IRIS UniCatt

Tasca, Giorgio
 Distribuzione geografica
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Continente #
NA - Nord America 3.406
EU - Europa 3.235
AS - Asia 2.490
SA - Sud America 554
AF - Africa 69
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 2
Totale 9.768
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Nazione #
US - Stati Uniti d'America 3.326
SG - Singapore 1.225
DE - Germania 873
CN - Cina 674
IT - Italia 551
SE - Svezia 492
BR - Brasile 471
PL - Polonia 310
UA - Ucraina 193
FI - Finlandia 163
IE - Irlanda 146
GB - Regno Unito 129
FR - Francia 128
VN - Vietnam 125
ID - Indonesia 104
IN - India 86
RU - Federazione Russa 72
HK - Hong Kong 44
AR - Argentina 39
ES - Italia 36
NL - Olanda 35
CA - Canada 34
BD - Bangladesh 33
TR - Turchia 31
ZA - Sudafrica 28
BE - Belgio 26
JP - Giappone 25
AT - Austria 24
IQ - Iraq 17
IR - Iran 17
KR - Corea 16
MX - Messico 15
VE - Venezuela 13
CI - Costa d'Avorio 12
CL - Cile 12
PK - Pakistan 12
CZ - Repubblica Ceca 11
RO - Romania 11
AE - Emirati Arabi Uniti 10
CH - Svizzera 10
SA - Arabia Saudita 10
UZ - Uzbekistan 10
EC - Ecuador 9
AU - Australia 8
DZ - Algeria 6
IL - Israele 6
LT - Lituania 6
PH - Filippine 6
HN - Honduras 5
KZ - Kazakistan 5
PA - Panama 5
TN - Tunisia 5
AZ - Azerbaigian 4
TT - Trinidad e Tobago 4
BG - Bulgaria 3
BN - Brunei Darussalam 3
BY - Bielorussia 3
BZ - Belize 3
CR - Costa Rica 3
JM - Giamaica 3
JO - Giordania 3
LB - Libano 3
MN - Mongolia 3
NZ - Nuova Zelanda 3
PE - Perù 3
PR - Porto Rico 3
PT - Portogallo 3
PY - Paraguay 3
SK - Slovacchia (Repubblica Slovacca) 3
TH - Thailandia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AM - Armenia 2
AO - Angola 2
BW - Botswana 2
DO - Repubblica Dominicana 2
KE - Kenya 2
LV - Lettonia 2
MA - Marocco 2
MY - Malesia 2
OM - Oman 2
SN - Senegal 2
SY - Repubblica araba siriana 2
AL - Albania 1
BB - Barbados 1
BO - Bolivia 1
CO - Colombia 1
DK - Danimarca 1
EG - Egitto 1
GA - Gabon 1
GE - Georgia 1
GP - Guadalupe 1
GR - Grecia 1
GY - Guiana 1
IS - Islanda 1
KW - Kuwait 1
LK - Sri Lanka 1
LY - Libia 1
MD - Moldavia 1
MG - Madagascar 1
ML - Mali 1
Totale 9.758
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Città #
Singapore 548
Chandler 532
Ashburn 373
Warsaw 296
Munich 226
Beijing 145
Dublin 142
San Mateo 136
Jacksonville 115
Rome 98
New York 97
Ann Arbor 95
Helsinki 94
Jakarta 94
Wilmington 91
Nanjing 78
Woodbridge 78
Fairfield 73
Milan 72
Los Angeles 70
Boston 69
Hefei 60
Houston 60
Cattolica 57
Moscow 53
Seattle 50
Princeton 43
São Paulo 42
Chicago 41
Dallas 40
Nürnberg 40
Lawrence 38
Hong Kong 34
Dearborn 33
Redwood City 33
Hanoi 32
Ho Chi Minh City 32
Nanchang 32
Boardman 25
Cambridge 25
Santa Clara 24
Nuremberg 22
Buffalo 21
Frankfurt am Main 21
Johannesburg 21
Bremen 20
Izmir 20
Stockholm 19
Brooklyn 18
Brussels 18
Tokyo 18
Changsha 17
Hangzhou 17
Jiaxing 16
Seoul 16
Shenyang 16
Washington 16
Curitiba 15
London 15
Madrid 15
The Dalles 15
San Jose 14
Shanghai 14
Inverigo 13
Kent 13
Leawood 13
Marseille 13
Mountain View 13
Mumbai 13
Phoenix 13
Rio de Janeiro 13
Vienna 13
Abidjan 12
Augusta 12
Detroit 12
Hebei 12
Kunming 12
Palermo 12
Belo Horizonte 11
Poplar 11
San Francisco 11
Toronto 11
Amsterdam 10
Chennai 10
Denver 10
Düsseldorf 10
North Bergen 10
Orem 10
Atlanta 9
Campinas 9
Guarulhos 9
Jyväskylä 9
Lappeenranta 9
Las Vegas 9
Montreal 9
Norwalk 9
Tashkent 9
University Park 9
Lancaster 8
Manchester 8
Totale 5.099
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Nome #
Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions 396
Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients 380
Upper body involvement in GNE myopathy assessed by muscle imaging 236
Hospital admissions from the emergency department of adult patients affected by myopathies 217
CD8(+) T Cells in Facioscapulohumeral Muscular Dystrophy Patients with Inflammatory Features at Muscle MRI 205
Tracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imaging 184
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients. 172
Muscle imaging findings in GNE myopathy 167
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 167
Non-myogenic mesenchymal cells contribute to muscle degeneration in facioscapulohumeral muscular dystrophy patients 165
Matrin 3 variants are frequent in Italian ALS patients 158
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 156
An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene 146
Muscle MRI in Becker muscular dystrophy 145
New ALS-related genes expand the spectrum paradigm of amyotrophic lateral sclerosis 145
Myotonic dystrophy type 1 and de novo FSHD mutation double trouble: A clinical and muscle MRI study 140
Muscle MRI in female carriers of dystrophinopathy 139
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 133
Different molecular signatures in magnetic resonance imaging-staged facioscapulohumeral muscular dystrophy muscles 132
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy 129
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
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 121
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation 118
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 118
SOD1 p.D12Y variant is associated with ALS/distal myopathy spectrum 117
Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity 115
Diagnostic magnetic resonance imaging biomarkers for facioscapulohumeral muscular dystrophy identified by machine learning 112
Limb-girdle muscular dystrophy with α-dystroglycan deficiency and mutations in the ISPD gene 111
Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2 109
Dynamic magnetic resonance imaging of muscle contraction in facioscapulohumeral muscular dystrophy 108
