IRIS UniCatt

Sabatelli, Mario
 Distribuzione geografica
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Continente #
NA - Nord America 10.943
EU - Europa 9.066
AS - Asia 7.500
SA - Sud America 1.457
AF - Africa 249
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 12
Totale 29.251
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Nazione #
US - Stati Uniti d'America 10.646
SG - Singapore 3.425
DE - Germania 3.234
CN - Cina 1.795
SE - Svezia 1.272
BR - Brasile 1.203
IT - Italia 863
VN - Vietnam 784
UA - Ucraina 723
FR - Francia 639
PL - Polonia 577
GB - Regno Unito 548
IE - Irlanda 364
FI - Finlandia 303
IN - India 247
ID - Indonesia 240
RU - Federazione Russa 192
JP - Giappone 183
CA - Canada 168
HK - Hong Kong 152
TR - Turchia 136
BD - Bangladesh 110
AR - Argentina 89
ZA - Sudafrica 86
BE - Belgio 84
IQ - Iraq 74
NL - Olanda 72
MX - Messico 70
PK - Pakistan 48
CI - Costa d'Avorio 44
KR - Corea 43
ES - Italia 40
SA - Arabia Saudita 35
AT - Austria 33
CO - Colombia 33
EC - Ecuador 31
PY - Paraguay 30
MA - Marocco 29
CH - Svizzera 25
IR - Iran 25
CL - Cile 23
VE - Venezuela 23
AU - Australia 22
PH - Filippine 22
AE - Emirati Arabi Uniti 21
JO - Giordania 21
UZ - Uzbekistan 19
TN - Tunisia 18
KE - Kenya 17
RO - Romania 15
IL - Israele 14
AZ - Azerbaigian 11
CZ - Repubblica Ceca 10
DO - Repubblica Dominicana 10
KZ - Kazakistan 10
TH - Thailandia 10
EG - Egitto 9
ET - Etiopia 9
LT - Lituania 9
PE - Perù 9
PT - Portogallo 9
CR - Costa Rica 8
GR - Grecia 8
NP - Nepal 8
TT - Trinidad e Tobago 8
HN - Honduras 7
JM - Giamaica 7
KG - Kirghizistan 7
LK - Sri Lanka 7
OM - Oman 7
UY - Uruguay 7
DK - Danimarca 6
EU - Europa 6
SN - Senegal 6
TW - Taiwan 6
BY - Bielorussia 5
DZ - Algeria 5
HR - Croazia 5
LB - Libano 5
MY - Malesia 5
PS - Palestinian Territory 5
AO - Angola 4
BB - Barbados 4
BG - Bulgaria 4
BO - Bolivia 4
CG - Congo 4
GY - Guiana 4
NO - Norvegia 4
PA - Panama 4
XK - ???statistics.table.value.countryCode.XK??? 4
AL - Albania 3
AM - Armenia 3
BH - Bahrain 3
GE - Georgia 3
GT - Guatemala 3
MD - Moldavia 3
MM - Myanmar 3
MN - Mongolia 3
NG - Nigeria 3
NI - Nicaragua 3
Totale 29.200
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Città #
Singapore 1.838
Chandler 1.310
Ashburn 1.133
San Jose 944
Warsaw 510
Dublin 354
Beijing 345
Jacksonville 337
Ann Arbor 322
San Mateo 320
New York 311
Redmond 284
Ho Chi Minh City 272
Nanjing 262
Munich 224
Nürnberg 219
Wilmington 219
Jakarta 218
Los Angeles 213
Lauterbourg 201
Fairfield 199
Hanoi 197
Houston 185
Boston 175
Woodbridge 174
Seattle 157
Milan 148
Tokyo 147
Cattolica 136
Hefei 135
Dearborn 129
Hong Kong 126
Frankfurt am Main 120
Moscow 115
Chicago 113
Lawrence 113
Nanchang 112
Rome 110
São Paulo 104
Helsinki 102
Redwood City 93
Izmir 86
Buffalo 83
Santa Clara 83
Dallas 76
Princeton 72
Marseille 69
Detroit 64
London 60
Bremen 59
Cambridge 59
Brussels 58
Kraków 53
Norwalk 49
Shenyang 49
Council Bluffs 45
Abidjan 44
Hangzhou 44
Paris 44
Orem 43
Hebei 42
Phoenix 42
Boardman 40
Seoul 40
Jiaxing 39
Lappeenranta 39
University Park 39
Guangzhou 38
Leawood 38
Atlanta 37
Changsha 37
Kent 36
Mountain View 36
North Bergen 36
Johannesburg 35
Rio de Janeiro 35
The Dalles 35
Nuremberg 34
Tianjin 34
Montreal 33
Philadelphia 33
Ottawa 32
Pune 32
Kunming 31
Zhengzhou 31
Baghdad 30
Brooklyn 30
Stockholm 30
Da Nang 29
Shanghai 29
Denver 28
San Francisco 28
Chennai 27
Curitiba 27
Toronto 27
Belo Horizonte 26
Fremont 25
Manchester 24
Dhaka 23
Haiphong 22
Totale 15.175
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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 739
Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients 419
Clinical–neurophysiological correlations in a series of patients with IgM-related neuropathy 376
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 360
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 315
Histamine beyond its effects on allergy: Potential therapeutic benefits for the treatment of Amyotrophic Lateral Sclerosis (ALS) 269
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 267
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 260
Hospital admissions from the emergency department of adult patients affected by myopathies 257
Teaching neuroimages: Peroneal intraneural ganglion cyst: a rare cause of drop foot in a child. 250
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 248
Proteostasis and ALS: Protocol for a phase II, randomised, double-blind, placebo-controlled, multicentre clinical trial for colchicine in ALS (Co-ALS) 247
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 244
Relations between C9orf72 expansion size in blood, age at onset, age at collection and transmission across generations in patients and presymptomatic carriers 222
Retinal detachment with an unusual shape. 219
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 213
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 205
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 195
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. 195
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS 191
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients. 190
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 188
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 187
Chronic GM2 gangliosidosis type Sandhoff associated with a novel missense HEXB gene mutaton causing a double patogenetic effect 186
Flow Cytofluorimetric Analysis of Anti-LRP4 (LDL Receptor-Related Protein 4) Autoantibodies in Italian Patients with Myasthenia Gravis 186
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 183
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 183
Matrin 3 variants are frequent in Italian ALS patients 182
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 180
A Genome-wide Association Study of Myasthenia Gravis 176
Efficacy of lenalidomide plus dexamethasone for POEMS syndrome relapsed after autologous peripheral stem-cell transplantation 172
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 170
