Zobrazeno 1 - 7
of 7
pro vyhledávání: '"ROSANNA MONETTA"'
Autor:
Mariafrancesca Hyeraci, Elena Sofia Papanikolau, Marta Grimaldi, Francesco Ricci, Sabatino Pallotta, Rosanna Monetta, Ylenia Aura Minafò, Giovanni Di Lella, Giovanna Galdo, Damiano Abeni, Luca Fania, Elena Dellambra
Publikováno v:
Biomolecules, Vol 13, Iss 7, p 1067 (2023)
Non-melanoma skin cancers (NMSCs), which include basal cell carcinoma (BCC), squamous cell carcinoma (SCC), and actinic keratosis (AK), are the most common cancer diseases in the Caucasian race. If diagnosed late and improperly treated, BCC and SCC c
Externí odkaz:
https://doaj.org/article/5e6517ee98d54188be5090b29ddbb0f0
Autor:
Liliana Guerra, Fabio Bergamo, Maria Rosaria D'Apice, Francesco Angelucci, Stefano di Girolamo, Letizia Camerota, Rosanna Monetta, Giorgio Annessi, Daniele Castiglia, Giuseppe Novelli, Mauro Paradisi, Francesco Brancati
Publikováno v:
Acta Dermato-Venereologica, Vol 99, Iss 12, Pp 1192-1194 (2019)
Abstract is missing (Short communication)
Externí odkaz:
https://doaj.org/article/5d19b1bd99194a1c91b73384cc4ca428
Autor:
Paola Fortugno, Rosanna Monetta, Valeria Cinquina, Chiara Rigon, Francesca Boaretto, Chiara De Luca, Nicoletta Zoppi, Luana Di Leandro, Emanuela De Domenico, Arianna Di Daniele, Rodolfo Ippoliti, Francesco Angelucci, Ernesto Di Cesare, Ruggero De Paulis, Leonardo Salviati, Marina Colombi, Francesco Brancati, Marco Ritelli
Pathogenic variants in TGFBR1 are a common cause of Loeys-Dietz syndrome (LDS) characterized by life-threatening aortic and arterial disease. Generally, these are missense changes in highly conserved amino acids in the serine-threonine kinase domain.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bec70ccd70c2800c09ed3cc7c1a0d8d
https://hdl.handle.net/11697/205221
https://hdl.handle.net/11697/205221
Autor:
MARCO INFANTE, PASQUALE DIPERNA, MARINA PASSERI, ROSANNA MONETTA, FRANCO PAPOLA, FRANCESCO BRANCATI, MASSIMILIANO CAPRIO, ANDREA FABBRI
Publikováno v:
Diabetes. 71
KPD is classically regarded as an atypical form of diabetes caused by near-complete beta-cell failure. A 37-year-old Egyptian man (BMI: 27.7 Kg/m2) presented with hyperglycemia (362 mg/dL) and DKA (arterial pH 7.20, ketonemia 5.0 mmol/L, ketonuria 80
Autor:
Edwin P. Kirk, Patrick M. A. Sleiman, Meredith Wilson, Alicia R. P. Aycinena, Rosanna Monetta, Michael Buckley, Oana Caluseriu, Paola Fortugno, Anne M. Turner, Louise C. Pyle, María José Sánchez-Soler, Elaine H. Zackai, Yiran Guo, Liza L Cox, Leticia S. Matsuoka, Emma Bedoukian, Letizia Camerota, Timothy C. Cox, Benjamin Kamien, Christoph Seiler, Tony Roscioli, Allison Tam, Dong Li, Chirag Patel, Annelies Dheedene, Michael E. March, Candy Kumps, Elizabeth J. Bhoj, John Christodoulou, Hakon Hakonarson, Francesco Brancati, Katheryn Grand, Bert Callewaert
Publikováno v:
Hum Genet
Human genetics, vol 140, iss 7
Human genetics, vol 140, iss 7
Teebi hypertelorism syndrome (THS; OMIM 145420) is a rare craniofacial disorder characterized by hypertelorism, prominent forehead, short nose with broad or depressed nasal root. Some cases of THS have been attributed to SPECC1L variants. Homozygous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::030edbe721add081a2170d0dc3066dce
http://hdl.handle.net/11697/179001
http://hdl.handle.net/11697/179001
Autor:
Giuseppe Novelli, Fabio Bergamo, Maria Rosaria D'Apice, Mauro Paradisi, Daniele Castiglia, Francesco Angelucci, Rosanna Monetta, Giorgio Annessi, Liliana Guerra, Letizia Camerota, Francesco Brancati, Stefano Di Girolamo
Publikováno v:
Acta Dermato-Venereologica, Vol 99, Iss 12, Pp 1192-1194 (2019)
is missing (Short communication)
Autor:
Francesca Moretti, Paola Fortugno, Francesco Brancati, Luca Bianchi, Daniele Castiglia, Francesco Angelucci, Letizia Camerota, B. Didona, Rosanna Monetta, Elisabetta Botti
Publikováno v:
Journal of Investigative Dermatology. 139:S230