Zobrazeno 1 - 7
of 7
pro vyhledávání: '"M. F. Roversi"'
Autor:
S. Palma, M. F. Roversi, M. Bettini, S. Mazzoni, P. Pietrosemoli, L. Lucaccioni, A. Berardi, E. Genovese
Publikováno v:
Acta Otorhinolaryngologica Italica, Vol 39, Iss 1, Pp 40-45 (2019)
Externí odkaz:
https://doaj.org/article/eb715ba4b61442fcb734fe1eaed26b80
Autor:
M, Portolani, A M, Bartoletti, P, Pietrosemoli, F, Beretti, E, Della Casa Muttini, M F, Roversi, L, Livio, F, Ferrari
A case of non-specific febrile illness by Coxsackievirus A 16 (CA 16) in a 6-day-old newborn whose mother had developed hand, foot and mouth disease manifestations 2 days after delivery is reported. Notwithstanding the concurrence of negative circums
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3b9c2a3f7d9399da1829fc5971d97ab0
https://hdl.handle.net/11380/741192
https://hdl.handle.net/11380/741192
General movements detect early signs of hemiplegia in term infants with neonatal cerebral infarction
Autor:
Heinz F.R. Prechtl, Christa Einspieler, G. Rapisardi, Eugenio Mercuri, M. F. Roversi, Frances M. Cowan, Fabrizio Ferrari, Mary A. Rutherford, Antonio Boldrini, Lilly Dubowitz, Andrea Guzzetta, P. B. Paolicelli, Giovanni Cioni
Publikováno v:
Neuropediatrics. 34(2)
Background. Studies have reported that infants with hemiplegia of congenital origin may have a period between birth and up to 12 months when clinical signs of hemiplegia are not evident. The aim of this study was to establish whether the assessment o
Autor:
M. F. Roversi, P. B. Paolicelli, Christa Einspieler, Anastasia Dressler, Arend F. Bos, Giovanni Cioni, Heinz F.R. Prechtl, Fabrizio Ferrari
Publikováno v:
Neuropediatrics, 33(2), 73-78. GEORG THIEME VERLAG KG
Qualitative abnormalities of spontaneous motor activity in new-borns and young infants are early predictive markers for later spastic cerebral palsy. Aim of this research was to identify which motor patterns may be specific for later dyskinetic cereb
Autor:
E, Della Casa Muttini, M, Pancaldi, M F, Roversi, M, Pugliese, B, Mordini, O, Biagioni, G, Gargano, P L, Ceccarelli, S, Cattani, F, Ferrari, G B, Cavazzuti
Publikováno v:
Acta bio-medica de L'Ateneo parmense : organo della Societa di medicina e scienze naturali di Parma. 71
Cystic fibrosis is the most common life-limiting recessive genetic disorder in Caucasian. It is caused by mutations of CFTR gene (cystic fibrosis transmembrane conductance regulator); at present over 500 mutations are known. Cystic fibrosis as a caus
Autor:
Fabio Facchinetti, M F Roversi, K Rossi, L Lugli, A Berardi, Elisabetta Tridapalli, F Ferrari
Publikováno v:
Pediatric Research. 58:360-360
Background Group B streptococcus (GBS) is the leading cause of early-onset infections (EOI) in the developed world. Few data are available in Europe about incidence and clinical findings of neonatal disease. We reviewed cases occurred in the last 2 y