IRIS PubliCatt

Ricci, Enzo
 Distribuzione geografica
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Continente #
EU - Europa 4.537
NA - Nord America 4.236
AS - Asia 1.281
AF - Africa 22
OC - Oceania 22
SA - Sud America 9
Continente sconosciuto - Info sul continente non disponibili 5
Totale 10.112
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Nazione #
US - Stati Uniti d'America 4.151
DE - Germania 1.536
SE - Svezia 741
CN - Cina 633
IT - Italia 462
PL - Polonia 433
UA - Ucraina 430
SG - Singapore 289
IE - Irlanda 228
GB - Regno Unito 205
FR - Francia 178
ID - Indonesia 148
FI - Finlandia 104
RU - Federazione Russa 83
IN - India 79
CA - Canada 60
TR - Turchia 49
BE - Belgio 31
ES - Italia 27
JP - Giappone 24
NL - Olanda 22
AU - Australia 21
CI - Costa d'Avorio 20
MX - Messico 18
HK - Hong Kong 16
IR - Iran 16
CH - Svizzera 14
CZ - Repubblica Ceca 9
AT - Austria 8
VN - Vietnam 7
RO - Romania 6
KR - Corea 4
AR - Argentina 3
BZ - Belize 3
CL - Cile 3
DK - Danimarca 3
PR - Porto Rico 3
PT - Portogallo 3
SK - Slovacchia (Repubblica Slovacca) 3
TH - Thailandia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AE - Emirati Arabi Uniti 2
BG - Bulgaria 2
BR - Brasile 2
EE - Estonia 2
EU - Europa 2
GR - Grecia 2
HU - Ungheria 2
IL - Israele 2
MN - Mongolia 2
SA - Arabia Saudita 2
A1 - Anonimo 1
BD - Bangladesh 1
BN - Brunei Darussalam 1
DZ - Algeria 1
HN - Honduras 1
IS - Islanda 1
KE - Kenya 1
KZ - Kazakistan 1
LU - Lussemburgo 1
MY - Malesia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PE - Perù 1
PH - Filippine 1
Totale 10.112
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Città #
Chandler 779
Warsaw 422
Ashburn 382
Jacksonville 253
San Mateo 237
Dublin 221
Singapore 188
Nanjing 152
Wilmington 147
Jakarta 146
Ann Arbor 145
Woodbridge 122
Houston 114
Nürnberg 114
Fairfield 111
New York 103
Boston 99
Dearborn 94
Rome 74
Moscow 68
Lawrence 67
Seattle 66
Milan 63
Princeton 63
Redwood City 63
Nanchang 61
Cattolica 59
Beijing 46
Bremen 46
Izmir 43
Chicago 42
Munich 40
Marseille 37
Chengdu 35
Cambridge 34
Ottawa 34
Shenyang 34
Hebei 31
Redmond 29
Mountain View 27
University Park 27
Hangzhou 26
Jiaxing 26
Kunming 26
Boardman 25
Los Angeles 25
San Jose 25
Leawood 23
Norwalk 22
Changsha 21
Detroit 21
Abidjan 20
Lancaster 20
Washington 20
Brussels 18
Sydney 18
Madrid 17
Tianjin 17
Fremont 16
Saint Louis 15
Shanghai 15
Helsinki 14
Toronto 14
Zhengzhou 14
Inverigo 13
Las Vegas 12
London 10
Pune 10
Berlin 9
Guangzhou 9
Kraków 9
Augusta 8
Hong Kong 8
Kish 8
Lanzhou 8
Ningbo 8
Philadelphia 8
Andover 7
Antwerp 7
Busto Arsizio 7
Oristano 7
Phoenix 7
Auburn Hills 6
Brno 6
Cuauhtémoc 6
Jinan 6
Bologna 5
Falls Church 5
Florence 5
Hounslow 5
Naples 5
San Diego 5
Vienna 5
Amsterdam 4
Ardabil 4
Arezzo 4
Changchun 4
Dong Ket 4
Essen 4
Frattamaggiore 4
Totale 5.618
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Nome #
MyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle. 318
Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients 316
An immunological analysis of dystroglycan subunits: lessons learned from a small cohort of non-congenital dystrophic patients. 283
Balance and walking in facioscapulohumeral muscular dystrophy: multiperspective assessment 200
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 195
Sleeep quality in Facioscapulohumeral muscular dystrophy. 194
Alternative splicing alterations of Ca(2+) handling genes are associated with Ca(2+) signal dysregulation in DM1 and DM2 myotubes 190
CD8(+) T Cells in Facioscapulohumeral Muscular Dystrophy Patients with Inflammatory Features at Muscle MRI 158
Cephalometric findings in facioscapulohumeral muscular dystrophy patients with obstructive sleep apneas 144
alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy 142
Balance and walking involvement in Facioscapulohumeral Muscular Dystrophy (FSHD): a pilot study on the effects of custom lower limb orthoses 140
Pain and the Alpha-Sleep Anomaly: A Mechanism of Sleep Disruption in Facioscapulohumeral Muscular Dystrophy 138
