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Clinical and molecular spectra in galactosemic patients from neonatal screening in northeastern Italy: structural and functional characterization of new variations in the galactose-1-phosphate uridyltransferase (GALT) gene.
Viggiano E, Marabotti A, Burlina AP, Cazzorla C, D'Apice MR, Giordano L, Fasan I, Novelli G, Facchiano A, Burlina AB. Viggiano E, et al. Gene. 2015 Apr 1;559(2):112-8. doi: 10.1016/j.gene.2015.01.013. Epub 2015 Jan 13. Gene. 2015. PMID: 25592817
Molecular Research in Medical Genetics.
Viggiano E. Viggiano E. Int J Mol Sci. 2022 Jun 14;23(12):6625. doi: 10.3390/ijms23126625. Int J Mol Sci. 2022. PMID: 35743065 Free PMC article.
Genetic counseling in Pompe disease.
Taglia A, Picillo E, D'Ambrosio P, Cecio MR, Viggiano E, Politano L. Taglia A, et al. Among authors: viggiano e. Acta Myol. 2011 Dec;30(3):179-81. Acta Myol. 2011. PMID: 22616199 Free PMC article.
Cardiac involvement in patients with spinal muscular atrophies.
Palladino A, Passamano L, Taglia A, D'Ambrosio P, Scutifero M, Cecio MR, Picillo E, Viggiano E, Torre V, De Luca F, Nigro G, Politano L. Palladino A, et al. Among authors: viggiano e. Acta Myol. 2011 Dec;30(3):175-8. Acta Myol. 2011. PMID: 22616198 Free PMC article.
62 results