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World Journal of Pediatrics : WJP|March 11, 2015
Newborn screening for galactosemia: a 30-year single center experienceFrancesco Porta, Severo Pagliardini, Veronica Pagliardini, et al.
Molecular Genetics and Metabolism Reports|October 4, 2017
Neonatal screening for biotinidase deficiency: A 30-year single center experienceFrancesco Porta, Veronica Pagliardini, Isabella Celestino, et al.
American Journal of Human Genetics|June 15, 2006
High incidence of later-onset fabry disease revealed by newborn screeningMarco Spada, Severo Pagliardini, Makiko Yasuda, et al.
Pediatric Research|August 29, 2014
α-Fetoprotein assay on dried blood spot for hepatoblastoma screening in children with overgrowth-cancer predisposition syndromesAlessandro Mussa, Severo Pagliardini, Veronica Pagliardini, et al.
Journal of the Neurological Sciences|January 8, 2015
Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: a survey clinic-based studyVeronica Pagliardini, Severo Pagliardini, Lucia Corrado, et al.
Molecular Genetics and Metabolism|April 10, 2013
Screening for later-onset Pompe's disease in patients with paucisymptomatic hyperCKemiaMarco Spada, Francesco Porta, Liliana Vercelli, et al.
Cancers|January 17, 2019
Longitudinal Monitoring of Alpha-Fetoprotein by Dried Blood Spot for Hepatoblastoma Screening in Beckwith⁻Wiedemann SyndromeAlessandro Mussa, Valentina Pia Ciuffreda, Pina Sauro, et al.
Nutrients|October 9, 2019
Daily Fructose Traces Intake and Liver Injury in Children with Hereditary Fructose IntoleranceFabiola Di Dato, Simona Spadarella, Maria Giovanna Puoti, et al.
Pediatric Research|January 28, 2006
Cryptogenic liver disease in four children: a novel congenital disorder of glycosylationClaudia Mandato, Lena Brive, Yoshiaki Miura, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 24, 2012
First pilot newborn screening for four lysosomal storage diseases in an Italian region: identification and analysis of a putative causative mutation in the GBA geneSilvia Paciotti, Emanuele Persichetti, Severo Pagliardini, et al.
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