IRIS UniCatt

Ricci, Enzo
 Distribuzione geografica
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Continente #
NA - Nord America 7.032
EU - Europa 5.892
AS - Asia 5.095
SA - Sud America 1.065
AF - Africa 143
OC - Oceania 29
Continente sconosciuto - Info sul continente non disponibili 5
Totale 19.261
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Nazione #
US - Stati Uniti d'America 6.808
SG - Singapore 2.406
DE - Germania 1.886
CN - Cina 1.242
BR - Brasile 874
SE - Svezia 779
IT - Italia 747
PL - Polonia 464
UA - Ucraina 445
VN - Vietnam 427
FR - Francia 400
GB - Regno Unito 290
IE - Irlanda 236
FI - Finlandia 230
IN - India 191
ID - Indonesia 172
JP - Giappone 133
RU - Federazione Russa 111
CA - Canada 108
HK - Hong Kong 97
TR - Turchia 76
AR - Argentina 71
BD - Bangladesh 70
NL - Olanda 67
MX - Messico 59
ES - Italia 50
IQ - Iraq 47
ZA - Sudafrica 40
AT - Austria 35
BE - Belgio 34
EC - Ecuador 31
PK - Pakistan 28
VE - Venezuela 26
AU - Australia 25
KR - Corea 23
SA - Arabia Saudita 23
CI - Costa d'Avorio 22
UZ - Uzbekistan 22
MA - Marocco 18
CH - Svizzera 17
CL - Cile 17
IR - Iran 17
KE - Kenya 16
CO - Colombia 12
CR - Costa Rica 12
PY - Paraguay 11
CZ - Repubblica Ceca 10
JO - Giordania 10
LT - Lituania 10
PH - Filippine 10
RO - Romania 10
AE - Emirati Arabi Uniti 9
DZ - Algeria 9
EG - Egitto 9
IL - Israele 9
LV - Lettonia 9
PA - Panama 9
PE - Perù 9
TN - Tunisia 9
JM - Giamaica 8
KZ - Kazakistan 8
OM - Oman 8
UY - Uruguay 8
GR - Grecia 7
MY - Malesia 7
AZ - Azerbaigian 6
BG - Bulgaria 6
ET - Etiopia 6
HN - Honduras 6
LB - Libano 6
PS - Palestinian Territory 6
PT - Portogallo 6
SK - Slovacchia (Repubblica Slovacca) 6
TH - Thailandia 6
DO - Repubblica Dominicana 5
AL - Albania 4
AM - Armenia 4
BN - Brunei Darussalam 4
BO - Bolivia 4
DK - Danimarca 4
EE - Estonia 4
NP - Nepal 4
SI - Slovenia 4
AO - Angola 3
BZ - Belize 3
GE - Georgia 3
HU - Ungheria 3
KG - Kirghizistan 3
LU - Lussemburgo 3
MD - Moldavia 3
MN - Mongolia 3
NI - Nicaragua 3
NO - Norvegia 3
NZ - Nuova Zelanda 3
PR - Porto Rico 3
SN - Senegal 3
TW - Taiwan 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BA - Bosnia-Erzegovina 2
BW - Botswana 2
Totale 19.222
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Città #
Singapore 1.286
Ashburn 844
Chandler 779
San Jose 761
Warsaw 443
Munich 259
Jacksonville 258
San Mateo 237
Dublin 229
Beijing 226
New York 162
Nanjing 153
Jakarta 148
Wilmington 147
Ann Arbor 145
Lauterbourg 142
Rome 136
Ho Chi Minh City 134
Houston 127
Woodbridge 122
Nürnberg 114
Fairfield 111
Helsinki 109
Boston 108
Los Angeles 108
Milan 107
Tokyo 106
Hefei 103
Dallas 94
Dearborn 94
Hanoi 85
Chicago 75
Moscow 75
São Paulo 75
Hong Kong 73
Seattle 72
Lawrence 67
Frankfurt am Main 66
Princeton 63
Redwood City 63
Nanchang 61
Cattolica 59
Santa Clara 54
Buffalo 47
Bremen 46
Council Bluffs 44
Izmir 44
Chengdu 39
Marseille 37
Cambridge 35
The Dalles 35
Ottawa 34
Shenyang 34
Boardman 33
Hebei 31
Nuremberg 31
Belo Horizonte 29
Redmond 29
Atlanta 28
Hangzhou 28
Brooklyn 27
Mountain View 27
Rio de Janeiro 27
University Park 27
Chennai 26
Jiaxing 26
Kunming 26
London 26
Johannesburg 25
Madrid 25
Orem 25
Shanghai 25
Washington 25
Detroit 24
Norwalk 24
Phoenix 24
Changsha 23
Kent 23
Leawood 23
Paris 23
Abidjan 22
Da Nang 21
St Louis 21
Toronto 21
Brussels 20
Haiphong 20
Lancaster 20
Sydney 20
Biên Hòa 19
Düsseldorf 19
Montreal 19
Seoul 19
Tashkent 19
Vienna 19
Curitiba 18
Denver 18
Mexico City 18
Tianjin 18
Baghdad 17
Porto Alegre 17
Totale 10.170
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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 421
MyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle. 410
An immunological analysis of dystroglycan subunits: lessons learned from a small cohort of non-congenital dystrophic patients. 346
Balance and walking in facioscapulohumeral muscular dystrophy: multiperspective assessment 269
Upper body involvement in GNE myopathy assessed by muscle imaging 265
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 264
Hospital admissions from the emergency department of adult patients affected by myopathies 259
