[HTML][HTML] Reliability of the Performance of Upper Limb assessment in Duchenne muscular dystrophy

…, G Colia, M Catteruccia, C Palermo, G D'Angelo… - Neuromuscular …, 2014 - Elsevier
The Performance of Upper Limb was specifically designed to assess upper limb function in
Duchenne muscular dystrophy. The aim of this study was to assess (1) a cohort of typically …

Early neurodevelopmental assessment in Duchenne muscular dystrophy

M Pane, R Scalise, A Berardinelli, G D'Angelo… - Neuromuscular …, 2013 - Elsevier
The aim of this study was to assess neurodevelopmental profile in young boys affected by
Duchenne muscular dystrophy and to establish the correlation between neurodevelopmental …

[HTML][HTML] A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes

…, E Bucci, M Cao, MC D'Amico, G D'Angelo… - Journal of …, 2016 - Springer
Based on the 7-year experience of the Italian Clinical Network for FSHD, we revised the FSHD
clinical form to describe, in a harmonized manner, the phenotypic spectrum observed in …

Assessing mental health in boys with Duchenne muscular dystrophy: Emotional, behavioural and neurodevelopmental profile in an Italian clinical sample

…, E Mani, M Molteni, N Bresolin, G D'Angelo - European Journal of …, 2017 - Elsevier
Objective To evaluate through a comprehensive protocol, the psychopathological profile of
DMD boys. The primary aim of this observational study was to describe the emotional and …

Nusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patients

…, N Stocchetti, E Calderini, G D'Angelo… - Journal of Cellular …, 2020 - Wiley Online Library
The antisense oligonucleotide Nusinersen has been recently licensed to treat spinal
muscular atrophy (SMA). Since SMA type 3 is characterized by variable phenotype and milder …

Genetic modifiers of respiratory function in Duchenne muscular dystrophy

L Bello, G D'Angelo, M Villa, A Fusto… - Annals of clinical …, 2020 - Wiley Online Library
Objective Respiratory insufficiency is a major complication of Duchenne muscular dystrophy
(DMD). Its progression shows considerable interindividual variability, which has been less …

[HTML][HTML] Benefits of glucocorticoids in non-ambulant boys/men with Duchenne muscular dystrophy: A multicentric longitudinal study using the Performance of Upper …

…, S Bonfiglio, E Rolle, C Palermo, G D'Angelo… - Neuromuscular …, 2015 - Elsevier
The aim of this study was to establish the possible effect of glucocorticoid treatment on upper
limb function in a cohort of 91 non-ambulant DMD boys and adults of age between 11 and …

Multiparametric quantitative MRI assessment of thigh muscles in limb‐girdle muscular dystrophy 2A and 2B

…, A Leemans, N Bresolin, G D'angelo - Muscle & …, 2018 - Wiley Online Library
Introduction: The aim of this study was to apply quantitative MRI (qMRI) to assess structural
modifications in thigh muscles of subjects with limb girdle muscular dystrophy (LGMD) 2A …

Nitric oxide deficiency determines global chromatin changes in Duchenne muscular dystrophy

…, M Moggio, C Lamperti, G D'Angelo… - The FASEB …, 2009 - Wiley Online Library
The present study provides evidence that abnormal patterns of global histone modification
are present in the skeletal muscle nuclei of mdx mice and Duchenne muscular dystrophy (…

Spectroscopic identification and anti-biofilm properties of polar metabolites from the medicinal plant Helichrysum italicum against Pseudomonas aeruginosa

B D'Abrosca, E Buommino, G D'Angelo… - Bioorganic & medicinal …, 2013 - Elsevier
Two new acylated styrylpyrones, one 5-methoxy-1(3H)-isobenzofuranone glucoside and a
hydroxymethyl-orcinol derivative, along with sixteen known aromatic metabolites, including …