IRIS
RUFA, ALESSANDRA
 Distribuzione geografica
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Continente #
NA - Nord America 20.892
EU - Europa 13.992
AS - Asia 7.425
SA - Sud America 1.196
AF - Africa 479
OC - Oceania 22
Continente sconosciuto - Info sul continente non disponibili 21
Totale 44.027
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Nazione #
US - Stati Uniti d'America 20.657
GB - Regno Unito 3.701
CN - Cina 2.786
RU - Federazione Russa 2.671
SG - Singapore 2.317
IE - Irlanda 1.723
IT - Italia 1.239
UA - Ucraina 1.106
BR - Brasile 1.011
SE - Svezia 1.006
FR - Francia 785
DE - Germania 771
VN - Vietnam 612
HK - Hong Kong 520
FI - Finlandia 459
KR - Corea 397
ZA - Sudafrica 275
IN - India 178
CA - Canada 136
TR - Turchia 116
ES - Italia 97
NL - Olanda 96
BD - Bangladesh 83
IQ - Iraq 78
NG - Nigeria 71
MX - Messico 60
PL - Polonia 57
BE - Belgio 56
JP - Giappone 54
AR - Argentina 53
PK - Pakistan 53
CI - Costa d'Avorio 31
EC - Ecuador 31
CZ - Repubblica Ceca 28
SA - Arabia Saudita 28
BG - Bulgaria 27
CL - Cile 25
CO - Colombia 25
UZ - Uzbekistan 25
AT - Austria 24
MA - Marocco 23
RO - Romania 23
LT - Lituania 21
AU - Australia 19
KE - Kenya 19
EU - Europa 17
ID - Indonesia 17
IR - Iran 15
IL - Israele 14
PH - Filippine 14
VE - Venezuela 14
EG - Egitto 13
GR - Grecia 12
HU - Ungheria 11
JO - Giordania 11
NO - Norvegia 11
PY - Paraguay 11
TN - Tunisia 11
UY - Uruguay 11
DZ - Algeria 10
KG - Kirghizistan 10
AZ - Azerbaigian 9
DK - Danimarca 9
AE - Emirati Arabi Uniti 8
BO - Bolivia 8
DO - Repubblica Dominicana 8
ET - Etiopia 8
MY - Malesia 8
EE - Estonia 7
NP - Nepal 7
OM - Oman 7
PS - Palestinian Territory 7
PT - Portogallo 7
JM - Giamaica 6
KZ - Kazakistan 6
PE - Perù 6
TW - Taiwan 6
AL - Albania 5
CH - Svizzera 5
HN - Honduras 5
LB - Libano 5
LV - Lettonia 5
SI - Slovenia 5
SN - Senegal 5
GE - Georgia 4
KW - Kuwait 4
LK - Sri Lanka 4
MD - Moldavia 4
PA - Panama 4
RS - Serbia 4
SK - Slovacchia (Repubblica Slovacca) 4
SY - Repubblica araba siriana 4
TT - Trinidad e Tobago 4
AM - Armenia 3
AO - Angola 3
HR - Croazia 3
LA - Repubblica Popolare Democratica del Laos 3
LU - Lussemburgo 3
MK - Macedonia 3
NZ - Nuova Zelanda 3
Totale 43.984
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Città #
Menlo Park 4.450
Southend 3.333
Dallas 2.816
Dublin 1.716
Fairfield 1.363
Singapore 1.280
Ashburn 1.192
Chandler 1.127
Jacksonville 915
Santa Clara 791
Moscow 680
Beijing 660
Houston 653
Wilmington 622
Woodbridge 621
Hong Kong 493
San Jose 491
Hefei 488
Seattle 487
Cambridge 457
Ann Arbor 437
Seoul 396
Princeton 351
Nanjing 285
Siena 267
Johannesburg 247
The Dalles 240
Los Angeles 221
Helsinki 220
New York 193
Ho Chi Minh City 185
Lauterbourg 182
Boardman 152
San Mateo 150
Hanoi 147
Nanchang 119
Buffalo 114
Munich 111
Council Bluffs 107
São Paulo 103
Shenyang 86
Milan 81
Orem 78
Rome 78
San Diego 77
Florence 74
Venezia 68
Izmir 67
Abuja 66
Düsseldorf 66
Shanghai 63
Málaga 62
Dong Ket 60
Tianjin 56
Turku 55
Kunming 54
London 53
Tokyo 53
Frankfurt am Main 51
Toronto 47
Chennai 45
Jiaxing 45
Hebei 44
Warsaw 44
Columbus 41
Bengaluru 40
Changsha 40
Dearborn 38
Rio de Janeiro 38
San Francisco 38
Brussels 36
Brooklyn 35
Atlanta 32
Abidjan 31
Washington 31
Manchester 30
Belo Horizonte 29
Fremont 29
Jinan 29
Mestre 29
Montreal 29
Redondo Beach 29
Norwalk 28
Amsterdam 27
Lancaster 27
Phoenix 27
Naples 26
Sofia 26
Chicago 25
Redwood City 25
Brasília 24
Haiphong 24
Tashkent 24
Bologna 23
Denver 23
Hangzhou 23
Stockholm 23
Curitiba 22
Da Nang 21
Dhaka 21
Totale 31.378
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Nome #
A CASE OF CEREBROTENDINOUS XANTHOMATOSIS PRESENTING WITH PARKINSONISM IN THE SEVENTH DECADE 390
A case of bilateral facial palsy with detection of herpes simplex virus type 1 DNA in the cerebrospinal fluid and serum anti-gm1 antibodies. 366
A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case 366
A case of ethambutol-induced optic neuropathy harbouring the primary mitochondrial LHON mutation at nt 11778 358
A new family with CADASIL: presentation of an homozygous patient and comparison with heterozigous phenotypes. 353
Hemodynamic evaluation of the optic nerve head in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. 351
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients 339
AARS2-related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases 333
Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R gene 332
