IRIS
GIANNINI, FABIO
 Distribuzione geografica
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Continente #
NA - Nord America 14.823
EU - Europa 10.654
AS - Asia 5.853
SA - Sud America 918
AF - Africa 315
OC - Oceania 30
Continente sconosciuto - Info sul continente non disponibili 17
Totale 32.610
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Nazione #
US - Stati Uniti d'America 14.664
GB - Regno Unito 2.704
CN - Cina 2.216
RU - Federazione Russa 2.089
SG - Singapore 1.783
IE - Irlanda 1.442
UA - Ucraina 841
SE - Svezia 834
IT - Italia 822
BR - Brasile 766
FR - Francia 618
DE - Germania 595
VN - Vietnam 508
HK - Hong Kong 464
FI - Finlandia 367
KR - Corea 257
ZA - Sudafrica 153
IN - India 138
TR - Turchia 127
CA - Canada 82
ES - Italia 73
NG - Nigeria 62
AR - Argentina 58
NL - Olanda 54
BD - Bangladesh 49
IQ - Iraq 48
MX - Messico 46
JP - Giappone 45
BE - Belgio 44
PL - Polonia 43
PK - Pakistan 36
SA - Arabia Saudita 27
CI - Costa d'Avorio 25
AU - Australia 24
AT - Austria 23
VE - Venezuela 22
EC - Ecuador 21
CZ - Repubblica Ceca 19
MA - Marocco 15
CL - Cile 14
ID - Indonesia 14
EG - Egitto 13
EU - Europa 13
JO - Giordania 13
AE - Emirati Arabi Uniti 12
CO - Colombia 12
NP - Nepal 12
AZ - Azerbaigian 11
LT - Lituania 11
UZ - Uzbekistan 11
IL - Israele 10
IR - Iran 10
PH - Filippine 10
KE - Kenya 9
PY - Paraguay 9
TN - Tunisia 9
PE - Perù 8
AL - Albania 7
DZ - Algeria 7
RO - Romania 7
RS - Serbia 7
UY - Uruguay 7
BG - Bulgaria 6
ET - Etiopia 6
GR - Grecia 6
KZ - Kazakistan 6
MY - Malesia 6
PT - Portogallo 6
JM - Giamaica 5
MK - Macedonia 5
NZ - Nuova Zelanda 5
OM - Oman 5
CH - Svizzera 4
DO - Repubblica Dominicana 4
EE - Estonia 4
GE - Georgia 4
MD - Moldavia 4
MM - Myanmar 4
NI - Nicaragua 4
AO - Angola 3
CR - Costa Rica 3
CY - Cipro 3
DK - Danimarca 3
GT - Guatemala 3
HR - Croazia 3
HU - Ungheria 3
KG - Kirghizistan 3
KW - Kuwait 3
LB - Libano 3
LU - Lussemburgo 3
PA - Panama 3
SN - Senegal 3
SY - Repubblica araba siriana 3
XK - ???statistics.table.value.countryCode.XK??? 3
HN - Honduras 2
KH - Cambogia 2
LK - Sri Lanka 2
PS - Palestinian Territory 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
Totale 32.581
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Città #
Southend 2.451
Dallas 1.967
Fairfield 1.565
Dublin 1.433
Ashburn 1.142
Singapore 963
Chandler 825
Woodbridge 686
Jacksonville 681
Seattle 638
Wilmington 603
Santa Clara 592
Moscow 570
Houston 566
Cambridge 547
Beijing 543
Menlo Park 503
Hong Kong 442
Ann Arbor 434
San Jose 354
Hefei 328
Siena 325
Princeton 304
The Dalles 254
Seoul 244
Nanjing 231
Los Angeles 205
New York 165
Helsinki 158
Lauterbourg 139
Johannesburg 138
Ho Chi Minh City 136
Hanoi 126
Boardman 123
Council Bluffs 112
Munich 110
Dearborn 101
Buffalo 95
Nanchang 88
Izmir 84
San Diego 83
San Mateo 64
Shanghai 61
Abuja 60
Shenyang 58
São Paulo 58
Orem 54
Dong Ket 51
Columbus 50
Málaga 47
Changsha 46
San Francisco 43
Tianjin 43
Frankfurt am Main 42
London 41
Norwalk 41
Hebei 40
Milan 40
Brussels 39
Tokyo 39
Turku 37
Jiaxing 35
Lappeenranta 35
Warsaw 35
Rome 33
Toronto 33
Chennai 32
Bengaluru 30
Kunming 29
Brooklyn 28
Florence 27
Redondo Beach 26
Abidjan 25
Baghdad 25
Denver 25
Jinan 25
Stockholm 25
Montreal 22
Nuremberg 22
Haiphong 21
Hangzhou 21
Amsterdam 20
Atlanta 20
Da Nang 20
Philadelphia 20
Zhengzhou 20
Guangzhou 19
Poplar 18
Washington 17
Chicago 16
Mexico City 16
Belo Horizonte 15
Brasília 15
Falls Church 15
Manchester 15
Mumbai 15
Ningbo 15
Porto Alegre 15
Redwood City 15
Rio de Janeiro 15
Totale 22.883
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Nome #
Neurological adverse events of ICI therapy: A ten-year comprehensive management from a multidisciplinary team 471
Eosinophilia-associated muscle disorders:an immunohistological study with tissue localisation of major basic protein in distinct clinicopathological forms 350
Antiangiogenic VEGF isoform in inflammatory myopathies 346
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients 339
Altered CSF protein pattern in a case of mycosis fungoides with nervous system involvement 334
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 323
Rhabdomyolysis in an elderly multitreated patient: multiple drug interactions after statin withdrawal 318
A new mutation in DNM2 gene in a large Italian family 316
