IRIS
GIANNINI, FABIO
 Distribuzione geografica
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Continente #
NA - Nord America 15.373
EU - Europa 11.299
AS - Asia 5.941
SA - Sud America 933
AF - Africa 315
OC - Oceania 31
Continente sconosciuto - Info sul continente non disponibili 17
Totale 33.909
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Nazione #
US - Stati Uniti d'America 15.187
GB - Regno Unito 2.706
CN - Cina 2.230
RU - Federazione Russa 2.090
SG - Singapore 1.797
IT - Italia 1.448
IE - Irlanda 1.442
UA - Ucraina 841
SE - Svezia 837
BR - Brasile 775
FR - Francia 619
DE - Germania 595
VN - Vietnam 509
HK - Hong Kong 466
FI - Finlandia 367
KR - Corea 257
ZA - Sudafrica 153
IN - India 139
TR - Turchia 127
BD - Bangladesh 100
CA - Canada 98
ES - Italia 76
NG - Nigeria 62
AR - Argentina 60
NL - Olanda 60
MX - Messico 50
IQ - Iraq 48
BE - Belgio 45
JP - Giappone 45
PL - Polonia 43
PK - Pakistan 36
SA - Arabia Saudita 27
AU - Australia 25
CI - Costa d'Avorio 25
AT - Austria 23
EC - Ecuador 23
VE - Venezuela 23
CZ - Repubblica Ceca 19
ID - Indonesia 15
MA - Marocco 15
CL - Cile 14
CO - Colombia 13
EG - Egitto 13
EU - Europa 13
JO - Giordania 13
AE - Emirati Arabi Uniti 12
LT - Lituania 12
NP - Nepal 12
AZ - Azerbaigian 11
UZ - Uzbekistan 11
IL - Israele 10
IR - Iran 10
PH - Filippine 10
KE - Kenya 9
PY - Paraguay 9
TN - Tunisia 9
MY - Malesia 8
PE - Perù 8
AL - Albania 7
BG - Bulgaria 7
DZ - Algeria 7
RO - Romania 7
RS - Serbia 7
UY - Uruguay 7
ET - Etiopia 6
GR - Grecia 6
JM - Giamaica 6
KZ - Kazakistan 6
PT - Portogallo 6
MK - Macedonia 5
NZ - Nuova Zelanda 5
OM - Oman 5
CH - Svizzera 4
CR - Costa Rica 4
DO - Repubblica Dominicana 4
EE - Estonia 4
GE - Georgia 4
MD - Moldavia 4
MM - Myanmar 4
NI - Nicaragua 4
TH - Thailandia 4
AO - Angola 3
CY - Cipro 3
DK - Danimarca 3
GT - Guatemala 3
HN - Honduras 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
SV - El Salvador 3
SY - Repubblica araba siriana 3
XK - ???statistics.table.value.countryCode.XK??? 3
KH - Cambogia 2
LK - Sri Lanka 2
PR - Porto Rico 2
Totale 33.877
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Città #
Southend 2.451
Dallas 1.972
Fairfield 1.565
Dublin 1.433
Ashburn 1.185
Singapore 969
Chandler 825
Woodbridge 686
Jacksonville 682
Seattle 639
Santa Clara 614
Wilmington 603
Moscow 570
Houston 567
Cambridge 547
Beijing 544
Menlo Park 503
San Jose 499
Hong Kong 443
Ann Arbor 434
Milan 374
Hefei 328
Siena 325
Princeton 304
The Dalles 257
Seoul 244
Nanjing 231
Los Angeles 206
Council Bluffs 193
New York 185
Helsinki 158
Lauterbourg 139
Johannesburg 138
Ho Chi Minh City 137
Hanoi 126
Boardman 123
Rome 123
Munich 110
Dearborn 101
Buffalo 97
Nanchang 88
Izmir 84
San Diego 83
San Mateo 64
Shanghai 63
Abuja 60
São Paulo 59
Shenyang 58
Orem 54
Dong Ket 51
Columbus 50
Changsha 47
Málaga 47
San Francisco 44
Tianjin 43
Frankfurt am Main 42
London 41
Norwalk 41
Brussels 40
Figino 40
Hebei 40
Tokyo 39
Turku 37
Toronto 36
Jiaxing 35
Lappeenranta 35
Warsaw 35
Chennai 32
Florence 32
Bengaluru 30
Brooklyn 29
Kunming 29
Denver 26
Redondo Beach 26
Abidjan 25
Baghdad 25
Jinan 25
Stockholm 25
Atlanta 24
Turin 24
Montreal 23
Philadelphia 23
Amsterdam 22
Hangzhou 22
Nuremberg 22
Chicago 21
Haiphong 21
Da Nang 20
Zhengzhou 20
Guangzhou 19
Mexico City 18
Poplar 18
Washington 17
Manchester 16
Belo Horizonte 15
Brasília 15
Falls Church 15
Mumbai 15
Ningbo 15
Porto Alegre 15
Totale 23.710
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Nome #
Neurological adverse events of ICI therapy: A ten-year comprehensive management from a multidisciplinary team 504
Antiangiogenic VEGF isoform in inflammatory myopathies 364
Eosinophilia-associated muscle disorders:an immunohistological study with tissue localisation of major basic protein in distinct clinicopathological forms 362
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients 345
Altered CSF protein pattern in a case of mycosis fungoides with nervous system involvement 341
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 333
Rhabdomyolysis in an elderly multitreated patient: multiple drug interactions after statin withdrawal 328
