IRIS UniCatt

Sabatelli, Mario
 Distribuzione geografica
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Continente #
NA - Nord America 12.435
EU - Europa 9.286
AS - Asia 7.634
SA - Sud America 1.481
Continente sconosciuto - Info sul continente non disponibili 388
AF - Africa 249
OC - Oceania 29
Totale 31.502
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Nazione #
US - Stati Uniti d'America 12.069
SG - Singapore 3.440
DE - Germania 3.238
CN - Cina 1.816
SE - Svezia 1.272
BR - Brasile 1.216
IT - Italia 1.026
VN - Vietnam 784
UA - Ucraina 723
FR - Francia 644
PL - Polonia 587
GB - Regno Unito 559
IE - Irlanda 365
FI - Finlandia 303
IN - India 251
ID - Indonesia 240
CA - Canada 207
RU - Federazione Russa 194
BD - Bangladesh 192
JP - Giappone 187
HK - Hong Kong 153
TR - Turchia 137
AR - Argentina 91
ZA - Sudafrica 86
BE - Belgio 84
NL - Olanda 80
IQ - Iraq 74
MX - Messico 72
PK - Pakistan 48
CI - Costa d'Avorio 44
ES - Italia 43
KR - Corea 43
CO - Colombia 36
SA - Arabia Saudita 35
AT - Austria 33
EC - Ecuador 33
PY - Paraguay 30
CH - Svizzera 29
MA - Marocco 29
VE - Venezuela 26
IR - Iran 25
AE - Emirati Arabi Uniti 23
AU - Australia 23
CL - Cile 23
PH - Filippine 22
JO - Giordania 21
UZ - Uzbekistan 19
TN - Tunisia 18
KE - Kenya 17
IL - Israele 15
RO - Romania 15
JM - Giamaica 14
PT - Portogallo 13
AZ - Azerbaigian 11
DO - Repubblica Dominicana 11
TH - Thailandia 11
CR - Costa Rica 10
CZ - Repubblica Ceca 10
KZ - Kazakistan 10
PE - Perù 10
EG - Egitto 9
ET - Etiopia 9
HN - Honduras 9
LT - Lituania 9
TT - Trinidad e Tobago 9
GR - Grecia 8
NP - Nepal 8
KG - Kirghizistan 7
LK - Sri Lanka 7
MY - Malesia 7
OM - Oman 7
UY - Uruguay 7
BB - Barbados 6
BY - Bielorussia 6
DK - Danimarca 6
EU - Europa 6
HR - Croazia 6
NI - Nicaragua 6
SN - Senegal 6
TW - Taiwan 6
DZ - Algeria 5
LB - Libano 5
NZ - Nuova Zelanda 5
PS - Palestinian Territory 5
AL - Albania 4
AO - Angola 4
BG - Bulgaria 4
BO - Bolivia 4
CG - Congo 4
GT - Guatemala 4
GY - Guiana 4
NO - Norvegia 4
PA - Panama 4
SV - El Salvador 4
XK - ???statistics.table.value.countryCode.XK??? 4
AM - Armenia 3
BH - Bahrain 3
GE - Georgia 3
MD - Moldavia 3
MM - Myanmar 3
Totale 31.063
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Città #
Singapore 1.849
Ashburn 1.330
Chandler 1.310
San Jose 1.032
Warsaw 515
Beijing 356
Dublin 355
New York 340
Jacksonville 338
Ann Arbor 322
San Mateo 320
Redmond 284
Ho Chi Minh City 272
Nanjing 262
Los Angeles 239
Munich 225
Wilmington 220
Nürnberg 219
Jakarta 218
Lauterbourg 201
Fairfield 199
Hanoi 197
Houston 192
Boston 175
Woodbridge 174
Milan 162
Seattle 160
Tokyo 148
Cattolica 136
Hefei 135
Rome 133
Dearborn 129
Hong Kong 127
Chicago 121
Frankfurt am Main 120
Moscow 116
Lawrence 113
Nanchang 112
São Paulo 105
Helsinki 102
Santa Clara 98
Dallas 93
Redwood City 93
Buffalo 91
Izmir 86
Princeton 73
Marseille 69
Detroit 68
London 62
Bremen 59
Cambridge 59
Atlanta 58
Brussels 58
Phoenix 54
Kraków 53
Norwalk 49
Shenyang 49
Boardman 48
Council Bluffs 45
Hangzhou 45
Orem 45
Abidjan 44
Paris 44
Philadelphia 44
San Francisco 43
Hebei 42
North Bergen 42
The Dalles 41
Seoul 40
Jiaxing 39
Lappeenranta 39
Toronto 39
University Park 39
Guangzhou 38
Leawood 38
Montreal 38
Rio de Janeiro 38
Changsha 37
Brooklyn 36
Kent 36
Mountain View 36
Johannesburg 35
Nuremberg 34
Tianjin 34
Denver 32
Ottawa 32
Pune 32
Kunming 31
Shanghai 31
Zhengzhou 31
Baghdad 30
Stockholm 30
Da Nang 29
Belo Horizonte 28
Chennai 28
Curitiba 27
Memphis 27
Fremont 25
Manchester 24
Dhaka 23
Totale 15.774
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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 743
Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients 428
Clinical–neurophysiological correlations in a series of patients with IgM-related neuropathy 384
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 363
Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis: a Single-Centre Experience 328
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 321
Exploring the Role of CCNF Variants in Italian ALS Patients 311
ALS skin fibroblasts reveal oxidative stress and ERK1/2-mediated cytoplasmic localization of TDP-43 299
Histamine beyond its effects on allergy: Potential therapeutic benefits for the treatment of Amyotrophic Lateral Sclerosis (ALS) 286
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 274
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 266
Hospital admissions from the emergency department of adult patients affected by myopathies 261
Teaching neuroimages: Peroneal intraneural ganglion cyst: a rare cause of drop foot in a child. 254
Proteostasis and ALS: Protocol for a phase II, randomised, double-blind, placebo-controlled, multicentre clinical trial for colchicine in ALS (Co-ALS) 254
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 253
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 247
Relations between C9orf72 expansion size in blood, age at onset, age at collection and transmission across generations in patients and presymptomatic carriers 240
Retinal detachment with an unusual shape. 220
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 220
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. 210
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 209
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 199
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS 197
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients. 196
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 195
Flow Cytofluorimetric Analysis of Anti-LRP4 (LDL Receptor-Related Protein 4) Autoantibodies in Italian Patients with Myasthenia Gravis 194
Matrin 3 variants are frequent in Italian ALS patients 191
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 191
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 190
Chronic GM2 gangliosidosis type Sandhoff associated with a novel missense HEXB gene mutaton causing a double patogenetic effect 188
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 186
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 184
