Luigetti, Marco
 Distribuzione geografica
Continente #
NA - Nord America 11.864
EU - Europa 8.944
AS - Asia 7.744
SA - Sud America 1.596
AF - Africa 269
OC - Oceania 25
Continente sconosciuto - Info sul continente non disponibili 12
Totale 30.454
Nazione #
US - Stati Uniti d'America 11.520
SG - Singapore 3.559
DE - Germania 3.268
CN - Cina 1.843
BR - Brasile 1.315
SE - Svezia 1.148
IT - Italia 1.006
VN - Vietnam 737
UA - Ucraina 711
FR - Francia 703
GB - Regno Unito 514
IE - Irlanda 388
PL - Polonia 311
IN - India 282
FI - Finlandia 276
ID - Indonesia 249
CA - Canada 209
RU - Federazione Russa 194
JP - Giappone 179
BD - Bangladesh 170
HK - Hong Kong 145
TR - Turchia 121
AR - Argentina 97
ZA - Sudafrica 96
BE - Belgio 92
IQ - Iraq 87
NL - Olanda 85
MX - Messico 68
ES - Italia 55
EC - Ecuador 50
CI - Costa d'Avorio 46
PK - Pakistan 46
KR - Corea 42
SA - Arabia Saudita 41
AT - Austria 35
CO - Colombia 34
PY - Paraguay 32
MA - Marocco 30
JO - Giordania 26
KE - Kenya 26
CL - Cile 25
PH - Filippine 25
AU - Australia 24
IR - Iran 24
AE - Emirati Arabi Uniti 23
RO - Romania 21
CH - Svizzera 20
TN - Tunisia 19
UZ - Uzbekistan 19
LT - Lituania 18
JM - Giamaica 16
PT - Portogallo 16
IL - Israele 15
VE - Venezuela 14
TH - Thailandia 13
CZ - Repubblica Ceca 12
KZ - Kazakistan 12
AZ - Azerbaigian 10
DK - Danimarca 10
DO - Repubblica Dominicana 10
EG - Egitto 10
PE - Perù 10
UY - Uruguay 10
DZ - Algeria 9
SN - Senegal 9
BY - Bielorussia 8
NP - Nepal 8
BO - Bolivia 7
KG - Kirghizistan 7
OM - Oman 7
PS - Palestinian Territory 7
ET - Etiopia 6
HR - Croazia 6
LB - Libano 6
LK - Sri Lanka 6
TT - Trinidad e Tobago 6
A2 - ???statistics.table.value.countryCode.A2??? 5
GR - Grecia 5
GT - Guatemala 5
HN - Honduras 5
MY - Malesia 5
NI - Nicaragua 5
NO - Norvegia 5
SI - Slovenia 5
AL - Albania 4
AM - Armenia 4
LA - Repubblica Popolare Democratica del Laos 4
MD - Moldavia 4
MM - Myanmar 4
PR - Porto Rico 4
QA - Qatar 4
RS - Serbia 4
AO - Angola 3
CR - Costa Rica 3
EU - Europa 3
GE - Georgia 3
GM - Gambi 3
IS - Islanda 3
LV - Lettonia 3
PA - Panama 3
Totale 30.400
Città #
Singapore 1.891
Chandler 1.414
Ashburn 1.161
San Jose 995
New York 414
Redmond 404
Dublin 377
Beijing 373
Jacksonville 348
San Mateo 333
Ann Arbor 303
Ho Chi Minh City 263
Nanjing 240
Warsaw 236
Los Angeles 232
Nürnberg 231
Jakarta 226
Lauterbourg 199
Wilmington 199
Hanoi 189
Boston 175
Rome 159
Woodbridge 152
Hefei 151
Tokyo 147
Munich 138
Houston 136
Hong Kong 132
Dearborn 128
São Paulo 125
Milan 124
Moscow 120
Dallas 119
Chicago 118
Frankfurt am Main 118
Lawrence 112
Buffalo 105
Seattle 103
Nanchang 99
Redwood City 87
Cattolica 82
Fairfield 79
Santa Clara 79
Helsinki 74
Marseille 73
Princeton 73
The Dalles 71
Bremen 69
Brussels 69
Detroit 69
Izmir 68
Boardman 65
Kraków 57
Norwalk 56
Paris 52
Shenyang 50
Council Bluffs 49
London 47
Abidjan 46
Hebei 45
Orem 45
Brooklyn 44
Kent 44
Toronto 44
Guangzhou 43
Atlanta 42
Changsha 42
Phoenix 41
Rio de Janeiro 41
Johannesburg 40
San Francisco 39
Baghdad 38
Ottawa 38
Seoul 38
St Louis 38
Montreal 37
Hangzhou 35
Lappeenranta 35
Philadelphia 35
Stockholm 35
Da Nang 34
Leawood 34
Denver 33
Jiaxing 33
Nuremberg 32
Pune 32
Kunming 31
Shanghai 30
Dhaka 29
Haiphong 29
University Park 29
Belo Horizonte 28
Tianjin 28
Turku 28
Zhengzhou 27
Brasília 26
North Bergen 26
Mountain View 25
Amman 24
Cambridge 24
Totale 15.225
Nome #
Real-life experience with inotersen in hereditary transthyretin amyloidosis with late-onset phenotype: Data from an early-access program in Italy 740
Clinical–neurophysiological correlations in a series of patients with IgM-related neuropathy 380
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 361
Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: Pitfalls and tips in the diagnosis 335
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 318
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 273
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 265
Teaching neuroimages: Peroneal intraneural ganglion cyst: a rare cause of drop foot in a child. 252
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 252
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 246
Persistence of abnormal electrophysiological findings after carpal tunnel release 223
Retinal detachment with an unusual shape. 220
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 216
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 215
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 208
Bilateral thalamic stroke transiently reduces arousals and NREM sleep instability. 206
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 198
Nerve ultrasound in hereditary transthyretin amyloidosis: red flags and possible progression biomarkers 198
null 198
Distinctive clinical and neuroimaging characteristics of longitudinally extensive transverse myelitis associated with aquaporin-4 autoantibodies 197
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 194
Chronic inflammatory demyelinating polyradiculoneuropathy: can a diagnosis be made in patients not fulfilling electrodiagnostic criteria? 191
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 186
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 185
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 183
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 178
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 177
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
Restless leg syndrome in different types of demyelinating neuropathies: a single-center pilot study 173
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 170
Epstein-Barr virus antibodies in serum and cerebrospinal fluid from Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculoneuropathy and Amyotrophic Lateral 169
