IRIS
PELUSO, SILVIO
 Distribuzione geografica
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Continente #
NA - Nord America 1.252
EU - Europa 461
AS - Asia 316
AF - Africa 31
SA - Sud America 1
Totale 2.061
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Nazione #
US - Stati Uniti d'America 1.223
IT - Italia 252
CN - Cina 146
SG - Singapore 137
NL - Olanda 86
IE - Irlanda 31
FI - Finlandia 29
CA - Canada 28
DE - Germania 28
CI - Costa d'Avorio 26
IN - India 14
VN - Vietnam 12
FR - Francia 8
GB - Regno Unito 6
UA - Ucraina 6
ZA - Sudafrica 5
JP - Giappone 4
IR - Iran 3
SE - Svezia 3
BE - Belgio 2
ES - Italia 2
GR - Grecia 2
BG - Bulgaria 1
BZ - Belize 1
CH - Svizzera 1
CO - Colombia 1
DK - Danimarca 1
RO - Romania 1
RS - Serbia 1
SI - Slovenia 1
Totale 2.061
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Città #
Chandler 314
Singapore 115
Ashburn 110
Amsterdam 82
Millbury 55
Beijing 52
Santa Clara 39
Princeton 38
Nanjing 37
Des Moines 36
Naples 31
Napoli 29
Seattle 28
Ottawa 27
Boston 22
Lawrence 15
Dallas 14
Dong Ket 12
Pune 12
Washington 12
San Jose 11
Hebei 10
Norwalk 10
San Mateo 10
Helsinki 9
Houston 9
Jacksonville 8
Jiaxing 8
Nanchang 8
Nola 8
Wilmington 8
Redwood City 7
Shenyang 7
Changsha 6
Dearborn 6
Los Angeles 6
Paris 6
Dublin 5
Munich 5
Augusta 4
Campagna 4
Guangzhou 4
Milan 4
Portici 4
Rome 4
Telese 4
Torre Annunziata 4
Ardabil 3
Buffalo 3
Böblingen 3
Cape Town 3
Genoa 3
Kronberg 3
Leawood 3
Nuremberg 3
Poli 3
Saint Louis 3
Atlanta 2
Caserta 2
Chengdu 2
Davis 2
Las Vegas 2
León 2
Marsala 2
Monmouth Junction 2
Mugnano Di Napoli 2
Muizenberg 2
New York 2
Sacile 2
Sciacca 2
Simi Valley 2
Tianjin 2
Torre Del Greco 2
Waanrode 2
Woodbridge 2
Acerra 1
Adelfia 1
Albuquerque 1
Ann Arbor 1
Belgrade 1
Belize City 1
Boardman 1
Castellana Grotte 1
Cerro Maggiore 1
Chicago 1
Columbus 1
Costa Mesa 1
Decatur 1
Esslingen am Neckar 1
Ferrara 1
Florence 1
Fuzhou 1
Hamm 1
Horia 1
Kunming 1
Lanzhou 1
Lappeenranta 1
Ljubljana 1
London 1
Lviv 1
Totale 1.350
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Nome #
DNA damage signatures in peripheral blood cells as biomarkers in prodromal huntington disease 74
Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study 73
SPG5 and multiple sclerosis: clinical and genetic overlap? 63
Cognitive decline in Huntington's disease expansion gene carriers 62
Parkinsonism in adult-onset Rasmussens's encephalitis: a clinical picture presenting as corticobasal syndrome 60
Pathological laughter as onset symptom in atypical parkinsonisms 58
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study 54
Cervical dystonia patients display subclinical gait changes 53
Emotion Recognition and Psychological Comorbidity in Friedreich’s Ataxia 53
Application of the p9NORM correction method to timed neuropsychological tests in Parkinson's disease and multiple system atrophy. 53
Closing-in Phenomenon in Huntington's Disease: A Neuropsychological Marker of Frontal/Executive Dysfunction 52
Frontal defect contribution to decreasing of body mass index in Parkinson's disease patients 49
Autonomic disorders and myocardial 123I-metaiodobenzylguanidine scintigraphy in Huntington's disease 49
Chorea-acanthocytosis without chorea: Expanding the clinical phenotype 48
Perseverative Behavior on Verbal Fluency Task in Patients with Huntington's Disease: a Retrospective Study on a Large Patient Sample 48
The Treatment of Hypersalivation in Rett Syndrome with Botulinum Toxin: Efficacy and Clinical Implications 47
Complex phenotype in an Italian family with a novel mutation in SPG3A. 46
Predictors of survival in spinocerebellar ataxia type 2 population from Southern Italy. 45