Adult Alexander disease with de novo c.1193C>T heterozygous variant in GFAP gene 325
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: Update on clinical, diagnostic, and management aspects 325
A two-layered diffusion model traces the dynamics of information processing in the valuation-and-choice circuit of decision making 321
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy. 320
Cerebellum and neuropsychiatric disorders: insights from ARSACS 314
Cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies: a case report 303
Transient supranuclear paresis of the abduction in viral encephalitis of the brainstem 300
A novel point mutation in the mitochondrial tRNA((Trp)) gene produces late-onset encephalomyopathy, plus additional features 294
Visual impairment in FOXG1-mutated individuals and mice 294
A case report of transient posterior internuclear ophthalmoplegia (PINO) associated with encephalitis of ponto-mesencephalic junction 291
Eye movement abnormalities in a patient with Zellweger spectrum disorder 287
Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 287
Two novel HTRA1 mutations in a European CARASIL patient. 286
Frequency of OPA1 and OPTN gene variations in 18 patients with normal tension glaucoma 285
Automatic eye fixations identification based on analysis of variance and covariance, 284
A case of ovarioleukodystrophy without elF2B mutations 284
Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias. 282
The role of dentate nuclei in human oculomotor control: Insights from cerebrotendinous xanthomatosis 277
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families 277
Typical pathological changes of CADASIL in the optic nerve 276
Clinical and MRI improvement in a case of progressive multifocal leukoencephalopathy 273
Clinical Course of Two Italian Siblings with Ataxia-Telangiectasia-Like Disorder. 273
Systemic blood pressure profile in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 271
Homozygosity and severity of phenotypic presentation in a CADASIL family 269
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 266
Wilson's disease with Leu492Ser mutation and arylsulfatase A pseudodeficiency: just a coincidence? 266
Acute vestibular syndrome in a patient with cerebral autosomal dominant leukoencephalopathy with subcortical infarcts and leukoencephalopathy (CADASIL) 266
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy. 266
Anti-saccades in cerebellar ataxias reveal a contribution of the cerebellum in executive functions 263
Blinking Rate Comparison Between Patients with Chronic Pain and Parkinson's Disease 262
Spatial ranking strategy and enhanced peripheral vision discrimination optimize performance and efficiency of visual sequential search. 257
Alu-Element Insertion In The Opa1 Intron Sequence Associated With ADOA 255
A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosis 254
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene. 254
Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). 253
Toscana itaca (Italian CADASIL) registry: an implementable online database for CADASIL (Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy). 252
Vertical supranuclear gaze palsy in Niemann-Pick type C disease 252
GABAAergic dysfunction in the olivary-cerebellar-brainstem network may cause eye oscillations and body tremor 252
Visual System Involvement in CADASIL. 247
Genetic leukoencephalopaties with unknown metabolic pathogenesis 245
Alu-element insertion in the OPA1 intron sequence associated with ADOA. 244
Characteristic eye movements in ataxia-telangiectasia-like disorder: An explanatory hypothesis 244
Impairment of vertical saccades from an acute pontine lesion in multiple sclerosis 243
A novel OPA1 mutation resulting in atypical dominant optic atrophy with NTG “Like” phenotype. 243
CADASIL and cerebrovascular diseases 242
Evaluating the human ongoing visual search performance by eye tracking application and sequencing tests 242
Sixth nerve and superior division of third nerve palsy due to intracranial extension of multiple myeloma. A diagnostic challenge and differential diagnosis 242
Trigeminal-Nociceptive Activation And Pupillary Changes In Two Patients With Wernicke’s Encephalopathy 241
Evaluating gaze control on a multi-target sequencing task: The distribution of fixations is evidence of exploration optimisation. 240
Type I sialidosis: a clinical, biochemical and neuroradiological study 240
