IRIS
RUFA, ALESSANDRA
 Distribuzione geografica
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Continente #
NA - Nord America 15.645
EU - Europa 10.933
AS - Asia 1.920
AF - Africa 37
SA - Sud America 33
Continente sconosciuto - Info sul continente non disponibili 19
OC - Oceania 18
Totale 28.605
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Nazione #
US - Stati Uniti d'America 15.582
GB - Regno Unito 3.593
IE - Irlanda 1.744
CN - Cina 1.306
UA - Ucraina 1.099
SE - Svezia 993
IT - Italia 955
RU - Federazione Russa 733
DE - Germania 624
FR - Francia 534
SG - Singapore 366
FI - Finlandia 338
TR - Turchia 80
VN - Vietnam 74
ES - Italia 69
BE - Belgio 55
CA - Canada 50
NL - Olanda 48
CI - Costa d'Avorio 27
CZ - Repubblica Ceca 25
BG - Bulgaria 23
BR - Brasile 19
EU - Europa 18
AU - Australia 16
RO - Romania 16
IN - India 15
IR - Iran 15
GR - Grecia 11
LT - Lituania 10
HU - Ungheria 9
JP - Giappone 9
IL - Israele 8
HK - Hong Kong 7
EE - Estonia 6
TW - Taiwan 6
CH - Svizzera 5
DK - Danimarca 5
AR - Argentina 4
AT - Austria 4
CL - Cile 4
EG - Egitto 4
MX - Messico 4
NO - Norvegia 4
PL - Polonia 4
PT - Portogallo 4
AZ - Azerbaigian 3
DO - Repubblica Dominicana 3
IQ - Iraq 3
LA - Repubblica Popolare Democratica del Laos 3
LK - Sri Lanka 3
LU - Lussemburgo 3
LV - Lettonia 3
MK - Macedonia 3
PH - Filippine 3
PK - Pakistan 3
RS - Serbia 3
SI - Slovenia 3
BO - Bolivia 2
EC - Ecuador 2
GE - Georgia 2
ID - Indonesia 2
KR - Corea 2
MD - Moldavia 2
NG - Nigeria 2
NZ - Nuova Zelanda 2
PE - Perù 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
BD - Bangladesh 1
BS - Bahamas 1
BY - Bielorussia 1
GL - Groenlandia 1
HR - Croazia 1
KG - Kirghizistan 1
KW - Kuwait 1
MA - Marocco 1
MM - Myanmar 1
MS - Montserrat 1
MT - Malta 1
MY - Malesia 1
PA - Panama 1
TJ - Tagikistan 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
UZ - Uzbekistan 1
Totale 28.605
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Città #
Menlo Park 4.569
Southend 3.376
Dublin 1.739
Fairfield 1.381
Chandler 1.138
Jacksonville 927
Ashburn 864
Santa Clara 760
Houston 638
Wilmington 627
Woodbridge 626
Seattle 490
Cambridge 459
Ann Arbor 443
Princeton 354
Beijing 311
Nanjing 290
Singapore 265
Siena 258
Helsinki 154
Boardman 152
San Mateo 151
Nanchang 120
New York 107
Moscow 86
Shenyang 84
San Diego 77
Venezia 68
Izmir 67
Düsseldorf 65
Málaga 62
Dong Ket 60
Rome 57
Kunming 54
Shanghai 52
Tianjin 52
Jiaxing 46
Hebei 45
Changsha 38
Dearborn 38
Florence 37
Brussels 36
Milan 35
Toronto 30
Washington 30
Fremont 29
London 29
Mestre 29
Norwalk 28
Abidjan 27
Jinan 26
Lancaster 25
Los Angeles 25
Redwood City 25
Sofia 23
Dallas 21
Hangzhou 20
Ningbo 20
Renton 18
San Francisco 17
Waanrode 17
Frankfurt am Main 16
Bologna 14
Brno 14
Falls Church 14
Munich 14
St Louis 14
Lanzhou 13
Zhengzhou 13
Changchun 12
Naples 12
Guangzhou 11
Amsterdam 10
Chicago 10
Auburn Hills 9
Budapest 9
Taizhou 9
Tokyo 9
Edinburgh 8
Hefei 8
Olomouc 8
Pescara 8
Chengdu 7
Costa Mesa 7
Grosseto 7
Phoenix 7
Pisa 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
Ancona 5
Bonndorf 5
Totale 22.044
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Nome #
Hemodynamic evaluation of the optic nerve head in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. 308
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients 290
Visual impairment in FOXG1-mutated individuals and mice 228
The role of dentate nuclei in human oculomotor control: Insights from cerebrotendinous xanthomatosis 224
Cerebellum and neuropsychiatric disorders: insights from ARSACS 222
Two novel HTRA1 mutations in a European CARASIL patient. 219
Wilson's disease with Leu492Ser mutation and arylsulfatase A pseudodeficiency: just a coincidence? 218
Adult Alexander disease with de novo c.1193C>T heterozygous variant in GFAP gene 217
Transient supranuclear paresis of the abduction in viral encephalitis of the brainstem 215
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: Update on clinical, diagnostic, and management aspects 211
