IRIS UniCatt

Sabatelli, Mario
 Distribuzione geografica
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Continente #
NA - Nord America 9.244
EU - Europa 8.634
AS - Asia 6.003
SA - Sud America 1.388
AF - Africa 224
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 12
Totale 25.529
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Nazione #
US - Stati Uniti d'America 8.978
DE - Germania 3.191
SG - Singapore 2.822
CN - Cina 1.633
SE - Svezia 1.272
BR - Brasile 1.169
IT - Italia 782
UA - Ucraina 719
PL - Polonia 576
GB - Regno Unito 529
FR - Francia 408
IE - Irlanda 360
VN - Vietnam 348
FI - Finlandia 283
ID - Indonesia 240
IN - India 219
RU - Federazione Russa 188
CA - Canada 152
TR - Turchia 122
BD - Bangladesh 94
HK - Hong Kong 88
JP - Giappone 84
AR - Argentina 81
ZA - Sudafrica 81
BE - Belgio 77
NL - Olanda 64
MX - Messico 63
IQ - Iraq 59
CI - Costa d'Avorio 44
KR - Corea 41
ES - Italia 37
AT - Austria 32
PK - Pakistan 31
SA - Arabia Saudita 28
MA - Marocco 27
PY - Paraguay 26
CH - Svizzera 25
EC - Ecuador 25
IR - Iran 25
AU - Australia 22
CO - Colombia 22
CL - Cile 21
VE - Venezuela 21
AE - Emirati Arabi Uniti 20
JO - Giordania 18
PH - Filippine 17
KE - Kenya 15
UZ - Uzbekistan 15
RO - Romania 14
TN - Tunisia 14
IL - Israele 12
KZ - Kazakistan 10
AZ - Azerbaigian 9
CZ - Repubblica Ceca 9
DO - Repubblica Dominicana 9
LT - Lituania 9
TT - Trinidad e Tobago 8
GR - Grecia 7
LK - Sri Lanka 7
NP - Nepal 7
PE - Perù 7
PT - Portogallo 7
UY - Uruguay 7
CR - Costa Rica 6
DK - Danimarca 6
EG - Egitto 6
ET - Etiopia 6
EU - Europa 6
HN - Honduras 6
OM - Oman 6
BY - Bielorussia 5
DZ - Algeria 5
HR - Croazia 5
JM - Giamaica 5
KG - Kirghizistan 5
PS - Palestinian Territory 5
TW - Taiwan 5
AO - Angola 4
BB - Barbados 4
BG - Bulgaria 4
BO - Bolivia 4
CG - Congo 4
GY - Guiana 4
LB - Libano 4
NO - Norvegia 4
PA - Panama 4
SN - Senegal 4
TH - Thailandia 4
XK - ???statistics.table.value.countryCode.XK??? 4
AM - Armenia 3
GE - Georgia 3
GT - Guatemala 3
MD - Moldavia 3
MM - Myanmar 3
MY - Malesia 3
SI - Slovenia 3
SK - Slovacchia (Repubblica Slovacca) 3
SY - Repubblica araba siriana 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AL - Albania 2
Totale 25.486
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Città #
Chandler 1.310
Singapore 1.294
Ashburn 828
Warsaw 509
Dublin 351
Beijing 337
Jacksonville 337
Ann Arbor 322
San Mateo 320
New York 300
Redmond 284
Nanjing 261
Munich 224
Nürnberg 219
Wilmington 219
Jakarta 218
Los Angeles 200
Fairfield 199
Houston 184
Boston 175
Woodbridge 174
Seattle 157
Milan 141
Cattolica 136
Hefei 135
Dearborn 129
Ho Chi Minh City 120
Moscow 115
Lawrence 113
Nanchang 112
Chicago 103
São Paulo 102
Hanoi 98
Redwood City 93
Frankfurt am Main 91
Rome 90
Izmir 86
Helsinki 82
Buffalo 81
Dallas 76
Hong Kong 75
Princeton 72
Marseille 67
Detroit 64
Cambridge 59
Santa Clara 59
Bremen 58
Brussels 58
London 58
Kraków 53
Tokyo 50
Norwalk 49
Shenyang 48
Abidjan 44
Hebei 42
Boardman 40
Seoul 40
Jiaxing 39
Lappeenranta 39
Phoenix 39
University Park 39
Leawood 38
Changsha 37
Hangzhou 36
Kent 36
Mountain View 36
North Bergen 35
Rio de Janeiro 35
Guangzhou 32
Ottawa 32
Philadelphia 32
Atlanta 31
Brooklyn 31
Johannesburg 31
Kunming 31
Montreal 31
Nuremberg 31
Pune 31
Tianjin 31
Zhengzhou 31
Stockholm 30
San Francisco 28
Curitiba 27
Toronto 26
Belo Horizonte 25
Denver 25
Fremont 25
Orem 25
Baghdad 23
Manchester 23
Dhaka 22
Lancaster 22
Simi Valley 22
Brasília 21
Chennai 21
Cape Town 20
The Dalles 20
Turku 20
Düsseldorf 19
Amman 18
Totale 12.507
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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 722
Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients 383
Clinical–neurophysiological correlations in a series of patients with IgM-related neuropathy 354
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 334
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 292
Histamine beyond its effects on allergy: Potential therapeutic benefits for the treatment of Amyotrophic Lateral Sclerosis (ALS) 246
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 244
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 241
Teaching neuroimages: Peroneal intraneural ganglion cyst: a rare cause of drop foot in a child. 240
Proteostasis and ALS: Protocol for a phase II, randomised, double-blind, placebo-controlled, multicentre clinical trial for colchicine in ALS (Co-ALS) 235
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 231
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 226
Hospital admissions from the emergency department of adult patients affected by myopathies 220
Retinal detachment with an unusual shape. 202
Relations between C9orf72 expansion size in blood, age at onset, age at collection and transmission across generations in patients and presymptomatic carriers 201
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 192
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 189
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 178
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 177
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
Chronic GM2 gangliosidosis type Sandhoff associated with a novel missense HEXB gene mutaton causing a double patogenetic effect 169
Flow Cytofluorimetric Analysis of Anti-LRP4 (LDL Receptor-Related Protein 4) Autoantibodies in Italian Patients with Myasthenia Gravis 167
A Genome-wide Association Study of Myasthenia Gravis 167
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. 166
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 162
Efficacy of lenalidomide plus dexamethasone for POEMS syndrome relapsed after autologous peripheral stem-cell transplantation 161
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 161
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 159
Matrin 3 variants are frequent in Italian ALS patients 159
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS 156
Demyelinating Encephalomyeloradiculitis with Balò-like lesions 152
