Zobrazeno 1 - 10
of 303
pro vyhledávání: '"Francesco Tonelli"'
Publikováno v:
Pharmaceutics, Vol 16, Iss 5, p 640 (2024)
Familial adenomatous polyposis (FAP) is a rare disease characterized by the development of adenomatous polyps in the colon and rectum already in adolescence. If left untreated, patients develop colorectal cancer (CRC) with a 100% probability. To date
Externí odkaz:
https://doaj.org/article/969f7d722b044b2f87c4a1f56a48dfec
Autor:
Francesco Tonelli, Francesca Marini, Francesca Giusti, Teresa Iantomasi, Francesco Giudici, Maria Luisa Brandi
Publikováno v:
Cancers, Vol 15, Iss 20, p 4919 (2023)
Pancreatic neuroendocrine neoplasms (PNENs) affect over 80% of patients with multiple endocrine neoplasia type 1 (MEN1). Surgery is usually the therapy of choice, but the real immediate and long-term therapeutic benefit of a partial extensive pancrea
Externí odkaz:
https://doaj.org/article/fe1da800f74b4d3aaaf56d4165d8cc47
Autor:
Leonardo Guasti, Luisella Cianferotti, Barbara Pampaloni, Francesco Tonelli, Francesco Martelli, Teresa Iantomasi, Maria Luisa Brandi
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionBoth osteoporosis and periodontitis are pathologies characterized by an imbalance in the bone tissue. Vitamin C is an important factor involved in maintaining the health of the periodontium; its deficiency causes characteristic lesions to
Externí odkaz:
https://doaj.org/article/fea569148cf24bf4b4143dc3f77054df
Publikováno v:
European Physical Journal C: Particles and Fields, Vol 81, Iss 11, Pp 1-23 (2021)
Abstract The oscillation of neutron n into mirror neutron $$n'$$ n ′ , its mass degenerate partner from dark mirror sector, can gradually transform the neutron stars into the mixed stars consisting in part of mirror dark matter. In quark stars $$n-
Externí odkaz:
https://doaj.org/article/2b8bbe9e261b41fcb36ac06f39a0a888
Autor:
Francesca Giusti, Federica Cioppi, Caterina Fossi, Francesca Marini, Laura Masi, Francesco Tonelli, Maria Luisa Brandi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-15 (2021)
Abstract Background MEN1 is a complex, rare, syndrome inherited in an autosomal dominant tract and characterized by the development of multiple neuroendocrine tumors, requiring lifelong surveillance and multiple medical and surgical therapies through
Externí odkaz:
https://doaj.org/article/56fd11c71a6d4e5fb557bcf613968d65
Autor:
Francesco Giudici, Tiziana Cavalli, Cristina Luceri, Edda Russo, Daniela Zambonin, Stefano Scaringi, Ferdinando Ficari, Marilena Fazi, Amedeo Amedei, Francesco Tonelli, Cecilia Malentacchi
Publikováno v:
Mediators of Inflammation, Vol 2021 (2021)
Background. CARD15/NOD2 is the most significant genetic susceptibility in Crohn’s disease (CD) even though a relationship between the different polymorphisms and clinical phenotype has not been described yet. The study is aimed at analyzing, in a g
Externí odkaz:
https://doaj.org/article/9f4acd5a3ba74e2883ca3e54184e4edf
Autor:
Francesca Marini, Francesca Giusti, Federica Cioppi, Davide Maraghelli, Tiziana Cavalli, Francesco Tonelli, Maria Luisa Brandi
Publikováno v:
Cells, Vol 10, Iss 8, p 1895 (2021)
Primary hyperparathyroidism (PHPT) is the most common endocrinopathy in multiple endocrine neoplasia type 1 (MEN1). Persistent levels of increased parathyroid hormone (PTH) result in a higher incidence of osteopenia and osteoporosis compared to the g
Externí odkaz:
https://doaj.org/article/3f71393f5b0848a1a4862b8015d3bffe
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 8, p 4041 (2021)
Pancreatic neuroendocrine tumors (pNETs) are a rare group of cancers accounting for about 1–2% of all pancreatic neoplasms. About 10% of pNETs arise within endocrine tumor syndromes, such as Multiple Endocrine Neoplasia type 1 (MEN1). pNETs affect
Externí odkaz:
https://doaj.org/article/1986a01facad42378411a0766db5bd2c
Publikováno v:
Frontiers in Endocrinology, Vol 9 (2018)
Multiple Endocrine Neoplasia Type 1 (MEN1) is a rare inherited endocrine tumor syndrome principally affecting parathyroid glands, neuroendocrine tissues of the gastro-entero-pancreatic and thoracic tracts, and anterior pituitary, caused by germline i
Externí odkaz:
https://doaj.org/article/ace91b03ce394fb699505ba5ad7a73cd
Publikováno v:
Frontiers in Endocrinology, Vol 9 (2018)
Background: The choice of surgical treatment for patients with Multiple Endocrine Neoplasia type 1 (MEN1)-related primary hyperparathyroidism (PHPT) remains controversial and it has not been specifically addressed in young patients.Methods: This is a
Externí odkaz:
https://doaj.org/article/8237bf5a9d574bf0b1adc8679e3350ce