IRIS UniCatt

Ricci, Enzo
 Distribuzione geografica
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Continente #
NA - Nord America 8.635
EU - Europa 6.068
AS - Asia 5.137
SA - Sud America 1.128
Continente sconosciuto - Info sul continente non disponibili 250
AF - Africa 143
OC - Oceania 31
Totale 21.392
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Nazione #
US - Stati Uniti d'America 8.316
SG - Singapore 2.414
DE - Germania 1.886
CN - Cina 1.248
BR - Brasile 901
IT - Italia 882
SE - Svezia 779
PL - Polonia 464
UA - Ucraina 448
VN - Vietnam 428
FR - Francia 406
GB - Regno Unito 301
IE - Irlanda 237
FI - Finlandia 230
IN - India 192
ID - Indonesia 174
CA - Canada 155
JP - Giappone 134
RU - Federazione Russa 111
HK - Hong Kong 100
BD - Bangladesh 80
TR - Turchia 77
AR - Argentina 75
NL - Olanda 74
MX - Messico 64
ES - Italia 50
IQ - Iraq 47
EC - Ecuador 40
ZA - Sudafrica 40
AT - Austria 35
BE - Belgio 34
VE - Venezuela 30
PK - Pakistan 29
AU - Australia 27
CO - Colombia 26
SA - Arabia Saudita 24
KR - Corea 23
CI - Costa d'Avorio 22
UZ - Uzbekistan 22
CR - Costa Rica 21
CL - Cile 19
JM - Giamaica 19
MA - Marocco 18
CH - Svizzera 17
IR - Iran 17
KE - Kenya 16
PY - Paraguay 12
RO - Romania 12
PH - Filippine 11
PT - Portogallo 11
AE - Emirati Arabi Uniti 10
CZ - Repubblica Ceca 10
JO - Giordania 10
LT - Lituania 10
PE - Perù 10
DZ - Algeria 9
EG - Egitto 9
IL - Israele 9
LV - Lettonia 9
PA - Panama 9
TH - Thailandia 9
TN - Tunisia 9
UY - Uruguay 9
EE - Estonia 8
GR - Grecia 8
KZ - Kazakistan 8
MY - Malesia 8
OM - Oman 8
PR - Porto Rico 7
SK - Slovacchia (Repubblica Slovacca) 7
TT - Trinidad e Tobago 7
AZ - Azerbaigian 6
BG - Bulgaria 6
ET - Etiopia 6
HN - Honduras 6
LB - Libano 6
NI - Nicaragua 6
PS - Palestinian Territory 6
DO - Repubblica Dominicana 5
AL - Albania 4
AM - Armenia 4
BN - Brunei Darussalam 4
BO - Bolivia 4
BZ - Belize 4
DK - Danimarca 4
GT - Guatemala 4
NP - Nepal 4
SI - Slovenia 4
AO - Angola 3
GE - Georgia 3
HU - Ungheria 3
KG - Kirghizistan 3
LU - Lussemburgo 3
MD - Moldavia 3
MN - Mongolia 3
NO - Norvegia 3
NZ - Nuova Zelanda 3
SN - Senegal 3
SV - El Salvador 3
TW - Taiwan 3
Totale 21.100
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Città #
Singapore 1.291
Ashburn 1.077
San Jose 904
Chandler 780
Warsaw 443
Jacksonville 267
Munich 259
San Mateo 237
Dublin 230
Beijing 227
Council Bluffs 183
New York 177
Nanjing 153
Rome 151
Wilmington 149
Jakarta 148
Ann Arbor 145
Lauterbourg 142
Ho Chi Minh City 135
Houston 131
Los Angeles 126
Woodbridge 124
Milan 120
Nürnberg 114
Fairfield 111
Boston 110
Helsinki 109
Dallas 107
Tokyo 107
Hefei 103
Dearborn 95
Hanoi 85
Chicago 82
São Paulo 79
Hong Kong 76
Moscow 75
Seattle 73
Santa Clara 71
Lawrence 68
Frankfurt am Main 66
Princeton 63
Redwood City 63
Nanchang 61
Cattolica 59
Atlanta 51
Buffalo 49
Phoenix 49
Bremen 46
Izmir 44
Chengdu 39
Marseille 37
Ottawa 36
Cambridge 35
The Dalles 35
Boardman 34
Shenyang 34
Hebei 31
Nuremberg 31
Belo Horizonte 30
Brooklyn 30
London 29
Redmond 29
Toronto 29
Washington 29
Detroit 28
Hangzhou 28
Mountain View 27
Rio de Janeiro 27
University Park 27
Chennai 26
Denver 26
Jiaxing 26
Kunming 26
Orem 26
Johannesburg 25
Madrid 25
Shanghai 25
Norwalk 24
Paris 24
Changsha 23
Kent 23
Leawood 23
Abidjan 22
Las Vegas 22
Montreal 22
Sydney 22
Da Nang 21
San Francisco 21
St Louis 21
Brussels 20
Haiphong 20
Lancaster 20
Biên Hòa 19
Düsseldorf 19
Seoul 19
Tashkent 19
Vienna 19
Curitiba 18
Mexico City 18
Porto Alegre 18
Totale 10.922
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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 438
MyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle. 428
An immunological analysis of dystroglycan subunits: lessons learned from a small cohort of non-congenital dystrophic patients. 351
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 330
Balance and walking in facioscapulohumeral muscular dystrophy: multiperspective assessment 301
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 274
Upper body involvement in GNE myopathy assessed by muscle imaging 274