Decreased nocturnal movements in patients with facioscapulohumeral muscular dystrophy 136
Chronic GM2 gangliosidosis type Sandhoff associated with a novel missense HEXB gene mutaton causing a double patogenetic effect 134
Tracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imaging 132
Heart rate variability in facioscapulohumeral muscular dystrophy. 131
Analysis of ryanodine receptor 1 (RyR1) and voltage-gated Ca2+ channel (VGCC) alpha1S subunit (Cav1.1) pre-mRNA splicing and correlation with intracellular calcium signals in myotonic dystrophy type 1 (DM1) and in myotonic dystrophy type 2 (DM2) myotubes. 129
Muscle imaging findings in GNE myopathy 124
Quality of Life and Pain assessment in patients with facioscapulohumeral muscular dystrophy 123
Sleep quality in Facioscapulohumeral muscular dystrophy 123
Alternative splicing alterations of Ca2+ handling genes are associated with Ca2+ signal dysregulation in myotonic dystrophy type 1 (DM1) and type 2 (DM2) myotubes. 118
Muscle MRI in Becker muscular dystrophy 117
Myotonic dystrophy type 1 and de novo FSHD mutation double trouble: A clinical and muscle MRI study 113
Monoclonal antibody fragment from combinatorial phage display library neutralizes alpha-latrotoxin activity and abolishes black widow spider venom lethality, in mice 112
Mesoangioblasts from Facioscapulohumeral Muscular Dystrophy display in vivo a variable myogenic ability predictable by their in vitro behavior. 111
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients. 107
Muscle MRI in female carriers of dystrophinopathy 102
Muscle MRI in Becker muscular dystrophy 102
Congenital muscular dystrophies with cognitive impairment. A population study 100
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study 99
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 98
Upper Girdle Imaging in Facioscapulohumeral Muscular Dystrophy 97
Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle 95
Different molecular signatures in magnetic resonance imaging-staged facioscapulohumeral muscular dystrophy muscles 94
Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease 91
Coeliac disease presenting with acute disseminated encephalomyelitis 89
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 89
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy 87
Ocular palsies in the absence of other neurological or ocular symptoms: analysis of 105 cases 85
Limb-girdle muscular dystrophy with α-dystroglycan deficiency and mutations in the ISPD gene 85
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 85
Magnetic Resonance Imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: pattern refinement and implications for clinical trials 84
Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity 83
Sleep disordered breathing in facioscapulohumeral muscular dystrophy. 82
Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis. 81
New phenotype and pathology features in MYH7-related distal myopathy 80
Calf muscle involvement in Becker muscular dystrophy: When size does not matter 78
Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma. 76
Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2 76
Remitting-Relapsing Carbamazepine Overdosage Mimicking Vertebrobasilar Transient Ischemic Attacks 74
Coeliac disease presenting with acute disseminated encephalomyelitis. 73
Analysis of MTMR1 expression and correlation with muscle pathological features in juvenile/adult onset myotonic dystrophy type 1 (DM1) and in myotonic dystrophy type 2 (DM2). 72
Non-myogenic mesenchymal cells contribute to muscle degeneration in facioscapulohumeral muscular dystrophy patients 71
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation 71
An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene 70
Teaching video neuroimages: complicated scapular winging 70
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 70
Severe 5,10-methylenetetrahydrofolate reductase deficiency: A rare, treatable cause of complicated hereditary spastic paraplegia 70
