IRIS PubliCatt

Tasca, Giorgio
 Distribuzione geografica
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Continente #
NA - Nord America 2.543
EU - Europa 2.392
AS - Asia 553
AF - Africa 13
SA - Sud America 8
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 2
Totale 5.518
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Nazione #
US - Stati Uniti d'America 2.521
DE - Germania 604
SE - Svezia 455
IT - Italia 371
CN - Cina 335
PL - Polonia 290
UA - Ucraina 184
IE - Irlanda 142
SG - Singapore 103
FR - Francia 88
GB - Regno Unito 81
FI - Finlandia 53
IN - India 34
RU - Federazione Russa 32
BE - Belgio 24
TR - Turchia 24
ES - Italia 22
IR - Iran 16
CA - Canada 14
CI - Costa d'Avorio 12
NL - Olanda 12
HK - Hong Kong 11
CZ - Repubblica Ceca 9
JP - Giappone 9
CH - Svizzera 8
RO - Romania 6
AT - Austria 5
AU - Australia 5
CL - Cile 4
ID - Indonesia 4
VN - Vietnam 4
BZ - Belize 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
GR - Grecia 1
IL - Israele 1
IS - Islanda 1
KE - Kenya 1
MY - Malesia 1
PE - Perù 1
PT - Portogallo 1
Totale 5.518
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Città #
Chandler 532
Warsaw 280
Ashburn 237
Dublin 138
San Mateo 136
Jacksonville 113
Ann Arbor 95
Wilmington 91
Woodbridge 78
Nanjing 77
Fairfield 73
New York 68
Boston 65
Singapore 55
Cattolica 53
Rome 53
Houston 51
Milan 47
Seattle 45
Princeton 43
Nürnberg 40
Lawrence 38
Dearborn 33
Redwood City 33
Nanchang 32
Moscow 27
Beijing 25
Cambridge 25
Chicago 21
Boardman 20
Bremen 20
Izmir 20
Munich 17
Brussels 16
Hangzhou 16
Jiaxing 16
Shenyang 16
Changsha 15
Madrid 15
Washington 15
Inverigo 13
Leawood 13
Marseille 13
Mountain View 13
Abidjan 12
Hebei 12
Kunming 12
San Jose 11
Shanghai 11
Augusta 10
Detroit 9
London 9
Norwalk 9
University Park 9
Lancaster 8
Los Angeles 8
Andover 7
Bologna 7
Helsinki 7
Las Vegas 7
Ningbo 7
Tianjin 7
Berlin 6
Brno 6
Falls Church 6
Hong Kong 6
Kish 6
Kraków 6
Redmond 6
Toronto 6
Zhengzhou 6
Ardabil 5
Guangzhou 5
Lanzhou 5
Mumbai 5
Pune 5
Arezzo 4
Auburn Hills 4
Essen 4
Hadamar 4
Jinan 4
Oristano 4
Philadelphia 4
Renton 4
Simi Valley 4
Tower Hamlets 4
Waanrode 4
Amsterdam 3
Belize City 3
Busto Arsizio 3
Caguas 3
Cava de' Tirreni 3
Changchun 3
Chengdu 3
Decollatura 3
Dong Ket 3
Indiana 3
Ottawa 3
Pamplona 3
Phoenix 3
Totale 3.166
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Nome #
Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions 359
Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients 313
CD8(+) T Cells in Facioscapulohumeral Muscular Dystrophy Patients with Inflammatory Features at Muscle MRI 155
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 129
Tracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imaging 125
Muscle imaging findings in GNE myopathy 122
Muscle MRI in Becker muscular dystrophy 112
Myotonic dystrophy type 1 and de novo FSHD mutation double trouble: A clinical and muscle MRI study 111
An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene 108
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients. 104
New ALS-related genes expand the spectrum paradigm of amyotrophic lateral sclerosis 103
Muscle MRI in female carriers of dystrophinopathy 98
Matrin 3 variants are frequent in Italian ALS patients 98
Different molecular signatures in magnetic resonance imaging-staged facioscapulohumeral muscular dystrophy muscles 91
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 88
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy 86
Limb-girdle muscular dystrophy with α-dystroglycan deficiency and mutations in the ISPD gene 84
Magnetic Resonance Imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: pattern refinement and implications for clinical trials 82
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 81
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 81
Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity 80
SOD1 p.D12Y variant is associated with ALS/distal myopathy spectrum 79
New phenotype and pathology features in MYH7-related distal myopathy 78
Calf muscle involvement in Becker muscular dystrophy: When size does not matter 76
Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2 74
ANCA-related vasculitic neuropathy mimicking motor neuron disease. 73
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation 70
Teaching video neuroimages: complicated scapular winging 68
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging 65
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 64
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 64
A man with sarcoidosis and slurred speech 62
Proteomics of muscle microdialysates identifies potential circulating biomarkers in facioscapulohumeral muscular dystrophy 61
MRI patterns of muscle involvement in type 2 and 3 spinal muscular atrophy patients 60
Magnetic resonance imaging pattern recognition in sporadic Inclusion-Body Myositis 59
Non-myogenic mesenchymal cells contribute to muscle degeneration in facioscapulohumeral muscular dystrophy patients 58
