Phenotypic spectrum of short-chain enoyl-Coa hydratase-1 (ECHS1) deficiencySilvia Masnada, Davide Tonduti, Marialuisa Valente et al.|European Journal of Paediatric Neurology|2020Cited by 33
Newborn screening for X-linked adrenoleukodystrophy in Italy: Diagnostic algorithm and disease monitoringEleonora Bonaventura, Luisella Alberti, Simona Lucchi et al.|Frontiers in Neurology|2023Cited by 26
Vitamin B12 deficiency in newborns: impact on individual’s health status and healthcare costsSimona Ferraro, Cristina Cereda, Simona Lucchi et al.|Clinical Chemistry and Laboratory Medicine (CCLM)|2024Cited by 10