IRIS
RUFA, ALESSANDRA
 Distribuzione geografica
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Continente #
NA - Nord America 14.755
EU - Europa 10.337
AS - Asia 1.621
Continente sconosciuto - Info sul continente non disponibili 19
OC - Oceania 18
SA - Sud America 15
AF - Africa 9
Totale 26.774
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Nazione #
US - Stati Uniti d'America 14.701
GB - Regno Unito 3.583
IE - Irlanda 1.743
CN - Cina 1.253
UA - Ucraina 1.099
SE - Svezia 992
IT - Italia 857
DE - Germania 612
FR - Francia 534
FI - Finlandia 328
RU - Federazione Russa 292
SG - Singapore 134
TR - Turchia 77
VN - Vietnam 73
ES - Italia 68
BE - Belgio 52
CA - Canada 44
NL - Olanda 40
CZ - Repubblica Ceca 25
BG - Bulgaria 23
EU - Europa 18
AU - Australia 16
RO - Romania 16
IR - Iran 15
IN - India 14
GR - Grecia 10
HU - Ungheria 9
JP - Giappone 9
IL - Israele 8
HK - Hong Kong 7
BR - Brasile 6
EE - Estonia 6
TW - Taiwan 6
CH - Svizzera 5
LT - Lituania 5
AT - Austria 4
CL - Cile 4
NO - Norvegia 4
PL - Polonia 4
AZ - Azerbaigian 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
EG - Egitto 3
IQ - Iraq 3
LU - Lussemburgo 3
MK - Macedonia 3
PK - Pakistan 3
RS - Serbia 3
SI - Slovenia 3
AR - Argentina 2
BO - Bolivia 2
ID - Indonesia 2
KR - Corea 2
LV - Lettonia 2
MD - Moldavia 2
NG - Nigeria 2
NZ - Nuova Zelanda 2
PH - Filippine 2
PT - Portogallo 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 2
ZA - Sudafrica 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
AN - Antille olandesi 1
BS - Bahamas 1
BY - Bielorussia 1
CI - Costa d'Avorio 1
GE - Georgia 1
GL - Groenlandia 1
HR - Croazia 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
MM - Myanmar 1
MS - Montserrat 1
MT - Malta 1
MX - Messico 1
PA - Panama 1
PE - Perù 1
TJ - Tagikistan 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
UZ - Uzbekistan 1
Totale 26.774
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Città #
Menlo Park 4.569
Southend 3.376
Dublin 1.738
Fairfield 1.381
Chandler 1.138
Jacksonville 927
Ashburn 833
Houston 638
Wilmington 627
Woodbridge 626
Seattle 490
Cambridge 459
Ann Arbor 443
Princeton 354
Beijing 309
Nanjing 290
Siena 238
Boardman 152
San Mateo 151
Helsinki 145
Nanchang 120
New York 107
Moscow 86
Singapore 86
Shenyang 83
San Diego 77
Venezia 68
Izmir 67
Düsseldorf 65
Málaga 62
Dong Ket 60
Kunming 54
Tianjin 52
Jiaxing 46
Shanghai 46
Hebei 45
Changsha 38
Dearborn 38
Rome 35
Florence 34
Brussels 33
Fremont 29
Mestre 29
Milan 29
Washington 29
Norwalk 28
Jinan 26
Lancaster 25
Redwood City 25
Toronto 25
London 23
Sofia 23
Dallas 21
Ningbo 20
Hangzhou 19
Renton 18
San Francisco 17
Waanrode 17
Los Angeles 16
Brno 14
Falls Church 14
St Louis 14
Bologna 13
Lanzhou 13
Changchun 12
Zhengzhou 12
Frankfurt am Main 11
Naples 11
Chicago 10
Amsterdam 9
Auburn Hills 9
Budapest 9
Guangzhou 9
Tokyo 9
Edinburgh 8
Hefei 8
Munich 8
Olomouc 8
Pescara 8
Taizhou 8
Chengdu 7
Costa Mesa 7
Grosseto 7
Phoenix 7
Saint Petersburg 7
Tappahannock 7
Canberra 6
Central 6
Livorno 6
Messina 6
Padova 6
Philadelphia 6
Tallinn 6
Zanjan 6
Aci Sant'Antonio 5
Bonndorf 5
Calenzano 5
Cluj-napoca 5
Falkenstein 5
Haikou 5
Totale 20.942
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Nome #
Hemodynamic evaluation of the optic nerve head in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. 301
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients 281
Visual impairment in FOXG1-mutated individuals and mice 220
The role of dentate nuclei in human oculomotor control: Insights from cerebrotendinous xanthomatosis 216
Cerebellum and neuropsychiatric disorders: insights from ARSACS 212
Two novel HTRA1 mutations in a European CARASIL patient. 212
Wilson's disease with Leu492Ser mutation and arylsulfatase A pseudodeficiency: just a coincidence? 210
Transient supranuclear paresis of the abduction in viral encephalitis of the brainstem 207
Adult Alexander disease with de novo c.1193C>T heterozygous variant in GFAP gene 207
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: Update on clinical, diagnostic, and management aspects 202
Eye movement abnormalities in a patient with Zellweger spectrum disorder 200
Cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies: a case report 199