Eye movement abnormalities in a patient with Zellweger spectrum disorder 210
Cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies: a case report 209
Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R gene 203
Visual System Involvement in CADASIL. 198
Systemic blood pressure profile in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 196
Type I sialidosis: a clinical, biochemical and neuroradiological study 196
Typical pathological changes of CADASIL in the optic nerve 196
A two-layered diffusion model traces the dynamics of information processing in the valuation-and-choice circuit of decision making 195
Video-based eye tracking: our experience with advanced stimuli design for eye tracking software 194
A CASE OF CEREBROTENDINOUS XANTHOMATOSIS PRESENTING WITH PARKINSONISM IN THE SEVENTH DECADE 194
Toscana itaca (Italian CADASIL) registry: an implementable online database for CADASIL (Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy). 192
Homozygosity and severity of phenotypic presentation in a CADASIL family 192
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy. 191
Clinical and MRI improvement in a case of progressive multifocal leukoencephalopathy 190
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families 190
Typical pathological changes of CADASIL in the optic nerve 189
A case of ethambutol-induced optic neuropathy harbouring the primary mitochondrial LHON mutation at nt 11778 187
Vertical supranuclear gaze palsy in Niemann-Pick type C disease 187
Sixth nerve and superior division of third nerve palsy due to intracranial extension of multiple myeloma. A diagnostic challenge and differential diagnosis 187
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene. 186
Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias. 185
A case of bilateral facial palsy with detection of herpes simplex virus type 1 DNA in the cerebrospinal fluid and serum anti-gm1 antibodies. 184
Frequency of OPA1 and OPTN gene variations in 18 patients with normal tension glaucoma 182
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation 179
AARS2-related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases 179
null 178
Spatial ranking strategy and enhanced peripheral vision discrimination optimize performance and efficiency of visual sequential search. 178
null 177
Using a simplified trail making test B to assess visuo-spatial and sequencing abilities in hereditary spinocerebellar ataxias (SCA) 177
Trigeminal-Nociceptive Activation And Pupillary Changes In Two Patients With Wernicke’s Encephalopathy 176
Sindrome di Goldman-Favre: descrizione di un caso 174
Ocular-motor profile and effects of memantine in a familial form of adult cerebellar ataxia with slow saccades and square wave saccadic intrusions. 174
Evaluating gaze control on a multi-target sequencing task: The distribution of fixations is evidence of exploration optimisation. 172
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy. 172
Vitamin-E serum level in LHON patients 171
Wernicke Encephalopathy After Gastrointestinal Surgery for Cancer: Causes of Diagnostic Failure or Delay. 168
The first cerebrotendinous xanthomatosis family from Argentina: a new mutation in CYP27A1 gene. 167
Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 167
GABAAergic dysfunction in the olivary-cerebellar-brainstem network may cause eye oscillations and body tremor 166
null 165
Pulsating enophthalmos in an adult patient with type 1 neurofibromatosis 165
A new family with CADASIL: presentation of an homozygous patient and comparison with heterozigous phenotypes. 165
null 165
Acute vestibular syndrome in a patient with cerebral autosomal dominant leukoencephalopathy with subcortical infarcts and leukoencephalopathy (CADASIL) 164
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telithromycin consumption 164
Transient periodic lateralised epileptiform discharges (PLEDs) following internal carotid artery stenting 163
Photophobia and bilateral pulvinar involvement in non-alcoholic Wernicke's encephalopathy. 163
