IRIS
PANICUCCI, CHIARA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 1.018
Totale 1.018
Salva come PNG Salva come JPEG
Nazione #
IT - Italia 1.018
Totale 1.018
Salva come PNG Salva come JPEG
Città #
Genova 348
Genoa 239
Vado Ligure 219
Rapallo 199
Bordighera 13
Totale 1.018
Salva come PNG Salva come JPEG
Nome #
Mutations in GMPPB Presenting with Pseudometabolic Myopathy 137
Enhancement of Muscle T Regulatory Cells and Improvement of Muscular Dystrophic Process in mdx Mice by Blockade of Extracellular ATP/P2X Axis. 126
The danger signal extracellular ATP is involved in the immunomediated damage of α-sarcoglycan deficient muscular dystrophy 109
Eatp/p2x7r axis: An orchestrated pathway triggering inflammasome activation in muscle diseases 63
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. 63
Novel TRIM32 mutation in sarcotubular myopathy 59
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 45
P2X7 Receptor Antagonist Reduces Fibrosis and Inflammation in a Mouse Model of Alpha-Sarcoglycan Muscular Dystrophy 44
The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatment 43
The Role of Muscle Biopsy in Diagnostic Process of Infant Hypotonia: From Clinical Classification to the Genetic Outcome 42
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 41
Muscle inflammatory pattern in alpha- and gamma-sarcoglycanopathies 36
Emergencies cards for neuromuscular disorders 1stConsensus Meeting from UILDM - Italian Muscular Dystrophy Association Workshop report 33
Management and outcome of benign acute childhood myositis in pediatric emergency department 33
Comprehensive Phenotyping of Peripheral Blood T Lymphocytes in Healthy Mice 30
Long-term clinical and MRI follow-up in two POMT2-related limb girdle muscular dystrophy (LGMDR14) patients 26
Age, corticosteroid treatment and site of mutations affect motor functional changes in young boys with Duchenne Muscular Dystrophy 21
Body mass index in type 2 spinal muscular atrophy: a longitudinal study 21
New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy 15
Digital health and Clinical Patient Management System (CPMS) platform utility for data sharing of neuromuscular patients: the Italian EURO-NMD experience 14
DAG1 haploinsufficiency is associated with sporadic and familial isolated or pauci-symptomatic hyperCKemia 14
Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy 14
Myopathologic trajectory in Duchenne muscular dystrophy (DMD) reveals lack of regeneration due to senescence in satellite cells 14
Structured Light Plethysmography for Non-Invasive Assessment of Respiratory Pattern in Spinal Muscular Atrophy Type 1 13
Nusinersen Induces Disease-Severity-Specific Neurometabolic Effects in Spinal Muscular Atrophy 13
Genetic modifiers of upper limb function in Duchenne muscular dystrophy 11
Totale 1.080
Salva come PNG Salva come JPEG
Categoria #
all - tutte 6.264
article - articoli 6.046
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 12.310
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020102 0 0 0 0 0 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
2024/2025259 45 38 17 41 62 56 0 0 0 0 0 0
Totale 1.080