Artificial Intelligence for Evaluation of Retinal Vasculopathy in Facioscapulohumeral Dystrophy Using OCT Angiography: A Case Series 266
Hospital admissions from the emergency department of adult patients affected by myopathies 265
Tracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imaging 262
Sleeep quality in Facioscapulohumeral muscular dystrophy. 252
CD8(+) T Cells in Facioscapulohumeral Muscular Dystrophy Patients with Inflammatory Features at Muscle MRI 252
Alternative splicing alterations of Ca(2+) handling genes are associated with Ca(2+) signal dysregulation in DM1 and DM2 myotubes 249
Pain and the Alpha-Sleep Anomaly: A Mechanism of Sleep Disruption in Facioscapulohumeral Muscular Dystrophy 238
Cephalometric findings in facioscapulohumeral muscular dystrophy patients with obstructive sleep apneas 230
Non-myogenic mesenchymal cells contribute to muscle degeneration in facioscapulohumeral muscular dystrophy patients 217
Balance and walking involvement in Facioscapulohumeral Muscular Dystrophy (FSHD): a pilot study on the effects of custom lower limb orthoses 214
Decreased nocturnal movements in patients with facioscapulohumeral muscular dystrophy 213
Alternative splicing alterations of Ca2+ handling genes are associated with Ca2+ signal dysregulation in myotonic dystrophy type 1 (DM1) and type 2 (DM2) myotubes. 213
An Exceptional Case of Acute Respiratory Failure Caused by Intra-Thoracic Gastric Perforation Secondary to Overeating 211
Heart rate variability in facioscapulohumeral muscular dystrophy. 209
alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy 207
Muscle imaging findings in GNE myopathy 200
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients. 199
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. 198
Quality of Life and Pain assessment in patients with facioscapulohumeral muscular dystrophy 198
Chronic GM2 gangliosidosis type Sandhoff associated with a novel missense HEXB gene mutaton causing a double patogenetic effect 193
Sleep quality in Facioscapulohumeral muscular dystrophy 192
Mesoangioblasts from Facioscapulohumeral Muscular Dystrophy display in vivo a variable myogenic ability predictable by their in vitro behavior. 188
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 187
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 187
Monoclonal antibody fragment from combinatorial phage display library neutralizes alpha-latrotoxin activity and abolishes black widow spider venom lethality, in mice 179
Muscle MRI in female carriers of dystrophinopathy 174
Muscle MRI in Becker muscular dystrophy 172
Muscle MRI in Becker muscular dystrophy 171
Myotonic dystrophy type 1 and de novo FSHD mutation double trouble: A clinical and muscle MRI study 171
Muscle fibrosis as a prognostic biomarker in facioscapulohumeral muscular dystrophy: a retrospective cohort study 170
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 161
Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease 160
New phenotype and pathology features in MYH7-related distal myopathy 160
Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle 159
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 158
Upper Girdle Imaging in Facioscapulohumeral Muscular Dystrophy 157
Different molecular signatures in magnetic resonance imaging-staged facioscapulohumeral muscular dystrophy muscles 156
Ocular palsies in the absence of other neurological or ocular symptoms: analysis of 105 cases 155
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study 155
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 152
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation 152
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 152
Diagnostic magnetic resonance imaging biomarkers for facioscapulohumeral muscular dystrophy identified by machine learning 151
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy 150
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 149
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 148
Magnetic Resonance Imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: pattern refinement and implications for clinical trials 145
Congenital muscular dystrophies with cognitive impairment. A population study 144
