Amelia Morrone
www.mendeley.com
0000-0003-2890-8179
Università di bologna
4 papers found
Refreshing results…
Identification of GM1-Ganglioside Secondary Accumulation in Fibroblasts from Neuropathic Gaucher Patients and Effect of a Trivalent Trihydroxypiperidine Iminosugar Compound on Its Storage Reduction
Fluorescent In Situ Staining and Flow Cytometric Procedures as New Pre-Diagnostic Tests for Sialidosis, GM1 Gangliosidosis and Niemann–Pick Type C
Expanded Newborn Screening in Italy Using Tandem Mass Spectrometry: Two Years of National Experience
PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutations
Missing publications? Search for publications with a matching author name.