IRIS PubliCatt

Ricci, Enzo
 Distribuzione geografica
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Continente #
EU - Europa 4.654
NA - Nord America 4.274
AS - Asia 1.471
AF - Africa 23
OC - Oceania 22
SA - Sud America 10
Continente sconosciuto - Info sul continente non disponibili 5
Totale 10.459
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Nazione #
US - Stati Uniti d'America 4.188
DE - Germania 1.546
SE - Svezia 748
CN - Cina 689
IT - Italia 509
PL - Polonia 433
UA - Ucraina 430
SG - Singapore 414
IE - Irlanda 229
GB - Regno Unito 209
FR - Francia 183
ID - Indonesia 148
FI - Finlandia 126
RU - Federazione Russa 83
IN - India 80
CA - Canada 61
TR - Turchia 49
BE - Belgio 32
ES - Italia 29
NL - Olanda 28
JP - Giappone 24
AU - Australia 21
CI - Costa d'Avorio 20
HK - Hong Kong 20
MX - Messico 18
IR - Iran 16
CH - Svizzera 15
AT - Austria 10
CZ - Repubblica Ceca 9
VN - Vietnam 8
RO - Romania 7
KR - Corea 4
LT - Lituania 4
SK - Slovacchia (Repubblica Slovacca) 4
AR - Argentina 3
BG - Bulgaria 3
BZ - Belize 3
CL - Cile 3
DK - Danimarca 3
GR - Grecia 3
PR - Porto Rico 3
PT - Portogallo 3
TH - Thailandia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AE - Emirati Arabi Uniti 2
BR - Brasile 2
EE - Estonia 2
EU - Europa 2
HU - Ungheria 2
IL - Israele 2
LU - Lussemburgo 2
MN - Mongolia 2
SA - Arabia Saudita 2
A1 - Anonimo 1
AM - Armenia 1
BD - Bangladesh 1
BN - Brunei Darussalam 1
DZ - Algeria 1
EC - Ecuador 1
GE - Georgia 1
HN - Honduras 1
IS - Islanda 1
KE - Kenya 1
KZ - Kazakistan 1
MA - Marocco 1
MY - Malesia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PE - Perù 1
PH - Filippine 1
UZ - Uzbekistan 1
Totale 10.459
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Città #
Chandler 779
Warsaw 422
Ashburn 382
Singapore 308
Jacksonville 253
San Mateo 237
Dublin 222
Nanjing 153
Wilmington 147
Jakarta 146
Ann Arbor 145
Woodbridge 122
Houston 114
Nürnberg 114
Fairfield 111
New York 104
Boston 99
Dearborn 94
Rome 88
Milan 78
Moscow 68
Lawrence 67
Seattle 66
Princeton 63
Redwood City 63
Nanchang 61
Cattolica 59
Beijing 48
Bremen 46
Munich 45
Izmir 43
Chicago 42
Chengdu 37
Marseille 37
Helsinki 36
Cambridge 34
Ottawa 34
Shenyang 34
Hebei 31
Redmond 29
Hangzhou 27
Mountain View 27
University Park 27
Jiaxing 26
Kunming 26
Los Angeles 26
Boardman 25
San Jose 25
Changsha 23
Leawood 23
Norwalk 22
Detroit 21
Abidjan 20
Lancaster 20
Washington 20
Brussels 19
Shanghai 19
Sydney 18
Madrid 17
Tianjin 17
Fremont 16
Saint Louis 15
Toronto 15
Zhengzhou 15
Inverigo 13
Las Vegas 12
Guangzhou 11
London 10
Pune 10
Berlin 9
Hong Kong 9
Kraków 9
Paris 9
Augusta 8
Bologna 8
Kish 8
Lanzhou 8
Ningbo 8
Philadelphia 8
Andover 7
Antwerp 7
Busto Arsizio 7
Oristano 7
Phoenix 7
Vienna 7
Auburn Hills 6
Brno 6
Cuauhtémoc 6
Jinan 6
Amsterdam 5
Falls Church 5
Florence 5
Hounslow 5
Naples 5
San Diego 5
Ardabil 4
Arezzo 4
Changchun 4
Dong Ket 4
Essen 4
Totale 5.826
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Nome #
Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients 323
MyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle. 320
An immunological analysis of dystroglycan subunits: lessons learned from a small cohort of non-congenital dystrophic patients. 286
Balance and walking in facioscapulohumeral muscular dystrophy: multiperspective assessment 206
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 198
Sleeep quality in Facioscapulohumeral muscular dystrophy. 197
Alternative splicing alterations of Ca(2+) handling genes are associated with Ca(2+) signal dysregulation in DM1 and DM2 myotubes 191
CD8(+) T Cells in Facioscapulohumeral Muscular Dystrophy Patients with Inflammatory Features at Muscle MRI 160
Cephalometric findings in facioscapulohumeral muscular dystrophy patients with obstructive sleep apneas 149
Balance and walking involvement in Facioscapulohumeral Muscular Dystrophy (FSHD): a pilot study on the effects of custom lower limb orthoses 145
alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy 143
Pain and the Alpha-Sleep Anomaly: A Mechanism of Sleep Disruption in Facioscapulohumeral Muscular Dystrophy 141
Heart rate variability in facioscapulohumeral muscular dystrophy. 140
Decreased nocturnal movements in patients with facioscapulohumeral muscular dystrophy 140
Tracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imaging 136
Chronic GM2 gangliosidosis type Sandhoff associated with a novel missense HEXB gene mutaton causing a double patogenetic effect 135
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. 133
Sleep quality in Facioscapulohumeral muscular dystrophy 131
Muscle imaging findings in GNE myopathy 125
Quality of Life and Pain assessment in patients with facioscapulohumeral muscular dystrophy 124
Alternative splicing alterations of Ca2+ handling genes are associated with Ca2+ signal dysregulation in myotonic dystrophy type 1 (DM1) and type 2 (DM2) myotubes. 119
Muscle MRI in Becker muscular dystrophy 118
Mesoangioblasts from Facioscapulohumeral Muscular Dystrophy display in vivo a variable myogenic ability predictable by their in vitro behavior. 115
Monoclonal antibody fragment from combinatorial phage display library neutralizes alpha-latrotoxin activity and abolishes black widow spider venom lethality, in mice 115
Myotonic dystrophy type 1 and de novo FSHD mutation double trouble: A clinical and muscle MRI study 115
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients. 108
Muscle MRI in female carriers of dystrophinopathy 106
Muscle MRI in Becker muscular dystrophy 103
Congenital muscular dystrophies with cognitive impairment. A population study 102
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 102
