Luigetti, Marco
 Distribuzione geografica
Continente #
NA - Nord America 7.405
EU - Europa 7.365
AS - Asia 2.232
AF - Africa 82
SA - Sud America 24
OC - Oceania 15
Continente sconosciuto - Info sul continente non disponibili 8
Totale 17.131
Nazione #
US - Stati Uniti d'America 7.315
DE - Germania 3.023
SE - Svezia 1.109
CN - Cina 974
UA - Ucraina 688
SG - Singapore 659
IT - Italia 618
IE - Irlanda 380
GB - Regno Unito 367
FR - Francia 352
PL - Polonia 257
ID - Indonesia 224
FI - Finlandia 193
IN - India 147
RU - Federazione Russa 143
BE - Belgio 86
CA - Canada 85
TR - Turchia 80
NL - Olanda 50
CI - Costa d'Avorio 45
JP - Giappone 36
ZA - Sudafrica 34
HK - Hong Kong 20
IR - Iran 19
RO - Romania 17
AU - Australia 15
CH - Svizzera 15
ES - Italia 15
KR - Corea 15
VN - Vietnam 14
BR - Brasile 11
PH - Filippine 10
AT - Austria 8
AE - Emirati Arabi Uniti 6
PT - Portogallo 6
TH - Thailandia 6
A2 - ???statistics.table.value.countryCode.A2??? 5
CZ - Repubblica Ceca 5
DK - Danimarca 5
CO - Colombia 4
HR - Croazia 4
IL - Israele 4
LT - Lituania 4
NO - Norvegia 4
AR - Argentina 3
CL - Cile 3
EU - Europa 3
MD - Moldavia 3
SI - Slovenia 3
SK - Slovacchia (Repubblica Slovacca) 3
BD - Bangladesh 2
GR - Grecia 2
JO - Giordania 2
KZ - Kazakistan 2
LK - Sri Lanka 2
MX - Messico 2
PK - Pakistan 2
PR - Porto Rico 2
SA - Arabia Saudita 2
AL - Albania 1
BO - Bolivia 1
BZ - Belize 1
DZ - Algeria 1
EC - Ecuador 1
EG - Egitto 1
HU - Ungheria 1
KG - Kirghizistan 1
LA - Repubblica Popolare Democratica del Laos 1
LU - Lussemburgo 1
LV - Lettonia 1
MA - Marocco 1
MC - Monaco 1
MM - Myanmar 1
MY - Malesia 1
OM - Oman 1
PE - Perù 1
TW - Taiwan 1
Totale 17.131
Città #
Chandler 1.414
Ashburn 539
Singapore 493
Redmond 404
Dublin 371
Jacksonville 339
San Mateo 333
Ann Arbor 303
New York 276
Nanjing 240
Nürnberg 231
Jakarta 223
Wilmington 197
Warsaw 194
Boston 157
Woodbridge 151
Dearborn 128
Moscow 115
Houston 114
Lawrence 112
Milan 99
Nanchang 99
Beijing 90
Seattle 89
Redwood City 87
Cattolica 82
Rome 81
Fairfield 79
Princeton 73
Marseille 72
Munich 70
Brussels 68
Chicago 67
Bremen 66
Izmir 66
Detroit 61
Kraków 57
Norwalk 56
Shenyang 49
Boardman 46
Helsinki 46
Abidjan 45
Hebei 45
Changsha 41
Los Angeles 40
Guangzhou 34
Leawood 34
Jiaxing 33
Ottawa 33
Kunming 30
University Park 29
London 27
Hangzhou 26
Zhengzhou 26
Mountain View 25
Pune 25
Cambridge 24
Phoenix 22
Tianjin 22
Fremont 21
Philadelphia 21
Hong Kong 18
Lancaster 18
Waanrode 18
Auburn Hills 17
Washington 17
Santa Clara 16
Shanghai 16
Simi Valley 16
Toronto 16
Trieste 16
Hefei 15
Millbury 15
Cape Town 14
Birmingham 13
Falkenstein 13
Seoul 13
Busto Arsizio 12
Las Vegas 12
Paris 11
Stockholm 11
Buffalo 10
Hanoi 10
Jinan 10
San Diego 10
San Francisco 10
Chengdu 9
Florence 9
Leeds 9
Nashville 9
Nuremberg 9
Amsterdam 8
Augusta 8
Frankfurt am Main 8
Lappeenranta 8
Manchester 8
Monza 8
The Bronx 8
Tokyo 8
Andover 7
Totale 8.903
Nome #
Real-life experience with inotersen in hereditary transthyretin amyloidosis with late-onset phenotype: Data from an early-access program in Italy 678
Clinical–neurophysiological correlations in a series of patients with IgM-related neuropathy 323
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 304
Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: Pitfalls and tips in the diagnosis 282
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 264
Teaching neuroimages: Peroneal intraneural ganglion cyst: a rare cause of drop foot in a child. 207
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 199
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 198
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 193
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 182
Retinal detachment with an unusual shape. 168
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 166
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 163
Persistence of abnormal electrophysiological findings after carpal tunnel release 156
Distinctive clinical and neuroimaging characteristics of longitudinally extensive transverse myelitis associated with aquaporin-4 autoantibodies 148
Bilateral thalamic stroke transiently reduces arousals and NREM sleep instability. 141
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 137
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 135
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 132
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 130
Efficacy of lenalidomide plus dexamethasone for POEMS syndrome relapsed after autologous peripheral stem-cell transplantation 129
A Case of Hemiabdominal Myoclonus 125
Epstein-Barr virus antibodies in serum and cerebrospinal fluid from Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculoneuropathy and Amyotrophic Lateral 120
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience 119
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 117
Assessment of neurological manifestations in hospitalized patients with COVID-19 117
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 116
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 114
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 114
Mitochondrial neuropathy: considerations on pathogenesis 114
Restless leg syndrome in different types of demyelinating neuropathies: a single-center pilot study 110
