IRIS PubliCatt

Sabatelli, Mario
 Distribuzione geografica
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Continente #
EU - Europa 7.491
NA - Nord America 7.201
AS - Asia 1.538
AF - Africa 78
OC - Oceania 19
SA - Sud America 18
Continente sconosciuto - Info sul continente non disponibili 8
Totale 16.353
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Nazione #
US - Stati Uniti d'America 7.122
DE - Germania 2.877
SE - Svezia 1.240
CN - Cina 948
UA - Ucraina 698
IT - Italia 598
PL - Polonia 525
GB - Regno Unito 398
IE - Irlanda 352
FR - Francia 296
SG - Singapore 212
FI - Finlandia 177
RU - Federazione Russa 152
IN - India 125
TR - Turchia 96
CA - Canada 72
BE - Belgio 69
CI - Costa d'Avorio 44
JP - Giappone 35
NL - Olanda 35
ZA - Sudafrica 31
HK - Hong Kong 27
CH - Svizzera 23
KR - Corea 23
IR - Iran 19
VN - Vietnam 19
AU - Australia 18
PH - Filippine 11
RO - Romania 11
BR - Brasile 7
ES - Italia 7
CL - Cile 6
CZ - Repubblica Ceca 6
EU - Europa 6
GR - Grecia 6
AE - Emirati Arabi Uniti 4
NO - Norvegia 4
SA - Arabia Saudita 4
HR - Croazia 3
ID - Indonesia 3
MX - Messico 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AR - Argentina 2
BZ - Belize 2
DK - Danimarca 2
KZ - Kazakistan 2
LU - Lussemburgo 2
LV - Lettonia 2
PE - Perù 2
TH - Thailandia 2
AL - Albania 1
AT - Austria 1
BD - Bangladesh 1
BY - Bielorussia 1
DZ - Algeria 1
EC - Ecuador 1
IL - Israele 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LI - Liechtenstein 1
LK - Sri Lanka 1
MD - Moldavia 1
MT - Malta 1
NG - Nigeria 1
NZ - Nuova Zelanda 1
OM - Oman 1
PA - Panama 1
PK - Pakistan 1
PR - Porto Rico 1
PT - Portogallo 1
SI - Slovenia 1
TN - Tunisia 1
TW - Taiwan 1
Totale 16.353
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Città #
Chandler 1.310
Ashburn 481
Warsaw 468
Dublin 344
Jacksonville 332
Ann Arbor 322
San Mateo 317
Redmond 284
Nanjing 261
New York 225
Nürnberg 219
Wilmington 218
Fairfield 199
Woodbridge 174
Houston 164
Boston 160
Seattle 139
Singapore 138
Cattolica 136
Dearborn 129
Lawrence 113
Moscow 113
Nanchang 112
Milan 96
Redwood City 93
Izmir 86
Beijing 82
Chicago 77
Princeton 71
Marseille 67
Detroit 61
Cambridge 59
Bremen 56
Munich 55
Kraków 53
Brussels 50
Rome 50
Norwalk 49
Shenyang 48
Abidjan 44
Hebei 42
Los Angeles 41
Jiaxing 39
University Park 39
Leawood 38
Boardman 37
Mountain View 36
Changsha 35
Hangzhou 33
Guangzhou 30
Kunming 30
London 30
Ottawa 29
Tianjin 28
Philadelphia 27
Zhengzhou 26
Fremont 25
Pune 25
Lappeenranta 24
Seoul 23
Lancaster 22
Simi Valley 22
Phoenix 21
Helsinki 18
Hong Kong 16
Waanrode 16
Auburn Hills 14
Hefei 14
Las Vegas 14
Birmingham 13
Cape Town 13
Edinburgh 13
Hanoi 13
Shanghai 12
San Diego 11
San Jose 11
Buffalo 10
Changchun 10
Greensboro 10
Jinan 10
Millbury 10
Nashville 10
Ningbo 10
Padova 10
Toronto 10
Falls Church 9
Leeds 9
Washington 9
Augusta 8
Busto Arsizio 8
Chengdu 8
Manchester 8
Monza 8
The Bronx 8
Berlin 7
Columbus 7
Indiana 7
Lanzhou 7
Liverpool 7
Miami 7
Totale 8.542
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Nome #
Real-life experience with inotersen in hereditary transthyretin amyloidosis with late-onset phenotype: Data from an early-access program in Italy 673
Clinical–neurophysiological correlations in a series of patients with IgM-related neuropathy 318
Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients 314
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 299
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 259
Histamine beyond its effects on allergy: Potential therapeutic benefits for the treatment of Amyotrophic Lateral Sclerosis (ALS) 212
Teaching neuroimages: Peroneal intraneural ganglion cyst: a rare cause of drop foot in a child. 201
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 193
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 193
Proteostasis and ALS: Protocol for a phase II, randomised, double-blind, placebo-controlled, multicentre clinical trial for colchicine in ALS (Co-ALS) 193
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 187
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 177
Relations between C9orf72 expansion size in blood, age at onset, age at collection and transmission across generations in patients and presymptomatic carriers 168
Retinal detachment with an unusual shape. 165