Type I sialidosis: a clinical, biochemical and neuroradiological study 191
Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R gene 188
Visual System Involvement in CADASIL. 188
Toscana itaca (Italian CADASIL) registry: an implementable online database for CADASIL (Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy). 187
Typical pathological changes of CADASIL in the optic nerve 187
Video-based eye tracking: our experience with advanced stimuli design for eye tracking software 186
Systemic blood pressure profile in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 183
Typical pathological changes of CADASIL in the optic nerve 183
Homozygosity and severity of phenotypic presentation in a CADASIL family 183
Clinical and MRI improvement in a case of progressive multifocal leukoencephalopathy 182
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy. 182
Vertical supranuclear gaze palsy in Niemann-Pick type C disease. 181
A two-layered diffusion model traces the dynamics of information processing in the valuation-and-choice circuit of decision making. 181
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families 179
Sixth nerve and superior division of third nerve palsy due to intracranial extension of multiple myeloma. A diagnostic challenge and differential diagnosis 179
A CASE OF CEREBROTENDINOUS XANTHOMATOSIS PRESENTING WITH PARKINSONISM IN THE SEVENTH DECADE 179
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Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene. 177
A case of ethambutol-induced optic neuropathy harbouring the primary mitochondrial LHON mutation at nt 11778 176
Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias. 175
A case of bilateral facial palsy with detection of herpes simplex virus type 1 DNA in the cerebrospinal fluid and serum anti-gm1 antibodies. 172
Frequency of OPA1 and OPTN gene variations in 18 patients with normal tension glaucoma 171
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation 170
AARS2-related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases 168
Trigeminal-Nociceptive Activation And Pupillary Changes In Two Patients With Wernicke’s Encephalopathy 167
Spatial ranking strategy and enhanced peripheral vision discrimination optimize performance and efficiency of visual sequential search. 166
Using a simplified trail making test B to assess visuo-spatial and sequencing abilities in hereditary spinocerebellar ataxias (SCA) 166
Evaluating gaze control on a multi-target sequencing task: The distribution of fixations is evidence of exploration optimisation. 165
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Sindrome di Goldman-Favre: descrizione di un caso 164
Ocular-motor profile and effects of memantine in a familial form of adult cerebellar ataxia with slow saccades and square wave saccadic intrusions. 164
Wernicke Encephalopathy After Gastrointestinal Surgery for Cancer: Causes of Diagnostic Failure or Delay. 162
Vitamin-E serum level in LHON patients 162
The first cerebrotendinous xanthomatosis family from Argentina: a new mutation in CYP27A1 gene. 160
Pulsating enophthalmos in an adult patient with type 1 neurofibromatosis 158
Acute vestibular syndrome in a patient with cerebral autosomal dominant leukoencephalopathy with subcortical infarcts and leukoencephalopathy (CADASIL) 157
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telithromycin consumption 157
Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 156
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy. 156
GABAAergic dysfunction in the olivary-cerebellar-brainstem network may cause eye oscillations and body tremor 156
Photophobia and bilateral pulvinar involvement in non-alcoholic Wernicke's encephalopathy. 156
Valutazione delle associazioni tra polimorfismi del gene OPA 1 e glaucoma normotensivo in Italia 156
Velocity profile and trajectory of saccades in different forms of cerebellar ataxia 155
Transient periodic lateralised epileptiform discharges (PLEDs) following internal carotid artery stenting 154
Wernicke Syndrome: Seven case reports. 152
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A new family with CADASIL: presentation of an homozygous patient and comparison with heterozigous phenotypes. 151
