IRIS
PELUSO, SILVIO
 Distribuzione geografica
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Continente #
NA - Nord America 1.214
EU - Europa 449
AS - Asia 270
AF - Africa 31
SA - Sud America 1
Totale 1.965
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Nazione #
US - Stati Uniti d'America 1.186
IT - Italia 252
CN - Cina 141
SG - Singapore 96
NL - Olanda 84
IE - Irlanda 31
CA - Canada 27
DE - Germania 27
CI - Costa d'Avorio 26
FI - Finlandia 22
IN - India 14
VN - Vietnam 12
FR - Francia 7
UA - Ucraina 6
GB - Regno Unito 5
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 1.965
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Città #
Chandler 314
Ashburn 108
Amsterdam 82
Singapore 75
Millbury 55
Beijing 52
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
Santa Clara 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
Los Angeles 6
Dublin 5
Paris 5
Augusta 4
Campagna 4
Guangzhou 4
Milan 4
Munich 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
Davis 2
Helsinki 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
Marigliano 1
Totale 1.270
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Nome #
DNA damage signatures in peripheral blood cells as biomarkers in prodromal huntington disease 73
Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study 69
SPG5 and multiple sclerosis: clinical and genetic overlap? 60
Cognitive decline in Huntington's disease expansion gene carriers 58
Parkinsonism in adult-onset Rasmussens's encephalitis: a clinical picture presenting as corticobasal syndrome 57
Pathological laughter as onset symptom in atypical parkinsonisms 57
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study 52
Closing-in Phenomenon in Huntington's Disease: A Neuropsychological Marker of Frontal/Executive Dysfunction 52
Cervical dystonia patients display subclinical gait changes 51
Emotion Recognition and Psychological Comorbidity in Friedreich’s Ataxia 51
Application of the p9NORM correction method to timed neuropsychological tests in Parkinson's disease and multiple system atrophy. 51
Frontal defect contribution to decreasing of body mass index in Parkinson's disease patients 48
Chorea-acanthocytosis without chorea: Expanding the clinical phenotype 46
Perseverative Behavior on Verbal Fluency Task in Patients with Huntington's Disease: a Retrospective Study on a Large Patient Sample 46
Complex phenotype in an Italian family with a novel mutation in SPG3A. 45
The Treatment of Hypersalivation in Rett Syndrome with Botulinum Toxin: Efficacy and Clinical Implications 45
Autonomic disorders and myocardial 123I-metaiodobenzylguanidine scintigraphy in Huntington's disease 45
Predictors of survival in spinocerebellar ataxia type 2 population from Southern Italy. 43
Cognitive profile and 18F-fluorodeoxyglucose PET study in LRRK2-related Parkinson's disease 42
Benign hereditary chorea: clinical and neuroimaging features in an Italian family. 42
A case of restless leg syndrome in a family with LRRK2 gene mutation. 42
Be aware of Wolfram syndrome when examining ataxic patients 42
The flavor test is a sensitive tool in identifying the flavor sensorineural dysfunction in Parkinson's disease 42
Peripheral markers of autophagy in polyglutamine diseases 42
Adult normative values for the PATA Rate Test 42
Myocardial (123)I-metaiodobenzylguanidine scintigraphy in patients with homozygous and heterozygous parkin mutations 41
Screening for dopa-responsive dystonia in patients with scans without evidence of dopaminergic deficiency (SWEDD). 40
Spatial and egocentric mental rotation in patients with cervical dystonia 38
Antiphospholipid-related chorea. 38
CCM3/PDCD10 gene mutation in cerebral cavernous malformations associated with hyperkeratotic cutaneous capillary venous malformations 38
Pseudo-orthostatic tremor: description of a not typical case 38
Animal-Assisted Therapy in Elderly Patients: Evidence and Controversies in Dementia and Psychiatric Disorders and Future Perspectives in Other Neurological Diseases 38
Disruption of GABA(A)-mediated intracortical inhibition in patients with chorea-acanthocytosis 37
Does motor cortex plasticity depend on the type of mutation in the leucine-rich repeat kinase 2 gene? 34
Efficacy of dopamine agonist treatment in delayed-onset parkinsonism due to midbrain hemorrhage. 33
Friedreich ataxia: 150 years of bench and bedside studies 33
The magnetic apraxia of Denny-Brown 32
Constructional Apraxia is related to Different Cognitive Defect's across Dementia 31
Cognitive correlates of prospective memory in dystonia 30
Parkinsonism in a pair of monozygotic CADASIL twins sharing the R1006C mutation: a transcranial sonography study 30
Reversible valproate-induced subacute encephalopathy associated with a MT-ATP8 variant in the mitochondrial genome 29
Metabolic Ataxias in Adults. 28
The occurrence of lateral shift in cervical dystonia 28
The Multiple Faces of Spinocerebellar Ataxia type 2 27
Jaw-Opening Oromandibular Dystonia Associated With Spinocerebellar Ataxia Type 2 27
Using global team science to identify genetic parkinson's disease worldwide 27
Correction to: Peripheral markers of autophagy in polyglutamine diseases (Neurological Sciences, (2018), 39, 1, (149-152), 10.1007/s10072-017-3156-6) 24
Clinical manifestations of intermediate allele carriers in Huntington disease 24
A Novel PSEN1 Mutation in a Patient with Sporadic Early-Onset Alzheimer's Disease and Prominent Cerebellar Ataxia. 23
Infusion treatments and deep brain stimulation in Parkinson's Disease: The role of nursing 23
The cerebellum in idiopathic cervical dystonia: A specific pattern of structural abnormalities? 20
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 12
Totale 2.099
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Categoria #
all - tutte 9.299
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 9.299
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020133 0 0 0 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
2023/2024370 21 50 30 37 24 56 7 76 3 5 46 15
2024/2025115 68 34 11 2 0 0 0 0 0 0 0 0
Totale 2.099