Sfoglia per Autore
Congenital midline cervical cleft: clinical approach to a congenital anterior neck defect
2015 B.L. Crippa, M.F. Bedeschi, G. Cantarella, L. Colombo, V. Agosti, I. Amodeo, M. Fumagalli, I. Mazzola, F. Mosca
STAR syndrome plus: The first description of a female patient with the lethal form
2017 B. Maria F., S. Giangiobbe, L. Paganini, S.M. Tabano, R. Silipigni, L.L. Colombo, B.L. Crippa, L. Faustina, G. Silvana, M.R. Miozzo
Abdominal cystic lymphangioma in a term newborn : A case report and update of new treatments
2017 I. Amodeo, G. Cavallaro, G. Raffaeli, L. Colombo, M. Fumagalli, R. Cavalli, E. Leva, F. Mosca
Sequence variants identification at the KCNQ1OT1: TSS differentially Methylated region in isolated omphalocele cases
2017 B. Maria Francesca, M. Calvello, L. Paganini, L. Pezzani, M. Baccarin, L. Fontana, S.M. Sirchia, G. Silvana, L. Canazza, L. Ernesto, L.L. Colombo, L. Faustina, F. Mosca, S.M. Tabano, M.R. Miozzo
Delayed cord clamping increased the need for phototherapy treatment in infants with AB0 alloimmunization born by cesarean section: A retrospective study
2018 S. Ghirardello, B.L. Crippa, V. Cortesi, E.D. Francesco, D. Consonni, L. Colombo, M. Fumagalli, A.B. te Pas, F. Mosca
Breastfeeding Determinants in Healthy Term Newborns
2018 L. Colombo, B.L. Crippa, D. Consonni, M.E. Bettinelli, V. Agosti, G. Mangino, E.N. Bezze, P.A. Mauri, L. Zanotta, P. Roggero, L. Plevani, D. Bertoli, M.L. Giannì, F. Mosca
Serum creatinine during physiological perinatal dehydration may estimate individual nephron endowment
2018 A. Gianluigi, F. Tel, P. Ilaria, P. Mariangela, P. Michela, F. Giulia, S. Patrizia, L.L. Colombo, G. Stefano, C. Bianca, C. Dario, B. Dario;, V. Daniela Li, L.M. Giancarlo, F. Mosca
Do a Few Weeks Matter? Late Preterm Infants and Breastfeeding Issues
2019 B.L. Crippa, L. Colombo, D. Morniroli, D. Consonni, M.E. Bettinelli, I. Spreafico, G. Vercesi, P. Sannino, P.A. Mauri, L. Zanotta, A. Canziani, P. Roggero, L. Plevani, D. Bertoli, S. Zorzan, M.L. Giannì, F. Mosca
Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations
2020 R. Villa, V.G.C. Fergnani, R. Silipigni, S. Guerneri, C. Cinnante, A. Guala, C. Danesino, E. Scola, G. Conte, M. Fumagalli, S. Gangi, L. Colombo, O. Picciolini, P.F. Ajmone, A. Accogli, F. Madia, E. Tassano, M. Scala, V. Capra, M. Srour, L. Spaccini, A. Righini, D. Greco, L. Castiglia, C. Romano, M.F. Bedeschi
CHARGE syndrome presenting with persistent hypoglycemia: case report and overview of the main genetic syndromes associated with neonatal hypoglycemia
2022 A. Consales, B.L. Crippa, L. Colombo, R. Villa, F. Menni, C. Giavoli, F. Mosca, M.F. Bedeschi
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