about
Assessment of patients with idiopathic inflammatory myopathies and isolated creatin-kinase elevation.Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2EGenetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy.Non-neural phenotype of spinal and bulbar muscular atrophy: results from a large cohort of Italian patients.Burden, professional support, and social network in families of children and young adults with muscular dystrophies."I have got something positive out of this situation": psychological benefits of caregiving in relatives of young people with muscular dystrophy.Enzyme replacement therapy for Pompe disease.Functional changes in Becker muscular dystrophy: implications for clinical trials in dystrophinopathiesProgress in Enzyme Replacement Therapy in Glycogen Storage Disease Type IIClinical phenotype, muscle MRI and muscle pathology of LGMD1F.Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years.Enzyme replacement therapy improves respiratory outcomes in patients with late-onset type II glycogenosis and high ventilator dependency.Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations.Spinal cord herniation: a missing piece in the pathogenesis of amyotrophic lateral sclerosis and multiple sclerosis?
P50
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P50
description
hulumtues
@sq
researcher
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wetenschapper
@nl
հետազոտող
@hy
name
Claudio Semplicini
@ast
Claudio Semplicini
@en
Claudio Semplicini
@es
Claudio Semplicini
@nl
Claudio Semplicini
@sl
type
label
Claudio Semplicini
@ast
Claudio Semplicini
@en
Claudio Semplicini
@es
Claudio Semplicini
@nl
Claudio Semplicini
@sl
prefLabel
Claudio Semplicini
@ast
Claudio Semplicini
@en
Claudio Semplicini
@es
Claudio Semplicini
@nl
Claudio Semplicini
@sl
P106
P1153
35759581600
P21
P31
P496
0000-0003-0870-1349