Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jessica Iacopelli"'
Autor:
Giulia Trippella, Jessica Iacopelli
Publikováno v:
Medico e Bambino pagine elettroniche. 24:157-157
The Authors describe the case of an 11-month-old infant with severe vitamin B12 deficiency consequent to a strict vegan diet followed by the mother during pregnancy and to a strictly vegan weaning. The child presented with food refusal, somatic growt
Autor:
Jessica Iacopelli, Daniela Gioè
Publikováno v:
Medico e Bambino pagine elettroniche. 23:216-216
Autor:
Simona Gambini, Angelo Vacca, Francesco Cinetto, Viviana Moschese, Baldassarre Martire, Maria Giovanna Danieli, Jessica Iacopelli, Marco De Carli, Carolina Marasco, Francesco Licciardi, Andrea Finocchi, Alessia Gatta, Antonino Trizzino, Clementina Canessa, Domenico De Mattia, Andrea Matucci, Alessandra Vultaggio, Antonio Pecoraro, Silvana Martino, Chiara Azzari, Giuseppe Spadaro, Mario Di Gioacchino, Carlo Agostini, Cinzia Milito, Alessandro Plebani
Publikováno v:
International Journal of Immunopathology and Pharmacology
In patients with primary antibody deficiencies, subcutaneous administration of IgG (SCIG) replacement is effective, safe, well-tolerated, and can be self-administered at home. A new SCIG replacement at 20% concentration (Hizentra®) has been develope
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed897a589075fd3200f04c00658a8c45
http://hdl.handle.net/11573/980478
http://hdl.handle.net/11573/980478
Autor:
Sara Sollai, Luisa Galli, Elena Chiappini, Maurizio de Martino, Manuela Prato, Mattia Giovannini, Jessica Iacopelli
Publikováno v:
Journal of chemotherapy (Florence, Italy). 28(5)
Accidental needle injury is a common but still discussed problem.We discuss possible options to optimize the management of injured children in light of the available literature findings.The risk of viral infection is low. However, blood investigation
Publikováno v:
Area Pediatrica. 13:59-62
Riassunto La sindrome di DiGeorge rappresenta una delle forme piu frequenti tra le immunodeficienze primitive. La mutazione responsabile e una delezione sul cromosoma 22. Il fenotipo clinico e variabile, tuttavia caratterizzabile da tratti patologic