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 68
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 68
Prevalence of congenital muscular dystrophy in Italy: a population study 66
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging 66
Increased aging in primary muscle cultures of sporadic inclusion-body myositis. 65
Proteomics of muscle microdialysates identifies potential circulating biomarkers in facioscapulohumeral muscular dystrophy 64
Magnetic resonance imaging pattern recognition in sporadic Inclusion-Body Myositis 62
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 61
Pilot trial of simvastatin in the treatment of sporadic inclusion-body myositis 60
To the Editor: Fasciculations in Late-Onset Pompe Disease: A Sign of Motor Neuron Involvement? 60
Mouth leaks may complicate positive airway pressure treatment of OSAS in facioscapulohumeral muscular dystrophy. 58
Upper girdle imaging in facioscapulohumeral muscular dystrophy 58
Mixed connective tissue disease presenting as a peculiar myositis with poor muscle regeneration 58
MRI in sarcoglycanopathies: a large international cohort study 57
Somatic mosaicism in TPM2-related myopathy with nemaline rods and cap structures. 56
'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1D 55
An Exceptional Case of Acute Respiratory Failure Caused by Intra-Thoracic Gastric Perforation Secondary to Overeating 55
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. 54
Muscle hypertrophy in amyloid myopathy 54
Diagnostic magnetic resonance imaging biomarkers for facioscapulohumeral muscular dystrophy identified by machine learning 54
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression. 52
European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) 52
Dynamic magnetic resonance imaging of muscle contraction in facioscapulohumeral muscular dystrophy 52
Upper body involvement in GNE myopathy assessed by muscle imaging 51
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials 50
The genetic basis of undiagnosed muscular dystrophies and myopathies 50
Technology outcome measures in neuromuscular disorders: A systematic review 50
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 49
Music exposure differentially alters the levels of brain-derived neurotrophic factor and nerve growth factor in the mouse hypothalamus. 48
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1 48
Concentric muscle involvement in POLG-related distal myopathy 48
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 48
Investigating the neurobiology of music: brain-derived neurotrophic factor modulation in the hippocampus of young adult mice. 47
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 47
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 47
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 47
Thymectomy in the treatment of myasthenia gravis: report of 247 patients 46
Surgical Decision-Making in Spinal Instability in Facioscapulohumeral Muscular Dystrophy Related with a Spinal Muscle Atrophy 46
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 45
Texture analysis and machine learning to predict water T2 and fat fraction from non-quantitative MRI of thigh muscles in Facioscapulohumeral muscular dystrophy 45
COVID-19 pandemic and days of absence from work in workers with flu-like symptoms in the City of Rome, Italy 44
Ultrasound Tissue Characterization Does Not Differentiate Genotype, But Indexes Ejection Fraction Deterioration in Becker Muscular Dystrophy 43
Totale 9.061
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Categoria #
all - tutte 41.326
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 41.326
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020910 0 0 0 106 109 104 127 52 88 71 142 111
2020/20211.109 36 113 26 118 146 45 139 22 161 54 211 38
2021/20221.235 92 94 30 87 49 70 22 194 88 61 213 235
2022/20232.272 283 289 193 330 178 298 76 177 302 29 57 60
2023/20241.317 50 340 40 81 37 167 115 72 20 54 174 167
2024/2025391 67 87 233 4 0 0 0 0 0 0 0 0
Totale 10.274