrospective, hospital-based studyMarco Spadafora, Beatrice Melli, Jonida Bardhushi, et al.
Rheumatology International|September 8, 2012
IL-23A, IL-23R, IL-17A and IL-17R polymorphisms in different psoriatic arthritis clinical manifestations in the northern Italian populationMaria Grazia Catanoso, Luigi Boiardi, Pierluigi Macchioni, et al.
Arthritis and Rheumatism|October 2, 2007
PlA1/A2 polymorphism of the platelet glycoprotein receptor IIIA and risk of cranial ischemic complications in giant cell arteritisCarlo Salvarani, Bruno Casali, Enrico Farnetti, et al.
Journal of Human Genetics|October 29, 2019
Alazami syndrome: the first case of papillary thyroid carcinomaIvan Ivanovski, Stefano Giuseppe Caraffi, Elisa Magnani, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|April 23, 2015
Polymorphisms in cyclooxygenase-2 gene in endometrial cancer patientsFederica Torricelli, Vincenzo Dario Mandato, Enrico Farnetti, et al.
BMC Cancer|April 18, 2015
HNF1B polymorphism influences the prognosis of endometrial cancer patients: a cohort studyVincenzo Dario Mandato, Enrico Farnetti, Federica Torricelli, et al.
Fetal and Pediatric Pathology|April 24, 2025
Thoracic Giant Venous Malformation in a Stillbirth with <i>Pik3ca</i> Somatic MutationNunzio Cosimo Mario Salfi, Sabrina Gismondi, Anna Martinelli, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|December 19, 2022
Mother-newborn ABO group discrepancy caused by a rare BW.17 variantChiara Marraccini, Barbara Iotti, Petronilla Vanzanelli, et al.
Annals of the Rheumatic Diseases|September 6, 2015
MicroRNA markers of inflammation and remodelling in temporal arteries from patients with giant cell arteritisStefania Croci, Alessandro Zerbini, Luigi Boiardi, et al.
Pageof 7