GC
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Projects
Identification of an intragenic deletion in the SGCB gene through a re-evaluation of negative next generation sequencing results
"Autori: Giugliano, T., Fan...
IRCCS Fondazione Ospedale San Camillo
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes
"Autori: Ricci, G., Ruggier...
IRCCS Fondazione Ospedale San Camillo
Effects of Functional Electrical Stimulation Lower Extremity Training in Myotonic Dystrophy Type I: A Pilot Controlled Study
Autori: Cudia, P., Weis, L....
IRCCS Fondazione Ospedale San Camillo
Challenges and progress in the diagnosis of Congenital Muscular Dystrophies
"Autore: Angelini, C"
IRCCS Fondazione Ospedale San Camillo
Mitochondrial neuropathies: A survey from the large cohort of the Italian Network
"Autori: Mancuso, M., Orsuc...
IRCCS Fondazione Ospedale San Camillo
Neuromuscular disease: Diagnosis and discovery in limb-girdle muscular dystrophy
"Autore: Angelini, C"
IRCCS Fondazione Ospedale San Camillo
Circulating microRNAs as biomarkers of muscle differentiation and atrophy in ALS
"Autori: Tasca, E., Pegorar...
IRCCS Fondazione Ospedale San Camillo
LOPED study: Looking for an early diagnosis in a late-onset Pompe disease high-risk population
"Autori: Musumeci, O., Marc...
IRCCS Fondazione Ospedale San Camillo
The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosis.
"Autori: Magri F, Nigro V, ...
IRCCS Fondazione Ospedale San Camillo
Progress and challenges in diagnosis of dysferlinopathy.
"Fanin M, Angelini C."
IRCCS Fondazione Ospedale San Camillo
Functional changes in Becker muscular dystrophy: implications for clinical trials in dystrophinopathies.
"Bello L, Campadello P, Bar...
IRCCS Fondazione Ospedale San Camillo
MicroRNA signatures predict dysregulated vitamin D receptor and calcium pathways status in limb girdle muscle dystrophies (LGMD) 2A/2B.
"Aguennouz M, Lo Giudice C,...
IRCCS Fondazione Ospedale San Camillo
Relationship between neuropsychological impairment and grey and white matter changes in adult-onset myotonic dystrophy type 1.
"Baldanzi S, Cecchi P, Fabb...
IRCCS Fondazione Ospedale San Camillo
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients.
"Savarese M, Di Fruscio G, ...
IRCCS Fondazione Ospedale San Camillo
Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study.
"Baldanzi S, Bevilacqua F, ...
IRCCS Fondazione Ospedale San Camillo
Giornata Nazionale Parkinson
L'Unità Operativa per la Ma...
IRCCS Fondazione Ospedale San Camillo
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gabriella.traviglia@unive.it / info@venezia86.it