Somatosensory Evoked Potentials of Inferior Alveolar Nerve: confirmation of a possible non-invasive neurophysiological approach 169
A Case of Hemiabdominal Myoclonus 166
Mitochondrial neuropathy: considerations on pathogenesis 166
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 165
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 162
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience 162
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 161
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 161
Neurologic improvement after peripheral blood stem cell transplantation in poems 160
Recurrent miller fisher: a new case report and a literature review 160
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 159
A novel L67P SOD1 mutation in an Italian ALS patient. 158
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 158
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 155
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience 155
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 154
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 154
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 154
Usefulness of F-18 FDG PET/CT in the follow-up of POEMS syndrome after autologous peripheral blood stem cell transplantation 152
Distinct lymphocytes subsets in IgM-related neuropathy: clinical-immunological correlations 152
Pathological findings in chronic inflammatory demyelinating polyradiculoneuropathy: A single-center experience 152
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 151
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 151
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 150
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 150
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 149
Serum Neurofilament and Free Light Chain Levels in Patients Undergoing Treatment for Chronic Inflammatory Demyelinating Polyneuropathy 148
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 148
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? 147
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 147
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 147
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 146
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 145
Clinical-neurophysiological correlations in a series of patients with IgM-related neuropathy 145
Restless Legs Syndrome and lateralized periodic movements due to a spinal schwannoma 145
Ocular involvement in hereditary transthyretin amyloidosis: A case series describing novel potential biomarkers 145
Ocular Morpho-Functional Evaluation in ATTRv Pre-Symptomatic Carriers: A Case Series 144
Pupillometric findings in ATTRv patients and carriers: results from a single-centre experience 144
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 144
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 144
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunction 143
Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis: a Single-Centre Experience 143
Vertebral artery dissection presenting with isolated occipital headache 142
Longitudinal assessments in discordant twins with SMA 142
Guillain–Barré syndrome from an emergency department view: how to better predict the outcome? 141
Mycosis fungoides as a cause of severe obstructive sleep apnea 140
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 138
Myasthenia gravis with presynaptic neurophysiological signs: Two case reports and literature review 138
Ocular Involvement in Hereditary Amyloidosis 137
Ultrasound evaluation in transthyretin-related amyloid neuropathy 136
Sural nerve pathology in ALS patients: a single-centre experience 135
Wernicke's encephalopathy following chronic diarrhoea 134
Posterior interosseous nerve syndrome due to radioulnar joint cyst 134
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 134
Nerve MR in the Differential Diagnosis of Neuropathies: A Case Series from a Single Center 133
A Case of Hemiabdominal Myoclonus 133
Clinical features and outcome of patients with autoimmune cerebellar ataxia evaluated with the Scale for the Assessment and Rating of Ataxia 133
Nerve conduction studies of the sural nerve: Normative data from a single-center experience 132
HFE p.H63D polymorphism does not influence ALS phenotype and survival 131
Improvement of obstructive sleep apneas caused by hydrocephalus associated with Chiari malformation Type II following surgery. 129
Benedictine hand of 'central' origin 129
Uncommon pathological findings in sural nerve biopsy from a patient with Churg-Strauss related multiple mononeuropathy 128
Teaching NeuroImages: Transient mutism associated with splenium lesion in capecitabine-induced leukoencephalopathy 128
Small fibre involvement in multifocal motor neuropathy explored with sudoscan: a single-centre experience 128
Early detection of nerve involvement in presymptomatic TTR mutation carriers: exploring potential markers of disease onset 127
Neuralgic Amyotrophy and Hourglass Nerve Constriction/Nerve Torsion: Two Sides of the Same Coin? A Clinical Review 127
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 127
Autonomic Dysfunction during Acute SARS-CoV-2 Infection: A Systematic Review 126
Totale 17.529
Categoria #
all - tutte 124.243
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 124.243


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.828 197 130 20 180 56 55 45 284 90 109 296 366
2022/20234.453 439 516 298 601 250 505 156 303 483 731 110 61
2023/20241.947 95 572 56 127 61 361 100 60 13 78 207 217
2024/20253.751 99 126 321 192 257 115 136 163 516 364 788 674
2025/202610.426 1.680 303 601 1.189 1.738 496 1.799 508 581 764 340 427
2026/2027434 434 0 0 0 0 0 0 0 0 0 0 0
Totale 30.906