IRIS UniCatt

Tasca, Giorgio
 Distribuzione geografica
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Continente #
NA - Nord America 4.265
EU - Europa 3.706
AS - Asia 3.200
SA - Sud America 616
AF - Africa 90
OC - Oceania 22
Continente sconosciuto - Info sul continente non disponibili 2
Totale 11.901
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Nazione #
US - Stati Uniti d'America 4.156
SG - Singapore 1.527
DE - Germania 1.120
CN - Cina 745
IT - Italia 609
BR - Brasile 504
SE - Svezia 492
PL - Polonia 313
VN - Vietnam 278
FR - Francia 231
UA - Ucraina 196
FI - Finlandia 166
GB - Regno Unito 148
IE - Irlanda 148
ID - Indonesia 109
IN - India 109
HK - Hong Kong 76
JP - Giappone 72
RU - Federazione Russa 72
ES - Italia 47
CA - Canada 45
NL - Olanda 44
AR - Argentina 43
BD - Bangladesh 40
TR - Turchia 40
IQ - Iraq 36
ZA - Sudafrica 32
BE - Belgio 27
AT - Austria 24
PK - Pakistan 23
MX - Messico 22
VE - Venezuela 19
AU - Australia 18
KR - Corea 18
IR - Iran 17
CL - Cile 15
EC - Ecuador 15
UZ - Uzbekistan 14
CI - Costa d'Avorio 13
SA - Arabia Saudita 13
RO - Romania 12
CZ - Repubblica Ceca 11
AE - Emirati Arabi Uniti 10
CH - Svizzera 10
LT - Lituania 9
PH - Filippine 9
CR - Costa Rica 8
DZ - Algeria 7
IL - Israele 7
JO - Giordania 7
KE - Kenya 7
PY - Paraguay 7
CO - Colombia 6
JM - Giamaica 6
TN - Tunisia 6
HN - Honduras 5
KZ - Kazakistan 5
MY - Malesia 5
PA - Panama 5
TH - Thailandia 5
AZ - Azerbaigian 4
BG - Bulgaria 4
MA - Marocco 4
MN - Mongolia 4
OM - Oman 4
PT - Portogallo 4
TT - Trinidad e Tobago 4
AL - Albania 3
AO - Angola 3
BN - Brunei Darussalam 3
BY - Bielorussia 3
BZ - Belize 3
GA - Gabon 3
LB - Libano 3
LV - Lettonia 3
NZ - Nuova Zelanda 3
PE - Perù 3
PR - Porto Rico 3
SK - Slovacchia (Repubblica Slovacca) 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AM - Armenia 2
BW - Botswana 2
DK - Danimarca 2
DO - Repubblica Dominicana 2
EG - Egitto 2
ET - Etiopia 2
GR - Grecia 2
KG - Kirghizistan 2
KH - Cambogia 2
MU - Mauritius 2
NI - Nicaragua 2
NP - Nepal 2
SN - Senegal 2
SY - Repubblica araba siriana 2
UY - Uruguay 2
BB - Barbados 1
BH - Bahrain 1
BO - Bolivia 1
BS - Bahamas 1
GE - Georgia 1
Totale 11.884
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Città #
Singapore 827
Chandler 532
Ashburn 505
San Jose 458
Warsaw 298
Frankfurt am Main 260
Munich 226
Beijing 147
Dublin 143
San Mateo 136
Jacksonville 115
Rome 108
New York 102
Ann Arbor 95
Helsinki 95
Jakarta 94
Wilmington 91
Ho Chi Minh City 86
Lauterbourg 85
Milan 80
Nanjing 78
Woodbridge 78
Los Angeles 76
Fairfield 73
Hanoi 71
Boston 70
Tokyo 64
Hong Kong 63
Hefei 60
Houston 60
Cattolica 57
Moscow 53
Seattle 50
Chicago 48
São Paulo 44
Princeton 43
Dallas 40
Nürnberg 40
Santa Clara 39
Council Bluffs 38
Lawrence 38
Dearborn 33
Redwood City 33
Nanchang 32
Boardman 25
Cambridge 25
Johannesburg 23
Madrid 23
Nuremberg 23
Buffalo 21
Izmir 21
Bremen 20
Paris 20
The Dalles 20
Brooklyn 19
Brussels 19
Shanghai 19
Stockholm 19
Hangzhou 18
London 18
Changsha 17
Da Nang 17
Orem 17
St Louis 17
Washington 17
Jiaxing 16
Mumbai 16
Seoul 16
Shenyang 16
Baghdad 15
Curitiba 15
Phoenix 15
Atlanta 14
Marseille 14
Abidjan 13
Inverigo 13
Kent 13
Leawood 13
Mountain View 13
Rio de Janeiro 13
Tashkent 13
Toronto 13
Vienna 13
Augusta 12
Chennai 12
Detroit 12
Hebei 12
Kunming 12
Montreal 12
Palermo 12
Amsterdam 11
Belo Horizonte 11
Denver 11
North Bergen 11
Poplar 11
San Francisco 11
Biên Hòa 10
Düsseldorf 10
Lappeenranta 10
Manchester 10
Totale 6.626
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Nome #
Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions 452
Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients 419
Upper body involvement in GNE myopathy assessed by muscle imaging 265
Hospital admissions from the emergency department of adult patients affected by myopathies 258
Novel missense variants associated with GNE myopathy 243
CD8(+) T Cells in Facioscapulohumeral Muscular Dystrophy Patients with Inflammatory Features at Muscle MRI 238
Tracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imaging 227
Non-myogenic mesenchymal cells contribute to muscle degeneration in facioscapulohumeral muscular dystrophy patients 193
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients. 191
Muscle imaging findings in GNE myopathy 190
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 185
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 184
Matrin 3 variants are frequent in Italian ALS patients 182
New ALS-related genes expand the spectrum paradigm of amyotrophic lateral sclerosis 165
An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene 163
Muscle MRI in female carriers of dystrophinopathy 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 160
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 152
Different molecular signatures in magnetic resonance imaging-staged facioscapulohumeral muscular dystrophy muscles 150
Muscle fibrosis as a prognostic biomarker in facioscapulohumeral muscular dystrophy: a retrospective cohort study 145
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy 144
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 143
Diagnostic magnetic resonance imaging biomarkers for facioscapulohumeral muscular dystrophy identified by machine learning 143
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation 142
New phenotype and pathology features in MYH7-related distal myopathy 140
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 137
SOD1 p.D12Y variant is associated with ALS/distal myopathy spectrum 136
Magnetic Resonance Imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: pattern refinement and implications for clinical trials 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
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 130
MRI patterns of muscle involvement in type 2 and 3 spinal muscular atrophy patients 129
Limb-girdle muscular dystrophy with α-dystroglycan deficiency and mutations in the ISPD gene 122
Artificial Intelligence for Evaluation of Retinal Vasculopathy in Facioscapulohumeral Dystrophy Using OCT Angiography: A Case Series 120
Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2 118
Deep learning for automatic segmentation of thigh and leg muscles 118
ANCA-related vasculitic neuropathy mimicking motor neuron disease. 117
A man with sarcoidosis and slurred speech 116
Teaching video neuroimages: complicated scapular winging 115
Calf muscle involvement in Becker muscular dystrophy: When size does not matter 115
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging 114
Proteomics of muscle microdialysates identifies potential circulating biomarkers in facioscapulohumeral muscular dystrophy 114
Anti-cN1A Antibodies Are Associated with More Severe Dysphagia in Sporadic Inclusion Body Myositis 110
Thr124Met myelin protein zero mutation mimicking motor neuron disease 110
An unusual ryanodine receptor 1 (RYR1) phenotype: Mild, calf-predominant myopathy. 109
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies 108
Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene 106
Upper girdle imaging in facioscapulohumeral muscular dystrophy 106
Mixed connective tissue disease presenting as a peculiar myositis with poor muscle regeneration 106
Technology outcome measures in neuromuscular disorders: A systematic review 106
'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1D 105
Muscle hypertrophy in amyloid myopathy 105
MRI in sarcoglycanopathies: a large international cohort study 103
High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients 103
Magnetic resonance imaging pattern recognition in sporadic Inclusion-Body Myositis 102
Muscle-MRI and Functional Levels for the Evaluation of Upper Limbs in Duchenne Muscular Dystrophy: A Critical Review of the Literature 102
Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy 99
Association study reveals novel risk loci for sporadic inclusion body myositis 98
European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) 97