Velocity profile and trajectory of saccades in different forms of cerebellar ataxia 162
Valutazione delle associazioni tra polimorfismi del gene OPA 1 e glaucoma normotensivo in Italia 162
Impairment of vertical saccades from an acute pontine lesion in multiple sclerosis 160
Clinical Course of Two Italian Siblings with Ataxia-Telangiectasia-Like Disorder. 160
Anti-saccades in cerebellar ataxias reveal a contribution of the cerebellum in executive functions 160
Wernicke Syndrome: Seven case reports. 158
High energy efficiency biped robot controlled by the human brain for people with ALS disease 158
A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case 157
Video-Based Eye-Tracking: one year of experience with astidet 156
Alu-element insertion in the OPA1 intron sequence associated with ADOA. 155
A novel point mutation in the mitochondrial tRNA((Trp)) gene produces late-onset encephalomyopathy, plus additional features 154
Idiopathic bilateral facial palsy: is a causative role of anti-GM1 ganglioside and herpes simplex type 1 possible? 153
Evaluating the human ongoing visual search performance by eye tracking application and sequencing tests 153
Four novel CYP27A1 mutations in seven Italian patients with CTX 153
Automatic eye fixations identification based on analysis of variance and covariance, 152
CADASIL and cerebrovascular diseases 152
null 152
Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiency 151
Increased QT variability in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. 151
Fast versus slow: different saccadic behavior in cerebellar ataxias 150
Characteristic eye movements in ataxia-telangiectasia-like disorder: An explanatory hypothesis 150
Molecular genetic study of Leber’s hereditary optic neurophaty (LHON): mutation screening by sequencing of ND1, ND4, ND%, ND6 genes 150
Retinochoroidal atrophy in two adult patients with Angelman syndrome 149
Lateral Medullary Ischemia Presenting with Persistent Hiccups and Vertigo 148
Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). 148
Adult-onset phenylketonuria revealed by acute reversible dementia, prosopagnosia and parkinsonism. 148
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 147
High frequency of exon 10 mutations in the NOTCH3 gene in Italian CADASIL families: phenotypic peculiarities. 146
Retinal nerve fiber layer thinning in CADASIL: an optical coherence tomography and MRI study. 145
Neuro-Ophthalmological findings in two adult siblings with ataxiatelangiectasia– like disorder 144
Alu-Element Insertion In The Opa1 Intron Sequence Associated With ADOA 142
Spike removal through multiscale wavelet and entropy analysis of ocular motor noise: a case study in patients with cerebellar disease. 142
Wernicke's encelophaty after gastro-intestinal surgery for cancer: a retrospective clinical study 142
Lithium neurotoxicity mimicking rapidly progressive dementia 141
The spectrum of NOTCH3 mutation and phonotype variability in fourteen Italian families with CADASIL. 140
Genetic leukoencephalopaties with unknown metabolic pathogenesis 140
null 140
The Primrose syndrome with progressive neurological involvement and cerebral calcification. 140
Human-Robotics Interface for the Interaction with Cognitive and Emotional Human Domains 136
Using simplified trial macking test B to evacuate ongoing learning capabilities on visual search. 136
Eight and a Half Syndrome with Hemiparesis and Hemihypesthesia: The Nine Syndrome? 136
Overconfident Behavior In Informational Cascades: An Eye-Tracking Study 135
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telythromicin consumption 135
Totale 17.263
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Categoria #
all - tutte 79.306
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 79.306
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.223 0 0 0 0 0 310 300 490 376 351 126 270
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
2024/20252.204 92 350 451 305 745 261 0 0 0 0 0 0
Totale 28.943