Video-based eye tracking: our experience with advanced stimuli design for eye tracking software 239
Acute visual loss due to anterior ischemic optic neuropathy as first symptom in a patient with CADASIL 238
Molecular genetic study of Leber’s hereditary optic neurophaty (LHON): mutation screening by sequencing of ND1, ND4, ND%, ND6 genes 238
Ocular-motor profile and effects of memantine in a familial form of adult cerebellar ataxia with slow saccades and square wave saccadic intrusions. 237
Fast versus slow: different saccadic behavior in cerebellar ataxias 236
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation 235
Using a simplified trail making test B to assess visuo-spatial and sequencing abilities in hereditary spinocerebellar ataxias (SCA) 232
Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy 229
Transient periodic lateralised epileptiform discharges (PLEDs) following internal carotid artery stenting 228
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telithromycin consumption 228
Eight and a Half Syndrome with Hemiparesis and Hemihypesthesia: The Nine Syndrome? 227
Sindrome di Goldman-Favre: descrizione di un caso 226
Eye movement recording and nonlinear dynamics analysis - The case of saccades 225
Adult-onset phenylketonuria revealed by acute reversible dementia, prosopagnosia and parkinsonism. 222
Analysis of opa1 isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 gene 221
Cognitive Biases and Gaze Direction: An Experimental Study 221
Hemodynamic evaluation at the papilla in CADASIL 220
Analisi quantitativa di saccadi orizzontali in disordini atassici degenerative 220
High energy efficiency biped robot controlled by the human brain for people with ALS disease 220
Vitamin-E serum level in LHON patients 220
High-Dose Methylprednisolone For Bickerstaff’s Brainstem Encephalitis. 219
Wernicke Encephalopathy After Gastrointestinal Surgery for Cancer: Causes of Diagnostic Failure or Delay. 219
Neuro-Ophthalmological findings in two adult siblings with ataxiatelangiectasia– like disorder 218
The first cerebrotendinous xanthomatosis family from Argentina: a new mutation in CYP27A1 gene. 217
Photophobia and bilateral pulvinar involvement in non-alcoholic Wernicke's encephalopathy. 217
Evaluating human visual search performance by Monte Carlo methods and heuristic model 216
Valutazione delle associazioni tra polimorfismi del gene OPA 1 e glaucoma normotensivo in Italia 214
Velocity profile and trajectory of saccades in different forms of cerebellar ataxia 212
Visual Sequencing Search Strategy in Parkinson's Disease 209
Pulsating enophthalmos in an adult patient with type 1 neurofibromatosis 209
Heterogeneity of retinal manifestations in mitochondrial myopathy: genotype/phenotype correlation in our experience. 208
Assessment of cognitive profile and visual spatial attention in autosomal dominant cerebellar ataxia type 2 (SCA2). Correlation between eye-tracking and neuroosychological studies. 208
Cognitive Biases And Gaze Direction. An Experimental Study. 208
Lateral Medullary Ischemia Presenting with Persistent Hiccups and Vertigo 206
Ischemic stroke as first clinical manifestation in alagille syndrome : a case report. 205
Dynamical complexity analysis of saccadic eye movements in two different psychological conditions 205
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telythromicin consumption 204
Lithium neurotoxicity mimicking rapidly progressive dementia 204
Increased QT variability in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. 203
Plasma levels of asymmetric dimethylarginine (ADMA) in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarct and Leukoencephalopathy (CADASIL) 203
Idiopathic bilateral facial palsy: is a causative role of anti-GM1 ganglioside and herpes simplex type 1 possible? 202
Totale 25.685
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Categoria #
all - tutte 117.536
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 117.536
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021792 0 0 0 0 0 0 0 0 0 169 400 223
2021/20222.365 146 295 201 189 128 59 100 78 110 251 260 548
2022/20233.901 233 254 541 507 466 736 67 339 434 93 161 70
2023/20242.645 122 78 217 107 104 712 884 114 43 40 36 188
2024/20255.353 92 346 437 294 738 273 192 328 405 189 541 1.518
2025/202612.704 1.021 2.214 1.968 1.403 2.620 457 1.388 466 423 744 0 0
Totale 44.401