A new mutation in DNM2 gene in a large Italian family 325
Rare POMC Mutation in a Patient With Myotonic Dystrophy Type 1 and Adrenocorticotropin Hyperresponse to Corticotropin-Releasing Hormone 321
A case of amyloid myopathy in a patient with familial Mediterranean fever 320
Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomised, double blind, placebo controlled, phase III study 308
Colchicine myopathy and neuromyopathy: two cases with different characteristics 306
A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia 292
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 287
Novel CSN syndrome and ectodermal dysplasia 287
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD 285
Oxidative stress-induced apoptosis in peripheral blood lymphocytes from patients with POLG-related disorders 281
Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients 280
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis 275
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 274
A new clinical scale of carpal tunnel syndrome: validation of the measurement and clinical-neurophysiological assessment 272
No association of MTHFR c.677C>T variant with sporadic ALS in an Italian population 268
Major motor-functional determinants associated with poor self-reported health-related quality of life in myasthenia gravis patients 268
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population 265
G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype 263
Italian multicentre study of peroneal mononeuropathy: Multiperspective follow-up 261
Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsies. 260
ANALYSIS OF THE HYPOXIA-RESPONSE ELEMENT OF THE VASCULAR ENDOTHELIAL GROWTH FACTOR PROMOTER IN SPORADIC ALS PATIENTS 257
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 256
Recurrent Miller Fisher syndrome in children 253
Diagnostic specificity of sensory and motor nerve conduction variables in early detection of carpal tunnel syndrome 252
Polysomnographic characterization of pergolide-induced sleep attacks in idiopathic PD. 252
Aperiodic alternating nystagmus: report of two cases and treatment by baclofen 252
Association of extrahepatic manifestations with HLA class II alleles and with virus genotype in HCV infected patients 251
PEG placement in patients with ALS 250
Genetic architecture of ALS in Sardinia 248
'NEUROPHYSIOLOGICAL STUDY OF ANTERIOR THORACIC WALL MUSCLES AFTER MODIFIED RADICAL MASTECTOMY 248
Trigeminal-Nociceptive Activation And Pupillary Changes In Two Patients With Wernicke’s Encephalopathy 246
Hereditary neuronal intranuclear inclusion disease with autonomic failure and cerebellar degeneration. 242
A new clinical scale to grade the impairment of median nerve in carpal tunnel syndrome 241
Multifocal neural conduction impairment in forestry workers exposed and not exposed to vibration 240
Carpal tunnel syndrome incidence in a general population 236
Clinical evidence of fluconazole-induced carbamazepine toxicity 236
Protein misfolding, amyotrophic lateral sclerosis and guanabenz: Protocol for a phase II RCT with futility design (ProMISe trial) 236
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] 235
Diagnosis of thoracic outlet syndrome. Relative value of electrophysiological studies 234
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis 233
Exome sequencing reveals VCP mutations as a cause of familial ALS. 232
Wernicke Encephalopathy After Gastrointestinal Surgery for Cancer: Causes of Diagnostic Failure or Delay. 230
Jitter of corticospinal neurons during repetitive transcranial magnetic stimulation. Method and possible clinical implications 229
Genotype–phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation 229
A novel exon 1 mutation (G10R) in the SOD1 gene in a patient with familial ALS 228
An electromyographic evaluation of motor complications in thoracic herpes zoster 228
Endothelins and endothelin receptors in vascultic neuropathies 227
Analysis of regulatory regions of macrophage migration inhibitory factor (MIF) gene in Italian ALS patients 227
