Ricci, Enzo
 Distribuzione geografica
Continente #
EU - Europa 4.404
NA - Nord America 4.189
AS - Asia 782
OC - Oceania 22
AF - Africa 21
SA - Sud America 9
Continente sconosciuto - Info sul continente non disponibili 5
Totale 9.432
Nazione #
US - Stati Uniti d'America 4.104
DE - Germania 1.533
SE - Svezia 740
CN - Cina 557
PL - Polonia 433
UA - Ucraina 430
IT - Italia 416
IE - Irlanda 228
GB - Regno Unito 204
FR - Francia 176
FI - Finlandia 103
IN - India 79
CA - Canada 60
TR - Turchia 48
BE - Belgio 31
ES - Italia 27
JP - Giappone 22
NL - Olanda 22
AU - Australia 21
CI - Costa d'Avorio 20
MX - Messico 18
HK - Hong Kong 16
IR - Iran 16
CH - Svizzera 14
SG - Singapore 14
RU - Federazione Russa 8
AT - Austria 7
CZ - Repubblica Ceca 7
VN - Vietnam 7
RO - Romania 6
KR - Corea 4
AR - Argentina 3
BZ - Belize 3
CL - Cile 3
DK - Danimarca 3
ID - Indonesia 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
HN - Honduras 1
IS - Islanda 1
KE - Kenya 1
KZ - Kazakistan 1
MY - Malesia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PE - Perù 1
PH - Filippine 1
Totale 9.432
Città #
Chandler 779
Warsaw 422
Ashburn 378
Jacksonville 253
San Mateo 237
Dublin 221
Nanjing 152
Wilmington 147
Ann Arbor 145
Woodbridge 122
Houston 114
Nürnberg 114
Fairfield 111
New York 103
Boston 99
Dearborn 94
Lawrence 67
Seattle 66
Milan 63
Princeton 63
Redwood City 63
Nanchang 61
Rome 59
Cattolica 55
Beijing 46
Bremen 46
Izmir 43
Munich 38
Marseille 37
Chengdu 35
Chicago 35
Cambridge 34
Ottawa 34
Shenyang 34
Hebei 31
Redmond 29
Mountain View 27
University Park 27
Hangzhou 26
Jiaxing 26
Kunming 26
San Jose 25
Leawood 23
Norwalk 22
Boardman 21
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
Los Angeles 14
Toronto 14
Zhengzhou 14
Helsinki 13
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
Busto Arsizio 7
Oristano 7
Phoenix 7
Auburn Hills 6
Cuauhtémoc 6
Jinan 6
Falls Church 5
Florence 5
Hounslow 5
Naples 5
San Diego 5
Singapore 5
Vienna 5
Amsterdam 4
Ardabil 4
Arezzo 4
Brno 4
Changchun 4
Dong Ket 4
Essen 4
Hadamar 4
Lausanne 4
Mumbai 4
Paris 4
Renton 4
Totale 5.175
Nome #
MyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle. 314
Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients 312
An immunological analysis of dystroglycan subunits: lessons learned from a small cohort of non-congenital dystrophic patients. 281
Balance and walking in facioscapulohumeral muscular dystrophy: multiperspective assessment 194
Sleeep quality in Facioscapulohumeral muscular dystrophy. 190
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 189
Alternative splicing alterations of Ca(2+) handling genes are associated with Ca(2+) signal dysregulation in DM1 and DM2 myotubes 185
CD8(+) T Cells in Facioscapulohumeral Muscular Dystrophy Patients with Inflammatory Features at Muscle MRI 153
Cephalometric findings in facioscapulohumeral muscular dystrophy patients with obstructive sleep apneas 139
alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy 136
Pain and the Alpha-Sleep Anomaly: A Mechanism of Sleep Disruption in Facioscapulohumeral Muscular Dystrophy 132
Decreased nocturnal movements in patients with facioscapulohumeral muscular dystrophy 131
Balance and walking involvement in Facioscapulohumeral Muscular Dystrophy (FSHD): a pilot study on the effects of custom lower limb orthoses 131
Heart rate variability in facioscapulohumeral muscular dystrophy. 128
Chronic GM2 gangliosidosis type Sandhoff associated with a novel missense HEXB gene mutaton causing a double patogenetic effect 128
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. 125
Muscle imaging findings in GNE myopathy 119
Sleep quality in Facioscapulohumeral muscular dystrophy 119
Tracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imaging 119
Quality of Life and Pain assessment in patients with facioscapulohumeral muscular dystrophy 115
Alternative splicing alterations of Ca2+ handling genes are associated with Ca2+ signal dysregulation in myotonic dystrophy type 1 (DM1) and type 2 (DM2) myotubes. 111
Muscle MRI in Becker muscular dystrophy 110
Monoclonal antibody fragment from combinatorial phage display library neutralizes alpha-latrotoxin activity and abolishes black widow spider venom lethality, in mice 108
Mesoangioblasts from Facioscapulohumeral Muscular Dystrophy display in vivo a variable myogenic ability predictable by their in vitro behavior. 107
Myotonic dystrophy type 1 and de novo FSHD mutation double trouble: A clinical and muscle MRI study 105
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients. 103
Muscle MRI in female carriers of dystrophinopathy 96
Muscle MRI in Becker muscular dystrophy 96
Congenital muscular dystrophies with cognitive impairment. A population study 94
Upper Girdle Imaging in Facioscapulohumeral Muscular Dystrophy 94
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study 92
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 90
Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle 89
Coeliac disease presenting with acute disseminated encephalomyelitis 87
Different molecular signatures in magnetic resonance imaging-staged facioscapulohumeral muscular dystrophy muscles 87
Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease 86
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 85
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy 84
Limb-girdle muscular dystrophy with α-dystroglycan deficiency and mutations in the ISPD gene 83
