IRIS UniCatt

Luigetti, Marco
 Distribuzione geografica
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Continente #
EU - Europa 7.776
NA - Nord America 7.758
AS - Asia 2.812
SA - Sud America 604
AF - Africa 101
OC - Oceania 19
Continente sconosciuto - Info sul continente non disponibili 8
Totale 19.078
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Nazione #
US - Stati Uniti d'America 7.649
DE - Germania 3.121
SE - Svezia 1.124
CN - Cina 1.089
SG - Singapore 996
UA - Ucraina 692
IT - Italia 686
BR - Brasile 554
FR - Francia 432
GB - Regno Unito 401
IE - Irlanda 382
PL - Polonia 272
ID - Indonesia 225
FI - Finlandia 205
RU - Federazione Russa 161
IN - India 154
CA - Canada 90
BE - Belgio 87
TR - Turchia 85
NL - Olanda 60
CI - Costa d'Avorio 45
KR - Corea 40
ZA - Sudafrica 40
JP - Giappone 38
HK - Hong Kong 31
VN - Vietnam 29
AT - Austria 27
AR - Argentina 22
AU - Australia 19
ES - Italia 19
IR - Iran 19
RO - Romania 19
CH - Svizzera 17
IQ - Iraq 14
PH - Filippine 12
PT - Portogallo 11
AE - Emirati Arabi Uniti 10
BD - Bangladesh 10
MX - Messico 10
CO - Colombia 8
CZ - Repubblica Ceca 8
DK - Danimarca 8
MA - Marocco 8
EC - Ecuador 7
LT - Lituania 7
LK - Sri Lanka 6
TH - Thailandia 6
A2 - ???statistics.table.value.countryCode.A2??? 5
KG - Kirghizistan 5
KZ - Kazakistan 5
NO - Norvegia 5
CL - Cile 4
HR - Croazia 4
IL - Israele 4
JO - Giordania 4
MD - Moldavia 4
PK - Pakistan 4
SA - Arabia Saudita 4
UZ - Uzbekistan 4
AZ - Azerbaigian 3
BO - Bolivia 3
BY - Bielorussia 3
DZ - Algeria 3
EU - Europa 3
IS - Islanda 3
LA - Repubblica Popolare Democratica del Laos 3
LV - Lettonia 3
PE - Perù 3
PY - Paraguay 3
SI - Slovenia 3
SK - Slovacchia (Repubblica Slovacca) 3
AM - Armenia 2
BG - Bulgaria 2
EG - Egitto 2
GR - Grecia 2
JM - Giamaica 2
PR - Porto Rico 2
AL - Albania 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BZ - Belize 1
CR - Costa Rica 1
CY - Cipro 1
DO - Repubblica Dominicana 1
GE - Georgia 1
HU - Ungheria 1
KE - Kenya 1
KH - Cambogia 1
KW - Kuwait 1
LB - Libano 1
LU - Lussemburgo 1
MC - Monaco 1
MM - Myanmar 1
MY - Malesia 1
OM - Oman 1
PA - Panama 1
QA - Qatar 1
SN - Senegal 1
TN - Tunisia 1
TW - Taiwan 1
Totale 19.078
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Città #
Chandler 1.414
Singapore 629
Ashburn 552
Redmond 404
Dublin 373
Jacksonville 341
San Mateo 333
Ann Arbor 303
New York 284
Nanjing 240
Nürnberg 231
Jakarta 223
Warsaw 204
Wilmington 197
Boston 161
Woodbridge 151
Dearborn 128
Houston 115
Moscow 115
Lawrence 112
Milan 105
Rome 100
Nanchang 99
Beijing 91
Seattle 91
Redwood City 87
Cattolica 82
Fairfield 79
Munich 75
Princeton 73
Marseille 72
Chicago 70
Brussels 69
Los Angeles 69
Izmir 67
Bremen 66
Detroit 62
Kraków 57
Frankfurt am Main 56
Norwalk 56
Shenyang 49
São Paulo 48
Helsinki 47
Boardman 46
Abidjan 45
Hebei 45
Hefei 45
Changsha 41
Seoul 38
Guangzhou 35
Leawood 34
Ottawa 34
Hangzhou 33
Jiaxing 33
The Dalles 32
Kunming 30
London 30
University Park 29
Hong Kong 28
Nuremberg 27
Zhengzhou 26
Mountain View 25
Pune 25
Cambridge 24
San Francisco 24
Düsseldorf 23
Phoenix 23
Philadelphia 22
Tianjin 22
Fremont 21
Santa Clara 21
North Bergen 19
Lancaster 18
Waanrode 18
Auburn Hills 17
Belo Horizonte 17
Hanoi 17
Toronto 17
Washington 17
Shanghai 16
Simi Valley 16
Stockholm 16
Trieste 16
Cape Town 15
Millbury 15
Rio de Janeiro 15
Las Vegas 14
Lauterbourg 14
Vienna 14
Birmingham 13
Brooklyn 13
Falkenstein 13
Paris 13
Portsmouth 13
Busto Arsizio 12
Bologna 11
Buffalo 11
Florence 11
Bexley 10
Brasília 10
Totale 9.462
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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 686
Clinical–neurophysiological correlations in a series of patients with IgM-related neuropathy 329
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 309
Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: Pitfalls and tips in the diagnosis 290
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 270
Teaching neuroimages: Peroneal intraneural ganglion cyst: a rare cause of drop foot in a child. 213
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 208
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 205
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 203
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 191
Retinal detachment with an unusual shape. 180
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 168
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 168
Persistence of abnormal electrophysiological findings after carpal tunnel release 166
Distinctive clinical and neuroimaging characteristics of longitudinally extensive transverse myelitis associated with aquaporin-4 autoantibodies 156
Bilateral thalamic stroke transiently reduces arousals and NREM sleep instability. 148
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 142
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 142
Efficacy of lenalidomide plus dexamethasone for POEMS syndrome relapsed after autologous peripheral stem-cell transplantation 139
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 137
Assessment of neurological manifestations in hospitalized patients with COVID-19 137
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 134
A Case of Hemiabdominal Myoclonus 131
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 127
Epstein-Barr virus antibodies in serum and cerebrospinal fluid from Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculoneuropathy and Amyotrophic Lateral 127
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience 127
Mitochondrial neuropathy: considerations on pathogenesis 127
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 125
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 121
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 120
