IRIS PubliCatt

Tasca, Giorgio
 Distribuzione geografica
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Continente #
NA - Nord America 2.589
EU - Europa 2.508
AS - Asia 837
AF - Africa 14
SA - Sud America 8
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 2
Totale 5.965
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Nazione #
US - Stati Uniti d'America 2.564
DE - Germania 607
SE - Svezia 457
IT - Italia 434
CN - Cina 358
PL - Polonia 290
SG - Singapore 267
UA - Ucraina 184
IE - Irlanda 143
ID - Indonesia 97
FR - Francia 91
GB - Regno Unito 83
RU - Federazione Russa 59
FI - Finlandia 58
IN - India 35
BE - Belgio 25
TR - Turchia 24
ES - Italia 22
CA - Canada 17
IR - Iran 16
NL - Olanda 14
CI - Costa d'Avorio 12
HK - Hong Kong 11
CZ - Repubblica Ceca 10
JP - Giappone 9
CH - Svizzera 8
RO - Romania 7
AT - Austria 6
AU - Australia 5
VN - Vietnam 5
CL - Cile 4
BZ - Belize 3
LT - Lituania 3
PR - Porto Rico 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AE - Emirati Arabi Uniti 2
AR - Argentina 2
BG - Bulgaria 2
KR - Corea 2
MN - Mongolia 2
MX - Messico 2
NZ - Nuova Zelanda 2
SA - Arabia Saudita 2
TH - Thailandia 2
BD - Bangladesh 1
BR - Brasile 1
DK - Danimarca 1
DZ - Algeria 1
GE - Georgia 1
GR - Grecia 1
IL - Israele 1
IS - Islanda 1
KE - Kenya 1
MY - Malesia 1
PE - Perù 1
PT - Portogallo 1
SK - Slovacchia (Repubblica Slovacca) 1
UZ - Uzbekistan 1
Totale 5.965
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Città #
Chandler 532
Warsaw 280
Ashburn 238
Singapore 200
Dublin 139
San Mateo 136
Jacksonville 113
Ann Arbor 95
Jakarta 94
Wilmington 91
Nanjing 78
Woodbridge 78
Rome 76
Fairfield 73
New York 68
Boston 65
Cattolica 57
Milan 55
Houston 51
Moscow 50
Seattle 45
Princeton 43
Nürnberg 40
Lawrence 38
Dearborn 33
Redwood City 33
Nanchang 32
Chicago 28
Beijing 25
Cambridge 25
Boardman 20
Bremen 20
Izmir 20
Munich 20
Brussels 17
Changsha 16
Hangzhou 16
Jiaxing 16
Shenyang 16
Madrid 15
Washington 15
Los Angeles 14
Inverigo 13
Leawood 13
Marseille 13
Mountain View 13
Abidjan 12
Hebei 12
Helsinki 12
Kunming 12
San Jose 11
Shanghai 11
Augusta 10
London 10
Detroit 9
Norwalk 9
University Park 9
Lancaster 8
Toronto 8
Andover 7
Bologna 7
Brno 7
Las Vegas 7
Ningbo 7
Tianjin 7
Antwerp 6
Berlin 6
Falls Church 6
Guangzhou 6
Hong Kong 6
Kish 6
Kraków 6
Redmond 6
Zhengzhou 6
Ardabil 5
Lanzhou 5
Mumbai 5
Pune 5
Arezzo 4
Auburn Hills 4
Chengdu 4
Essen 4
Frattamaggiore 4
Genoa 4
Hadamar 4
Jinan 4
Oristano 4
Ottawa 4
Philadelphia 4
Renton 4
Simi Valley 4
Tower Hamlets 4
Vienna 4
Waanrode 4
Amsterdam 3
Belize City 3
Busto Arsizio 3
Caguas 3
Cava de' Tirreni 3
Changchun 3
Totale 3.499
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Nome #
Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions 363
Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients 321
CD8(+) T Cells in Facioscapulohumeral Muscular Dystrophy Patients with Inflammatory Features at Muscle MRI 160
Tracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imaging 135
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 134
Muscle imaging findings in GNE myopathy 125
Muscle MRI in Becker muscular dystrophy 118
Myotonic dystrophy type 1 and de novo FSHD mutation double trouble: A clinical and muscle MRI study 115
An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene 113
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients. 108
New ALS-related genes expand the spectrum paradigm of amyotrophic lateral sclerosis 108
Muscle MRI in female carriers of dystrophinopathy 106
Matrin 3 variants are frequent in Italian ALS patients 103
Different molecular signatures in magnetic resonance imaging-staged facioscapulohumeral muscular dystrophy muscles 95
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 91
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 91
SOD1 p.D12Y variant is associated with ALS/distal myopathy spectrum 91
Magnetic Resonance Imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: pattern refinement and implications for clinical trials 90
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy 88
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 86
Limb-girdle muscular dystrophy with α-dystroglycan deficiency and mutations in the ISPD gene 85
Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity 85
New phenotype and pathology features in MYH7-related distal myopathy 82
Calf muscle involvement in Becker muscular dystrophy: When size does not matter 79
Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2 77
Non-myogenic mesenchymal cells contribute to muscle degeneration in facioscapulohumeral muscular dystrophy patients 75
ANCA-related vasculitic neuropathy mimicking motor neuron disease. 75
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation 72
Teaching video neuroimages: complicated scapular winging 71
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 71
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 70
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging 69
MRI patterns of muscle involvement in type 2 and 3 spinal muscular atrophy patients 67
A man with sarcoidosis and slurred speech 66
