IRIS PubliCatt

Luigetti, Marco
 Distribuzione geografica
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Continente #
NA - Nord America 7.237
EU - Europa 7.129
AS - Asia 1.484
AF - Africa 80
SA - Sud America 19
OC - Oceania 15
Continente sconosciuto - Info sul continente non disponibili 8
Totale 15.972
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Nazione #
US - Stati Uniti d'America 7.165
DE - Germania 2.983
SE - Svezia 1.106
CN - Cina 908
UA - Ucraina 688
IT - Italia 556
IE - Irlanda 380
GB - Regno Unito 359
FR - Francia 341
PL - Polonia 256
SG - Singapore 212
FI - Finlandia 162
IN - India 144
RU - Federazione Russa 86
BE - Belgio 82
TR - Turchia 79
CA - Canada 67
CI - Costa d'Avorio 45
NL - Olanda 45
JP - Giappone 36
ZA - Sudafrica 33
IR - Iran 19
HK - Hong Kong 18
AU - Australia 15
CH - Svizzera 15
KR - Corea 15
RO - Romania 15
ES - Italia 12
VN - Vietnam 12
PH - Filippine 10
BR - Brasile 7
AE - Emirati Arabi Uniti 6
AT - Austria 6
PT - Portogallo 6
TH - Thailandia 6
A2 - ???statistics.table.value.countryCode.A2??? 5
CZ - Repubblica Ceca 5
DK - Danimarca 5
CO - Colombia 4
NO - Norvegia 4
CL - Cile 3
EU - Europa 3
HR - Croazia 3
IL - Israele 3
MD - Moldavia 3
AR - Argentina 2
GR - Grecia 2
ID - Indonesia 2
JO - Giordania 2
KZ - Kazakistan 2
MX - Messico 2
PK - Pakistan 2
PR - Porto Rico 2
SA - Arabia Saudita 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
AL - Albania 1
BO - Bolivia 1
BZ - Belize 1
DZ - Algeria 1
EC - Ecuador 1
EG - Egitto 1
HU - Ungheria 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
LU - Lussemburgo 1
LV - Lettonia 1
MC - Monaco 1
MM - Myanmar 1
MY - Malesia 1
OM - Oman 1
PE - Perù 1
TW - Taiwan 1
Totale 15.972
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Città #
Chandler 1.414
Ashburn 535
Redmond 404
Dublin 371
Jacksonville 339
San Mateo 333
Ann Arbor 303
New York 276
Nanjing 240
Nürnberg 231
Wilmington 197
Warsaw 194
Boston 157
Woodbridge 151
Singapore 131
Dearborn 128
Houston 114
Lawrence 112
Nanchang 99
Milan 93
Beijing 89
Redwood City 87
Cattolica 80
Seattle 80
Fairfield 79
Princeton 73
Marseille 72
Moscow 72
Chicago 67
Bremen 66
Izmir 66
Brussels 64
Detroit 61
Kraków 57
Norwalk 56
Rome 55
Munich 50
Shenyang 49
Boardman 46
Abidjan 45
Hebei 45
Changsha 40
Leawood 34
Guangzhou 33
Jiaxing 32
Kunming 29
University Park 29
Hangzhou 26
Mountain View 25
Ottawa 25
Pune 25
Cambridge 24
London 23
Tianjin 22
Zhengzhou 22
Fremont 21
Philadelphia 21
Phoenix 21
Los Angeles 20
Lancaster 18
Waanrode 18
Auburn Hills 17
Washington 17
Helsinki 16
Hong Kong 16
Simi Valley 16
Trieste 16
Millbury 15
Hefei 14
Birmingham 13
Cape Town 13
Seoul 13
Busto Arsizio 12
Las Vegas 12
Shanghai 12
Buffalo 10
Hanoi 10
Jinan 10
San Diego 10
San Francisco 10
Stockholm 10
Toronto 10
Leeds 9
Nashville 9
Amsterdam 8
Augusta 8
Lappeenranta 8
Manchester 8
Monza 8
The Bronx 8
Tokyo 8
Andover 7
Berlin 7
Chengdu 7
Liverpool 7
Miami 7
Plantation 7
San Antonio 7
Bologna 6
Changchun 6
Totale 8.096
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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 673
Clinical–neurophysiological correlations in a series of patients with IgM-related neuropathy 318
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 298
Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: Pitfalls and tips in the diagnosis 275
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 259
Teaching neuroimages: Peroneal intraneural ganglion cyst: a rare cause of drop foot in a child. 201
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 193
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 193
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 185
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 176
Retinal detachment with an unusual shape. 165
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 162
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 159
Persistence of abnormal electrophysiological findings after carpal tunnel release 149
Distinctive clinical and neuroimaging characteristics of longitudinally extensive transverse myelitis associated with aquaporin-4 autoantibodies 142
Bilateral thalamic stroke transiently reduces arousals and NREM sleep instability. 135
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 130
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 129
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 127
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 124
Efficacy of lenalidomide plus dexamethasone for POEMS syndrome relapsed after autologous peripheral stem-cell transplantation 123
A Case of Hemiabdominal Myoclonus 119
Epstein-Barr virus antibodies in serum and cerebrospinal fluid from Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculoneuropathy and Amyotrophic Lateral 116
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 112
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience 111
Assessment of neurological manifestations in hospitalized patients with COVID-19 111
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 109
Mitochondrial neuropathy: considerations on pathogenesis 109
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 107
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 107
Restless leg syndrome in different types of demyelinating neuropathies: a single-center pilot study 106
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 105
