Mariano Pomata
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Mariano Pomata has a total of 10 co-authors. Here are the top co-authors by number of shared publications:
- Angelo Nicolosi
Department of Surgical Sciences, University of Cagliari, S. S. 554, Bivio Sestu, 09042 Monserrato, CA, Italy
1 shared publication - Antonello Cappai
Endocrinology Unit, Department of Medical Sciences and Public Health, University of Cagliari, 09100 Cagliari, Italy
1 shared publication - Elena Pardi
Dipartimento di Medicina Clinica e Sperimentale, Università di Pisa, Pisa, Italia
1 shared publication - Enrico Erdas
Department of Surgical Sciences, University of Cagliari, Cagliari, Italy
1 shared publication - Filomena Cetani
Department of Clinical and Experimental Medicine, University of Pisa
1 shared publication - Luca Pilloni
Division of Pathology, Department of Medical Sciences and Public Health, University Hospital of Cagliari, 09124 Cagliari, Italy
1 shared publication
Latest Publications
- Open Access
- 22 December 2012
- Published by Springer Nature in BMC Cancer
- Vol. 12 (1) , 614
Functioning glucagonoma associated with primary hyperparathyroidism: multiple endocrine neoplasia type 1 or incidental association?
Diagnosis of multiple endocrine neoplasia type 1 (MEN1) is commonly based on clinical criteria, and confirmed by genetic testing. In patients without known MEN1-related germline mutations, the possibility of a casual association between two or more endocrine tumors cannot be excluded and subsequent management may be difficult to plan. We describe a very uncommon case of functioning glucagonoma associated with primary hyperparathyroidism (pHPT) in which genetic testing failed to detect germline mutations of MEN-1 and other known genes responsible for MEN1.
- 22 December 2012
- Published by Springer Nature in BMC Cancer
- Vol. 12 (1) , 614
Open AccessFunctioning glucagonoma associated with primary hyperparathyroidism: multiple endocrine neoplasia type 1 or incidental association?
Diagnosis of multiple endocrine neoplasia type 1 (MEN1) is commonly based on clinical criteria, and confirmed by genetic testing. In patients without known MEN1-related germline mutations, the possibility of a casual association between two or more endocrine tumors cannot be excluded and subsequent management may be difficult to plan. We describe a very uncommon case of functioning glucagonoma associated with primary hyperparathyroidism (pHPT) in which genetic testing failed to detect germline mutations of MEN-1 and other known genes responsible for MEN1.