Vitamin B12 deficiency in newborns: impact on individual’s health status and healthcare costs
Simona Ferraro(Ospedale dei Bambini Vittore Buzzi), Cristina Cereda(University of Milan), Davide Biganzoli(University of Milan), Simona Lucchi(IRCCS Istituto Auxologico Italiano), Laura Saielli(Ospedale dei Bambini Vittore Buzzi), Martina Tosi(University of Modena and Reggio Emilia), Stephana Carelli(ASST Fatebenefratelli Sacco), C Montanari(University of Milan), Luisella Alberti(Ospedale dei Bambini Vittore Buzzi), Gianvincenzo Zuccotti(University of Milan), Marta Marsilio(University of Milan), Elvira Verduci(University of Milan), Letizia Magnani(University of Milan), Elisa Pratiffi(Ospedale dei Bambini Vittore Buzzi), Andrea Lugotti(Ospedale dei Bambini Vittore Buzzi), Alessia Poli(University of Milan), Laura Cappelletti(Ospedale dei Bambini Vittore Buzzi)
Cited by 10
Related Papers
Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>
|American Journal of Medical Genetics Part A|2015|617
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
|Nature Genetics|2021|567
Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study
|The Lancet Neurology|2013|441