Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Giuseppina Renzulli"'
Autor:
Vincenzo Triggiani, Giuseppe Lisco, Giuseppina Renzulli, Andrea Frasoldati, Rinaldo Guglielmi, Jeffrey Garber, Enrico Papini
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2023)
BackgroundThe detection of thyroid nodules has been increasing over time, resulting in an extensive use of fine-needle aspiration (FNA) and cytology. Tailored methods are required to improve the management of thyroid nodules, including algorithms and
Externí odkaz:
https://doaj.org/article/3c4a4eb049c4457d9897f66985ac6358
Autor:
Valentina Ferraro, Lucia Ilaria Sgaramella, Giovanna Di Meo, Francesco Paolo Prete, Francesco Logoluso, Francesco Minerva, Marica Noviello, Giuseppina Renzulli, Angela Gurrado, Mario Testini
Publikováno v:
BMC Endocrine Disorders, Vol 19, Iss S1, Pp 1-9 (2019)
Abstract Background Parathyroid carcinoma is a rare neoplasm that may present sporadically or in the context of a genetic syndrome. Diagnosis and management are challenging due to the lack of clinical and pathological features that may reliably disti
Externí odkaz:
https://doaj.org/article/6e2245b0c9cf4695ae26e0232d1e3e49
Autor:
Giuseppe Lisco, Giuseppina Renzulli, Andrea Frasoldati, Rinaldo Guglielmi, Giagulli Vito Angelo, Edoardo Guastamacchia, Garber Jeffrey R, Vincenzo Triggiani, Enrico Papini
Publikováno v:
Endocrine Abstracts.
Autor:
Angela Gurrado, Giovanna Di Meo, Giuseppina Renzulli, Francesco Minerva, Valentina Ferraro, Lucia Ilaria Sgaramella, Mario Testini, Marica Noviello, Francesco Logoluso, Francesco Paolo Prete
Publikováno v:
BMC Endocrine Disorders, Vol 19, Iss S1, Pp 1-9 (2019)
BMC Endocrine Disorders
BMC Endocrine Disorders
Background Parathyroid carcinoma is a rare neoplasm that may present sporadically or in the context of a genetic syndrome. Diagnosis and management are challenging due to the lack of clinical and pathological features that may reliably distinguish ma
Autor:
Vincenzo Triggiani, Marco Castellana, Paolo Basile, Vito Angelo Giagulli, Giuseppina Renzulli
Publikováno v:
Endocrine, Metabolic & Immune Disorders Drug Targets
Background:Neurofibromatosis type 1 is an autosomal dominant disorder characterized by an increased incidence of tumors, including endocrine ones. Primary hyperparathyroidism can be rarely caused by a parathyroid carcinoma; these patients are general
Autor:
Gaetano Paolino, Giuseppe Zamboni, Ada Maria Florena, Aldo Scarpa, Paola Capelli, Claudio Doglioni, Giuseppina Renzulli, Sara Pecori, Giuseppe Ingravallo, Claudio Luchini, Matteo Fassan
Publikováno v:
Pathologica
Summary Inflammatory/tumor-like lesions of the pancreas represent a heterogeneous group of diseases that can variably involve the pancreatic gland determining different signs and symptoms. In the category of inflammatory/tumor-like lesions of the pan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac4a06ad12df667303c9ef9d27f8c621
http://hdl.handle.net/11577/3363293
http://hdl.handle.net/11577/3363293
Autor:
Ada Maria Florena, Paola Parente, Aldo Scarpa, Claudio Doglioni, Giuseppina Renzulli, Matteo Fassan, Giuseppe Zamboni, Paola Mattiolo, Giuseppe Ingravallo, Alessandro D'Amuri, Sara Pecori, Alessandro Vanoli, Gaetano Paolino, Claudio Luchini, Federica Grillo, Paola Capelli
Publikováno v:
Pathologica
Summary Pancreatic malignant exocrine tumors represent the most important cause of cancer-related death for pancreatic neoplasms. The most common tumor type in this category is represented by pancreatic ductal adenocarcinoma (PDAC), an ill defined, s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef876ea4e6f4cc527ed88161ffde6e74
http://hdl.handle.net/11577/3363292
http://hdl.handle.net/11577/3363292
Publikováno v:
Endocrine, metabolicimmune disorders drug targets. 20(2)
Introduction: Medullary thyroid carcinoma (MTC) is an infrequent thyroid malignancy rarely observed and managed during pregnancy. An accurate diagnostic workup is extremely important in this clinical setting to correctly diagnose and treat the diseas
Autor:
Andrea Madaro, Angela Pezzolla, Giovanni Docimo, Giuseppina Renzulli, Francesco Paolo Prete, Emanuela Lacalendola, Rinaldo Marzaioli, Serafina Lattarulo
Publikováno v:
Minerva Surgery. 72
Autor:
Rosanna Bagnulo, Edoardo Guastamacchia, E. Tafaro, Vito Angelo Giagulli, Francesco Resta, Alessandro Stella, Vincenzo Triggiani, Giuseppina Renzulli, Brunella Licchelli, Nicoletta Resta, Patrizia Lastella, Carlo Sabbà
Publikováno v:
Thyroid. 21:1273-1277
Peutz-Jeghers syndrome (PJS) is a rare dominantly inherited disease characterized by the association of gastrointestinal hamartomatous polyposis, mucocutaneous hyperpigmentation, and increased risk of cancer at different target organs. Its occurrence