Frequency and time to relapse after discontinuing 6-month therapy with IVIg or pulsed methylprednisolone in CIDP 226
D90A-SOD1 mutation in ALS: The first report of heterozigous Italian patients and unusual findings 225
Clinical Features and Outcome of the Guillain–Barre Syndrome: A Single-Center 11-Year Experience 223
Electrodiagnosis in cranial botulism 223
Lack of association of PON polymorphisms with sporadic ALS in an Italian population 217
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 217
A self-administered questionnaire of ulnar neuropathy at the elbow 216
Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years 216
A novel SOD1 gene mutation in a familial ALS patient 215
Activity of protein phosphatase calcineurin is decreased in sporadic and familial amyotrophic lateral sclerosis patients 215
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis 211
A novel variant in superoxide dismutase 1 gene (P.V119M) in als patients with pure lower motor neuron presentation 208
Differences between surface EMG in male and female subjects evidenced by automatic analysis 207
FUS mutations in sporadic amyotrophic lateral sclerosis 203
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] 203
Treatment for ulnar neuropathy at the elbow 202
Wernicke Syndrome: Seven case reports. 201
Abdominal weakness following herpes zoster 200
Thalidomide-induced neuropathy: a ganglionopathy? 200
The MITOS system predicts long-term survival in amyotrophic lateral sclerosis 200
Relationship between thresholds detection of vibratory sensation and sensory nerve electrophysiology 197
BDNF and Pro-BDNF in Amyotrophic Lateral Sclerosis: A New Perspective for Biomarkers of Neurodegeneration 195
Sensory neural conduction of median nerve from digits and palm stimulation in carpal tunnel syndrome 195
Cervical and scalp recorded short latency somatosensory evoked potentials in response to epidural spinal cord stimulation in patients with peripheral vascular disease 195
Ulnar neuropathy at the elbow: how frequent is the idiopathic form? An ultrasonographic study in a cohort of patients. 193
Italian multicentre study of peroneal mononeuropathy at the fibular head: study design and preliminary results 193
Brain-stem compression in vertebrobasilar dolichoectasia. A multimodal electrophysiological study 191
Functioning and quality of life in patients with neuropathy associated with anti-MAG antibodies 191
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 190
Wernicke's encelophaty after gastro-intestinal surgery for cancer: a retrospective clinical study 189
Incidence of ulnar neuropathy at the elbow in the province of Siena (Italy) 188
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population 188
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 188
Treatment for ulnar neuropathy at the elbow 188
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation 188
Rituximab in patients with chronic inflammatory demyelinating polyradiculoneuropathy: a report of 13 cases and review of the literature 188
SOD1 GENE MUTATIONS IN AMYOTROPHIC LATERAL SCLEROSIS: A RETROSPECTIVE ITALIAN STUDY 185
Next-generation sequencing approach to hyperCKemia: A 2-year cohort study 185
Role of neurophysiological assessment of pectoralis major musce after Pateyand Madden's radical mmastectomy 183
Ultrasonographic and electrophysiological findings of NF1-associated diffuse polyneuropathy. Case report 183
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72 183
C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten 183
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data 182
Effects of immunotherapy on motor cortex excitability in Stiff Person Syndrome 182
Toxic polyneuropathy of shoe workers in Italy. A clinical, neurophysiological and follow-up study 181
Totale 23.935
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Categoria #
all - tutte 99.500
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 99.500
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/202610.827 816 1.546 1.657 1.041 1.920 412 1.135 318 393 545 221 823
2026/2027200 200 0 0 0 0 0 0 0 0 0 0 0
Totale 34.183