IRIS UniCatt

Tasca, Giorgio
 Distribuzione geografica
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Continente #
NA - Nord America 4.884
EU - Europa 3.882
AS - Asia 3.245
SA - Sud America 636
Continente sconosciuto - Info sul continente non disponibili 200
AF - Africa 90
OC - Oceania 22
Totale 12.959
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Nazione #
US - Stati Uniti d'America 4.739
SG - Singapore 1.533
DE - Germania 1.120
IT - Italia 764
CN - Cina 750
BR - Brasile 513
SE - Svezia 492
PL - Polonia 314
VN - Vietnam 279
FR - Francia 232
UA - Ucraina 196
FI - Finlandia 166
GB - Regno Unito 150
IE - Irlanda 148
IN - India 111
ID - Indonesia 109
HK - Hong Kong 79
JP - Giappone 72
RU - Federazione Russa 72
BD - Bangladesh 63
CA - Canada 63
NL - Olanda 52
ES - Italia 51
AR - Argentina 45
TR - Turchia 40
IQ - Iraq 36
ZA - Sudafrica 32
BE - Belgio 27
MX - Messico 26
AT - Austria 24
PK - Pakistan 23
VE - Venezuela 19
AU - Australia 18
KR - Corea 18
CL - Cile 17
IR - Iran 17
EC - Ecuador 16
SA - Arabia Saudita 16
UZ - Uzbekistan 14
CI - Costa d'Avorio 13
RO - Romania 13
CZ - Repubblica Ceca 11
JM - Giamaica 11
AE - Emirati Arabi Uniti 10
CH - Svizzera 10
CO - Colombia 10
CR - Costa Rica 10
LT - Lituania 9
PH - Filippine 9
IL - Israele 8
PY - Paraguay 8
DZ - Algeria 7
JO - Giordania 7
KE - Kenya 7
PT - Portogallo 7
TH - Thailandia 6
TN - Tunisia 6
HN - Honduras 5
KZ - Kazakistan 5
MY - Malesia 5
PA - Panama 5
TT - Trinidad e Tobago 5
AZ - Azerbaigian 4
BG - Bulgaria 4
MA - Marocco 4
MN - Mongolia 4
OM - Oman 4
PR - Porto Rico 4
SK - Slovacchia (Repubblica Slovacca) 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
A2 - ???statistics.table.value.countryCode.A2??? 2
AM - Armenia 2
BB - Barbados 2
BO - Bolivia 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
SV - El Salvador 2
SY - Repubblica araba siriana 2
UY - Uruguay 2
BH - Bahrain 1
BS - Bahamas 1
Totale 12.741
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Città #
Singapore 831
Ashburn 605
Chandler 533
San Jose 487
Warsaw 298
Frankfurt am Main 260
Munich 226
Beijing 147
Dublin 144
San Mateo 136
Rome 134
Jacksonville 115
New York 111
Milan 96
Ann Arbor 95
Helsinki 95
Jakarta 94
Wilmington 92
Ho Chi Minh City 87
Lauterbourg 85
Los Angeles 85
Woodbridge 79
Nanjing 78
Fairfield 73
Hanoi 71
Boston 70
Hong Kong 66
Houston 64
Tokyo 64
Hefei 60
Cattolica 57
Dallas 54
Moscow 53
Chicago 51
Seattle 51
Santa Clara 49
São Paulo 46
Council Bluffs 44
Princeton 43
Nürnberg 40
Lawrence 38
Dearborn 33
Redwood City 33
Nanchang 32
Boardman 29
Atlanta 27
Cambridge 25
Brooklyn 23
Buffalo 23
Johannesburg 23
Madrid 23
Nuremberg 23
Izmir 21
The Dalles 21
Bremen 20
Paris 20
Brussels 19
Shanghai 19
Stockholm 19
Hangzhou 18
London 18
Orem 18
Phoenix 18
Washington 18
Changsha 17
Da Nang 17
Mumbai 17
St Louis 17
Jiaxing 16
Seoul 16
Shenyang 16
Toronto 16
Baghdad 15
Curitiba 15
Rio de Janeiro 15
Kent 14
Marseille 14
Palermo 14
Abidjan 13
Inverigo 13
Leawood 13
Montreal 13
Mountain View 13
Tashkent 13
Vienna 13
Augusta 12
Chennai 12
Denver 12
Detroit 12
Hebei 12
Kunming 12
Las Vegas 12
North Bergen 12
Amsterdam 11
Belo Horizonte 11
Poplar 11
San Francisco 11
Biên Hòa 10
Düsseldorf 10
Hyderabad 10
Totale 6.910
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Nome #
Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions 471
Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients 428
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 292
Upper body involvement in GNE myopathy assessed by muscle imaging 269
Artificial Intelligence for Evaluation of Retinal Vasculopathy in Facioscapulohumeral Dystrophy Using OCT Angiography: A Case Series 263
Hospital admissions from the emergency department of adult patients affected by myopathies 261
Tracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imaging 252
CD8(+) T Cells in Facioscapulohumeral Muscular Dystrophy Patients with Inflammatory Features at Muscle MRI 248
Novel missense variants associated with GNE myopathy 247
Non-myogenic mesenchymal cells contribute to muscle degeneration in facioscapulohumeral muscular dystrophy patients 206
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients. 197
Muscle imaging findings in GNE myopathy 194
Matrin 3 variants are frequent in Italian ALS patients 194
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 186
New ALS-related genes expand the spectrum paradigm of amyotrophic lateral sclerosis 169
Muscle MRI in female carriers of dystrophinopathy 168
Muscle MRI in Becker muscular dystrophy 165
Myotonic dystrophy type 1 and de novo FSHD mutation double trouble: A clinical and muscle MRI study 165
An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene 164
Muscle fibrosis as a prognostic biomarker in facioscapulohumeral muscular dystrophy: a retrospective cohort study 163
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 156
New phenotype and pathology features in MYH7-related distal myopathy 156
Different molecular signatures in magnetic resonance imaging-staged facioscapulohumeral muscular dystrophy muscles 150
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 149
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy 146
Diagnostic magnetic resonance imaging biomarkers for facioscapulohumeral muscular dystrophy identified by machine learning 146
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation 145
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 143
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 142
SOD1 p.D12Y variant is associated with ALS/distal myopathy spectrum 140
Magnetic Resonance Imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: pattern refinement and implications for clinical trials 137
Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity 136
Dynamic magnetic resonance imaging of muscle contraction in facioscapulohumeral muscular dystrophy 134