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience 152
Epstein-Barr virus antibodies in serum and cerebrospinal fluid from Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculoneuropathy and Amyotrophic Lateral 150
Restless leg syndrome in different types of demyelinating neuropathies: a single-center pilot study 150
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 149
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 148
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
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 146
ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis 143
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 142
Mechanically assisted cough in amyotrophic lateral sclerosis: Effect on vital capacity decline and timing of non invasive ventilation onset 142
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 139
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 139
A novel L67P SOD1 mutation in an Italian ALS patient. 138
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 138
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 137
ATXN2 polyQ intermediate repeats are a modifier of ALS survival 137
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 134
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 134
Neurologic improvement after peripheral blood stem cell transplantation in poems 134
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 133
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 133
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 133
ALS skin fibroblasts reveal oxidative stress and ERK1/2-mediated cytoplasmic localization of TDP-43 133
ORal anticoagulants In fraGile patients with percutAneous endoscopic gastrostoMy and atrIal fibrillation: the (ORIGAMI) study 133
Usefulness of F-18 FDG PET/CT in the follow-up of POEMS syndrome after autologous peripheral blood stem cell transplantation 132
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? 132
Neuromyelitis optica spectrum disorder as a paraneoplastic manifestation of lung adenocarcinoma expressing aquaporin-4. 131
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 130
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 130
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 129
Ultrasound evaluation in transthyretin-related amyloid neuropathy 129
Clinical-neurophysiological correlations in a series of patients with IgM-related neuropathy 128
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 128
Distinct lymphocytes subsets in IgM-related neuropathy: clinical-immunological correlations 128
Guillain-Barre' syndrome following Varicella zoster reactivation in Chronic Lymphocytic Leukemia treated with fludarabine 127
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 127
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 127
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 127
Repeated courses of granulocyte colony-stimulating factor in amyotrophic lateral sclerosis: clinical and biological results from a prospective multicenter study. 126
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 126
Characterization of SOD1-DT, a Divergent Long Non-Coding RNA in the Locus of the SOD1 Human Gene 125
Botulinum toxin B ultrasound-guided injections for sialorrhea in amyotrophic lateral sclerosis and Parkinson's disease. 125
Letter: faecal microbiota transplantation in combination with fidaxomicin to treat severe complicated recurrent Clostridium difficile infection 125
Long-term motor cortex stimulation for amyotrophic lateral sclerosis 124
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 123
A useful electrophysiological test for diagnosis of minimal conduction block 123
Pathological findings in chronic inflammatory demyelinating polyradiculoneuropathy: A single-center experience 123
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 121
Pure motor chronic inlammatory demyelinating polyneuropathy 119
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
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 118
Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis: a Single-Centre Experience 118
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 117
High-throughput genetic testing in ALS: The challenging path of variant classification considering the acmg guidelines 117
Exome sequencing reveals VCP mutations as a cause of familial ALS 116
Wernicke's encephalopathy following chronic diarrhoea 116
Sural nerve pathology in ALS patients: a single-centre experience 115
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 114
Novel variants and cellular studies on patients' primary fibroblasts support a role for NEK1 missense variants in ALS pathogenesis 114
HFE p.H63D polymorphism does not influence ALS phenotype and survival 113
ORal anticoagulants In fraGile patients with percutAneous endoscopic gastrostoMy and atrIal fibrillation: the (ORIGAMI) study 113
Botulinum toxin-B ultrasound-guided injections for sialorrhea in amytrophic lateral sclerosis and Parkinson's disease 112
Guillain–Barré syndrome from an emergency department view: how to better predict the outcome? 112
Evaluating the contribution of the gene TARDBP in Italian patients with amyotrophic lateral sclerosis 111
Nerve ultrasound in CMT2E/CMT1F due to NEFL mutation: Confirmation of an axonal pathology 111
Teaching NeuroImage: MRI of diabetic lumbar plexopathy treated with local steroid injection. 110
Totale 15.970
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Categoria #
all - tutte 103.548
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 103.548
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021910 0 0 0 0 0 89 190 38 192 110 262 29
2021/20221.846 185 147 27 207 62 57 49 263 99 90 298 362
2022/20234.306 453 545 323 516 284 453 156 273 422 732 87 62
2023/20241.813 82 569 48 111 65 308 95 63 11 89 165 207
2024/20253.646 100 111 284 186 289 155 156 176 580 273 726 610
2025/20265.648 1.488 275 576 1.171 1.749 389 0 0 0 0 0 0
Totale 25.818