If you made any changes in Pure these will be visible here soon.

Fingerprint Dive into the research topics where Enrico Farnetti is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 3 Similar Profiles
Giant Cell Arteritis Medicine & Life Sciences
Genes Medicine & Life Sciences
Intercellular Adhesion Molecule-1 Medicine & Life Sciences
Alleles Medicine & Life Sciences
Liddle Syndrome Medicine & Life Sciences
Polymyalgia Rheumatica Medicine & Life Sciences
CCR5 Receptors Medicine & Life Sciences
Endometrial Neoplasms Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 1999 2019

Concurrent heterozygous Von-Hippel-Lindau and transmembrane-protein-127 gene mutation causing an erythropoietin-secreting pheochromocytoma in a normotensive patient with severe erythrocytosis

Negro, A., Graiani, G., Nicoli, D., Farnetti, E., Casali, B., Verzicco, I., Tedeschi, S., Ghirarduzzi, A., Cannone, V., Marco, L. D. E., Filice, A., Gemelli, G., Giunta, A. & Cabassi, A., Jan 1 2019, (Accepted/In press) In : Journal of Hypertension.

Research output: Contribution to journalArticle

Polycythemia
Pheochromocytoma
Erythropoietin
Mutation
Proteins

Co-occurrence of an HSPG2 Missense Variant and Functional Polymorphisms in Atypical Schwartz-Jampel Syndrome Type 1 with Obesity: A Case Report

Maini, I., Farnetti, E., Nicoli, D., Pavlidis, E., Spagnoli, C., Salerno, G. G., Frattini, D., Iodice, A. & Fusco, C., Jan 1 2019, In : Journal of Pediatric Neurology. 17, 4, p. 149-152 4 p.

Research output: Contribution to journalArticle

Osteochondrodysplasias
Obesity
Exome
Phenotype
perlecan

The clinical relevance of multiple DPYD polymorphisms on patients candidate for fluoropyrimidine based-chemotherapy. An Italian case-control study

Iachetta, F., Bonelli, C., Romagnani, A., Zamponi, R., Tofani, L., Farnetti, E., Nicoli, D., Damato, A., Banzi, M., Casali, B. & Pinto, C., Apr 16 2019, In : British Journal of Cancer. 120, 8, p. 834-839 6 p.

Research output: Contribution to journalArticle

Single Nucleotide Polymorphism
Case-Control Studies
Drug Therapy
Neutropenia
Fluorouracil

A Novel CCND2 Mutation in a Previously Reported Case of Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and Hydrocephalus

Maini, I., Farnetti, E., Caraffi, S. G., Ivanovski, I., de Bernardi, M. L., Gelmini, C., Pollazzon, M., Rosato, S., Laurie, S., Matalonga, L., Baldo, C. & Garavelli, L., Apr 11 2018, (Accepted/In press) In : Neuropediatrics.

Research output: Contribution to journalArticle

Computational development of a molecular-based approach to improve risk stratification of endometrial cancer patients

Torricelli, F., Nicoli, D., Bellazzi, R., Ciarrocchi, A., Farnetti, E., Mastrofilippo, V., Zamponi, R., La Sala, G. B., Casali, B. & Mandato, V. D., May 22 2018, In : Oncotarget. 9, 39, p. 25517-25528 12 p.

Research output: Contribution to journalArticle

Endometrial Neoplasms
Cluster Analysis
Data Mining
Neoplasm Genes
Histology