Associated Papers
Genetic analysis reveals novel variants for vascular cognitive impairment.
Mönkäre S et al.
Acta Neurologica Scandinavica, 2022
35307828 (PubMed )
Supplement: ANE-146-42-s001.docx
Neonatal Screening on Tandem Mass Spectrometry as a Powerful Tool for the Reassessment of the Prevalence of Underestimated Diseases in Newborns and Their Family Members: A Focus on Short Chain Acyl-CoA Dehydrogenase Deficiency.
Messina M et al.
International Journal of Neonatal Screening, 2020
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