ANCA-related vasculitic neuropathy mimicking motor neuron disease. 107
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 107
Muscle fibrosis as a prognostic biomarker in facioscapulohumeral muscular dystrophy: a retrospective cohort study 106
Calf muscle involvement in Becker muscular dystrophy: When size does not matter 102
MRI patterns of muscle involvement in type 2 and 3 spinal muscular atrophy patients 102
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging 101
Teaching video neuroimages: complicated scapular winging 97
A man with sarcoidosis and slurred speech 96
Thr124Met myelin protein zero mutation mimicking motor neuron disease 96
Upper girdle imaging in facioscapulohumeral muscular dystrophy 93
Proteomics of muscle microdialysates identifies potential circulating biomarkers in facioscapulohumeral muscular dystrophy 93
MRI in sarcoglycanopathies: a large international cohort study 92
Muscle hypertrophy in amyloid myopathy 92
Deep learning for automatic segmentation of thigh and leg muscles 92
Artificial Intelligence for Evaluation of Retinal Vasculopathy in Facioscapulohumeral Dystrophy Using OCT Angiography: A Case Series 92
'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1D 91
An unusual ryanodine receptor 1 (RYR1) phenotype: Mild, calf-predominant myopathy. 91
Mixed connective tissue disease presenting as a peculiar myositis with poor muscle regeneration 90
Anti-cN1A Antibodies Are Associated with More Severe Dysphagia in Sporadic Inclusion Body Myositis 89
Magnetic resonance imaging pattern recognition in sporadic Inclusion-Body Myositis 88
Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene 85
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients 84
High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients 84
Muscle-MRI and Functional Levels for the Evaluation of Upper Limbs in Duchenne Muscular Dystrophy: A Critical Review of the Literature 81
Rinsing after spinning: plasmapheresis in EBV-related post-infectious cerebellitis 80
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials 79
Technology outcome measures in neuromuscular disorders: A systematic review 79
Somatic mosaicism in TPM2-related myopathy with nemaline rods and cap structures. 78
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies 77
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression. 76
Multi-organ investigation in 16 CADASIL families from central Italy sharing the same R1006C mutation 76
European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) 76
Mosaic caveolin-3 expression in acquired rippling muscle disease without evidence of myasthenia gravis or acetylcholine receptor autoantibodies 75
To the Editor: Fasciculations in Late-Onset Pompe Disease: A Sign of Motor Neuron Involvement? 75
The genetic basis of undiagnosed muscular dystrophies and myopathies 75
Texture analysis and machine learning to predict water T2 and fat fraction from non-quantitative MRI of thigh muscles in Facioscapulohumeral muscular dystrophy 75
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1 73
Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy 72
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 72
Association study reveals novel risk loci for sporadic inclusion body myositis 71
MRI in sarcoglycanopathies: A large international cohort study 70
Redox homeostasis in muscular dystrophies 69
Concentric muscle involvement in POLG-related distal myopathy 68
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 68
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 68
Start codon mutation of GYG1 causing late-onset polyglucosan body myopathy with nemaline rods 65
Peculiar muscle imaging findings in a patient with alphaB-crystallinopathy and axial myopathy 65
Fast Open-Source Toolkit for Water T2 Mapping in the Presence of Fat From Multi-Echo Spin-Echo Acquisitions for Muscle MRI 65
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy 64
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression 63
MYO-MRI diagnostic protocols in genetic myopathies 62
MYH7-related myopathies: Clinical, histopathological and imaging findings in a cohort of Italian patients 57
Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study 55
Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy 55
Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy 55
The variability of SMCHD1 gene in FSHD patients: Evidence of new mutations 54
Genotype-phenotype correlations in recessive titinopathies 53
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1 53
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 51
An immunological analysis of dystroglycan subunits: Lessons learned from a small cohort of non-congenital dystrophic patients 48
The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosis 48
Centronuclear myopathies: genotype–phenotype correlation and frequency of defined genetic forms in an Italian cohort 47
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations 46
D4Z4 Methylation Levels Combined with a Machine Learning Pipeline Highlight Single CpG Sites as Discriminating Biomarkers for FSHD Patients 43
Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane trafficking 40
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations 40
Totale 9.918
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Categoria #
all - tutte 43.326
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 43.326
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021339 0 0 0 0 0 27 60 9 86 32 106 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
2025/20262.300 661 139 255 491 715 39 0 0 0 0 0 0
Totale 9.918