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 103
Ultrasound evaluation in transthyretin-related amyloid neuropathy 102
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 101
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 100
A novel L67P SOD1 mutation in an Italian ALS patient. 99
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 95
Posterior interosseous nerve syndrome due to radioulnar joint cyst 95
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? 94
Clinical-neurophysiological correlations in a series of patients with IgM-related neuropathy 94
Vertebral artery dissection presenting with isolated occipital headache 93
Neurologic improvement after peripheral blood stem cell transplantation in poems 93
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 93
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 91
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 91
Usefulness of F-18 FDG PET/CT in the follow-up of POEMS syndrome after autologous peripheral blood stem cell transplantation 90
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 90
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 90
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience 90
Somatosensory Evoked Potentials of Inferior Alveolar Nerve: confirmation of a possible non-invasive neurophysiological approach 90
Mycosis fungoides as a cause of severe obstructive sleep apnea 89
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 89
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 88
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 88
Wernicke's encephalopathy following chronic diarrhoea 87
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 87
Teaching NeuroImage: MRI of diabetic lumbar plexopathy treated with local steroid injection. 85
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 85
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 85
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 84
Nerve ultrasound in CMT2E/CMT1F due to NEFL mutation: Confirmation of an axonal pathology 84
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 83
Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients 82
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 81
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 81
Teaching NeuroImages: Transient mutism associated with splenium lesion in capecitabine-induced leukoencephalopathy 81
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 81
HFE p.H63D polymorphism does not influence ALS phenotype and survival 79
Improvement of obstructive sleep apneas caused by hydrocephalus associated with Chiari malformation Type II following surgery. 78
Restless Legs Syndrome and lateralized periodic movements due to a spinal schwannoma 78
Sural nerve pathology in ALS patients: a single-centre experience 77
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 77
Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs. 75
Myasthenia gravis with presynaptic neurophysiological signs: Two case reports and literature review 75
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 74
Nerve ultrasound in patients with CMT1C: Description of three cases 74
Distinct lymphocytes subsets in IgM-related neuropathy: clinical-immunological correlations 74
ANCA-related vasculitic neuropathy mimicking motor neuron disease. 73
Benedictine hand of 'central' origin 73
Bilateral thoracic long nerve involvement in motor multifocal neuropathy 73
A Case of Hemiabdominal Myoclonus 73
Post-Encephalitic Parkinsonism and Sleep Disorder Responsive to Immunological Treatment: A Case Report 73
Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma. 72
A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease 72
Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity 71
Nerve conduction studies of the sural nerve: Normative data from a single-center experience 71
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 71
Ultrasound evaluation in transthyretin-related amyloid neuropathy 70
Oculopharyngeal muscular dystrophy: Clinical and neurophysiological features 70
An uncommon cause of headache resolution: spontaneous ventriculostomy in obstructive hydrocephalus 70
Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis: a Single-Centre Experience 70
Low rate repetitive nerve stimulation in Lambert-Eaton myasthenic syndrome: Peculiar characteristics of decremental pattern from a single-centre experience 69
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 69
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)) 68
A novel GJB1 mutation in an Italian patient with Charcot-Marie-Tooth disease and pyramidal signs 67
Lower motor neuron involvement in longitudinally extensive transverse myelitis with and without aquaporin-4 antibodies 67
Ultrasound visualization of nerve morphological alteration at the site of conduction block. 66
Teaching neuroimages: Peroneal intraneural ganglion cyst: a rare cause of drop foot in a child 66
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 66
Totale 11.063
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Categoria #
all - tutte 58.320
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 58.320
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.055 424 121 112 103 168 179 212 67 111 151 223 184
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
2024/202521 21 0 0 0 0 0 0 0 0 0 0 0
Totale 16.316