Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Celeste Casto"'
Autor:
Giovanni Luppino, Malgorzata Wasniewska, Celeste Casto, Chiara Ferraloro, Alessandra Li Pomi, Giorgia Pepe, Letteria Anna Morabito, Angela Alibrandi, Domenico Corica, Tommaso Aversa
Publikováno v:
Children, Vol 11, Iss 2, p 205 (2024)
Background: Possible therapeutic failure of pediatric obesity is influenced by the high dropout rate. The aim of this study was to evaluate the rate of dropout and the rate of weight loss over the 24 months of follow-up. Methods: The retrospective, s
Externí odkaz:
https://doaj.org/article/402e8bea03394405bf54340de740daaf
Autor:
Antonella Gambadauro, Giorgia Pepe, Celeste Casto, Angelo Tropeano, Carmelo Romeo, Malgorzata Wasniewska
Publikováno v:
Atti della Accademia Peloritana dei Pericolanti - Classe di Scienze Medico-Biologiche, Vol 109, Iss 2, Pp 1-5 (2021)
NR5A1 gene mutations are associated principally to 46,XY DSD (Disorders of Sex Development), with an extensive range of phenotypic variability in patients, comprising gonadal dysgenesis and male infertility. NR5A1 gene plays a crucial role in reprodu
Externí odkaz:
https://doaj.org/article/dc8b1da367c04705be89e6d69957d740
Autor:
Celeste Casto, Valeria Dipasquale, Ida Ceravolo, Antonella Gambadauro, Emanuela Aliberto, Karol Galletta, Francesca Granata, Giorgia Ceravolo, Emanuela Falzia, Antonella Riva, Gianluca Piccolo, Maria Concetta Cutrupi, Pasquale Striano, Andrea Accogli, Federico Zara, Gabriella Di Rosa, Eloisa Gitto, Elisa Calì, Stephanie Efthymiou, Vincenzo Salpietro, Henry Houlden, Roberto Chimenz
Publikováno v:
Brain Sciences, Vol 11, Iss 9, p 1150 (2021)
Nance-Horan syndrome (NHS) is a rare X-linked developmental disorder caused mainly by loss of function variants in the NHS gene. NHS is characterized by congenital cataracts, dental anomalies, and distinctive facial features, and a proportion of the
Externí odkaz:
https://doaj.org/article/89759c36717a4e648545340fe0b0820a
Autor:
Giorgia Ceravolo, Tommaso La Macchia, Caterina Cuppari, Valeria Dipasquale, Antonella Gambadauro, Celeste Casto, Maria Domenica Ceravolo, Maricia Cutrupi, Maria Pia Calabrò, Paola Borgia, Gianluca Piccolo, Alessio Mancuso, Remo Albiero, Roberto Chimenz
Publikováno v:
Children, Vol 8, Iss 7, p 528 (2021)
Cardiorenal syndrome (CRS) is defined as a disorder resulting from the abnormal interaction between the heart and kidney, in which acute or chronic dysfunction of one organ may lead to acute and/or chronic dysfunction of the other. The functional int
Externí odkaz:
https://doaj.org/article/201b2f8ab6eb4aad8a933323cefc2531
Autor:
Antonella Riva, Antonella Gambadauro, Valeria Dipasquale, Celeste Casto, Maria Domenica Ceravolo, Andrea Accogli, Marcello Scala, Giorgia Ceravolo, Michele Iacomino, Federico Zara, Pasquale Striano, Caterina Cuppari, Gabriella Di Rosa, Maria Concetta Cutrupi, Vincenzo Salpietro, Roberto Chimenz
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 9, p 4471 (2021)
Microphthalmia, anophthalmia, and coloboma (MAC) are a group of congenital eye anomalies that can affect one or both eyes. Patients can present one or a combination of these ocular abnormalities in the so called “MAC spectrum”. The KIF17 gene enc
Externí odkaz:
https://doaj.org/article/18d935bf736340a09615435c56d75318
Autor:
Chiara Cuzzupè, Simona Santucci, Elda Pitrolo, Celeste Casto, Irene Viola, Claudio Romano, Mariella Valenzise, Filippo De Luca
Publikováno v:
