IRIS UniCatt

Ricci, Enzo
 Distribuzione geografica
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Continente #
NA - Nord America 5.527
EU - Europa 5.496
AS - Asia 4.054
SA - Sud America 979
AF - Africa 125
OC - Oceania 27
Continente sconosciuto - Info sul continente non disponibili 5
Totale 16.213
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Nazione #
US - Stati Uniti d'America 5.339
SG - Singapore 1.934
DE - Germania 1.855
CN - Cina 1.136
BR - Brasile 819
SE - Svezia 779
IT - Italia 619
PL - Polonia 461
UA - Ucraina 442
GB - Regno Unito 272
FR - Francia 245
IE - Irlanda 233
FI - Finlandia 220
VN - Vietnam 215
ID - Indonesia 165
IN - India 155
RU - Federazione Russa 102
CA - Canada 97
TR - Turchia 69
AR - Argentina 63
HK - Hong Kong 62
BD - Bangladesh 56
NL - Olanda 53
JP - Giappone 49
MX - Messico 49
ES - Italia 47
ZA - Sudafrica 35
AT - Austria 34
IQ - Iraq 34
BE - Belgio 33
EC - Ecuador 25
AU - Australia 23
VE - Venezuela 22
CI - Costa d'Avorio 21
KR - Corea 19
PK - Pakistan 19
UZ - Uzbekistan 18
CH - Svizzera 17
IR - Iran 17
MA - Marocco 16
SA - Arabia Saudita 16
CL - Cile 14
KE - Kenya 12
CZ - Repubblica Ceca 10
RO - Romania 10
AE - Emirati Arabi Uniti 9
DZ - Algeria 9
PA - Panama 9
PY - Paraguay 9
EG - Egitto 8
IL - Israele 8
KZ - Kazakistan 8
LT - Lituania 8
TN - Tunisia 8
UY - Uruguay 8
CO - Colombia 7
JO - Giordania 7
PE - Perù 7
AZ - Azerbaigian 6
CR - Costa Rica 6
HN - Honduras 6
LV - Lettonia 6
OM - Oman 6
PT - Portogallo 6
SK - Slovacchia (Repubblica Slovacca) 6
BG - Bulgaria 5
DO - Repubblica Dominicana 5
LB - Libano 5
MY - Malesia 5
PS - Palestinian Territory 5
AM - Armenia 4
BN - Brunei Darussalam 4
GR - Grecia 4
JM - Giamaica 4
PH - Filippine 4
TH - Thailandia 4
AO - Angola 3
BO - Bolivia 3
BZ - Belize 3
DK - Danimarca 3
ET - Etiopia 3
HU - Ungheria 3
LU - Lussemburgo 3
NO - Norvegia 3
NZ - Nuova Zelanda 3
PR - Porto Rico 3
SI - Slovenia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AL - Albania 2
BA - Bosnia-Erzegovina 2
BW - Botswana 2
BY - Bielorussia 2
EE - Estonia 2
EU - Europa 2
GE - Georgia 2
GY - Guiana 2
MD - Moldavia 2
ML - Mali 2
MN - Mongolia 2
NI - Nicaragua 2
Totale 16.186
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Città #
Singapore 856
Chandler 779
Ashburn 607
Warsaw 441
Munich 259
Jacksonville 258
San Mateo 237
Dublin 226
Beijing 218
Nanjing 153
Wilmington 147
Jakarta 146
Ann Arbor 145
New York 145
Houston 125
Woodbridge 122
Nürnberg 114
Fairfield 111
Rome 110
Boston 107
Los Angeles 101
Helsinki 100
Hefei 97
Dearborn 94
Dallas 91
Milan 91
Moscow 74
Seattle 72
São Paulo 70
Lawrence 67
Ho Chi Minh City 64
Princeton 63
Redwood City 63
Chicago 62
Nanchang 61
Cattolica 59
Bremen 46
Hong Kong 46
Buffalo 44
Izmir 43
Frankfurt am Main 42
Hanoi 41
Chengdu 37
Marseille 37
Cambridge 34
Ottawa 34
Shenyang 34
Hebei 31
Boardman 30
Belo Horizonte 29
Nuremberg 29
Redmond 29
San Jose 28
Hangzhou 27
Mountain View 27
Rio de Janeiro 27
Tokyo 27
University Park 27
Jiaxing 26
Kunming 26
Brooklyn 25
Detroit 24
Johannesburg 24
London 24
Madrid 24
Changsha 23
Leawood 23
Norwalk 23
Santa Clara 23
Kent 22
Washington 22
Abidjan 21
Phoenix 21
Shanghai 21
Chennai 20
Lancaster 20
Brussels 19
Düsseldorf 19
Toronto 19
Sydney 18
Tianjin 18
Vienna 18
Curitiba 17
Montreal 17
Porto Alegre 17
Seoul 17
Stockholm 17
The Dalles 17
Fremont 16
Las Vegas 16
Denver 15
North Bergen 15
Orem 15
Saint Louis 15
San Francisco 15
Tashkent 15
Zhengzhou 15
Biên Hòa 14
Campinas 14
Dhaka 14
Totale 8.088
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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 383
MyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle. 363
An immunological analysis of dystroglycan subunits: lessons learned from a small cohort of non-congenital dystrophic patients. 329
Balance and walking in facioscapulohumeral muscular dystrophy: multiperspective assessment 246
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 241
Upper body involvement in GNE myopathy assessed by muscle imaging 239
Sleeep quality in Facioscapulohumeral muscular dystrophy. 230
