IRIS
PELUSO, SILVIO
 Distribuzione geografica
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Continente #
NA - Nord America 1.149
EU - Europa 431
AS - Asia 175
AF - Africa 28
SA - Sud America 1
Totale 1.784
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Nazione #
US - Stati Uniti d'America 1.121
IT - Italia 243
CN - Cina 141
NL - Olanda 84
IE - Irlanda 31
CA - Canada 27
CI - Costa d'Avorio 26
DE - Germania 21
FI - Finlandia 20
IN - India 14
VN - Vietnam 12
FR - Francia 7
UA - Ucraina 6
GB - Regno Unito 4
JP - Giappone 4
IR - Iran 3
SE - Svezia 3
BE - Belgio 2
ES - Italia 2
GR - Grecia 2
ZA - Sudafrica 2
BG - Bulgaria 1
BZ - Belize 1
CH - Svizzera 1
CO - Colombia 1
DK - Danimarca 1
RO - Romania 1
RS - Serbia 1
SG - Singapore 1
SI - Slovenia 1
Totale 1.784
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Città #
Chandler 314
Ashburn 108
Amsterdam 82
Millbury 55
Beijing 52
Princeton 38
Nanjing 37
Des Moines 36
Naples 30
Napoli 29
Seattle 28
Ottawa 27
Boston 22
Lawrence 15
Dong Ket 12
Pune 12
Washington 12
San Jose 11
Hebei 10
Norwalk 10
San Mateo 10
Houston 9
Jacksonville 8
Jiaxing 8
Nanchang 8
Nola 8
Wilmington 8
Redwood City 7
Shenyang 7
Changsha 6
Dearborn 6
Dublin 5
Paris 5
Augusta 4
Campagna 4
Guangzhou 4
Portici 4
Rome 4
Telese 4
Torre Annunziata 4
Ardabil 3
Buffalo 3
Böblingen 3
Genoa 3
Kronberg 3
Leawood 3
Nuremberg 3
Poli 3
Saint Louis 3
Atlanta 2
Caserta 2
Davis 2
Las Vegas 2
León 2
Marsala 2
Monmouth Junction 2
Mugnano Di Napoli 2
Muizenberg 2
New York 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
Horia 1
Kunming 1
Lanzhou 1
Lappeenranta 1
Ljubljana 1
London 1
Los Angeles 1
Lviv 1
Marigliano 1
Massa 1
Milan 1
New Delhi 1
Newark 1
Ottaviano 1
Pioltello 1
Poggiomarino 1
Qualiano 1
Reggio Emilia 1
Totale 1.157
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Nome #
DNA damage signatures in peripheral blood cells as biomarkers in prodromal huntington disease 71
Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study 64
SPG5 and multiple sclerosis: clinical and genetic overlap? 58
Parkinsonism in adult-onset Rasmussens's encephalitis: a clinical picture presenting as corticobasal syndrome 54
Pathological laughter as onset symptom in atypical parkinsonisms 51
Cognitive decline in Huntington's disease expansion gene carriers 50
Application of the p9NORM correction method to timed neuropsychological tests in Parkinson's disease and multiple system atrophy. 49
Emotion Recognition and Psychological Comorbidity in Friedreich’s Ataxia 48
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study 48
Closing-in Phenomenon in Huntington's Disease: A Neuropsychological Marker of Frontal/Executive Dysfunction 45
Frontal defect contribution to decreasing of body mass index in Parkinson's disease patients 44
Chorea-acanthocytosis without chorea: Expanding the clinical phenotype 44
Cervical dystonia patients display subclinical gait changes 44
Perseverative Behavior on Verbal Fluency Task in Patients with Huntington's Disease: a Retrospective Study on a Large Patient Sample 44
Complex phenotype in an Italian family with a novel mutation in SPG3A. 43
The Treatment of Hypersalivation in Rett Syndrome with Botulinum Toxin: Efficacy and Clinical Implications 43
Autonomic disorders and myocardial 123I-metaiodobenzylguanidine scintigraphy in Huntington's disease 43
Predictors of survival in spinocerebellar ataxia type 2 population from Southern Italy. 42
Peripheral markers of autophagy in polyglutamine diseases 41
Benign hereditary chorea: clinical and neuroimaging features in an Italian family. 40
Adult normative values for the PATA Rate Test 40
Cognitive profile and 18F-fluorodeoxyglucose PET study in LRRK2-related Parkinson's disease 39
A case of restless leg syndrome in a family with LRRK2 gene mutation. 39
Be aware of Wolfram syndrome when examining ataxic patients 39
The flavor test is a sensitive tool in identifying the flavor sensorineural dysfunction in Parkinson's disease 37
Screening for dopa-responsive dystonia in patients with scans without evidence of dopaminergic deficiency (SWEDD). 36
CCM3/PDCD10 gene mutation in cerebral cavernous malformations associated with hyperkeratotic cutaneous capillary venous malformations 36
Myocardial (123)I-metaiodobenzylguanidine scintigraphy in patients with homozygous and heterozygous parkin mutations 36
Pseudo-orthostatic tremor: description of a not typical case 36
Antiphospholipid-related chorea. 35
Spatial and egocentric mental rotation in patients with cervical dystonia 34
Does motor cortex plasticity depend on the type of mutation in the leucine-rich repeat kinase 2 gene? 33
Disruption of GABA(A)-mediated intracortical inhibition in patients with chorea-acanthocytosis 33
Efficacy of dopamine agonist treatment in delayed-onset parkinsonism due to midbrain hemorrhage. 31
The magnetic apraxia of Denny-Brown 29
Cognitive correlates of prospective memory in dystonia 28
Friedreich ataxia: 150 years of bench and bedside studies 28
Parkinsonism in a pair of monozygotic CADASIL twins sharing the R1006C mutation: a transcranial sonography study 27
Constructional Apraxia is related to Different Cognitive Defect's across Dementia 27
Metabolic Ataxias in Adults. 26
The Multiple Faces of Spinocerebellar Ataxia type 2 26
Using global team science to identify genetic parkinson's disease worldwide 25
The occurrence of lateral shift in cervical dystonia 25
Animal-Assisted Therapy in Elderly Patients: Evidence and Controversies in Dementia and Psychiatric Disorders and Future Perspectives in Other Neurological Diseases 25
Jaw-Opening Oromandibular Dystonia Associated With Spinocerebellar Ataxia Type 2 23
Reversible valproate-induced subacute encephalopathy associated with a MT-ATP8 variant in the mitochondrial genome 22
Clinical manifestations of intermediate allele carriers in Huntington disease 22
Correction to: Peripheral markers of autophagy in polyglutamine diseases (Neurological Sciences, (2018), 39, 1, (149-152), 10.1007/s10072-017-3156-6) 21
A Novel PSEN1 Mutation in a Patient with Sporadic Early-Onset Alzheimer's Disease and Prominent Cerebellar Ataxia. 20
Infusion treatments and deep brain stimulation in Parkinson's Disease: The role of nursing 19
The cerebellum in idiopathic cervical dystonia: A specific pattern of structural abnormalities? 18
Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement 14
Unusual white matter involvement in EAST syndrome associated with novel KCNJ10 mutations 12
Personality traits associated with blepharospasm: A comparison with healthy subjects, patients with facial hemispasm and patients with hyperhidrosis 11
Totale 1.918
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Categoria #
all - tutte 6.914
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 6.914
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201918 0 0 0 0 0 0 0 0 0 7 10 1
2019/2020236 81 17 5 10 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
2023/2024304 21 50 30 37 24 56 7 76 3 0 0 0
Totale 1.918