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Enrico Farnetti

Showing results (31-40 of 46) with videos related to

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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.
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.
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.
Arthritis & Rheumatology (Hoboken, N.J.)|October 6, 2021
VEXAS Syndrome: A Case Series From a Single-Center Cohort of Italian Patients With VasculitisFrancesco Muratore, Chiara Marvisi, Paola Castrignanò, et al.
Hypertension (Dallas, Tex. : 1979)|December 13, 2017
Three Reportedly Unrelated Families With Liddle Syndrome Inherited From a Common AncestorLuca Pagani, Yoan Diekmann, Marco Sazzini, 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.
Frontiers in Endocrinology|April 5, 2021
Case Report: Irreversible Watery Diarrhea, Severe Metabolic Acidosis, Hypokalemia and Achloridria Syndrome Related to Vasoactive Intestinal Peptide Secreting Malignant PheochromocytomaAurelio Negro, Ignazio Verzicco, Stefano Tedeschi, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
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.
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.
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.
Arthritis & Rheumatology (Hoboken, N.J.)|October 6, 2021
VEXAS Syndrome: A Case Series From a Single-Center Cohort of Italian Patients With VasculitisFrancesco Muratore, Chiara Marvisi, Paola Castrignanò, et al.
Hypertension (Dallas, Tex. : 1979)|December 13, 2017
Three Reportedly Unrelated Families With Liddle Syndrome Inherited From a Common AncestorLuca Pagani, Yoan Diekmann, Marco Sazzini, 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.
Frontiers in Endocrinology|April 5, 2021
Case Report: Irreversible Watery Diarrhea, Severe Metabolic Acidosis, Hypokalemia and Achloridria Syndrome Related to Vasoactive Intestinal Peptide Secreting Malignant PheochromocytomaAurelio Negro, Ignazio Verzicco, Stefano Tedeschi, et al.
Pageof 5