IRIS UniCatt

Luigetti, Marco
 Distribuzione geografica
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Continente #
NA - Nord America 9.310
EU - Europa 8.298
AS - Asia 6.192
SA - Sud America 1.490
AF - Africa 242
OC - Oceania 23
Continente sconosciuto - Info sul continente non disponibili 10
Totale 25.565
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Nazione #
US - Stati Uniti d'America 9.060
DE - Germania 3.226
SG - Singapore 2.953
CN - Cina 1.667
BR - Brasile 1.264
SE - Svezia 1.145
IT - Italia 762
UA - Ucraina 707
GB - Regno Unito 485
FR - Francia 466
IE - Irlanda 385
VN - Vietnam 351
PL - Polonia 306
IN - India 254
FI - Finlandia 250
ID - Indonesia 246
RU - Federazione Russa 191
CA - Canada 152
TR - Turchia 105
BD - Bangladesh 100
ZA - Sudafrica 90
BE - Belgio 87
AR - Argentina 84
HK - Hong Kong 79
JP - Giappone 72
NL - Olanda 69
IQ - Iraq 66
MX - Messico 57
ES - Italia 47
CI - Costa d'Avorio 46
KR - Corea 40
EC - Ecuador 38
AT - Austria 34
SA - Arabia Saudita 32
MA - Marocco 28
PK - Pakistan 27
PY - Paraguay 26
CO - Colombia 24
IR - Iran 24
JO - Giordania 23
AU - Australia 22
KE - Kenya 22
AE - Emirati Arabi Uniti 21
CL - Cile 20
RO - Romania 19
CH - Svizzera 17
LT - Lituania 17
PH - Filippine 14
PT - Portogallo 14
UZ - Uzbekistan 14
IL - Israele 13
KZ - Kazakistan 12
TN - Tunisia 12
CZ - Repubblica Ceca 11
VE - Venezuela 11
AZ - Azerbaigian 10
DK - Danimarca 10
DZ - Algeria 9
DO - Repubblica Dominicana 8
TH - Thailandia 8
UY - Uruguay 8
BO - Bolivia 7
EG - Egitto 7
KG - Kirghizistan 7
PS - Palestinian Territory 7
SN - Senegal 7
LK - Sri Lanka 6
PE - Perù 6
A2 - ???statistics.table.value.countryCode.A2??? 5
BY - Bielorussia 5
ET - Etiopia 5
HR - Croazia 5
JM - Giamaica 5
NI - Nicaragua 5
NO - Norvegia 5
NP - Nepal 5
OM - Oman 5
SI - Slovenia 5
TT - Trinidad e Tobago 5
AM - Armenia 4
HN - Honduras 4
LA - Repubblica Popolare Democratica del Laos 4
MD - Moldavia 4
MM - Myanmar 4
AO - Angola 3
EU - Europa 3
GE - Georgia 3
GM - Gambi 3
GR - Grecia 3
IS - Islanda 3
LB - Libano 3
LV - Lettonia 3
PA - Panama 3
PR - Porto Rico 3
QA - Qatar 3
SK - Slovacchia (Repubblica Slovacca) 3
AL - Albania 2
BA - Bosnia-Erzegovina 2
BB - Barbados 2
BG - Bulgaria 2
Totale 25.526
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Città #
Chandler 1.414
Singapore 1.323
Ashburn 853
Redmond 404
Dublin 374
Beijing 355
New York 348
Jacksonville 343
San Mateo 333
Ann Arbor 303
Nanjing 240
Warsaw 232
Nürnberg 231
Jakarta 225
Wilmington 198
Los Angeles 184
Boston 173
Hefei 151
Woodbridge 151
Munich 138
Dearborn 128
Houston 128
Ho Chi Minh City 127
Moscow 119
São Paulo 117
Lawrence 112
Rome 111
Milan 108
Dallas 102
Hanoi 101
Chicago 99
Nanchang 99
Seattle 98
Frankfurt am Main 88
Redwood City 87
Cattolica 82
Fairfield 79
Hong Kong 75
Buffalo 73
Princeton 73
Marseille 72
Brussels 69
Bremen 68
Izmir 68
Detroit 66
Kraków 57
Norwalk 56
Helsinki 49
Shenyang 49
Abidjan 46
Boardman 46
Hebei 45
Santa Clara 45
Kent 44
Tokyo 44
Changsha 42
The Dalles 42
London 40
Seoul 38
Brooklyn 37
Ottawa 37
Rio de Janeiro 37
San Francisco 36
Guangzhou 35
Phoenix 35
Hangzhou 34
Johannesburg 34
Lappeenranta 34
Leawood 34
Jiaxing 33
Stockholm 32
Nuremberg 31
Kunming 30
Pune 30
Montreal 29
University Park 29
Philadelphia 28
Turku 28
Atlanta 27
Baghdad 27
Belo Horizonte 27
Denver 27
Dhaka 27
Brasília 26
Tianjin 26
Toronto 26
Zhengzhou 26
Mountain View 25
Orem 25
Cambridge 24
Cape Town 23
Düsseldorf 23
Amman 21
Chennai 21
Curitiba 21
Fremont 21
North Bergen 21
Poplar 19
Guarulhos 18
Lancaster 18
Totale 12.107
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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
Clinical–neurophysiological correlations in a series of patients with IgM-related neuropathy 354
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 334
Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: Pitfalls and tips in the diagnosis 313
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 292
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
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
Retinal detachment with an unusual shape. 202
Persistence of abnormal electrophysiological findings after carpal tunnel release 198
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
Distinctive clinical and neuroimaging characteristics of longitudinally extensive transverse myelitis associated with aquaporin-4 autoantibodies 185
Bilateral thalamic stroke transiently reduces arousals and NREM sleep instability. 184
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 178
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 177
Assessment of neurological manifestations in hospitalized patients with COVID-19 172
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 170