Ocular palsies in the absence of other neurological or ocular symptoms: analysis of 105 cases 82
Magnetic Resonance Imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: pattern refinement and implications for clinical trials 80
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 79
Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity 77
Sleep disordered breathing in facioscapulohumeral muscular dystrophy. 76
New phenotype and pathology features in MYH7-related distal myopathy 75
Calf muscle involvement in Becker muscular dystrophy: When size does not matter 75
Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis. 74
Remitting-Relapsing Carbamazepine Overdosage Mimicking Vertebrobasilar Transient Ischemic Attacks 73
Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2 72
Coeliac disease presenting with acute disseminated encephalomyelitis. 71
Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma. 70
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation 67
An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene 66
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). 66
Teaching video neuroimages: complicated scapular winging 65
Severe 5,10-methylenetetrahydrofolate reductase deficiency: A rare, treatable cause of complicated hereditary spastic paraplegia 65
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 64
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging 64
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 63
Prevalence of congenital muscular dystrophy in Italy: a population study 62
Increased aging in primary muscle cultures of sporadic inclusion-body myositis. 61
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 61
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 58
Magnetic resonance imaging pattern recognition in sporadic Inclusion-Body Myositis 58
To the Editor: Fasciculations in Late-Onset Pompe Disease: A Sign of Motor Neuron Involvement? 58
Pilot trial of simvastatin in the treatment of sporadic inclusion-body myositis 57
Proteomics of muscle microdialysates identifies potential circulating biomarkers in facioscapulohumeral muscular dystrophy 56
Non-myogenic mesenchymal cells contribute to muscle degeneration in facioscapulohumeral muscular dystrophy patients 54
Mouth leaks may complicate positive airway pressure treatment of OSAS in facioscapulohumeral muscular dystrophy. 54
Upper girdle imaging in facioscapulohumeral muscular dystrophy 53
Mixed connective tissue disease presenting as a peculiar myositis with poor muscle regeneration 52
Diagnostic magnetic resonance imaging biomarkers for facioscapulohumeral muscular dystrophy identified by machine learning 52
'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1D 51
An Exceptional Case of Acute Respiratory Failure Caused by Intra-Thoracic Gastric Perforation Secondary to Overeating 51
Somatic mosaicism in TPM2-related myopathy with nemaline rods and cap structures. 50
MRI in sarcoglycanopathies: a large international cohort study 50
European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) 50
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression. 48
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials 48
Music exposure differentially alters the levels of brain-derived neurotrophic factor and nerve growth factor in the mouse hypothalamus. 47
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. 47
Muscle hypertrophy in amyloid myopathy 47
Dynamic magnetic resonance imaging of muscle contraction in facioscapulohumeral muscular dystrophy 47
The genetic basis of undiagnosed muscular dystrophies and myopathies 46
Upper body involvement in GNE myopathy assessed by muscle imaging 46
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
Investigating the neurobiology of music: brain-derived neurotrophic factor modulation in the hippocampus of young adult mice. 44
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1 44
Concentric muscle involvement in POLG-related distal myopathy 44
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 44
Thymectomy in the treatment of myasthenia gravis: report of 247 patients 43
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 43
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 42
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 42
Ultrasound Tissue Characterization Does Not Differentiate Genotype, But Indexes Ejection Fraction Deterioration in Becker Muscular Dystrophy 41
Biochemical characterization of patients with in-frame or out-of-frame DMD deletions pertinent to exon 44 or 45 skipping 41
COVID-19 pandemic and days of absence from work in workers with flu-like symptoms in the City of Rome, Italy 41
Texture analysis and machine learning to predict water T2 and fat fraction from non-quantitative MRI of thigh muscles in Facioscapulohumeral muscular dystrophy 40
Surgical Decision-Making in Spinal Instability in Facioscapulohumeral Muscular Dystrophy Related with a Spinal Muscle Atrophy 40
Peculiar muscle imaging findings in a patient with alphaB-crystallinopathy and axial myopathy 39
Totale 8.568
Categoria #
all - tutte 34.269
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 34.269


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019289 0 0 0 0 0 0 0 0 0 0 146 143
2019/20201.315 231 78 96 106 109 104 127 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
2023/20241.028 50 340 40 81 37 167 115 72 20 54 52 0
Totale 9.594