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 108
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 107
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 107
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 105
Ultrasound evaluation in transthyretin-related amyloid neuropathy 105
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? 104
A novel L67P SOD1 mutation in an Italian ALS patient. 103
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 102
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 101
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 100
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 100
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 99
Neurologic improvement after peripheral blood stem cell transplantation in poems 99
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 98
Clinical-neurophysiological correlations in a series of patients with IgM-related neuropathy 98
Posterior interosseous nerve syndrome due to radioulnar joint cyst 98
Usefulness of F-18 FDG PET/CT in the follow-up of POEMS syndrome after autologous peripheral blood stem cell transplantation 97
Vertebral artery dissection presenting with isolated occipital headache 97
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience 97
Somatosensory Evoked Potentials of Inferior Alveolar Nerve: confirmation of a possible non-invasive neurophysiological approach 96
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 95
Mycosis fungoides as a cause of severe obstructive sleep apnea 94
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 93
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 93
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 93
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 92
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 91
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 91
Wernicke's encephalopathy following chronic diarrhoea 91
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 91
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 90
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 89
Teaching NeuroImage: MRI of diabetic lumbar plexopathy treated with local steroid injection. 89
Teaching NeuroImages: Transient mutism associated with splenium lesion in capecitabine-induced leukoencephalopathy 87
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 86
Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients 86
Nerve ultrasound in CMT2E/CMT1F due to NEFL mutation: Confirmation of an axonal pathology 86
HFE p.H63D polymorphism does not influence ALS phenotype and survival 85
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 84
Restless Legs Syndrome and lateralized periodic movements due to a spinal schwannoma 84
Sural nerve pathology in ALS patients: a single-centre experience 83
Distinct lymphocytes subsets in IgM-related neuropathy: clinical-immunological correlations 83
Improvement of obstructive sleep apneas caused by hydrocephalus associated with Chiari malformation Type II following surgery. 80
A Case of Hemiabdominal Myoclonus 80
Myasthenia gravis with presynaptic neurophysiological signs: Two case reports and literature review 80
Post-Encephalitic Parkinsonism and Sleep Disorder Responsive to Immunological Treatment: A Case Report 80
ANCA-related vasculitic neuropathy mimicking motor neuron disease. 79
Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs. 79
Nerve conduction studies of the sural nerve: Normative data from a single-center experience 78
Benedictine hand of 'central' origin 78
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 77
Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma. 77
Bilateral thoracic long nerve involvement in motor multifocal neuropathy 77
An uncommon cause of headache resolution: spontaneous ventriculostomy in obstructive hydrocephalus 77
Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity 76
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 76
Nerve ultrasound in patients with CMT1C: Description of three cases 75
Gadolinium enhancement of the lumbar leptomeninges and roots in a case of ALS 74
Low rate repetitive nerve stimulation in Lambert-Eaton myasthenic syndrome: Peculiar characteristics of decremental pattern from a single-centre experience 74
A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease 74
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 74
Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis: a Single-Centre Experience 74
Oculopharyngeal muscular dystrophy: Clinical and neurophysiological features 73
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 73
A novel GJB1 mutation in an Italian patient with Charcot-Marie-Tooth disease and pyramidal signs 72
Ultrasound evaluation in transthyretin-related amyloid neuropathy 72
Sjögren's syndrome presenting with isolated sensory axonal polyneuropathy 72
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)) 72
Post-Encephalitic Parkinsonism and Sleep Disorder Responsive to Immunological Treatment: A Case Report 72
Totale 11.623
Categoria #
all - tutte 72.912
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 72.912


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020948 0 0 0 0 0 0 212 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
2024/20251.189 99 126 321 192 257 115 79 0 0 0 0 0
Totale 17.484