Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Cinzia Carrozza"'
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Copy Number Variations (CNVs) account for a large proportion of human genome and are a primary contributor to human phenotypic variation, in addition to being the molecular basis of a wide spectrum of disease. Multiallelic CNVs represent a considerab
Externí odkaz:
https://doaj.org/article/1cf6fd7578c849be8bdf588ee15703b2
Autor:
Andrea Tamburrano, Doriana Vallone, Cinzia Carrozza, Andrea Urbani, Maurizio Sanguinetti, Nicola Nicolotti, Andrea Cambieri, Patrizia Laurenti
Publikováno v:
PLoS ONE, Vol 15, Iss 8, p e0237159 (2020)
BackgroundComputerized Clinical Decision Support Systems (CCDSS) have become increasingly important in ensuring patient safety and supporting all phases of clinical decision making. The aim of this study is to evaluate, through a CCDSS, the rate of t
Externí odkaz:
https://doaj.org/article/4f62f2d77f874b51b7fe2ea78a42c3ce
Autor:
Maurizio Delvecchio, Francesca Bizzoco, Rosa Lapolla, Antonia Gentile, Cinzia Carrozza, Michele Barone, Simonetta Simonetti, Paola Giordano, Vanessa Nadia Dargenio, Fernanda Cristofori, Ruggiero Francavilla
Publikováno v:
Nutrients, Vol 13, Iss 3, p 808 (2021)
Background: non-autoimmune thyroid disorder is a common finding in celiac patients, more frequent than in the general population. An impairment of iodine absorption has been hypothesized, but it has never been investigated so far. We aimed to evaluat
Externí odkaz:
https://doaj.org/article/88722f87f4834ca280a3f2f525fe8be7
Autor:
Lucia Lisi, Giovanni Camardese, Mariangela Treglia, Giuseppe Tringali, Cinzia Carrozza, Luigi Janiri, Cinzia Dello Russo, Pierluigi Navarra
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e52585 (2013)
It is now well established that major depression is accompanied and characterized by altered responses of the immune-inflammatory system. In this study we investigated the pro-inflammatory activation of monocytes isolated from depressed patients as a
Externí odkaz:
https://doaj.org/article/d53d7bca35a247e3abce8f9a915ab9d1
Autor:
Gregorio Spagni, Matteo Gastaldi, Pietro Businaro, Zeineb Chemkhi, Cinzia Carrozza, Giovanni Mascagna, Silvia Falso, Silvia Scaranzin, Diego Franciotta, Amelia Evoli, Valentina Damato
Publikováno v:
Neurology(R) neuroimmunologyneuroinflammation. 10(1)
Background and ObjectivesLive cell-based assay (CBA) can detect acetylcholine receptors (AChRs) or muscle-specific tyrosine kinase (MuSK) antibodies (Abs) in a proportion of patients with radioimmunoassay (RIA)-double seronegative myasthenia gravis (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15d31bdddf89250f5919d6b39418bbf1
https://pubmed.ncbi.nlm.nih.gov/36270951
https://pubmed.ncbi.nlm.nih.gov/36270951
Publikováno v:
Expert review of endocrinologymetabolism. 17(3)
Acromegaly is a rare disorder characterized by the excessive secretion of growth hormone (GH), mostly caused by pituitary adenomas. While in full-blown cases the diagnosis is easy to establish, milder cases are more challenging. Additionally, establi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23d8bcd3a88353d8e2fefe2e6ff8ca2c
https://pubmed.ncbi.nlm.nih.gov/35485763
https://pubmed.ncbi.nlm.nih.gov/35485763
Autor:
Andrea Urbani, Cinzia Carrozza, Andrea Corsello, Giampaolo Papi, Rosa Maria Paragliola, Salvatore Maria Corsello, Alfredo Pontecorvi, Eleonora Melfa
Publikováno v:
Thyroid. 30:1091-1094
Background: Immune checkpoint inhibitors (ICIs) are associated with several endocrine side effects. In particular, the use of programmed cell death protein-1 (PD-1)/programmed cell death-ligand 1 (PD-L1) inhibitors is related to a higher incidence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39a4ea3d686363abef461a5896fdbd03
https://doi.org/10.1089/thy.2019.0799
https://doi.org/10.1089/thy.2019.0799
Autor:
Paola Concolino, Linda Tartaglione, Elisa De Paolis, Cinzia Carrozza, Andrea Urbani, Angelo Minucci, Dario Pitocco, Concetta Santonocito
Publikováno v:
Genes. 13:2104
Maturity-onset diabetes of the young (MODY) is a rare form of non-autoimmune diabetes with an autosomal dominant inheritance. To date, 14 genes have been reported as genetic basis of MODY. GCK gene, encoding the glucokinase enzyme, was the first MODY
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8301620f27276f2a737065ed26f53123
https://doi.org/10.3390/genes13112104
https://doi.org/10.3390/genes13112104
Autor:
Chiara Mura, Cinzia Carrozza, Pietro Locantore, Roberto Novizio, Laura Rossi, Sara Menotti, Lorenzo Zelano, Corsello Salvatore Maria
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52cadfc2ed3d62e15fc9093fc46cfaca
https://doi.org/10.1530/endoabs.75.t08
https://doi.org/10.1530/endoabs.75.t08
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Frontiers in Endocrinology
Frontiers in Endocrinology
Copy Number Variations (CNVs) account for a large proportion of human genome and are a primary contributor to human phenotypic variation, in addition to being the molecular basis of a wide spectrum of disease. Multiallelic CNVs represent a considerab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b69354f31489a9a1544160a70c128850
https://www.frontiersin.org/articles/10.3389/fendo.2021.709758/full
https://www.frontiersin.org/articles/10.3389/fendo.2021.709758/full