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 163
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 160
Chronic GM2 gangliosidosis type Sandhoff associated with a novel missense HEXB gene mutaton causing a double patogenetic effect 131
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 130
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 129
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 127
Efficacy of lenalidomide plus dexamethasone for POEMS syndrome relapsed after autologous peripheral stem-cell transplantation 125
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 124
Epstein-Barr virus antibodies in serum and cerebrospinal fluid from Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculoneuropathy and Amyotrophic Lateral 116
Botulinum toxin A versus B in sialorrhea: A prospective, randomized, double-blind, crossover pilot study in patients with amyotrophic lateral sclerosis or Parkinson's disease. 114
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 112
Demyelinating Encephalomyeloradiculitis with Balò-like lesions 111
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience 111
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 110
An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene 109
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 107
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 107
Mechanically assisted cough in amyotrophic lateral sclerosis: Effect on vital capacity decline and timing of non invasive ventilation onset 107
Restless leg syndrome in different types of demyelinating neuropathies: a single-center pilot study 106
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 105
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients. 104
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 103
New ALS-related genes expand the spectrum paradigm of amyotrophic lateral sclerosis 103
Ultrasound evaluation in transthyretin-related amyloid neuropathy 102
Guillain-Barre' syndrome following Varicella zoster reactivation in Chronic Lymphocytic Leukemia treated with fludarabine 101
A useful electrophysiological test for diagnosis of minimal conduction block 101
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 101
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 100
A novel L67P SOD1 mutation in an Italian ALS patient. 100
Letter: faecal microbiota transplantation in combination with fidaxomicin to treat severe complicated recurrent Clostridium difficile infection 99
Matrin 3 variants are frequent in Italian ALS patients 99
ATXN2 polyQ intermediate repeats are a modifier of ALS survival 97
Flow Cytofluorimetric Analysis of Anti-LRP4 (LDL Receptor-Related Protein 4) Autoantibodies in Italian Patients with Myasthenia Gravis 97
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 96
Is it the use of Non Invasive Ventilation for less than four hours in the day sufficient to prolong survival in patients with Amyotrophic Lateral Sclerosis? 96
A Genome-wide Association Study of Myasthenia Gravis 95
Clinical-neurophysiological correlations in a series of patients with IgM-related neuropathy 94
Neurologic improvement after peripheral blood stem cell transplantation in poems 93
Usefulness of F-18 FDG PET/CT in the follow-up of POEMS syndrome after autologous peripheral blood stem cell transplantation 91
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 91
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 91
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 91
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 90
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 89
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 89
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 88
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 88
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 88
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 87
Long-term motor cortex stimulation for amyotrophic lateral sclerosis 87
Wernicke's encephalopathy following chronic diarrhoea 87
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 86
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 86
ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis 86
