IRIS
PANICUCCI, CHIARA
 Distribuzione geografica
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Continente #
EU - Europa 873
Totale 873
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Nazione #
IT - Italia 873
Totale 873
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Città #
Genova 348
Genoa 232
Rapallo 199
Vado Ligure 81
Bordighera 13
Totale 873
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Nome #
Mutations in GMPPB Presenting with Pseudometabolic Myopathy 128
Enhancement of Muscle T Regulatory Cells and Improvement of Muscular Dystrophic Process in mdx Mice by Blockade of Extracellular ATP/P2X Axis. 119
The danger signal extracellular ATP is involved in the immunomediated damage of α-sarcoglycan deficient muscular dystrophy 102
Eatp/p2x7r axis: An orchestrated pathway triggering inflammasome activation in muscle diseases 57
The role of inflammation on disease progression in alpha-sarcoglycan-related limb girdle muscular dystrophy (LGMDR3): new insights from human histological analysis and in vivo studies on Sgca-null mice. 57
Novel TRIM32 mutation in sarcotubular myopathy 53
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 41
The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatment 38
The Role of Muscle Biopsy in Diagnostic Process of Infant Hypotonia: From Clinical Classification to the Genetic Outcome 38
P2X7 Receptor Antagonist Reduces Fibrosis and Inflammation in a Mouse Model of Alpha-Sarcoglycan Muscular Dystrophy 37
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 34
Muscle inflammatory pattern in alpha- and gamma-sarcoglycanopathies 30
Emergencies cards for neuromuscular disorders 1stConsensus Meeting from UILDM - Italian Muscular Dystrophy Association Workshop report 29
Comprehensive Phenotyping of Peripheral Blood T Lymphocytes in Healthy Mice 26
Management and outcome of benign acute childhood myositis in pediatric emergency department 25
Long-term clinical and MRI follow-up in two POMT2-related limb girdle muscular dystrophy (LGMDR14) patients 19
Age, corticosteroid treatment and site of mutations affect motor functional changes in young boys with Duchenne Muscular Dystrophy 17
Body mass index in type 2 spinal muscular atrophy: a longitudinal study 17
New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy 11
Digital health and Clinical Patient Management System (CPMS) platform utility for data sharing of neuromuscular patients: the Italian EURO-NMD experience 9
Structured Light Plethysmography for Non-Invasive Assessment of Respiratory Pattern in Spinal Muscular Atrophy Type 1 9
Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy 9
Nusinersen Induces Disease-Severity-Specific Neurometabolic Effects in Spinal Muscular Atrophy 9
DAG1 haploinsufficiency is associated with sporadic and familial isolated or pauci-symptomatic hyperCKemia 8
Genetic modifiers of upper limb function in Duchenne muscular dystrophy 7
Myopathologic trajectory in Duchenne muscular dystrophy (DMD) reveals lack of regeneration due to senescence in satellite cells 6
Totale 935
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Categoria #
all - tutte 5.439
article - articoli 5.237
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 10.676
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020122 0 0 0 8 12 15 26 20 12 17 9 3
2020/202152 1 3 6 10 3 1 4 11 1 8 1 3
2021/2022139 9 4 4 8 2 6 11 22 5 14 19 35
2022/2023227 15 34 1 28 30 31 0 11 38 5 33 1
2023/2024210 2 15 23 33 14 24 18 22 8 7 19 25
2024/2025114 45 38 17 14 0 0 0 0 0 0 0 0
Totale 935