Rinsing after spinning: plasmapheresis in EBV-related post-infectious cerebellitis 95
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients 94
Multi-organ investigation in 16 CADASIL families from central Italy sharing the same R1006C mutation 93
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials 92
The genetic basis of undiagnosed muscular dystrophies and myopathies 92
MRI in sarcoglycanopathies: A large international cohort study 91
Redox homeostasis in muscular dystrophies 91
Mosaic caveolin-3 expression in acquired rippling muscle disease without evidence of myasthenia gravis or acetylcholine receptor autoantibodies 90
Texture analysis and machine learning to predict water T2 and fat fraction from non-quantitative MRI of thigh muscles in Facioscapulohumeral muscular dystrophy 90
Fast Open-Source Toolkit for Water T2 Mapping in the Presence of Fat From Multi-Echo Spin-Echo Acquisitions for Muscle MRI 89
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression. 86
Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study 84
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy 84
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1 84
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 84
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 84
Somatic mosaicism in TPM2-related myopathy with nemaline rods and cap structures. 83
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 83
Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane trafficking 82
Concentric muscle involvement in POLG-related distal myopathy 82
MYO-MRI diagnostic protocols in genetic myopathies 82
To the Editor: Fasciculations in Late-Onset Pompe Disease: A Sign of Motor Neuron Involvement? 81
MYH7-related myopathies: Clinical, histopathological and imaging findings in a cohort of Italian patients 78
Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy 77
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression 77
Peculiar muscle imaging findings in a patient with alphaB-crystallinopathy and axial myopathy 76
Start codon mutation of GYG1 causing late-onset polyglucosan body myopathy with nemaline rods 72
The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosis 70
Genotype-phenotype correlations in recessive titinopathies 69
The variability of SMCHD1 gene in FSHD patients: Evidence of new mutations 68
A Recurrent Pathogenic Variant of INPP5K Underlies Autosomal Recessive Congenital Muscular Dystrophy With Cataracts and Intellectual Disability: Evidence for a Founder Effect in Southern Italy 66
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1 66
An immunological analysis of dystroglycan subunits: Lessons learned from a small cohort of non-congenital dystrophic patients 65
Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy 64
D4Z4 Methylation Levels Combined with a Machine Learning Pipeline Highlight Single CpG Sites as Discriminating Biomarkers for FSHD Patients 63
Centronuclear myopathies: genotype–phenotype correlation and frequency of defined genetic forms in an Italian cohort 58
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations 58
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations 52
Natural history of facioscapulohumeral muscular dystrophy evaluated by multiparametric quantitative MRI: a prospective cohort study 17
265th ENMC International Workshop: Muscle imaging in Facioscapulohumeral Muscular Dystrophy (FSHD): relevance for clinical trials. 22–24 April 2022, Hoofddorp, The Netherlands 8
Totale 12.095
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Categoria #
all - tutte 48.164
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 48.164
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021125 0 0 0 0 0 0 0 0 0 0 106 19
2021/2022778 67 51 18 58 34 25 15 131 51 47 127 154
2022/20231.469 193 194 137 216 115 201 37 113 180 12 29 42
2023/2024917 41 238 26 49 29 112 73 66 12 34 122 115
2024/20251.955 52 64 151 49 140 128 146 148 300 154 338 285
2025/20264.477 661 139 255 491 715 467 849 234 300 325 41 0
Totale 12.095