A Genome-wide Association Study of Myasthenia Gravis 182
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 180
ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis 180
Restless leg syndrome in different types of demyelinating neuropathies: a single-center pilot study 178
Sural nerve biopsy in peripheral neuropathies: 30-year experience from a single center 175
Efficacy of lenalidomide plus dexamethasone for POEMS syndrome relapsed after autologous peripheral stem-cell transplantation 174
Evaluating the contribution of the gene TARDBP in Italian patients with amyotrophic lateral sclerosis 173
Novel variants and cellular studies on patients' primary fibroblasts support a role for NEK1 missense variants in ALS pathogenesis 173
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 172
Recurrent miller fisher: a new case report and a literature review 172
Epstein-Barr virus antibodies in serum and cerebrospinal fluid from Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculoneuropathy and Amyotrophic Lateral 170
New ALS-related genes expand the spectrum paradigm of amyotrophic lateral sclerosis 168
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 166
Mechanically assisted cough in amyotrophic lateral sclerosis: Effect on vital capacity decline and timing of non invasive ventilation onset 166
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 165
Demyelinating Encephalomyeloradiculitis with Balò-like lesions 164
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 163
An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene 163
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 163
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience 163
Characterization of SOD1-DT, a Divergent Long Non-Coding RNA in the Locus of the SOD1 Human Gene 161
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 160
Neurologic improvement after peripheral blood stem cell transplantation in poems 160
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 160
A novel L67P SOD1 mutation in an Italian ALS patient. 159
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 158
ORal anticoagulants In fraGile patients with percutAneous endoscopic gastrostoMy and atrIal fibrillation: the (ORIGAMI) study 158
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 157
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 156
Repeated courses of granulocyte colony-stimulating factor in amyotrophic lateral sclerosis: clinical and biological results from a prospective multicenter study. 155
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia. 155
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 154
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 154
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 154
Pathological findings in chronic inflammatory demyelinating polyradiculoneuropathy: A single-center experience 154
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 153
Usefulness of F-18 FDG PET/CT in the follow-up of POEMS syndrome after autologous peripheral blood stem cell transplantation 153
Distinct lymphocytes subsets in IgM-related neuropathy: clinical-immunological correlations 153
ATXN2 polyQ intermediate repeats are a modifier of ALS survival 152
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 151
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 150
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 150
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? 150
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 150
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 149
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 147
Ocular involvement in hereditary transthyretin amyloidosis: A case series describing novel potential biomarkers 147
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 146
Clinical-neurophysiological correlations in a series of patients with IgM-related neuropathy 146
Pupillometric findings in ATTRv patients and carriers: results from a single-centre experience 145
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 145
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation 145
A useful electrophysiological test for diagnosis of minimal conduction block 144
Neuromyelitis optica spectrum disorder as a paraneoplastic manifestation of lung adenocarcinoma expressing aquaporin-4. 144
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 144
Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis 143
High-throughput genetic testing in ALS: The challenging path of variant classification considering the acmg guidelines 143
Pure motor chronic inlammatory demyelinating polyneuropathy 142
Guillain-Barre' syndrome following Varicella zoster reactivation in Chronic Lymphocytic Leukemia treated with fludarabine 142
Long-term motor cortex stimulation for amyotrophic lateral sclerosis 142
Guillain–Barré syndrome from an emergency department view: how to better predict the outcome? 142
Botulinum toxin B ultrasound-guided injections for sialorrhea in amyotrophic lateral sclerosis and Parkinson's disease. 140
SOD1 p.D12Y variant is associated with ALS/distal myopathy spectrum 140
Exome sequencing reveals VCP mutations as a cause of familial ALS 139
SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration 139
Effect of RNS60 in amyotrophic lateral sclerosis: a phase II multicentre, randomized, double-blind, placebo-controlled trial 138
Ultrasound evaluation in transthyretin-related amyloid neuropathy 138
Letter: faecal microbiota transplantation in combination with fidaxomicin to treat severe complicated recurrent Clostridium difficile infection 138
Totale 19.037
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Categoria #
all - tutte 123.838
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 123.838
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.661 0 147 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
2025/202610.072 1.488 275 576 1.171 1.748 496 1.877 513 571 696 352 309
2026/20271.260 474 786 0 0 0 0 0 0 0 0 0 0
Totale 31.502