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Enrico Farnetti

Showing results (21-30 of 46) with videos related to

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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.
American Journal of Hypertension|April 29, 2011
A clinical phenotype mimicking essential hypertension in a newly discovered family with Liddle's syndromeErmanno Rossi, Enrico Farnetti, Davide Nicoli, 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.
Life (Basel, Switzerland)|October 23, 2021
Cutaneous Localization of Classic Hodgkin Lymphoma Associated with Mycosis Fungoides: Report of a Rare Event and Review of the LiteratureMagda Zanelli, Stefano Ricci, Francesca Sanguedolce, 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.
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.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
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.
American Journal of Hypertension|April 29, 2011
A clinical phenotype mimicking essential hypertension in a newly discovered family with Liddle's syndromeErmanno Rossi, Enrico Farnetti, Davide Nicoli, 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.
Life (Basel, Switzerland)|October 23, 2021
Cutaneous Localization of Classic Hodgkin Lymphoma Associated with Mycosis Fungoides: Report of a Rare Event and Review of the LiteratureMagda Zanelli, Stefano Ricci, Francesca Sanguedolce, 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.
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.
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