Zobrazeno 1 - 10 of 26 pro vyhledávání: '"M R, Ambrosio"'
1
Akademický článek
Tumour-induced osteomalacia: 18 months of 2-weekly burosumab treatment
Autor: L Aliberti, I Gagliardi, M Pontrelli, M C Zatelli, M R Ambrosio
Publikováno v: Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-7 (2023)
Tumour-induced osteomalacia (TIO) is due to an overproduction of fibroblast growth factor 23 (FGF23) by mesenchymal tumours, causing hypophosphatemia, osteomalacia and muscle weakness. TIO is usually cured by tumour resection, but neoplasms may be
Externí odkaz: https://doaj.org/article/6c9828172b9c47508f7d50cf76fd7412
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2
Protein kinase C delta mediates Pasireotide effects in an ACTH-secreting pituitary tumor cell line
Autor: E. Gentilin, P. Borges De Souza, M. R. Ambrosio, M. Bondanelli, I. Gagliardi, M. C. Zatelli
Publikováno v: Journal of Endocrinological Investigation.
Purpose Clinical control of corticotroph tumors is difficult to achieve since they usually persist or relapse after surgery. Pasireotide is approved to treat patients with Cushing’s disease for whom surgical therapy is not an option. However, Pasir
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ab293f3db1afd728310f0a5a96d0971e
https://doi.org/10.1007/s40618-023-02117-0
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4
GH/IGF-1 axis in a large cohort of ß-thalassemia major adult patients: a cross-sectional study
Autor: I. Gagliardi, R. Mungari, M. R. Gamberini, M. Fortini, F. Dassie, M. C. Putti, P. Maffei, L. Aliberti, M. Bondanelli, M. C. Zatelli, M. R. Ambrosio
Publikováno v: Journal of Endocrinological Investigation. 45:1439-1445
Purpose GH deficit (GHD) could represent an endocrine issue in ß-Thalassemia Major (ßTM) patients. GH/IGF-1 axis has not been extensively explored in ßTM adults, so far. We aim to assess GHD and IGF-1 deficiency prevalence in ßTM adult population
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f13e3ac8c88732cbcba669c50dcf9966
https://doi.org/10.1007/s40618-022-01780-z
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5
Investigation of COVID‑19 infection in subjects with Klinefelter syndrome
Autor: L. Aliberti, I. Gagliardi, S. Lupo, M. Verrienti, M. Bondanelli, M. C. Zatelli, M. R. Ambrosio
Publikováno v: Journal of Endocrinological Investigation
Purpose COVID-19 has worse clinical outcomes in males compared with females and testosterone may determine gender differences. Hypogonadism and supernumerary X chromosome may have a role in the SARS-CoV-2 infection in Klinefelter syndrome (KS). Aim o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c169b3b692e62c87da4cc5dfc922b1f
http://hdl.handle.net/11392/2488901
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6
Communicating the diagnosis of Klinefelter syndrome to children and adolescents: when, how, and who?
