IRIS
DE MICHELE, GIUSEPPE
 Distribuzione geografica
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Continente #
NA - Nord America 5.725
EU - Europa 2.940
AS - Asia 1.069
AF - Africa 82
SA - Sud America 14
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 2
Totale 9.838
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Nazione #
US - Stati Uniti d'America 5.598
IT - Italia 945
CN - Cina 860
NL - Olanda 427
UA - Ucraina 390
FI - Finlandia 346
IE - Irlanda 241
DE - Germania 226
SE - Svezia 139
CA - Canada 125
GB - Regno Unito 94
IN - India 83
CI - Costa d'Avorio 69
VN - Vietnam 58
FR - Francia 33
ES - Italia 30
IR - Iran 19
BE - Belgio 18
TR - Turchia 12
ZA - Sudafrica 12
BR - Brasile 11
GR - Grecia 9
JP - Giappone 8
SG - Singapore 8
BG - Bulgaria 7
EU - Europa 6
IL - Israele 5
KR - Corea 5
PT - Portogallo 5
RO - Romania 5
HK - Hong Kong 4
MK - Macedonia 4
PH - Filippine 4
CH - Svizzera 3
AT - Austria 2
AU - Australia 2
DK - Danimarca 2
LU - Lussemburgo 2
NO - Norvegia 2
RS - Serbia 2
SI - Slovenia 2
TH - Thailandia 2
AL - Albania 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BZ - Belize 1
CL - Cile 1
CO - Colombia 1
HU - Ungheria 1
LT - Lituania 1
MT - Malta 1
MX - Messico 1
PL - Polonia 1
SD - Sudan 1
UY - Uruguay 1
Totale 9.838
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Città #
Chandler 1.262
Millbury 456
Jacksonville 438
Amsterdam 398
Ashburn 397
Princeton 365
Nanjing 263
Naples 186
Beijing 165
Napoli 154
Wilmington 154
Boston 149
Ottawa 111
Des Moines 89
Nanchang 88
Woodbridge 82
Shenyang 65
Hebei 59
Dong Ket 58
Jiaxing 56
Norwalk 56
Houston 54
Seattle 50
Tianjin 33
Falls Church 32
Redwood City 32
Washington 32
Lawrence 30
Boardman 28
Changsha 28
San Mateo 28
Pune 26
Augusta 25
Kunming 25
Kronberg 24
Rome 21
Shanghai 21
Nola 18
Dublin 16
San Jose 16
Indiana 15
Ardabil 13
Dearborn 13
Milan 13
Telese 12
Leawood 11
Orange 11
Saint Louis 11
Toronto 10
Waanrode 10
Ann Arbor 9
Madrid 9
Gricignano di Aversa 8
Monmouth Junction 8
Muizenberg 8
Paris 8
Caserta 7
Changchun 7
Sofia 7
Torre Del Greco 7
Fairfield 6
Guangzhou 6
London 6
New York 6
Ankara 5
Atlanta 5
Bengaluru 5
Bristol 5
Florence 5
Hangzhou 5
Lanzhou 5
Monteforte Irpino 5
New Delhi 5
Pontelandolfo 5
Portici 5
Redmond 5
Salerno 5
Sassari 5
Torre Annunziata 5
Acerra 4
Barcelona 4
Battipaglia 4
Campagna 4
Hong Kong 4
Izmir 4
Modena 4
Mugnano di Napoli 4
Pavia 4
Pozzuoli 4
San Diego 4
Simi Valley 4
Adelfia 3
Aversa 3
Bitola 3
Buffalo 3
Chicago 3
Contursi 3
Edmonton 3
Eugene 3
Fremont 3
Totale 5.961
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Nome #
Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion. 136
Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutations 112
Pelizaeus-Merzbacher-Like disease presentation of MCT8 mutated male subjects. 84
Alteration of endosomal trafficking is associated with neurodegenerative diseases 82
DNA damage signatures in peripheral blood cells as biomarkers in prodromal huntington disease 71
Brain structural damage in Friedreich's ataxia. 68
The Italian version of the quick mild cognitive impairment (Qmci-I) screen: normative study on 307 healthy subjects 68
Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study 64
A novel mutation in SACS gene in a family from southern Italy 61
Epoetin alfa increases frataxin production in Friedreich's ataxia without affecting hematocrit. 61
Modifications of resting state networks in spinocerebellar ataxia type 2 58
SPG5 and multiple sclerosis: clinical and genetic overlap? 58
PINK1 homozygous W437X mutation in a patient with apparent dominant transmission of parkinsonism. 57
Ataxia with oculomotor apraxia type 1 in southern italy: late onset and variable phenotype. 55
Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa. 55
Impulsive-compulsive behaviors in parkin-associated Parkinson disease 54
Parkinsonism in adult-onset Rasmussens's encephalitis: a clinical picture presenting as corticobasal syndrome 54
Behavioral disorder, dementia, ataxia and rigidity in a large family with Tata box-Binding Protein mutation 53
Reduced striatal [123I]FP-CIT binding in SCA2 patients without parkinsonism 52
The Heterogeneity of Early Parkinson?s Disease: A Cluster Analysis on Newly Diagnosed Untreated Patients 52
PERK-mediated unfolded protein response activation and oxidative stress in PARK20 fibroblasts 52
Short-term continuous infusion of apomorphine hydrochloride for treatment of Huntington's chorea: A double blind, randomized cross-over trial 51
A randomized controlled pilot trial of lithium in spinocerebellar ataxia type 2. 51
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
Neurophysiological study in a Spanish family with recessive spastic ataxia of Charlevoix-Saguenay 48
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study 48
Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17 48
Non-motor symptoms and cardiac innervation in SYNJ1-related parkinsonism 48
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
Electrophysiologic characterization in spinocerebellar ataxia 17 47
Very late onset in ataxia oculomotor apraxia type I. 47
The Sepiapterin Reductase Gene Region Reveals Association in the PARK3 locus: Analysis of Familial and Sporadic Parkinson Disease in European Populations. 46
Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian families 46
Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis of SPG4 reveals eleven novel mutations. 45
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. 45
