Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Davide Nicoli

Showing results (41-50 of 64) with videos related to

Pageof 7
Sort By:
Experimental and Therapeutic Medicine|January 8, 2025
Clinical exome next‑generation sequencing panel for hereditary pheochromocytoma and paraganglioma diagnosisBeatrice Melli, Vincenza Ylenia Cusenza, Sandra Martinelli, et al.
Journal of Clinical Pathology|November 11, 2015
Diamond: immunohistochemistry versus sequencing in EGFR analysis of lung adenocarcinomasMoira Ragazzi, Ione Tamagnini, Alessandra Bisagni, et al.
Journal of Cancer|September 21, 2017
Prognostic Impact of ABO Blood Group on Type I Endometrial Cancer Patients- Results from Our Own and Other StudiesVincenzo Dario Mandato, Federica Torricelli, Valentina Mastrofilippo, et al.
The Journal of Rheumatology|March 23, 2002
Endothelial nitric oxide synthase gene polymorphisms in Behçet's diseaseCarlo Salvarani, Luigi Boiardi, Bruno Casali, et al.
Anticancer Research|October 13, 2012
Haptoglobin phenotype and epithelial ovarian cancerVincenzo Dario Mandato, Elena Magnani, Martino Abrate, et al.
Journal of Hypertension|October 1, 2019
Concurrent heterozygous Von-Hippel-Lindau and transmembrane-protein-127 gene mutation causing an erythropoietin-secreting pheochromocytoma in a normotensive patient with severe erythrocytosisAurelio Negro, Gallia Graiani, Davide Nicoli, et al.
Clinical Neurology and Neurosurgery|February 28, 2015
Prognostic value of MGMT promoter status in non-resectable glioblastoma after adjuvant therapyCorrado Iaccarino, Elena Orlandi, Francesco Ruggeri, et al.
Medicine|December 23, 2025
Variant analysis and biochemical investigation in two siblings with late onset idiopathic secondary erythrocytosis: A case reportVincenza Ylenia Cusenza, Beatrice Melli, Chiara Marraccini, et al.
Clinical and Experimental Rheumatology|October 5, 2011
PLA1/A2 polymorphism of the platelet glycoprotein receptors IIIA in Behçet's diseaseFabiola Atzeni, Luigi Boiardi, Davide Nicoli, et al.
Rheumatology (Oxford, England)|September 12, 2012
CC chemokine receptor 5 polymorphism in Italian patients with Behcet's diseaseFabiola Atzeni, Luigi Boiardi, Bruno Casali, et al.
Pageof 7

Showing results (41-50 of 64) with videos related to

Sort By:
Pageof 7
Experimental and Therapeutic Medicine|January 8, 2025
Clinical exome next‑generation sequencing panel for hereditary pheochromocytoma and paraganglioma diagnosisBeatrice Melli, Vincenza Ylenia Cusenza, Sandra Martinelli, et al.
Journal of Clinical Pathology|November 11, 2015
Diamond: immunohistochemistry versus sequencing in EGFR analysis of lung adenocarcinomasMoira Ragazzi, Ione Tamagnini, Alessandra Bisagni, et al.
Journal of Cancer|September 21, 2017
Prognostic Impact of ABO Blood Group on Type I Endometrial Cancer Patients- Results from Our Own and Other StudiesVincenzo Dario Mandato, Federica Torricelli, Valentina Mastrofilippo, et al.
The Journal of Rheumatology|March 23, 2002
Endothelial nitric oxide synthase gene polymorphisms in Behçet's diseaseCarlo Salvarani, Luigi Boiardi, Bruno Casali, et al.
Anticancer Research|October 13, 2012
Haptoglobin phenotype and epithelial ovarian cancerVincenzo Dario Mandato, Elena Magnani, Martino Abrate, et al.
Journal of Hypertension|October 1, 2019
Concurrent heterozygous Von-Hippel-Lindau and transmembrane-protein-127 gene mutation causing an erythropoietin-secreting pheochromocytoma in a normotensive patient with severe erythrocytosisAurelio Negro, Gallia Graiani, Davide Nicoli, et al.
Clinical Neurology and Neurosurgery|February 28, 2015
Prognostic value of MGMT promoter status in non-resectable glioblastoma after adjuvant therapyCorrado Iaccarino, Elena Orlandi, Francesco Ruggeri, et al.
Medicine|December 23, 2025
Variant analysis and biochemical investigation in two siblings with late onset idiopathic secondary erythrocytosis: A case reportVincenza Ylenia Cusenza, Beatrice Melli, Chiara Marraccini, et al.
Clinical and Experimental Rheumatology|October 5, 2011
PLA1/A2 polymorphism of the platelet glycoprotein receptors IIIA in Behçet's diseaseFabiola Atzeni, Luigi Boiardi, Davide Nicoli, et al.
Rheumatology (Oxford, England)|September 12, 2012
CC chemokine receptor 5 polymorphism in Italian patients with Behcet's diseaseFabiola Atzeni, Luigi Boiardi, Bruno Casali, et al.
Pageof 7