Restless leg syndrome in different types of demyelinating neuropathies: a single-center pilot study 119
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 119
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 117
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 117
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 116
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 114
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 114
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? 112
Ultrasound evaluation in transthyretin-related amyloid neuropathy 111
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 109
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 109
Neurologic improvement after peripheral blood stem cell transplantation in poems 109
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 108
Usefulness of F-18 FDG PET/CT in the follow-up of POEMS syndrome after autologous peripheral blood stem cell transplantation 107
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 107
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 107
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience 107
A novel L67P SOD1 mutation in an Italian ALS patient. 106
Clinical-neurophysiological correlations in a series of patients with IgM-related neuropathy 106
Somatosensory Evoked Potentials of Inferior Alveolar Nerve: confirmation of a possible non-invasive neurophysiological approach 106
Posterior interosseous nerve syndrome due to radioulnar joint cyst 104
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 103
Vertebral artery dissection presenting with isolated occipital headache 102
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 101
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 100
Mycosis fungoides as a cause of severe obstructive sleep apnea 100
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 100
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 99
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 98
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 97
Distinct lymphocytes subsets in IgM-related neuropathy: clinical-immunological correlations 97
Wernicke's encephalopathy following chronic diarrhoea 96
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 96
Teaching NeuroImage: MRI of diabetic lumbar plexopathy treated with local steroid injection. 95
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 94
Teaching NeuroImages: Transient mutism associated with splenium lesion in capecitabine-induced leukoencephalopathy 94
Restless Legs Syndrome and lateralized periodic movements due to a spinal schwannoma 93
Nerve conduction studies of the sural nerve: Normative data from a single-center experience 92
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 92
Nerve ultrasound in CMT2E/CMT1F due to NEFL mutation: Confirmation of an axonal pathology 92
Sural nerve pathology in ALS patients: a single-centre experience 91
Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients 90
HFE p.H63D polymorphism does not influence ALS phenotype and survival 90
Benedictine hand of 'central' origin 89
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 89
Clinical features and outcome of patients with autoimmune cerebellar ataxia evaluated with the Scale for the Assessment and Rating of Ataxia 89
Myasthenia gravis with presynaptic neurophysiological signs: Two case reports and literature review 88
Post-Encephalitic Parkinsonism and Sleep Disorder Responsive to Immunological Treatment: A Case Report 88
ANCA-related vasculitic neuropathy mimicking motor neuron disease. 87
Improvement of obstructive sleep apneas caused by hydrocephalus associated with Chiari malformation Type II following surgery. 87
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 87
Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity 86
A Case of Hemiabdominal Myoclonus 86
Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma. 84
Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs. 84
Bilateral thoracic long nerve involvement in motor multifocal neuropathy 84
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 84
An uncommon cause of headache resolution: spontaneous ventriculostomy in obstructive hydrocephalus 84
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 83
Longitudinal assessments in discordant twins with SMA 83
A novel GJB1 mutation in an Italian patient with Charcot-Marie-Tooth disease and pyramidal signs 82
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 82
Gadolinium enhancement of the lumbar leptomeninges and roots in a case of ALS 81
Lower motor neuron involvement in longitudinally extensive transverse myelitis with and without aquaporin-4 antibodies 81
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 81
A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease 80
Erratum to “Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience” (Clinical Neurology and Neurosurgery (2016) 147 (117–118) (S030384671630097X) (10.1016/j.clineuro.2016.03.007)) 80
Post-Encephalitic Parkinsonism and Sleep Disorder Responsive to Immunological Treatment: A Case Report 80
Sural nerve biopsy in peripheral neuropathies: 30-year experience from a single center 80
Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis: a Single-Centre Experience 80
Totale 12.431
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Categoria #
all - tutte 83.633
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 83.633
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020184 0 0 0 0 0 0 0 0 0 0 0 184
2020/20211.489 61 161 55 209 211 63 155 43 170 86 248 27
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
2024/20253.158 99 126 321 192 257 115 136 163 516 364 788 81
Totale 19.453