Sleeep quality in Facioscapulohumeral muscular dystrophy. 245
Alternative splicing alterations of Ca(2+) handling genes are associated with Ca(2+) signal dysregulation in DM1 and DM2 myotubes 244
CD8(+) T Cells in Facioscapulohumeral Muscular Dystrophy Patients with Inflammatory Features at Muscle MRI 239
Tracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imaging 238
Cephalometric findings in facioscapulohumeral muscular dystrophy patients with obstructive sleep apneas 220
Pain and the Alpha-Sleep Anomaly: A Mechanism of Sleep Disruption in Facioscapulohumeral Muscular Dystrophy 210
Balance and walking involvement in Facioscapulohumeral Muscular Dystrophy (FSHD): a pilot study on the effects of custom lower limb orthoses 208
Decreased nocturnal movements in patients with facioscapulohumeral muscular dystrophy 207
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 206
Non-myogenic mesenchymal cells contribute to muscle degeneration in facioscapulohumeral muscular dystrophy patients 201
Heart rate variability in facioscapulohumeral muscular dystrophy. 200
Alternative splicing alterations of Ca2+ handling genes are associated with Ca2+ signal dysregulation in myotonic dystrophy type 1 (DM1) and type 2 (DM2) myotubes. 199
alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy 198
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. 195
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients. 193
Muscle imaging findings in GNE myopathy 192
Quality of Life and Pain assessment in patients with facioscapulohumeral muscular dystrophy 188
Chronic GM2 gangliosidosis type Sandhoff associated with a novel missense HEXB gene mutaton causing a double patogenetic effect 188
Sleep quality in Facioscapulohumeral muscular dystrophy 183
Mesoangioblasts from Facioscapulohumeral Muscular Dystrophy display in vivo a variable myogenic ability predictable by their in vitro behavior. 179
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 174
Monoclonal antibody fragment from combinatorial phage display library neutralizes alpha-latrotoxin activity and abolishes black widow spider venom lethality, in mice 166
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 166
Muscle MRI in female carriers of dystrophinopathy 164
Muscle MRI in Becker muscular dystrophy 163
Muscle MRI in Becker muscular dystrophy 162
Myotonic dystrophy type 1 and de novo FSHD mutation double trouble: A clinical and muscle MRI study 161
Muscle fibrosis as a prognostic biomarker in facioscapulohumeral muscular dystrophy: a retrospective cohort study 156
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 155
Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease 153
Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle 153
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 151
Different molecular signatures in magnetic resonance imaging-staged facioscapulohumeral muscular dystrophy muscles 150
Upper Girdle Imaging in Facioscapulohumeral Muscular Dystrophy 149
Diagnostic magnetic resonance imaging biomarkers for facioscapulohumeral muscular dystrophy identified by machine learning 145
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy 144
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study 144
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation 143
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 142
New phenotype and pathology features in MYH7-related distal myopathy 142
Congenital muscular dystrophies with cognitive impairment. A population study 138
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 138
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 137
Magnetic Resonance Imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: pattern refinement and implications for clinical trials 136
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 136
Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis. 135
Dynamic magnetic resonance imaging of muscle contraction in facioscapulohumeral muscular dystrophy 133
Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity 132
Proteomics of muscle microdialysates identifies potential circulating biomarkers in facioscapulohumeral muscular dystrophy 132