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
A Case of Hemiabdominal Myoclonus 157
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 157
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience 152
Mitochondrial neuropathy: considerations on pathogenesis 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
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 148
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 146
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 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
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience 138
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 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
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
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
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
Vertebral artery dissection presenting with isolated occipital headache 128
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
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
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 126
Somatosensory Evoked Potentials of Inferior Alveolar Nerve: confirmation of a possible non-invasive neurophysiological approach 126
Longitudinal assessments in discordant twins with SMA 124
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 123
Restless Legs Syndrome and lateralized periodic movements due to a spinal schwannoma 123
Pathological findings in chronic inflammatory demyelinating polyradiculoneuropathy: A single-center experience 123
Posterior interosseous nerve syndrome due to radioulnar joint cyst 122
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 121
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunction 121
Myasthenia gravis with presynaptic neurophysiological signs: Two case reports and literature review 120
Nerve conduction studies of the sural nerve: Normative data from a single-center experience 119
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 118
Mycosis fungoides as a cause of severe obstructive sleep apnea 118
Teaching NeuroImages: Transient mutism associated with splenium lesion in capecitabine-induced leukoencephalopathy 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
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 116
Wernicke's encephalopathy following chronic diarrhoea 116
Sural nerve pathology in ALS patients: a single-centre experience 115
A Case of Hemiabdominal Myoclonus 115
Clinical features and outcome of patients with autoimmune cerebellar ataxia evaluated with the Scale for the Assessment and Rating of Ataxia 115
Benedictine hand of 'central' origin 114
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 114
HFE p.H63D polymorphism does not influence ALS phenotype and survival 113
Improvement of obstructive sleep apneas caused by hydrocephalus associated with Chiari malformation Type II following surgery. 112
Guillain–Barré syndrome from an emergency department view: how to better predict the outcome? 112
Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma. 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
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 110
Post-Encephalitic Parkinsonism and Sleep Disorder Responsive to Immunological Treatment: A Case Report 110
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 109
Post-Encephalitic Parkinsonism and Sleep Disorder Responsive to Immunological Treatment: A Case Report 109
Ocular Involvement in Hereditary Amyloidosis 109
A novel GJB1 mutation in an Italian patient with Charcot-Marie-Tooth disease and pyramidal signs 108
Sural nerve biopsy in peripheral neuropathies: 30-year experience from a single center 108
Ocular involvement in hereditary transthyretin amyloidosis: A case series describing novel potential biomarkers 108
ANCA-related vasculitic neuropathy mimicking motor neuron disease. 107
Sudoscan in the evaluation and follow-up of patients and carriers with TTR mutations: experience from an Italian Centre 107
Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity 106
Bilateral thoracic long nerve involvement in motor multifocal neuropathy 106
An uncommon cause of headache resolution: spontaneous ventriculostomy in obstructive hydrocephalus 106
Totale 15.162
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Categoria #
all - tutte 106.722
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 106.722
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021792 0 0 0 0 0 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
2024/20253.751 99 126 321 192 257 115 136 163 516 364 788 674
2025/20265.895 1.680 303 601 1.189 1.738 384 0 0 0 0 0 0
Totale 25.941