Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bruna Loperfido"'
Autor:
Lorenzo Fiorica, Lina Cimminelli, Eleonora Tognato, Bruna Loperfido, Simone Ceratto, Paolo Manzoni, Anna Perona, Enrico Felici, Giorgia Enrico
Publikováno v:
Medico e Bambino pagine elettroniche. 24:277-279
Iron deficiency is the most commonly detected nutritional disorder in childhood and at the same time the most frequent cause of anaemia worldwide. In most cases it can go unnoticed, because it causes subtle symptoms and signs. Iron plays a key role i
Autor:
Francesco Savino, Lorenzo Fiorica, Paolo Manzoni, Francesca Giuliani, Giorgia Enrico, Lina Cimminelli, Mohammad Reza Eshraghy, Roberta Spola, Maria Angela Militello, Eleonora Tognato, Bruna Loperfido, Simone Ceratto, Anna Perona
Publikováno v:
American Journal of Perinatology. 37:S57-S60
Neonatal adrenal hemorrhage (NAH) in newborn infants is a rare event that is associated with specific anatomical and vascular characteristics. It is more common in term infants and occurs more often in neonates who feature perinatal asphyxia. Symptom
Publikováno v:
Pediatric Infectious Disease Journal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fca13248e1f7773589be567bac607b7b
http://hdl.handle.net/2318/1840863
http://hdl.handle.net/2318/1840863
Autor:
Mohammad Reza Eshraghy, Bruna Loperfido, Simone Ceratto, Lina Cimminelli, Roberta Spola, Anna Perona, Antonella Bertola, Lorenzo Fiorica, Alessia Pagani, Eleonora Tognato, Maria Angela Militello, Giorgia Enrico, Paolo Manzoni
Publikováno v:
Medico e Bambino. 40:193-194
The paper describes the case of two Caucasian brothers (11 and 12 years old resepctively) who for the first time presented with acute haemolysis due to glucose-6-phosphate dehydrogenase deficiency. The two brothers showed different severity of sympto
Autor:
G. Genoni, F. Prato, Paolo Manzoni, Anna Perona, M. De Curtis, C. Vivenza, Bruna Loperfido, R. Broglia Franchin
Publikováno v:
10th International Conference on Clinical Neonatology—Selected Abstracts.
Autor:
Antonella Bertola, Lina Cimminelli, Paolo Manzoni, Anna Perona, Bruna Loperfido, Eleonora Tognato, Mohammad Reza Eshraghy, Angela Aronica, Simona De Vecchi, Claudia Vivenza
Objective The Marfan syndrome (MFS) is an autosomal dominant disorder of connective tissue resulting from pathogenic variants of the fibrillin-1 gene (FBN1) with skeletal, cardiac, and ocular involvement. Study Design We report on a full-term male ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ef0c46bada20ec386767837b2f73718
http://hdl.handle.net/2318/1841012
http://hdl.handle.net/2318/1841012