Rare POMC Mutation in a Patient With Myotonic Dystrophy Type 1 and Adrenocorticotropin Hyperresponse to Corticotropin-Releasing Hormone 312
A case of amyloid myopathy in a patient with familial Mediterranean fever 309
Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomised, double blind, placebo controlled, phase III study 296
Colchicine myopathy and neuromyopathy: two cases with different characteristics 294
Novel CSN syndrome and ectodermal dysplasia 282
A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia 282
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 278
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD 276
Oxidative stress-induced apoptosis in peripheral blood lymphocytes from patients with POLG-related disorders 275
Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients 273
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis 269
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 267
A new clinical scale of carpal tunnel syndrome: validation of the measurement and clinical-neurophysiological assessment 265
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population 261
Italian multicentre study of peroneal mononeuropathy: Multiperspective follow-up 259
No association of MTHFR c.677C>T variant with sporadic ALS in an Italian population 259
G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype 253
Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsies. 253
ANALYSIS OF THE HYPOXIA-RESPONSE ELEMENT OF THE VASCULAR ENDOTHELIAL GROWTH FACTOR PROMOTER IN SPORADIC ALS PATIENTS 249
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 247
Diagnostic specificity of sensory and motor nerve conduction variables in early detection of carpal tunnel syndrome 246
Recurrent Miller Fisher syndrome in children 245
Polysomnographic characterization of pergolide-induced sleep attacks in idiopathic PD. 244
Association of extrahepatic manifestations with HLA class II alleles and with virus genotype in HCV infected patients 242
Genetic architecture of ALS in Sardinia 241
PEG placement in patients with ALS 241
Trigeminal-Nociceptive Activation And Pupillary Changes In Two Patients With Wernicke’s Encephalopathy 241
A new clinical scale to grade the impairment of median nerve in carpal tunnel syndrome 239
Aperiodic alternating nystagmus: report of two cases and treatment by baclofen 238
'NEUROPHYSIOLOGICAL STUDY OF ANTERIOR THORACIC WALL MUSCLES AFTER MODIFIED RADICAL MASTECTOMY 238
Major motor-functional determinants associated with poor self-reported health-related quality of life in myasthenia gravis patients 234
Diagnosis of thoracic outlet syndrome. Relative value of electrophysiological studies 231
Multifocal neural conduction impairment in forestry workers exposed and not exposed to vibration 231
Clinical evidence of fluconazole-induced carbamazepine toxicity 231
Hereditary neuronal intranuclear inclusion disease with autonomic failure and cerebellar degeneration. 231
CAT and MRI in the study of partial epilepsy: comparison of the 2 methods and correlations with EEG [TAC e RMN nello studio delle epilessie parziali: confronto tra le due metodiche e correlazioni con l'EEG] 229
Carpal tunnel syndrome incidence in a general population 228
Exome sequencing reveals VCP mutations as a cause of familial ALS. 228
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis 226
A novel exon 1 mutation (G10R) in the SOD1 gene in a patient with familial ALS 222
An electromyographic evaluation of motor complications in thoracic herpes zoster 222
Frequency and time to relapse after discontinuing 6-month therapy with IVIg or pulsed methylprednisolone in CIDP 222
Genotype–phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation 221
Jitter of corticospinal neurons during repetitive transcranial magnetic stimulation. Method and possible clinical implications 220
Clinical Features and Outcome of the Guillain–Barre Syndrome: A Single-Center 11-Year Experience 219
Electrodiagnosis in cranial botulism 219
Wernicke Encephalopathy After Gastrointestinal Surgery for Cancer: Causes of Diagnostic Failure or Delay. 219
Endothelins and endothelin receptors in vascultic neuropathies 217
Analysis of regulatory regions of macrophage migration inhibitory factor (MIF) gene in Italian ALS patients 215
D90A-SOD1 mutation in ALS: The first report of heterozigous Italian patients and unusual findings 215