Impairment of vertical saccades from an acute pontine lesion in multiple sclerosis 150
Four novel CYP27A1 mutations in seven Italian patients with CTX 148
Clinical Course of Two Italian Siblings with Ataxia-Telangiectasia-Like Disorder. 148
Video-Based Eye-Tracking: one year of experience with astidet 148
Idiopathic bilateral facial palsy: is a causative role of anti-GM1 ganglioside and herpes simplex type 1 possible? 146
High energy efficiency biped robot controlled by the human brain for people with ALS disease 146
Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiency 145
A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case 144
Automatic eye fixations identification based on analysis of variance and covariance, 143
CADASIL and cerebrovascular diseases 143
Characteristic eye movements in ataxia-telangiectasia-like disorder: An explanatory hypothesis 142
A novel point mutation in the mitochondrial tRNA((Trp)) gene produces late-onset encephalomyopathy, plus additional features 141
Evaluating the human ongoing visual search performance by eye tracking application and sequencing tests 141
Increased QT variability in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. 141
Alu-element insertion in the OPA1 intron sequence associated with ADOA. 141
Lateral Medullary Ischemia Presenting with Persistent Hiccups and Vertigo 140
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Retinochoroidal atrophy in two adult patients with Angelman syndrome 139
High frequency of exon 10 mutations in the NOTCH3 gene in Italian CADASIL families: phenotypic peculiarities. 139
Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). 139
Adult-onset phenylketonuria revealed by acute reversible dementia, prosopagnosia and parkinsonism. 139
Retinal nerve fiber layer thinning in CADASIL: an optical coherence tomography and MRI study. 138
Fast versus slow: different saccadic behavior in cerebellar ataxias. 138
Molecular genetic study of Leber’s hereditary optic neurophaty (LHON): mutation screening by sequencing of ND1, ND4, ND%, ND6 genes 137
Association in the same patient of autosomal dominant progressive external ophthalmoplegia with multiple mtDNA deletions and X-linked ichthyosis: clinical, biochemical, histological, submicroscopic and molecular genetic study 136
Spike removal through multiscale wavelet and entropy analysis of ocular motor noise: a case study in patients with cerebellar disease. 136
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Anti-saccades in cerebellar ataxias reveal a contribution of the cerebellum in executive functions 134
The spectrum of NOTCH3 mutation and phonotype variability in fourteen Italian families with CADASIL. 133
Alu-Element Insertion In The Opa1 Intron Sequence Associated With ADOA 133
Wernicke's encelophaty after gastro-intestinal surgery for cancer: a retrospective clinical study 133
The Primrose syndrome with progressive neurological involvement and cerebral calcification. 133
Lithium neurotoxicity mimicking rapidly progressive dementia 132
Neuro-Ophthalmological findings in two adult siblings with ataxiatelangiectasia– like disorder 132
Human-Robotics Interface for the Interaction with Cognitive and Emotional Human Domains 130
Genetic leukoencephalopaties with unknown metabolic pathogenesis 130
Overconfident Behavior In Informational Cascades: An Eye-Tracking Study 129
Using simplified trial macking test B to evacuate ongoing learning capabilities on visual search. 127
Plasma levels of asymmetric dimethylarginine (ADMA) in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarct and Leukoencephalopathy (CADASIL) 127
Totale 16.387
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Categoria #
all - tutte 71.049
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 71.049
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203.793 0 142 385 728 315 310 300 490 376 351 126 270
2020/20213.377 117 358 82 298 214 394 131 594 388 171 405 225
2021/20222.390 150 298 202 191 128 60 101 79 112 255 260 554
2022/20233.946 235 257 550 514 469 745 68 345 438 94 161 70
2023/20242.686 123 79 219 108 105 721 908 114 43 40 36 190
2024/2025369 92 277 0 0 0 0 0 0 0 0 0 0
Totale 27.108