Sleep disordered breathing in facioscapulohumeral muscular dystrophy. 131
Severe 5,10-methylenetetrahydrofolate reductase deficiency: A rare, treatable cause of complicated hereditary spastic paraplegia 130
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). 129
Ocular palsies in the absence of other neurological or ocular symptoms: analysis of 105 cases 127
Increased aging in primary muscle cultures of sporadic inclusion-body myositis. 124
Coeliac disease presenting with acute disseminated encephalomyelitis. 123
Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma. 123
Limb-girdle muscular dystrophy with α-dystroglycan deficiency and mutations in the ISPD gene 123
Surgical Decision-Making in Spinal Instability in Facioscapulohumeral Muscular Dystrophy Related with a Spinal Muscle Atrophy 123
Artificial Intelligence for Evaluation of Retinal Vasculopathy in Facioscapulohumeral Dystrophy Using OCT Angiography: A Case Series 123
Deep learning for automatic segmentation of thigh and leg muscles 120
Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2 119
Coeliac disease presenting with acute disseminated encephalomyelitis 118
An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene 116
Calf muscle involvement in Becker muscular dystrophy: When size does not matter 116
Teaching video neuroimages: complicated scapular winging 115
Pilot trial of simvastatin in the treatment of sporadic inclusion-body myositis 114
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging 114
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies 111
Thymectomy in the treatment of myasthenia gravis: report of 247 patients 111
Remitting-Relapsing Carbamazepine Overdosage Mimicking Vertebrobasilar Transient Ischemic Attacks 108
Technology outcome measures in neuromuscular disorders: A systematic review 108
Upper girdle imaging in facioscapulohumeral muscular dystrophy 107
Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene 106
Mixed connective tissue disease presenting as a peculiar myositis with poor muscle regeneration 106
'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1D 105
Muscle hypertrophy in amyloid myopathy 105
MRI in sarcoglycanopathies: a large international cohort study 104
High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients 104
Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy 103
An Exceptional Case of Acute Respiratory Failure Caused by Intra-Thoracic Gastric Perforation Secondary to Overeating 103
Magnetic resonance imaging pattern recognition in sporadic Inclusion-Body Myositis 102
Preparation for colonoscopy: Recommendations by an expert panel in Italy 101
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 100
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 100
Mouth leaks may complicate positive airway pressure treatment of OSAS in facioscapulohumeral muscular dystrophy. 99
European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) 99
Music exposure differentially alters the levels of brain-derived neurotrophic factor and nerve growth factor in the mouse hypothalamus. 98
COVID-19 pandemic and days of absence from work in workers with flu-like symptoms in the City of Rome, Italy 98
Investigating the neurobiology of music: brain-derived neurotrophic factor modulation in the hippocampus of young adult mice. 96
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials 95
Prevalence of congenital muscular dystrophy in Italy: a population study 95
The genetic basis of undiagnosed muscular dystrophies and myopathies 94
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. 91
Totale 15.504
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Categoria #
all - tutte 79.212
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 79.212
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202138 0 0 0 0 0 0 0 0 0 0 0 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
2023/20241.330 50 340 42 81 40 167 119 72 20 54 175 170
2024/20252.852 68 87 235 65 212 143 180 207 451 234 517 453
2025/20266.756 1.027 221 445 741 1.123 337 1.233 342 437 496 232 122
Totale 19.504