IRIS UniCatt

Tasca, Giorgio
 Distribuzione geografica
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Continente #
EU - Europa 3.480
NA - Nord America 3.447
AS - Asia 2.553
SA - Sud America 574
AF - Africa 79
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 2
Totale 10.147
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Nazione #
US - Stati Uniti d'America 3.358
SG - Singapore 1.231
DE - Germania 1.096
CN - Cina 685
IT - Italia 552
SE - Svezia 492
BR - Brasile 481
PL - Polonia 311
UA - Ucraina 193
FI - Finlandia 164
IE - Irlanda 146
VN - Vietnam 142
GB - Regno Unito 138
FR - Francia 128
ID - Indonesia 104
IN - India 93
RU - Federazione Russa 72
ES - Italia 44
HK - Hong Kong 44
AR - Argentina 41
BD - Bangladesh 37
CA - Canada 36
NL - Olanda 35
TR - Turchia 32
ZA - Sudafrica 29
IQ - Iraq 27
BE - Belgio 26
JP - Giappone 26
AT - Austria 24
MX - Messico 21
IR - Iran 17
KR - Corea 16
VE - Venezuela 16
PK - Pakistan 14
CL - Cile 13
CI - Costa d'Avorio 12
CZ - Repubblica Ceca 11
RO - Romania 11
AE - Emirati Arabi Uniti 10
CH - Svizzera 10
EC - Ecuador 10
SA - Arabia Saudita 10
UZ - Uzbekistan 10
AU - Australia 8
DZ - Algeria 7
LT - Lituania 7
IL - Israele 6
PH - Filippine 6
HN - Honduras 5
JO - Giordania 5
KE - Kenya 5
KZ - Kazakistan 5
PA - Panama 5
TN - Tunisia 5
AZ - Azerbaigian 4
MA - Marocco 4
PY - Paraguay 4
TT - Trinidad e Tobago 4
AO - Angola 3
BG - Bulgaria 3
BN - Brunei Darussalam 3
BY - Bielorussia 3
BZ - Belize 3
CR - Costa Rica 3
GA - Gabon 3
JM - Giamaica 3
LB - Libano 3
MN - Mongolia 3
MY - Malesia 3
NZ - Nuova Zelanda 3
PE - Perù 3
PR - Porto Rico 3
PT - Portogallo 3
SK - Slovacchia (Repubblica Slovacca) 3
TH - Thailandia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AM - Armenia 2
BW - Botswana 2
CO - Colombia 2
DO - Repubblica Dominicana 2
LV - Lettonia 2
OM - Oman 2
SN - Senegal 2
SY - Repubblica araba siriana 2
UY - Uruguay 2
AL - Albania 1
BB - Barbados 1
BO - Bolivia 1
DK - Danimarca 1
EG - Egitto 1
GE - Georgia 1
GP - Guadalupe 1
GR - Grecia 1
GY - Guiana 1
HR - Croazia 1
IS - Islanda 1
KG - Kirghizistan 1
KW - Kuwait 1
LK - Sri Lanka 1
LY - Libia 1
Totale 10.134
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Città #
Singapore 552
Chandler 532
Ashburn 383
Warsaw 296
Frankfurt am Main 244
Munich 226
Beijing 145
Dublin 142
San Mateo 136
Jacksonville 115
New York 98
Rome 98
Ann Arbor 95
Helsinki 94
Jakarta 94
Wilmington 91
Nanjing 78
Woodbridge 78
Los Angeles 74
Fairfield 73
Milan 72
Boston 70
Hefei 60
Houston 60
Cattolica 57
Moscow 53
Seattle 50
Princeton 43
São Paulo 42
Chicago 41
Ho Chi Minh City 41
Dallas 40
Nürnberg 40
Lawrence 38
Hanoi 34
Hong Kong 34
Dearborn 33
Redwood City 33
Nanchang 32
Boardman 25
Cambridge 25
Santa Clara 24
Johannesburg 22
Madrid 22
Nuremberg 22
Buffalo 21
Bremen 20
Izmir 20
Brooklyn 19
Stockholm 19
Tokyo 19
Brussels 18
Changsha 17
Hangzhou 17
Jiaxing 16
London 16
Seoul 16
Shenyang 16
Washington 16
Curitiba 15
Mumbai 15
Shanghai 15
The Dalles 15
San Jose 14
Baghdad 13
Inverigo 13
Kent 13
Leawood 13
Marseille 13
Mountain View 13
Phoenix 13
Rio de Janeiro 13
Vienna 13
Abidjan 12
Augusta 12
Detroit 12
Hebei 12
Kunming 12
Palermo 12
Belo Horizonte 11
Chennai 11
Montreal 11
North Bergen 11
Orem 11
Poplar 11
San Francisco 11
Toronto 11
Amsterdam 10
Atlanta 10
Denver 10
Düsseldorf 10
Lappeenranta 10
Campinas 9
Da Nang 9
Guarulhos 9
Jyväskylä 9
Las Vegas 9
Manchester 9
Norwalk 9
Tashkent 9
Totale 5.380
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Nome #
Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions 412
Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients 383
Upper body involvement in GNE myopathy assessed by muscle imaging 240
Novel missense variants associated with GNE myopathy 228
Hospital admissions from the emergency department of adult patients affected by myopathies 220
CD8(+) T Cells in Facioscapulohumeral Muscular Dystrophy Patients with Inflammatory Features at Muscle MRI 206
Tracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imaging 186
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients. 174
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 170
Muscle imaging findings in GNE myopathy 168
Non-myogenic mesenchymal cells contribute to muscle degeneration in facioscapulohumeral muscular dystrophy patients 167
Matrin 3 variants are frequent in Italian ALS patients 159
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 157
Muscle MRI in Becker muscular dystrophy 147
New ALS-related genes expand the spectrum paradigm of amyotrophic lateral sclerosis 147
An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene 146
Myotonic dystrophy type 1 and de novo FSHD mutation double trouble: A clinical and muscle MRI study 141
Muscle MRI in female carriers of dystrophinopathy 140
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 133
Different molecular signatures in magnetic resonance imaging-staged facioscapulohumeral muscular dystrophy muscles 133
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy 129
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 123
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
Diagnostic magnetic resonance imaging biomarkers for facioscapulohumeral muscular dystrophy identified by machine learning 121
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation 119
SOD1 p.D12Y variant is associated with ALS/distal myopathy spectrum 119
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 119
Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity 115