Teaching NeuroImage: MRI of diabetic lumbar plexopathy treated with local steroid injection. 85
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 85
Nerve ultrasound in CMT2E/CMT1F due to NEFL mutation: Confirmation of an axonal pathology 84
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 83
Repeated courses of granulocyte colony-stimulating factor in amyotrophic lateral sclerosis: clinical and biological results from a prospective multicenter study. 83
Pure motor chronic inlammatory demyelinating polyneuropathy 82
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 82
Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients 82
HFE p.H63D polymorphism does not influence ALS phenotype and survival 82
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 82
SOD1 p.D12Y variant is associated with ALS/distal myopathy spectrum 80
Sural nerve pathology in ALS patients: a single-centre experience 78
Neuromyelitis optica spectrum disorder as a paraneoplastic manifestation of lung adenocarcinoma expressing aquaporin-4. 78
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 78
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS 78
ORal anticoagulants In fraGile patients with percutAneous endoscopic gastrostoMy and atrIal fibrillation: the (ORIGAMI) study 78
Botulinum toxin B ultrasound-guided injections for sialorrhea in amyotrophic lateral sclerosis and Parkinson's disease. 77
ALS skin fibroblasts reveal oxidative stress and ERK1/2-mediated cytoplasmic localization of TDP-43 77
Monophasic demyelinating disease of the central nervous system associated with Hepatitis A infection 76
Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs. 75
Distinct lymphocytes subsets in IgM-related neuropathy: clinical-immunological correlations 75
Aims: The ORal anticoagulants In fraGile patients with percutAneous endoscopic gastrostoMy and atrIal fibrillation (ORIGAMI) study investigates the safety and efficacy of Edoxaban administered via PEG in patients with atrial fibrillation and a clinical indication for a long-term anticoagulation. Design: In this prospective, single-centre observational study, 12 PEG-treated patients with indication to anticoagulation will receive edoxaban via PEG and will be followed up to 6 months. Plasma antifactor Xa activity and edoxaban concentrations will be assessed. Thromboembolic (ischaemic stroke, systemic embolism, venous thromboembolism) and bleeding events (Bleeding Academic Research Consortium and Thrombolysis in Myocardial Infarction) will be recorded at 1 and 6 months. Preliminary results: A retrospective analysis of five atrial fibrillation cases undergoing PEG implantation at our Institution who received edoxaban via PEG showed plasma anti-FXa levels at a steady state of 146 ± 15 ng/ml, without major adverse event at a mean follow-up of 6 months. Conclusion: ORIGAMI prospectively investigates PEG-administration of edoxaban in PEG-treated patients requiring long-term anticoagulation. Our preliminary retrospective data support this route of DOAC administration. 75
ANCA-related vasculitic neuropathy mimicking motor neuron disease. 74
Botulinum toxin-B ultrasound-guided injections for sialorrhea in amytrophic lateral sclerosis and Parkinson's disease 74
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 74
Nerve ultrasound in patients with CMT1C: Description of three cases 74
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72 73
Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity 72
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 72
Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis: a Single-Centre Experience 71
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation 70
Ultrasound evaluation in transthyretin-related amyloid neuropathy 70
Totale 11.631
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Categoria #
all - tutte 60.325
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 60.325
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.043 0 136 157 225 193 234 260 93 139 171 246 189
2020/20211.624 79 169 65 178 226 89 189 38 191 110 261 29
2021/20221.841 185 146 27 207 62 57 49 260 99 90 298 361
2022/20234.304 452 545 323 515 284 453 156 273 422 732 87 62
2023/20241.807 81 567 48 111 65 308 94 63 11 89 164 206
2024/2025125 100 25 0 0 0 0 0 0 0 0 0 0
Totale 16.626