Dynamic magnetic resonance imaging of muscle contraction in facioscapulohumeral muscular dystrophy 141
Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis. 140
Sleep disordered breathing in facioscapulohumeral muscular dystrophy. 140
Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity 138
Severe 5,10-methylenetetrahydrofolate reductase deficiency: A rare, treatable cause of complicated hereditary spastic paraplegia 136
Proteomics of muscle microdialysates identifies potential circulating biomarkers in facioscapulohumeral muscular dystrophy 136
Limb-girdle muscular dystrophy with α-dystroglycan deficiency and mutations in the ISPD gene 135
Increased aging in primary muscle cultures of sporadic inclusion-body myositis. 132
Upper girdle imaging in facioscapulohumeral muscular dystrophy 132
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). 131
Surgical Decision-Making in Spinal Instability in Facioscapulohumeral Muscular Dystrophy Related with a Spinal Muscle Atrophy 129
Coeliac disease presenting with acute disseminated encephalomyelitis. 128
Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma. 127
Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2 127
Deep learning for automatic segmentation of thigh and leg muscles 127
An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene 125
Calf muscle involvement in Becker muscular dystrophy: When size does not matter 125
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies 122
Coeliac disease presenting with acute disseminated encephalomyelitis 122
Pilot trial of simvastatin in the treatment of sporadic inclusion-body myositis 122
Thymectomy in the treatment of myasthenia gravis: report of 247 patients 121
Technology outcome measures in neuromuscular disorders: A systematic review 121
Teaching video neuroimages: complicated scapular winging 120
Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene 118
Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy 118
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging 118
Remitting-Relapsing Carbamazepine Overdosage Mimicking Vertebrobasilar Transient Ischemic Attacks 114
'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1D 114
Mixed connective tissue disease presenting as a peculiar myositis with poor muscle regeneration 114
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 114
Muscle hypertrophy in amyloid myopathy 112
Magnetic resonance imaging pattern recognition in sporadic Inclusion-Body Myositis 110
High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients 110
MRI in sarcoglycanopathies: a large international cohort study 109
COVID-19 pandemic and days of absence from work in workers with flu-like symptoms in the City of Rome, Italy 108
Preparation for colonoscopy: Recommendations by an expert panel in Italy 107
Mouth leaks may complicate positive airway pressure treatment of OSAS in facioscapulohumeral muscular dystrophy. 107
European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) 107
Music exposure differentially alters the levels of brain-derived neurotrophic factor and nerve growth factor in the mouse hypothalamus. 106
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 106
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials 103
Prevalence of congenital muscular dystrophy in Italy: a population study 103
Investigating the neurobiology of music: brain-derived neurotrophic factor modulation in the hippocampus of young adult mice. 101
Texture analysis and machine learning to predict water T2 and fat fraction from non-quantitative MRI of thigh muscles in Facioscapulohumeral muscular dystrophy 101
The genetic basis of undiagnosed muscular dystrophies and myopathies 100
Totale 16.814
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Categoria #
all - tutte 87.152
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 87.152
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.019 0 0 0 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
2025/20266.785 1.027 221 445 741 1.123 337 1.233 342 437 496 232 151
2026/20271.859 451 423 464 521 0 0 0 0 0 0 0 0
Totale 21.392