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Giovanni Marrosu

University of Cagliari

51

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937

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Event-related potentials and deep grey matter atrophy in multiple sclerosis: Exploring the possible associations with cognition.

2021 Multiple sclerosis and related disorders
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Clinical and molecular features of a large cohort of Italian McArdle patients

2015 Neuromuscular Disorders
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Genotype-phenotype correlation in Pompe disease, a step forward

2014 Orphanet Journal of Rare Diseases
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This Provisional PDF corresponds to the article as it appeared upon acceptance. Fully formatted PDF and full text (HTML) versions will be made available soon.

2014
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Genetic and clinical characteristics of skeletal and cardiac muscle in patients with lamin A/C gene mutations.

2013 Muscle & Nerve
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Overlapping syndromes in laminopathies: a meta-analysis of the reported literature

2013
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Muscle MRI in female carriers of emerinopathy

2013 European Journal of Neurology
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Cardiac and muscle imaging findings in a family with X-linked Emery-Dreifuss muscular dystrophy

2012 Neuromuscular Disorders
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New motor outcome function measures in evaluation of Late‐Onset Pompe disease before and after enzyme replacement therapy

2012 Muscle & Nerve
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Mutations in the human isoprenoid synthase domain containing gene are a common cause of congenital and limb girdle muscular dystrophies

2012 Neuromuscular Disorders
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