MRI patterns of muscle involvement in type 2 and 3 spinal muscular atrophy patients 132
Proteomics of muscle microdialysates identifies potential circulating biomarkers in facioscapulohumeral muscular dystrophy 132
Limb-girdle muscular dystrophy with α-dystroglycan deficiency and mutations in the ISPD gene 127
Upper girdle imaging in facioscapulohumeral muscular dystrophy 127
ANCA-related vasculitic neuropathy mimicking motor neuron disease. 125
Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2 121
Deep learning for automatic segmentation of thigh and leg muscles 121
Calf muscle involvement in Becker muscular dystrophy: When size does not matter 120
A man with sarcoidosis and slurred speech 118
Teaching video neuroimages: complicated scapular winging 117
Anti-cN1A Antibodies Are Associated with More Severe Dysphagia in Sporadic Inclusion Body Myositis 116
Thr124Met myelin protein zero mutation mimicking motor neuron disease 116
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging 115
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies 114
Rinsing after spinning: plasmapheresis in EBV-related post-infectious cerebellitis 114
Technology outcome measures in neuromuscular disorders: A systematic review 114
Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene 113
An unusual ryanodine receptor 1 (RYR1) phenotype: Mild, calf-predominant myopathy. 110
'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1D 108
Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy 108
Mixed connective tissue disease presenting as a peculiar myositis with poor muscle regeneration 107
Muscle hypertrophy in amyloid myopathy 106
Muscle-MRI and Functional Levels for the Evaluation of Upper Limbs in Duchenne Muscular Dystrophy: A Critical Review of the Literature 106
Magnetic resonance imaging pattern recognition in sporadic Inclusion-Body Myositis 105
MRI in sarcoglycanopathies: a large international cohort study 105
High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients 105
European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) 102
Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane trafficking 101
Association study reveals novel risk loci for sporadic inclusion body myositis 101
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients 100
Multi-organ investigation in 16 CADASIL families from central Italy sharing the same R1006C mutation 99
Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study 98
The genetic basis of undiagnosed muscular dystrophies and myopathies 98
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials 97
MRI in sarcoglycanopathies: A large international cohort study 94
Mosaic caveolin-3 expression in acquired rippling muscle disease without evidence of myasthenia gravis or acetylcholine receptor autoantibodies 93
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression. 92
Texture analysis and machine learning to predict water T2 and fat fraction from non-quantitative MRI of thigh muscles in Facioscapulohumeral muscular dystrophy 92
Fast Open-Source Toolkit for Water T2 Mapping in the Presence of Fat From Multi-Echo Spin-Echo Acquisitions for Muscle MRI 92
Redox homeostasis in muscular dystrophies 91
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1 88
MYO-MRI diagnostic protocols in genetic myopathies 88
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy 87
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 87
Somatic mosaicism in TPM2-related myopathy with nemaline rods and cap structures. 86
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 86
To the Editor: Fasciculations in Late-Onset Pompe Disease: A Sign of Motor Neuron Involvement? 85
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 85
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression 84
Concentric muscle involvement in POLG-related distal myopathy 83
MYH7-related myopathies: Clinical, histopathological and imaging findings in a cohort of Italian patients 81
Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy 80
Peculiar muscle imaging findings in a patient with alphaB-crystallinopathy and axial myopathy 78
The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosis 75
D4Z4 Methylation Levels Combined with a Machine Learning Pipeline Highlight Single CpG Sites as Discriminating Biomarkers for FSHD Patients 72
Genotype-phenotype correlations in recessive titinopathies 72
Start codon mutation of GYG1 causing late-onset polyglucosan body myopathy with nemaline rods 72
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 71
The variability of SMCHD1 gene in FSHD patients: Evidence of new mutations 71
An immunological analysis of dystroglycan subunits: Lessons learned from a small cohort of non-congenital dystrophic patients 69
Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy 68
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1 67
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations 64
Centronuclear myopathies: genotype–phenotype correlation and frequency of defined genetic forms in an Italian cohort 61
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations 54
Natural history of facioscapulohumeral muscular dystrophy evaluated by multiparametric quantitative MRI: a prospective cohort study 34
Muscle Imaging in Inclusion Body Myositis: Refinement of MRI Criteria and Insights Into Upper Body Involvement 26
Totale 12.908
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Categoria #
all - tutte 53.840
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 53.840
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022660 0 0 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
2025/20264.730 661 139 255 491 715 467 849 234 300 325 178 116
2026/2027611 250 334 27 0 0 0 0 0 0 0 0 0
Totale 12.959