Autor: L. Aliberti, I. Gagliardi, S. Bigoni, S. Lupo, S. Caracciolo, A. Ferlini, A. M. Isidori, M. C. Zatelli, M. R. Ambrosio
Publikováno v: Journal of community genetics. 13(3)
Klinefelter syndrome (KS) is the most frequent sex chromosome aneuploidy in males. KS diagnosis disclosure has an important impact on diagnosis acceptance and the increase in prenatal diagnostic procedures raises questions regarding communication to
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc81af1952bdbe60896c33d9261f1cc8
https://pubmed.ncbi.nlm.nih.gov/35247190
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7
Akademický článek
PPARG in Human Adipogenesis: Differential Contribution of Canonical Transcripts and Dominant Negative Isoforms
Autor: M. Aprile, M. R. Ambrosio, V. D'Esposito, F. Beguinot, P. Formisano, V. Costa, A. Ciccodicola
Publikováno v: PPAR Research, Vol 2014 (2014)
The nuclear receptor PPARγ is a key regulator of adipogenesis, and alterations of its function are associated with different pathological processes related to metabolic syndrome. We recently identified two PPARG transcripts encoding dominant negativ
Externí odkaz: https://doaj.org/article/ea3552b547dd488694031e53be1cbc33
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8
Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH)
Autor: Marco Bonomi, Valeria Vezzoli, Csilla Krausz, Fabiana Guizzardi, Silvia Vezzani, Manuela Simoni, Ivan Bassi, Paolo Duminuco, Natascia Di Iorgi, Claudia Giavoli, Alessandro Pizzocaro, Gianni Russo, Mirella Moro, Letizia Fatti, Alberto Ferlin, Laura Mazzanti, Maria Chiara Zatelli, Salvo Cannavò, Andrea M Isidori, Angela Ida Pincelli, Flavia Prodam, Antonio Mancini, Paolo Limone, Maria Laura Tanda, Rossella Gaudino, Mariacarolina Salerno, Pregnolato Francesca, Mohamad Maghnie, Mario Maggi, Luca Persani, G Aimaretti, M Altobelli, M R Ambrosio, M Andrioli, G Angeletti, F Arecco, G Arnaldi, M Arosio, A Balsamo, M Baldassarri, L Bartalena, N Bazzoni, L Beccaria, P Beck-Peccoz, G Bellastella, M Bellizzi, F Benedicenti, S Bernasconi, C Bizzarri, G Bona, S Bonadonna, G Borretta, M Boschetti, A Brunani, V Brunelli, F Buzi, C Cacciatore, B Cangiano, M Cappa, R Casalone, A Cassio, P Cavarzere, V Cherubini, T Ciampani, D Cicognani, A Cignarelli, M Cisternino, P Colombo, S Corbetta, N Corciulo, G Corona, R Cozzi, C Crivellaro, I Dalle Mule, L Danesi, A V D’Elia, E degli Uberti, S De Leo, E Della Valle, M De Marchi, N Di Iorgi, A Di Mambro, A Fabbri, C Foresta, G Forti, A R Franceschi, A Garolla, M Ghezzi, C Giacomozzi, M Giusti, E Grosso, G Guabello, M P Guarneri, G Grugni, A M Isidori, F Lanfranco, A Lania, R Lanzi, L Larizza, A Lenzi, S Loche, P Loli, V Lombardi, M C Maggio, G Mandrile, C Manieri, G Mantovani, S Marelli, M Marzullo, M A Mencarelli, N Migone, G Motta, G Neri, G Padova, G Parenti, B Pasquino, A Pia, E Piantanida, E Pignatti, A Pilotta, B Pivetta, M Pollazzon, A Pontecorvi, P Porcelli, G B Pozzan, G Pozzobon, G Radetti, P Razzore, L Rocchetti, R Roncoroni, G Rossi, E Sala, A Salvatoni, F Salvini, A Secco, M Segni, R Selice, P Sgaramella, F Sileo, A A Sinisi, F Sirchia, A Spada, A Tresoldi, R Vigneri, G Weber, S Zucchini
Objective Isolated hypogonadotropic hypogonadism (IHH) is a rare disorder with pubertal delay, normal (normoosmic-IHH, nIHH) or defective sense of smell (Kallmann syndrome, KS). Other reproductive and non-reproductive anomalies might be present altho
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f800b3107977776e40dbca2a965ea877
http://hdl.handle.net/11383/2066625
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9
Leiomyomatosis peritonealis disseminata: an additional case
Autor: A, Barone, M R, Ambrosio, B J, Rocca, M G, Mastrogiulio, A, Ambrosio, R, Santopietro
Publikováno v: ResearcherID
Leiomyomatosis peritonealis disseminata (PPD) is a rare smooth muscle tumour of women in the reproductive age. It is characterized by multiple small nodules on the peritoneal surface, mimicking a metastatic process. To date, about 100 cases have been
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c351bf455dbaa923eca24c93343867a6
http://hdl.handle.net/11365/1007143
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