Closing-in Phenomenon in Huntington's Disease: A Neuropsychological Marker of Frontal/Executive Dysfunction 45
Genome-wide scan linkage analysis for Parkinson's disease: The European Genetic Study of Parkinson's disease. 44
Accuracy of clinical diagnostic criteria for Friedreich's ataxia. 44
A refined physical and transcriptional map of the SPG9 locus on 10q23.3[#150]q24.2 44
Cerebellar blood flow in spinocerebellar degenerations: a single photon emission tomography study in 28 patients. 44
Frontal defect contribution to decreasing of body mass index in Parkinson's disease patients 44
The Effect of Cerebellar Degeneration on Human Sensori-motor Plasticity 44
Chorea-acanthocytosis without chorea: Expanding the clinical phenotype 44
Perseverative Behavior on Verbal Fluency Task in Patients with Huntington's Disease: a Retrospective Study on a Large Patient Sample 44
Prevalence and features of non-motor symptoms in Wilson's disease 44
Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum 43
Long-term clinical experience with weekly interferon beta-1a in relapsing multiple sclerosis 43
A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2. 43
Complex phenotype in an Italian family with a novel mutation in SPG3A. 43
Why do some Friedreich's ataxia patients retain tendon reflexes? A clinical, neurophysiological and molecular study. 43
Electrophysiological characterisation in hereditary spastic paraplegia type 5. 43
Long-term effect of epoetin alfa on clinical and biochemical markers in friedreich ataxia 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
Longitudinal study of a cohort of MSA-C patients in South Italy: survival and clinical features 42
PARK11 is not linked with Parkinson's disease in European families. 41
Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease. 41
Ataxia with oculomotor apraxia type 1 in Southern Italy: late onset and variable phenotype 41
Ambulatory monitoring of left ventricular function in patients with Parkinson's disease and postural hypotension 41
DNA damage induced by polyglutamine-expanded proteins. 41
Novel mutation of SACS gene in a Spanish family with autosomal recessive spastic ataxia 41
A double-blind cross-over trial of amantadine hydrochloride in Friedreich's ataxia. 41
Auditory function and speech discrimination abilities are impaired in progressive supranuclear palsy 41
Normalization of timed neuropsychological tests with the PATA rate and nine-hole pegboard tests 41
Peripheral markers of autophagy in polyglutamine diseases 41
Influence of GAA expansion size and disease duration on Central Nervous System impairment in Friedreich's Ataxia. Contribution to the understanding of the pathophysiology of the disease 40
Benign hereditary chorea: clinical and neuroimaging features in an Italian family. 40
Functional MRI signal fluctuations highlight altered resting brain activity in Huntington’s disease 40
Adult normative values for the PATA Rate Test 40
Chronic Pachymeningitis: a case of neurosyphilis with spastic paraparesis. 39
Cognitive profile and 18F-fluorodeoxyglucose PET study in LRRK2-related Parkinson's disease 39
A randomized clinical trial of lithium in multiple system atrophy. 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
Cutaneous sensory and autonomic denervation in Progressive Supranuclear Palsy 39
Autonomic nervous system abnormalities in spinocerebellar ataxia type 2: a cardiovascular neurophysiologic study. 38
Genetic screening for LRRK2 gene G2019S mutation in Parkinson's disease patients from Southern Italy. 38
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. 38
Stability of erythropoietin repackaging in polypropylene syringes for clinical use 38
Case-control study of multiple system atrophy. 37
Adult-onset familial laryngeal abductor paralysis, cerebellar ataxia, and pure motor neuropathy. 37
INTERGENERATIONAL INSTABILITY AND MARKED ANTICIPATION IN SCA-17. 37
A randomized controlled clinical trial of growth hormone in amyotrophic lateral sclerosis: clinical, neuroimaging, and hormonal results. 37
Suicidal ideation in a European Huntington's disease population. 37
The flavor test is a sensitive tool in identifying the flavor sensorineural dysfunction in Parkinson's disease 37
Screening for Fabry disease in a series of Parkinson’s disease patients and literature review 36
Ambulatoy monitoring of left ventricular function in patients with Parkinson's disease and postural hypotension 36
A novel NKX2.1 mutation in a family with hypothyroidism and benign hereditary chorea. 36
Cerebral blood flow in spinocerebellar degenerations: a single photon emission tomography study in 28 patients. 36
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
Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian family. 36
Variable phenotype in a P102L Gerstmann-Straussler-Scheinker Italian family 35
A pathogenetic classification of hereditary ataxias: is the time ripe? 35
Evidence of a genetic marker for early onset in Friedreich's ataxia. 35
A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia. 35
Totale 4.698
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Categoria #
all - tutte 41.869
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 41.869
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201965 0 0 0 0 0 0 0 0 0 20 15 30
2019/20201.239 500 32 96 33 102 24 27 16 12 108 134 155
2020/20211.218 31 81 116 98 102 161 105 51 124 33 235 81
2021/20222.069 46 19 17 31 26 66 29 88 274 188 379 906
2022/20232.941 448 254 89 258 337 310 20 218 408 427 131 41
2023/20241.321 87 252 243 143 98 160 40 282 10 6 0 0
Totale 10.433