Atti della Accademia Peloritana dei Pericolanti - Classe di Scienze Medico-Biologiche, Vol 105, Iss 2 (2017)
Chronic granulomatous disease is a rare, inherited immunodeficiency caused by deletions or mutations in genes that encode subunits of the NADPH oxidase complex. The pattern of chronic granulomatous disease inheritance can be X-linked (about 70% of ca
Externí odkaz:
https://doaj.org/article/71dbed3b2a0746ce82ccf858d41ad4ff
Autor:
Giovanni Clemente Actis, Nusrat Ahsan, Rodolfo Alejandro, Angelo Armandi, Stefano Ascani, Tommaso Aversa, Mohammad Bashir, Danielle J. Beetler, Marina Beltrami, Nicola Bizzaro, Carmen Bonanno, Alexandro Bonifaz, Michael J. Brenner, Katelyn A. Bruno, Tess Moore Calcagno, Silvia Angélica Carmona-Cruz, Celeste Casto, Domenico Corica, Arianna Di Stadio, Andrea Fabbri, DeLisa Fairweather, Ahmed Fayed, María Teresa García-Romero, Antonio Greco, Mohamed Tharwat Hegazy, Callum Howard, Mohamed A. Hussein, Mohammed Idhrees, Marco Infante, Mahnaz Jamee, Prassana Karthik, Ilaria Maccora, Edoardo Marrani, Maria Vincenza Mastrolia, Nehman Meharban, Mehdi Mirsaeidi, Emmanuel Keddy Momoh, Wahaj Munir, Ilaria Pagnini, Farzad Pakdel, Andrea Palicelli, Giorgia Pepe, Leonardo Picca, Niloofar Pirmarzdashti, Theresa T. Pizarro, Alessandra Li Pomi, Luca Quartuccio, Gaafar Ragab, Massimo Ralli, Nima Rezaei, Davide Giuseppe Ribaldone, Camillo Ricordi, Francesca Sanguedolce, Jonathan D. Santoro, Jonathan Sheridan, Gabriele Simonini, Alessandra Soriano, Marco Soriano, Timothy J. Sullivan, Andrés Tirado-Sánchez, Renato Tozzoli, Angelo Tropeano, Mariella Valenzise, Malgorzata Wasniewska, Niloufar Yazdanpanah, Magda Zanelli, Maurizio Zizzo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0274c12a2c8750cb22cb48f3036638dd
https://doi.org/10.1016/b978-0-12-824466-1.09987-8
https://doi.org/10.1016/b978-0-12-824466-1.09987-8
Autor:
Antonella, Riva, Antonella, Gambadauro, Valeria, Dipasquale, Celeste, Casto, Maria Domenica, Ceravolo, Andrea, Accogli, Marcello, Scala, Giorgia, Ceravolo, Michele, Iacomino, Federico, Zara, Pasquale, Striano, Caterina, Cuppari, Gabriella, Di Rosa, Maria Concetta, Cutrupi, Vincenzo, Salpietro, Roberto, Chimenz
Publikováno v:
International Journal of Molecular Sciences
Microphthalmia, anophthalmia, and coloboma (MAC) are a group of congenital eye anomalies that can affect one or both eyes. Patients can present one or a combination of these ocular abnormalities in the so called “MAC spectrum”. The KIF17 gene enc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::859b125730460b1ec4ce08f2a34d9637
https://pubmed.ncbi.nlm.nih.gov/33922911
https://pubmed.ncbi.nlm.nih.gov/33922911
Autor:
Caterina Cuppari, Celeste Casto, Roberto Chimenz, Andrea Accogli, Valeria Dipasquale, Vincenzo Salpietro, Gabriella Di Rosa, Federico Zara, Maria Concetta Cutrupi, Pasquale Striano, Antonella Riva, G Ceravolo, Antonella Gambadauro, Michele Iacomino, M D Ceravolo, Marcello Scala
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 4471, p 4471 (2021)
International Journal of Molecular Sciences
Volume 22
Issue 9
International Journal of Molecular Sciences
Volume 22
Issue 9
Microphthalmia, anophthalmia, and coloboma (MAC) are a group of congenital eye anomalies that can affect one or both eyes. Patients can present one or a combination of these ocular abnormalities in the so called “MAC spectrum”. The KIF17 gene enc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb98d38aa65beb606cb0b610de3db6df
https://www.mdpi.com/1422-0067/22/9/4471
https://www.mdpi.com/1422-0067/22/9/4471