A case of restless leg syndrome in a family with LRRK2 gene mutation. 44
Myocardial (123)I-metaiodobenzylguanidine scintigraphy in patients with homozygous and heterozygous parkin mutations 44
Peripheral markers of autophagy in polyglutamine diseases 44
Adult normative values for the PATA Rate Test 44
Cognitive profile and 18F-fluorodeoxyglucose PET study in LRRK2-related Parkinson's disease 43
Benign hereditary chorea: clinical and neuroimaging features in an Italian family. 43
Be aware of Wolfram syndrome when examining ataxic patients 43
The flavor test is a sensitive tool in identifying the flavor sensorineural dysfunction in Parkinson's disease 43
Antiphospholipid-related chorea. 42
Screening for dopa-responsive dystonia in patients with scans without evidence of dopaminergic deficiency (SWEDD). 42
Spatial and egocentric mental rotation in patients with cervical dystonia 40
CCM3/PDCD10 gene mutation in cerebral cavernous malformations associated with hyperkeratotic cutaneous capillary venous malformations 40
Disruption of GABA(A)-mediated intracortical inhibition in patients with chorea-acanthocytosis 40
Pseudo-orthostatic tremor: description of a not typical case 40
Animal-Assisted Therapy in Elderly Patients: Evidence and Controversies in Dementia and Psychiatric Disorders and Future Perspectives in Other Neurological Diseases 40
Friedreich ataxia: 150 years of bench and bedside studies 36
Efficacy of dopamine agonist treatment in delayed-onset parkinsonism due to midbrain hemorrhage. 35
Does motor cortex plasticity depend on the type of mutation in the leucine-rich repeat kinase 2 gene? 35
The magnetic apraxia of Denny-Brown 34
Constructional Apraxia is related to Different Cognitive Defect's across Dementia 32
Cognitive correlates of prospective memory in dystonia 31
Parkinsonism in a pair of monozygotic CADASIL twins sharing the R1006C mutation: a transcranial sonography study 31
Reversible valproate-induced subacute encephalopathy associated with a MT-ATP8 variant in the mitochondrial genome 30
Metabolic Ataxias in Adults. 29
The Multiple Faces of Spinocerebellar Ataxia type 2 29
Jaw-Opening Oromandibular Dystonia Associated With Spinocerebellar Ataxia Type 2 29
The occurrence of lateral shift in cervical dystonia 29
Using global team science to identify genetic parkinson's disease worldwide 27
A Novel PSEN1 Mutation in a Patient with Sporadic Early-Onset Alzheimer's Disease and Prominent Cerebellar Ataxia. 25
Infusion treatments and deep brain stimulation in Parkinson's Disease: The role of nursing 25
Correction to: Peripheral markers of autophagy in polyglutamine diseases (Neurological Sciences, (2018), 39, 1, (149-152), 10.1007/s10072-017-3156-6) 25
Clinical manifestations of intermediate allele carriers in Huntington disease 25
The cerebellum in idiopathic cervical dystonia: A specific pattern of structural abnormalities? 22
Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement 18
Unusual white matter involvement in EAST syndrome associated with novel KCNJ10 mutations 15
Personality traits associated with blepharospasm: A comparison with healthy subjects, patients with facial hemispasm and patients with hyperhidrosis 14
Totale 2.195
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Categoria #
all - tutte 10.156
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 10.156
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020123 0 0 0 0 8 3 16 5 4 42 36 9
2020/2021131 12 2 7 9 9 5 9 19 12 3 29 15
2021/2022318 4 6 1 3 4 3 8 8 31 38 86 126
2022/2023663 68 65 31 64 82 76 1 54 108 83 24 7
2023/2024370 21 50 30 37 24 56 7 76 3 5 46 15
2024/2025211 68 34 11 14 84 0 0 0 0 0 0 0
Totale 2.195