Proteomics of muscle microdialysates identifies potential circulating biomarkers in facioscapulohumeral muscular dystrophy 65
Magnetic resonance imaging pattern recognition in sporadic Inclusion-Body Myositis 64
MRI in sarcoglycanopathies: a large international cohort study 62
Diagnostic magnetic resonance imaging biomarkers for facioscapulohumeral muscular dystrophy identified by machine learning 62
To the Editor: Fasciculations in Late-Onset Pompe Disease: A Sign of Motor Neuron Involvement? 61
Mixed connective tissue disease presenting as a peculiar myositis with poor muscle regeneration 60
Upper girdle imaging in facioscapulohumeral muscular dystrophy 59
Rinsing after spinning: plasmapheresis in EBV-related post-infectious cerebellitis 58
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients 58
Somatic mosaicism in TPM2-related myopathy with nemaline rods and cap structures. 57
'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1D 56
Dynamic magnetic resonance imaging of muscle contraction in facioscapulohumeral muscular dystrophy 56
Muscle hypertrophy in amyloid myopathy 55
Thr124Met myelin protein zero mutation mimicking motor neuron disease 55
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression. 52
European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) 52
Upper body involvement in GNE myopathy assessed by muscle imaging 52
Technology outcome measures in neuromuscular disorders: A systematic review 52
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials 50
The genetic basis of undiagnosed muscular dystrophies and myopathies 50
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 50
Concentric muscle involvement in POLG-related distal myopathy 49
Multi-organ investigation in 16 CADASIL families from central Italy sharing the same R1006C mutation 48
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1 48
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 48
Anti-cN1A Antibodies Are Associated with More Severe Dysphagia in Sporadic Inclusion Body Myositis 48
Mosaic caveolin-3 expression in acquired rippling muscle disease without evidence of myasthenia gravis or acetylcholine receptor autoantibodies 47
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 47
An unusual ryanodine receptor 1 (RYR1) phenotype: Mild, calf-predominant myopathy. 46
Texture analysis and machine learning to predict water T2 and fat fraction from non-quantitative MRI of thigh muscles in Facioscapulohumeral muscular dystrophy 46
Deep learning for automatic segmentation of thigh and leg muscles 44
Peculiar muscle imaging findings in a patient with alphaB-crystallinopathy and axial myopathy 43
Muscle fibrosis as a prognostic biomarker in facioscapulohumeral muscular dystrophy: a retrospective cohort study 42
Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy 41
MRI in sarcoglycanopathies: A large international cohort study 41
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy 40
Start codon mutation of GYG1 causing late-onset polyglucosan body myopathy with nemaline rods 39
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression 39
Redox homeostasis in muscular dystrophies 37
High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients 37
Fast Open-Source Toolkit for Water T2 Mapping in the Presence of Fat From Multi-Echo Spin-Echo Acquisitions for Muscle MRI 36
Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy 35
Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy 31
Artificial Intelligence for Evaluation of Retinal Vasculopathy in Facioscapulohumeral Dystrophy Using OCT Angiography: A Case Series 31
Association study reveals novel risk loci for sporadic inclusion body myositis 30
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations 29
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1 26
The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosis 25
MYO-MRI diagnostic protocols in genetic myopathies 23
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations 18
Hospital admissions from the emergency department of adult patients affected by myopathies 17
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 16
The variability of SMCHD1 gene in FSHD patients: Evidence of new mutations 16
Muscle-MRI and Functional Levels for the Evaluation of Upper Limbs in Duchenne Muscular Dystrophy: A Critical Review of the Literature 15
Centronuclear myopathies: genotype–phenotype correlation and frequency of defined genetic forms in an Italian cohort 14
An immunological analysis of dystroglycan subunits: Lessons learned from a small cohort of non-congenital dystrophic patients 13
Genotype-phenotype correlations in recessive titinopathies 12
Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene 10
MYH7-related myopathies: Clinical, histopathological and imaging findings in a cohort of Italian patients 8
Totale 6.106
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Categoria #
all - tutte 27.854
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 27.854
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020378 0 0 0 0 45 48 58 28 41 40 65 53
2020/2021584 20 59 30 62 74 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
2024/2025443 52 64 151 49 127 0 0 0 0 0 0 0
Totale 6.106