Veronica Pagliardini

Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy

Rossella Parini, Paola De Lorenzo, Andrea Dardis et al. · Orphanet Journal of Rare Diseases · 2018 · 88 citations · Full text

First pilot newborn screening for four lysosomal storage diseases in an Italian region: Identification and analysis of a putative causative mutation in the GBA gene

Silvia Paciotti, Emanuele Persichetti, Severo Pagliardini et al. · Clinica Chimica Acta · 2012 · 58 citations

Genetic Testing, Newborn Screening, Italian Region +12

Screening for later-onset Pompe's disease in patients with paucisymptomatic hyperCKemia

Marco Spada, Francesco Porta, Liliana Vercelli et al. · Molecular Genetics and Metabolism · 2013 · 57 citations

Later-onset Pompe, Clinical Epidemiology, Hematology +2

High Prevalence of Vitamin D Deficiency in Native versus Migrant Mothers and Newborns in the North of Italy: A Call to Act with a Stronger Prevention Program

Francesco Cadario, Silvia Savastio, Corrado Magnani et al. · PLoS ONE · 2015 · 44 citations · Full text

Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: A survey clinic-based study

Veronica Pagliardini, Severo Pagliardini, Lucia Corrado et al. · Journal of the Neurological Sciences · 2014 · 42 citations

Amyotrophic Lateral Sclerosis, Disease Progression, Neurochemical Biomarkers +5