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Showing results (121-130 of 124) with videos related to

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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.
European Journal of Neurology|July 23, 2020
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imagingG Giacomucci, M Monforte, J Diaz-Manera, et al.
Journal of Neurology|April 28, 2026
X-linked Emery-Dreifuss muscular dystrophy: a multicenter, Italian, cohort studyA Elkoush, R Giossi, G Gadaleta, et al.
Orphanet Journal of Rare Diseases|July 9, 2016
MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patientsC Fiorillo, G Astrea, M Savarese, et al.
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Showing results (121-130 of 124) with videos related to

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Pageof 13
You have reached the last page of results.This site can display upto 124 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.
European Journal of Neurology|July 23, 2020
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imagingG Giacomucci, M Monforte, J Diaz-Manera, et al.
Journal of Neurology|April 28, 2026
X-linked Emery-Dreifuss muscular dystrophy: a multicenter, Italian, cohort studyA Elkoush, R Giossi, G Gadaleta, et al.
Orphanet Journal of Rare Diseases|July 9, 2016
MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patientsC Fiorillo, G Astrea, M Savarese, et al.
Pageof 13