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 214
A novel SOD1 gene mutation in a familial ALS patient 213
Activity of protein phosphatase calcineurin is decreased in sporadic and familial amyotrophic lateral sclerosis patients 213
A self-administered questionnaire of ulnar neuropathy at the elbow 211
Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years 207
Lack of association of PON polymorphisms with sporadic ALS in an Italian population 205
A novel variant in superoxide dismutase 1 gene (P.V119M) in als patients with pure lower motor neuron presentation 202
FUS mutations in sporadic amyotrophic lateral sclerosis 200
Maps of somatosensory evoked potentials from the arm in patients with neoplasms and post-traumatic brain lesions [Mappe dei potenziali evocati somatosensoriali (PES) dall'arto superiore in pazienti affetti da neoplasia e lesioni post-traumatiche cerebrali] 200
Thalidomide-induced neuropathy: a ganglionopathy? 199
Differences between surface EMG in male and female subjects evidenced by automatic analysis 199
Wernicke Syndrome: Seven case reports. 196
Abdominal weakness following herpes zoster 195
Treatment for ulnar neuropathy at the elbow 195
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis 194
The MITOS system predicts long-term survival in amyotrophic lateral sclerosis 192
Sensory neural conduction of median nerve from digits and palm stimulation in carpal tunnel syndrome 190
Italian multicentre study of peroneal mononeuropathy at the fibular head: study design and preliminary results 189
Brain-stem compression in vertebrobasilar dolichoectasia. A multimodal electrophysiological study 188
Relationship between thresholds detection of vibratory sensation and sensory nerve electrophysiology 188
Cervical and scalp recorded short latency somatosensory evoked potentials in response to epidural spinal cord stimulation in patients with peripheral vascular disease 187
Treatment for ulnar neuropathy at the elbow 185
Ulnar neuropathy at the elbow: how frequent is the idiopathic form? An ultrasonographic study in a cohort of patients. 185
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation 185
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 184
Functioning and quality of life in patients with neuropathy associated with anti-MAG antibodies 184
Incidence of ulnar neuropathy at the elbow in the province of Siena (Italy) 182
Ultrasonographic and electrophysiological findings of NF1-associated diffuse polyneuropathy. Case report 182
Protein misfolding, amyotrophic lateral sclerosis and guanabenz: Protocol for a phase II RCT with futility design (ProMISe trial) 182
BDNF and Pro-BDNF in Amyotrophic Lateral Sclerosis: A New Perspective for Biomarkers of Neurodegeneration 181
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 181
Wernicke's encelophaty after gastro-intestinal surgery for cancer: a retrospective clinical study 181
Rituximab in patients with chronic inflammatory demyelinating polyradiculoneuropathy: a report of 13 cases and review of the literature 181
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population 180
Effects of immunotherapy on motor cortex excitability in Stiff Person Syndrome 179
Role of neurophysiological assessment of pectoralis major musce after Pateyand Madden's radical mmastectomy 178
CT and MRI of Wernicke's encephalopathy 177
C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten 177
Paraoxonase gene polymorphisms and susceptibility to sporadic ALS in Italian population. Preliminary results. 175
Next-generation sequencing approach to hyperCKemia: A 2-year cohort study 174
Anti-MAG IgM: differences in antibody tests and correlation with clinical findings 174
Macro-EMG and MUNE changes in patients with amyotrophic lateral sclerosis: one-year follow up 173
Totale 23.108
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Categoria #
all - tutte 94.025
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 94.025
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021663 0 0 0 0 0 0 0 0 0 238 230 195
2021/20222.134 136 258 105 243 91 68 116 80 106 226 227 478
2022/20232.994 193 239 389 424 321 600 57 238 311 69 99 54
2023/20242.160 88 50 171 147 52 608 750 51 6 71 24 142
2024/20253.917 88 229 360 217 522 194 66 202 382 158 456 1.043
2025/20269.728 816 1.546 1.657 1.041 1.920 412 1.135 318 393 490 0 0
Totale 32.884