Alternative splicing alterations of Ca(2+) handling genes are associated with Ca(2+) signal dysregulation in DM1 and DM2 myotubes 226
Hospital admissions from the emergency department of adult patients affected by myopathies 220
CD8(+) T Cells in Facioscapulohumeral Muscular Dystrophy Patients with Inflammatory Features at Muscle MRI 206
Cephalometric findings in facioscapulohumeral muscular dystrophy patients with obstructive sleep apneas 196
Tracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imaging 186
Balance and walking involvement in Facioscapulohumeral Muscular Dystrophy (FSHD): a pilot study on the effects of custom lower limb orthoses 184
Pain and the Alpha-Sleep Anomaly: A Mechanism of Sleep Disruption in Facioscapulohumeral Muscular Dystrophy 184
Decreased nocturnal movements in patients with facioscapulohumeral muscular dystrophy 183
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. 180
Heart rate variability in facioscapulohumeral muscular dystrophy. 178
alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy 178
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients. 173
Chronic GM2 gangliosidosis type Sandhoff associated with a novel missense HEXB gene mutaton causing a double patogenetic effect 169
Muscle imaging findings in GNE myopathy 168
Quality of Life and Pain assessment in patients with facioscapulohumeral muscular dystrophy 168
Non-myogenic mesenchymal cells contribute to muscle degeneration in facioscapulohumeral muscular dystrophy patients 167
Sleep quality in Facioscapulohumeral muscular dystrophy 163
Alternative splicing alterations of Ca2+ handling genes are associated with Ca2+ signal dysregulation in myotonic dystrophy type 1 (DM1) and type 2 (DM2) myotubes. 157
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 157
Mesoangioblasts from Facioscapulohumeral Muscular Dystrophy display in vivo a variable myogenic ability predictable by their in vitro behavior. 153
Monoclonal antibody fragment from combinatorial phage display library neutralizes alpha-latrotoxin activity and abolishes black widow spider venom lethality, in mice 151
Muscle MRI in Becker muscular dystrophy 147
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 147
Myotonic dystrophy type 1 and de novo FSHD mutation double trouble: A clinical and muscle MRI study 141
Muscle MRI in female carriers of dystrophinopathy 140
Muscle MRI in Becker muscular dystrophy 137
Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease 136
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 136
Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle 135
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 133
Different molecular signatures in magnetic resonance imaging-staged facioscapulohumeral muscular dystrophy muscles 133
Upper Girdle Imaging in Facioscapulohumeral Muscular Dystrophy 133
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study 130
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy 129
Congenital muscular dystrophies with cognitive impairment. A population study 124
Magnetic Resonance Imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: pattern refinement and implications for clinical trials 123
New phenotype and pathology features in MYH7-related distal myopathy 122
Diagnostic magnetic resonance imaging biomarkers for facioscapulohumeral muscular dystrophy identified by machine learning 121
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation 119
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 119
Sleep disordered breathing in facioscapulohumeral muscular dystrophy. 118
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 117
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 116
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). 115
Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis. 115
Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity 115
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 112
Coeliac disease presenting with acute disseminated encephalomyelitis 111
Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma. 111
Limb-girdle muscular dystrophy with α-dystroglycan deficiency and mutations in the ISPD gene 111