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study 100
Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle 98
Upper Girdle Imaging in Facioscapulohumeral Muscular Dystrophy 98
Different molecular signatures in magnetic resonance imaging-staged facioscapulohumeral muscular dystrophy muscles 95
Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease 93
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 92
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 91
Coeliac disease presenting with acute disseminated encephalomyelitis 90
Magnetic Resonance Imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: pattern refinement and implications for clinical trials 90
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy 88
Limb-girdle muscular dystrophy with α-dystroglycan deficiency and mutations in the ISPD gene 86
Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity 86
Ocular palsies in the absence of other neurological or ocular symptoms: analysis of 105 cases 85
Sleep disordered breathing in facioscapulohumeral muscular dystrophy. 84
Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis. 83
New phenotype and pathology features in MYH7-related distal myopathy 82
Non-myogenic mesenchymal cells contribute to muscle degeneration in facioscapulohumeral muscular dystrophy patients 81
Calf muscle involvement in Becker muscular dystrophy: When size does not matter 79
Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma. 77
Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2 77
Remitting-Relapsing Carbamazepine Overdosage Mimicking Vertebrobasilar Transient Ischemic Attacks 75
Coeliac disease presenting with acute disseminated encephalomyelitis. 74
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). 74
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 73
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation 72
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 72
Teaching video neuroimages: complicated scapular winging 71
Severe 5,10-methylenetetrahydrofolate reductase deficiency: A rare, treatable cause of complicated hereditary spastic paraplegia 71
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 71
An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene 70
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging 70
Increased aging in primary muscle cultures of sporadic inclusion-body myositis. 67
Prevalence of congenital muscular dystrophy in Italy: a population study 66
Proteomics of muscle microdialysates identifies potential circulating biomarkers in facioscapulohumeral muscular dystrophy 65
Magnetic resonance imaging pattern recognition in sporadic Inclusion-Body Myositis 64
MRI in sarcoglycanopathies: a large international cohort study 64
Diagnostic magnetic resonance imaging biomarkers for facioscapulohumeral muscular dystrophy identified by machine learning 64
Pilot trial of simvastatin in the treatment of sporadic inclusion-body myositis 62
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 61
To the Editor: Fasciculations in Late-Onset Pompe Disease: A Sign of Motor Neuron Involvement? 61
Mixed connective tissue disease presenting as a peculiar myositis with poor muscle regeneration 60
Mouth leaks may complicate positive airway pressure treatment of OSAS in facioscapulohumeral muscular dystrophy. 59
Upper girdle imaging in facioscapulohumeral muscular dystrophy 59
Upper body involvement in GNE myopathy assessed by muscle imaging 59
Dynamic magnetic resonance imaging of muscle contraction in facioscapulohumeral muscular dystrophy 58
Somatic mosaicism in TPM2-related myopathy with nemaline rods and cap structures. 57
'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1D 56
Muscle hypertrophy in amyloid myopathy 56
An Exceptional Case of Acute Respiratory Failure Caused by Intra-Thoracic Gastric Perforation Secondary to Overeating 56
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. 55
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 54
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression. 53
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 53
Technology outcome measures in neuromuscular disorders: A systematic review 53
European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) 52
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 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
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 50
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 49
Concentric muscle involvement in POLG-related distal myopathy 49
Surgical Decision-Making in Spinal Instability in Facioscapulohumeral Muscular Dystrophy Related with a Spinal Muscle Atrophy 49
Muscle fibrosis as a prognostic biomarker in facioscapulohumeral muscular dystrophy: a retrospective cohort study 48
Investigating the neurobiology of music: brain-derived neurotrophic factor modulation in the hippocampus of young adult mice. 48
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
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 48
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 47
Thymectomy in the treatment of myasthenia gravis: report of 247 patients 46
Texture analysis and machine learning to predict water T2 and fat fraction from non-quantitative MRI of thigh muscles in Facioscapulohumeral muscular dystrophy 46
Totale 9.315
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Categoria #
all - tutte 45.294
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 45.294
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020695 0 0 0 0 0 104 127 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
2024/2025738 67 87 233 62 207 82 0 0 0 0 0 0
Totale 10.621