To the Editor: Fasciculations in Late-Onset Pompe Disease: A Sign of Motor Neuron Involvement? 58
Upper girdle imaging in facioscapulohumeral muscular dystrophy 55
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients 55
Mixed connective tissue disease presenting as a peculiar myositis with poor muscle regeneration 55
Somatic mosaicism in TPM2-related myopathy with nemaline rods and cap structures. 54
'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1D 54
Rinsing after spinning: plasmapheresis in EBV-related post-infectious cerebellitis 54
Diagnostic magnetic resonance imaging biomarkers for facioscapulohumeral muscular dystrophy identified by machine learning 52
MRI in sarcoglycanopathies: a large international cohort study 51
European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) 51
Muscle hypertrophy in amyloid myopathy 51
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression. 49
Upper body involvement in GNE myopathy assessed by muscle imaging 49
Dynamic magnetic resonance imaging of muscle contraction in facioscapulohumeral muscular dystrophy 49
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials 48
The genetic basis of undiagnosed muscular dystrophies and myopathies 48
Mosaic caveolin-3 expression in acquired rippling muscle disease without evidence of myasthenia gravis or acetylcholine receptor autoantibodies 46
Concentric muscle involvement in POLG-related distal myopathy 46
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 46
Thr124Met myelin protein zero mutation mimicking motor neuron disease 46
Multi-organ investigation in 16 CADASIL families from central Italy sharing the same R1006C mutation 45
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1 45
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 45
Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy 45
An unusual ryanodine receptor 1 (RYR1) phenotype: Mild, calf-predominant myopathy. 42
Anti-cN1A Antibodies Are Associated with More Severe Dysphagia in Sporadic Inclusion Body Myositis 42
Texture analysis and machine learning to predict water T2 and fat fraction from non-quantitative MRI of thigh muscles in Facioscapulohumeral muscular dystrophy 41
Peculiar muscle imaging findings in a patient with alphaB-crystallinopathy and axial myopathy 40
Deep learning for automatic segmentation of thigh and leg muscles 40
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy 38
Technology outcome measures in neuromuscular disorders: A systematic review 38
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression 37
Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy 36
MRI in sarcoglycanopathies: A large international cohort study 36
Start codon mutation of GYG1 causing late-onset polyglucosan body myopathy with nemaline rods 35
Redox homeostasis in muscular dystrophies 33
High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients 33
Fast Open-Source Toolkit for Water T2 Mapping in the Presence of Fat From Multi-Echo Spin-Echo Acquisitions for Muscle MRI 31
Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy 29
Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy 28
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations 27
Association study reveals novel risk loci for sporadic inclusion body myositis 26
Artificial Intelligence for Evaluation of Retinal Vasculopathy in Facioscapulohumeral Dystrophy Using OCT Angiography: A Case Series 26
Muscle fibrosis as a prognostic biomarker in facioscapulohumeral muscular dystrophy: a retrospective cohort study 25
The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosis 23
MYO-MRI diagnostic protocols in genetic myopathies 22
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1 21
The variability of SMCHD1 gene in FSHD patients: Evidence of new mutations 15
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations 15
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 11
Muscle-MRI and Functional Levels for the Evaluation of Upper Limbs in Duchenne Muscular Dystrophy: A Critical Review of the Literature 11
Hospital admissions from the emergency department of adult patients affected by myopathies 10
Centronuclear myopathies: genotype–phenotype correlation and frequency of defined genetic forms in an Italian cohort 10
Genotype-phenotype correlations in recessive titinopathies 7
MYH7-related myopathies: Clinical, histopathological and imaging findings in a cohort of Italian patients 5
An immunological analysis of dystroglycan subunits: Lessons learned from a small cohort of non-congenital dystrophic patients 5
Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene 3
Totale 5.659
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Categoria #
all - tutte 22.724
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 22.724
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201957 0 0 0 0 0 0 0 0 0 0 0 57
2019/2020646 122 31 47 68 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
2023/2024913 41 238 26 49 29 112 73 66 12 34 122 111
Totale 5.659