about
Prevalence of congenital muscular dystrophy in Italy: a population studyMRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases.Upper girdle imaging in facioscapulohumeral muscular dystrophy.Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late-onset cerebellar ataxia.Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1.Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients.The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosis.Magnetic Resonance Imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: pattern refinement and implications for clinical trials.Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2.A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia.Teaching video neuroimages: complicated scapular winging.Muscle cramps and weakness after teriparatide therapy: a new drug-induced myopathy?Calf muscle involvement in Becker muscular dystrophy: when size does not matter.MRI in sarcoglycanopathies: a large international cohort study.Start codon mutation of GYG1 causing late-onset polyglucosan body myopathy with nemaline rods.Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort.Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy.Matrin 3 variants are frequent in Italian ALS patients.Muscle MRI in female carriers of dystrophinopathy.Muscle imaging findings in GNE myopathy.Rinsing after spinning: plasmapheresis in EBV-related post-infectious cerebellitis.New phenotype and pathology features in MYH7-related distal myopathySomatic mosaicism in TPM2-related myopathy with nemaline rods and cap structuresDysautonomia as Onset Symptom of Myotonic Dystrophy Type 2Concentric muscle involvement in POLG -related distal myopathyCD8(+) T cells in facioscapulohumeral muscular dystrophy patients with inflammatory features at muscle MRIMuscle MRI in Becker muscular dystrophyMixed connective tissue disease presenting as a peculiar myositis with poor muscle regenerationCase of postpartum Parsonage-Turner syndromeMagnetic resonance imaging pattern recognition in sporadic inclusion-body myositisOculopharyngeal muscular dystrophy: Clinical and neurophysiological featuresTuberculous nephritis accompanying neuromyelitis optica: causal or coincidental association?Isolated semitendinosus involvement in the initial stages of limb-girdle muscular dystrophy 2LTracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imagingTo the Editor
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description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Mauro Monforte
@ast
Mauro Monforte
@en
Mauro Monforte
@es
Mauro Monforte
@nl
type
label
Mauro Monforte
@ast
Mauro Monforte
@en
Mauro Monforte
@es
Mauro Monforte
@nl
prefLabel
Mauro Monforte
@ast
Mauro Monforte
@en
Mauro Monforte
@es
Mauro Monforte
@nl
P106
P1153
36056639400
P31
P496
0000-0002-4327-6969