Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Giovanna Paglietti"'
Autor:
Adele D’Amico, Antonella Longo, Fabiana Fattori, Michele Tosi, Luca Bosco, Maria Beatrice Chiarini Testa, Giovanna Paglietti, Claudio Cherchi, Adelina Carlesi, Irene Mizzoni, Enrico Bertini
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-7 (2021)
Abstract Background X-linked myotubular myopathy (XLMTM) is a rare congenital myopathy resulting from pathogenic variants in the MTM1 gene. Affected male subjects typically present with severe hypotonia and respiratory distress at birth and they ofte
Externí odkaz:
https://doaj.org/article/6c3ecfacd54d438aaffe437c59802931
Autor:
Valeria Fox, Gianluca Vrenna, Gianluca Foglietta, Luna Colagrossi, Barbara Lucignano, Manuela Onori, Venere Cortazzo, Marilena Agosta, Martina Rossitto, Maria del Carmen Pereyra Boza, Vanessa Fini, Annarita Granaglia, Maria Giovanna Paglietti, Elisabetta Verrillo, Renato Cutrera, Paola Bernaschi, Carlo Federico Perno
Publikováno v:
International Journal of Infectious Diseases, Vol 151, Iss , Pp 107320- (2025)
Objectives: Patients undergoing extracorporeal membrane oxygenation (ECMO) are susceptible to fungal infections, also from rare or emerging pathogens. We present a case of a 3-year-old male patient hospitalized for respiratory failure and subjected t
Externí odkaz:
https://doaj.org/article/0733bf8b5ad74a8d802a05a011de8f11
Autor:
Sergio Ghirardo, Letizia Sabatini, Alessandro Onofri, Maria Beatrice Chiarini Testa, Maria Giovanna Paglietti, Daria Diodato, Lorena Travaglini, Fabrizia Stregapede, Marta Luisa Ciofi degli Atti, Claudio Cherchi, Renato Cutrera
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-4 (2022)
Abstract Background Breathing disturbances are often a primary clinical concern especially during wakefulness of the classic form of Rett syndrome, but data for atypical forms are lacking. Case presentation We report the case of a 20-month-old female
Externí odkaz:
https://doaj.org/article/4fd327885e6d417784a818f981cc379f
Autor:
Maria Giovanna Paglietti, Claudio Cherchi, Federica Porcaro, Emanuele Agolini, Alessandra Schiavino, Francesca Petreschi, Antonio Novelli, Renato Cutrera
Publikováno v:
Italian Journal of Pediatrics, Vol 45, Iss 1, Pp 1-4 (2019)
Abstract Background Congenital central hypoventilation syndrome (CCHS) is characterized by alveolar hypoventilation increasing during sleep and affected patients are unable to perceive and respond to hypercarbia with increased ventilation and arousal
Externí odkaz:
https://doaj.org/article/fc74b8f0e5df46819aeb1c0ffd8a2679
Autor:
Federica Porcaro, Nicola Ullmann, Antonio Di Marco, Annalisa Allegorico, Claudio Cherchi, Maria Giovanna Paglietti, Renato Cutrera
Publikováno v:
Pediatric Pulmonology. 58:1640-1650
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db45887c54bf4d58046458b247710fc7
https://doi.org/10.1002/ppul.26387
https://doi.org/10.1002/ppul.26387
Autor:
Maria Giovanna Paglietti, Irene Esposito, Manuela Goia, Elvira Rizza, Renato Cutrera, Elisabetta Bignamini
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Central hypoventilation (CH) is a quite rare disorder caused by some congenital or acquired conditions. It is featured by increased arterial concentration of serum carbon dioxide related to an impairment of respiratory drive. Patients affected by CH
Externí odkaz:
https://doaj.org/article/ce1d5f8a1d2d434e97431386eb4875c2
Autor:
Federica Porcaro, Emidio Procaccini, Maria Giovanna Paglietti, Alessandra Schiavino, Francesca Petreschi, Renato Cutrera
Publikováno v:
Italian Journal of Pediatrics, Vol 44, Iss 1, Pp 1-6 (2018)
Abstract Background Pleural effusion is a rare complication of ventriculo-peritoneal (VP) cerebrospinal fluid (CSF) shunting and its diagnosis is difficult in patients with neurological and consciousness impairment. Case report Herein we report the c
Externí odkaz:
https://doaj.org/article/dcdd5278f7884da3afdaf7d56fb2ebf7
Autor:
Raffaele Piumelli, Riccardo Davanzo, Niccolò Nassi, Silvia Salvatore, Cinzia Arzilli, Marta Peruzzi, Massimo Agosti, Antonella Palmieri, Maria Giovanna Paglietti, Luana Nosetti, Raffaele Pomo, Francesco De Luca, Alessandro Rimini, Salvatore De Masi, Simona Costabel, Valeria Cavarretta, Anna Cremante, Fabio Cardinale, Renato Cutrera
Publikováno v:
Italian Journal of Pediatrics, Vol 43, Iss 1, Pp 1-23 (2017)
Abstract Five years after the first edition, we have revised and updated the guidelines, re-examining the queries and relative recommendations, expanding the issues addressed with the introduction of a new entity, recently proposed by the American Ac
Externí odkaz:
https://doaj.org/article/1510c951c86d4c62a54e8d79ec98849d
Autor:
Federica Porcaro, Maria Giovanna Paglietti, Antonella Diamanti, Francesca Petreschi, Alessandra Schiavino, Valentina Negro, Valentina Pecora, Alessandro Fiocchi, Renato Cutrera
Publikováno v:
Italian Journal of Pediatrics, Vol 43, Iss 1, Pp 1-3 (2017)
Abstract Background Medications with methyl-prednisolone sodium succinate containing lactose, which potentially contains traces of cow’s milk proteins (CMP), could cause allergic reactions or compromise treatment of acute allergic reactions in sens
Externí odkaz:
https://doaj.org/article/19baedae2efb4c7caa40b2567749648d
Autor:
Fabiana Fattori, Claudio Cherchi, Maria Beatrice Chiarini Testa, Enrico Bertini, Michele Tosi, Adele D'Amico, Adelina Carlesi, Giovanna Paglietti, Antonella Longo, Luca Bosco, Irene Mizzoni
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-7 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background X-linked myotubular myopathy (XLMTM) is a rare congenital myopathy resulting from pathogenic variants in the MTM1 gene. Affected male subjects typically present with severe hypotonia and respiratory distress at birth and they often require
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d83a1cb221d40ebd770b39afb91a1f01
https://doaj.org/article/6c3ecfacd54d438aaffe437c59802931
https://doaj.org/article/6c3ecfacd54d438aaffe437c59802931