Muscle fibrosis as a prognostic biomarker in facioscapulohumeral muscular dystrophy: a retrospective cohort study 110
Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2 109
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 109
Dynamic magnetic resonance imaging of muscle contraction in facioscapulohumeral muscular dystrophy 109
Ocular palsies in the absence of other neurological or ocular symptoms: analysis of 105 cases 108
Increased aging in primary muscle cultures of sporadic inclusion-body myositis. 107
Surgical Decision-Making in Spinal Instability in Facioscapulohumeral Muscular Dystrophy Related with a Spinal Muscle Atrophy 107
Coeliac disease presenting with acute disseminated encephalomyelitis. 106
An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene 106
Severe 5,10-methylenetetrahydrofolate reductase deficiency: A rare, treatable cause of complicated hereditary spastic paraplegia 106
Calf muscle involvement in Becker muscular dystrophy: When size does not matter 102
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging 101
Remitting-Relapsing Carbamazepine Overdosage Mimicking Vertebrobasilar Transient Ischemic Attacks 100
Teaching video neuroimages: complicated scapular winging 99
Upper girdle imaging in facioscapulohumeral muscular dystrophy 95
Deep learning for automatic segmentation of thigh and leg muscles 94
Artificial Intelligence for Evaluation of Retinal Vasculopathy in Facioscapulohumeral Dystrophy Using OCT Angiography: A Case Series 94
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 93
Proteomics of muscle microdialysates identifies potential circulating biomarkers in facioscapulohumeral muscular dystrophy 93
Pilot trial of simvastatin in the treatment of sporadic inclusion-body myositis 92
'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1D 92
MRI in sarcoglycanopathies: a large international cohort study 92
Muscle hypertrophy in amyloid myopathy 92
Thymectomy in the treatment of myasthenia gravis: report of 247 patients 91
Magnetic resonance imaging pattern recognition in sporadic Inclusion-Body Myositis 91
Mixed connective tissue disease presenting as a peculiar myositis with poor muscle regeneration 91
Prevalence of congenital muscular dystrophy in Italy: a population study 90
An Exceptional Case of Acute Respiratory Failure Caused by Intra-Thoracic Gastric Perforation Secondary to Overeating 90
Investigating the neurobiology of music: brain-derived neurotrophic factor modulation in the hippocampus of young adult mice. 88
Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene 87
High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients 87
Mouth leaks may complicate positive airway pressure treatment of OSAS in facioscapulohumeral muscular dystrophy. 86
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 85
Music exposure differentially alters the levels of brain-derived neurotrophic factor and nerve growth factor in the mouse hypothalamus. 84
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. 84
COVID-19 pandemic and days of absence from work in workers with flu-like symptoms in the City of Rome, Italy 83
Technology outcome measures in neuromuscular disorders: A systematic review 81
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies 79
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials 79
Somatic mosaicism in TPM2-related myopathy with nemaline rods and cap structures. 79
Ultrasound Tissue Characterization Does Not Differentiate Genotype, But Indexes Ejection Fraction Deterioration in Becker Muscular Dystrophy 78
European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) 78
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression. 76
Totale 13.427
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Categoria #
all - tutte 68.445
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 68.445
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021670 0 0 0 0 0 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
2024/20252.802 67 87 233 62 207 138 177 206 441 228 506 450
2025/20263.704 1.010 218 440 730 1.083 223 0 0 0 0 0 0
Totale 16.389