Restless leg syndrome in different types of demyelinating neuropathies: a single-center pilot study 169
Epstein-Barr virus antibodies in serum and cerebrospinal fluid from Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculoneuropathy and Amyotrophic Lateral 167
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 166
New ALS-related genes expand the spectrum paradigm of amyotrophic lateral sclerosis 165
Demyelinating Encephalomyeloradiculitis with Balò-like lesions 163
An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene 163
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 161
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 161
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 160
Mechanically assisted cough in amyotrophic lateral sclerosis: Effect on vital capacity decline and timing of non invasive ventilation onset 160
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience 160
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 159
ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis 159
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 158
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 157
Neurologic improvement after peripheral blood stem cell transplantation in poems 156
A novel L67P SOD1 mutation in an Italian ALS patient. 155
Characterization of SOD1-DT, a Divergent Long Non-Coding RNA in the Locus of the SOD1 Human Gene 154
Evaluating the contribution of the gene TARDBP in Italian patients with amyotrophic lateral sclerosis 153
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 153
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 153
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 152
ORal anticoagulants In fraGile patients with percutAneous endoscopic gastrostoMy and atrIal fibrillation: the (ORIGAMI) study 152
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 151
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 150
Distinct lymphocytes subsets in IgM-related neuropathy: clinical-immunological correlations 150
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 150
Repeated courses of granulocyte colony-stimulating factor in amyotrophic lateral sclerosis: clinical and biological results from a prospective multicenter study. 149
Usefulness of F-18 FDG PET/CT in the follow-up of POEMS syndrome after autologous peripheral blood stem cell transplantation 149
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 149
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 148
ATXN2 polyQ intermediate repeats are a modifier of ALS survival 148
Pathological findings in chronic inflammatory demyelinating polyradiculoneuropathy: A single-center experience 147
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 146
ALS skin fibroblasts reveal oxidative stress and ERK1/2-mediated cytoplasmic localization of TDP-43 146
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 145
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? 145
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 145
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 144
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 143
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 143
Clinical-neurophysiological correlations in a series of patients with IgM-related neuropathy 143
Recurrent miller fisher: a new case report and a literature review 143
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 142
Guillain-Barre' syndrome following Varicella zoster reactivation in Chronic Lymphocytic Leukemia treated with fludarabine 141
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation 141
A useful electrophysiological test for diagnosis of minimal conduction block 141
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 141
Neuromyelitis optica spectrum disorder as a paraneoplastic manifestation of lung adenocarcinoma expressing aquaporin-4. 141
Pure motor chronic inlammatory demyelinating polyneuropathy 139
Botulinum toxin B ultrasound-guided injections for sialorrhea in amyotrophic lateral sclerosis and Parkinson's disease. 139
Long-term motor cortex stimulation for amyotrophic lateral sclerosis 139
Ocular involvement in hereditary transthyretin amyloidosis: A case series describing novel potential biomarkers 139
Novel variants and cellular studies on patients' primary fibroblasts support a role for NEK1 missense variants in ALS pathogenesis 138
Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis: a Single-Centre Experience 137
Exome sequencing reveals VCP mutations as a cause of familial ALS 136
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 136
Ultrasound evaluation in transthyretin-related amyloid neuropathy 136
SOD1 p.D12Y variant is associated with ALS/distal myopathy spectrum 136
Guillain–Barré syndrome from an emergency department view: how to better predict the outcome? 136
Pupillometric findings in ATTRv patients and carriers: results from a single-centre experience 135
Letter: faecal microbiota transplantation in combination with fidaxomicin to treat severe complicated recurrent Clostridium difficile infection 135
High-throughput genetic testing in ALS: The challenging path of variant classification considering the acmg guidelines 135
ORal anticoagulants In fraGile patients with percutAneous endoscopic gastrostoMy and atrIal fibrillation: the (ORIGAMI) study 134
Sural nerve pathology in ALS patients: a single-centre experience 133
Wernicke's encephalopathy following chronic diarrhoea 133
Botulinum toxin-B ultrasound-guided injections for sialorrhea in amytrophic lateral sclerosis and Parkinson's disease 132
SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration 132
Totale 17.891
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Categoria #
all - tutte 111.779
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 111.779
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021291 0 0 0 0 0 0 0 0 0 0 262 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
2025/20269.454 1.488 275 576 1.171 1.748 496 1.877 513 571 696 43 0
Totale 29.624