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A Fiumara

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Journal of Neurology|July 11, 2025

Analysis of the Italian cohort of late-onset Pompe disease (LOPD) patients after 10 and 15 years of therapy with alglucosidase alfaT Mongini, G Gadaleta, P Alonge, et al.

Molecular Genetics and Metabolism Reports|July 14, 2017

Home infusion program with enzyme replacement therapy for Fabry disease: The experience of a large Italian collaborative groupD Concolino, L Amico, M D Cappellini, et al.

Glycoconjugate Journal|September 26, 2000

Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG. First International Workshop on CDGSM Aebi, A Helenius, B Schenk, et al.

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Search research articles

Showing results (71-80 of 73) with videos related to

Sort By:

Pageof 8

You have reached the last page of results.This site can display upto 73 results.

Journal of Neurology|July 11, 2025

Analysis of the Italian cohort of late-onset Pompe disease (LOPD) patients after 10 and 15 years of therapy with alglucosidase alfaT Mongini, G Gadaleta, P Alonge, et al.

Molecular Genetics and Metabolism Reports|July 14, 2017

Home infusion program with enzyme replacement therapy for Fabry disease: The experience of a large Italian collaborative groupD Concolino, L Amico, M D Cappellini, et al.

Glycoconjugate Journal|September 26, 2000

Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG. First International Workshop on CDGSM Aebi, A Helenius, B Schenk, et al.

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