Limb-girdle muscular dystrophy with α-dystroglycan deficiency and mutations in the ISPD gene 111
Muscle fibrosis as a prognostic biomarker in facioscapulohumeral muscular dystrophy: a retrospective cohort study 110
Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2 109
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 109
Dynamic magnetic resonance imaging of muscle contraction in facioscapulohumeral muscular dystrophy 109
ANCA-related vasculitic neuropathy mimicking motor neuron disease. 107
MRI patterns of muscle involvement in type 2 and 3 spinal muscular atrophy patients 104
Calf muscle involvement in Becker muscular dystrophy: When size does not matter 102
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging 102
Teaching video neuroimages: complicated scapular winging 100
A man with sarcoidosis and slurred speech 98
Thr124Met myelin protein zero mutation mimicking motor neuron disease 98
Upper girdle imaging in facioscapulohumeral muscular dystrophy 95
An unusual ryanodine receptor 1 (RYR1) phenotype: Mild, calf-predominant myopathy. 94
Proteomics of muscle microdialysates identifies potential circulating biomarkers in facioscapulohumeral muscular dystrophy 94
Deep learning for automatic segmentation of thigh and leg muscles 94
Artificial Intelligence for Evaluation of Retinal Vasculopathy in Facioscapulohumeral Dystrophy Using OCT Angiography: A Case Series 94
MRI in sarcoglycanopathies: a large international cohort study 93
Muscle hypertrophy in amyloid myopathy 93
'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1D 92
Mixed connective tissue disease presenting as a peculiar myositis with poor muscle regeneration 92
Magnetic resonance imaging pattern recognition in sporadic Inclusion-Body Myositis 91
Anti-cN1A Antibodies Are Associated with More Severe Dysphagia in Sporadic Inclusion Body Myositis 90
Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene 87
High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients 87
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients 84
Muscle-MRI and Functional Levels for the Evaluation of Upper Limbs in Duchenne Muscular Dystrophy: A Critical Review of the Literature 82
Technology outcome measures in neuromuscular disorders: A systematic review 81
Rinsing after spinning: plasmapheresis in EBV-related post-infectious cerebellitis 80
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies 79
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials 79
Somatic mosaicism in TPM2-related myopathy with nemaline rods and cap structures. 79
European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) 78
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression. 77
Multi-organ investigation in 16 CADASIL families from central Italy sharing the same R1006C mutation 76
Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy 76
The genetic basis of undiagnosed muscular dystrophies and myopathies 76
Texture analysis and machine learning to predict water T2 and fat fraction from non-quantitative MRI of thigh muscles in Facioscapulohumeral muscular dystrophy 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
Association study reveals novel risk loci for sporadic inclusion body myositis 74
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1 73
Concentric muscle involvement in POLG-related distal myopathy 72
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 72
MRI in sarcoglycanopathies: A large international cohort study 71
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 69
Redox homeostasis in muscular dystrophies 69
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
Fast Open-Source Toolkit for Water T2 Mapping in the Presence of Fat From Multi-Echo Spin-Echo Acquisitions for Muscle MRI 67
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy 66
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
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression 64
MYO-MRI diagnostic protocols in genetic myopathies 62
Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study 58
MYH7-related myopathies: Clinical, histopathological and imaging findings in a cohort of Italian patients 58
Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy 55
Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy 55
Genotype-phenotype correlations in recessive titinopathies 54
The variability of SMCHD1 gene in FSHD patients: Evidence of new mutations 54
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 52
An immunological analysis of dystroglycan subunits: Lessons learned from a small cohort of non-congenital dystrophic patients 50
Centronuclear myopathies: genotype–phenotype correlation and frequency of defined genetic forms in an Italian cohort 48
The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosis 48
D4Z4 Methylation Levels Combined with a Machine Learning Pipeline Highlight Single CpG Sites as Discriminating Biomarkers for FSHD Patients 47
Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane trafficking 47
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations 47
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations 40
Totale 10.298
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Categoria #
all - tutte 44.124
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 44.124
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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
2025/20262.680 661 139 255 491 715 419 0 0 0 0 0 0
Totale 10.298