IRIS
RUFA, ALESSANDRA
 Distribuzione geografica
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Continente #
NA - Nord America 15.766
EU - Europa 11.113
AS - Asia 2.311
SA - Sud America 355
AF - Africa 58
Continente sconosciuto - Info sul continente non disponibili 19
OC - Oceania 19
Totale 29.641
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Nazione #
US - Stati Uniti d'America 15.689
GB - Regno Unito 3.601
IE - Irlanda 1.744
CN - Cina 1.312
UA - Ucraina 1.105
IT - Italia 1.060
SE - Svezia 993
RU - Federazione Russa 744
SG - Singapore 690
DE - Germania 631
FR - Francia 538
FI - Finlandia 342
BR - Brasile 315
TR - Turchia 83
VN - Vietnam 75
ES - Italia 70
NL - Olanda 62
BE - Belgio 55
CA - Canada 55
CI - Costa d'Avorio 29
CZ - Repubblica Ceca 27
BG - Bulgaria 24
IN - India 19
EU - Europa 18
AU - Australia 16
RO - Romania 16
AT - Austria 15
IR - Iran 15
GR - Grecia 11
HK - Hong Kong 11
IL - Israele 11
LT - Lituania 10
UZ - Uzbekistan 10
AR - Argentina 9
HU - Ungheria 9
IQ - Iraq 9
JP - Giappone 9
BD - Bangladesh 8
EC - Ecuador 8
MX - Messico 8
EE - Estonia 7
PK - Pakistan 7
DK - Danimarca 6
EG - Egitto 6
KG - Kirghizistan 6
TW - Taiwan 6
ZA - Sudafrica 6
CH - Svizzera 5
CL - Cile 5
MA - Marocco 5
PT - Portogallo 5
AZ - Azerbaigian 4
DO - Repubblica Dominicana 4
LK - Sri Lanka 4
LV - Lettonia 4
NO - Norvegia 4
PH - Filippine 4
PL - Polonia 4
TN - Tunisia 4
UY - Uruguay 4
VE - Venezuela 4
AM - Armenia 3
BO - Bolivia 3
ID - Indonesia 3
LA - Repubblica Popolare Democratica del Laos 3
LU - Lussemburgo 3
MD - Moldavia 3
MK - Macedonia 3
NZ - Nuova Zelanda 3
PA - Panama 3
PE - Perù 3
RS - Serbia 3
SA - Arabia Saudita 3
SI - Slovenia 3
CO - Colombia 2
DZ - Algeria 2
GE - Georgia 2
KR - Corea 2
KZ - Kazakistan 2
NG - Nigeria 2
PY - Paraguay 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
AL - Albania 1
AN - Antille olandesi 1
BS - Bahamas 1
BY - Bielorussia 1
GL - Groenlandia 1
HN - Honduras 1
HR - Croazia 1
JM - Giamaica 1
JO - Giordania 1
KE - Kenya 1
KW - Kuwait 1
LB - Libano 1
MM - Myanmar 1
MS - Montserrat 1
MT - Malta 1
Totale 29.634
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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 761
Houston 638
Wilmington 627
Woodbridge 626
Seattle 490
Cambridge 459
Ann Arbor 443
Princeton 354
Beijing 311
Nanjing 290
Singapore 267
Siena 260
Helsinki 157
Boardman 152
San Mateo 151
Nanchang 120
New York 107
Moscow 87
Shenyang 84
San Diego 77
Rome 68
Venezia 68
Düsseldorf 67
Izmir 67
Florence 64
Málaga 62
Dong Ket 60
Council Bluffs 55
Kunming 54
Shanghai 53
Tianjin 52
Milan 48
Jiaxing 46
Hebei 45
Changsha 38
Dearborn 38
Brussels 36
Los Angeles 35
Toronto 32
London 30
Washington 30
Abidjan 29
Fremont 29
Mestre 29
Norwalk 28
Jinan 26
Lancaster 25
Redwood City 25
Sofia 24
Bologna 22
São Paulo 22
Dallas 21
Hangzhou 20
Ningbo 20
Naples 18
Renton 18
San Francisco 17
Waanrode 17
Frankfurt am Main 16
Brno 14
Falls Church 14
Munich 14
St Louis 14
The Dalles 14
Lanzhou 13
Zhengzhou 13
Changchun 12
Belo Horizonte 11
Guangzhou 11
Pescara 11
Rio de Janeiro 11
Amsterdam 10
Chicago 10
Tashkent 10
Vienna 10
Auburn Hills 9
Brasília 9
Budapest 9
Taizhou 9
Tokyo 9
Edinburgh 8
Hefei 8
Nuremberg 8
Olomouc 8
Phoenix 8
Chengdu 7
Costa Mesa 7
Curitiba 7
Grosseto 7
Pisa 7
Portsmouth 7
Saint Petersburg 7
Tallinn 7
Totale 22.242
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Nome #
Hemodynamic evaluation of the optic nerve head in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. 311
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients 293
Visual impairment in FOXG1-mutated individuals and mice 236
The role of dentate nuclei in human oculomotor control: Insights from cerebrotendinous xanthomatosis 231
Cerebellum and neuropsychiatric disorders: insights from ARSACS 230
Adult Alexander disease with de novo c.1193C>T heterozygous variant in GFAP gene 230
Wilson's disease with Leu492Ser mutation and arylsulfatase A pseudodeficiency: just a coincidence? 222
Two novel HTRA1 mutations in a European CARASIL patient. 221
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: Update on clinical, diagnostic, and management aspects 221
Transient supranuclear paresis of the abduction in viral encephalitis of the brainstem 220
Cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies: a case report 213
Eye movement abnormalities in a patient with Zellweger spectrum disorder 211
Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R gene 210
A two-layered diffusion model traces the dynamics of information processing in the valuation-and-choice circuit of decision making 206
A CASE OF CEREBROTENDINOUS XANTHOMATOSIS PRESENTING WITH PARKINSONISM IN THE SEVENTH DECADE 203
Typical pathological changes of CADASIL in the optic nerve 201
Type I sialidosis: a clinical, biochemical and neuroradiological study 200
Visual System Involvement in CADASIL. 199
Systemic blood pressure profile in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 198
Homozygosity and severity of phenotypic presentation in a CADASIL family 198
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy. 198
Video-based eye tracking: our experience with advanced stimuli design for eye tracking software 198
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families 195
Toscana itaca (Italian CADASIL) registry: an implementable online database for CADASIL (Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy). 194
Frequency of OPA1 and OPTN gene variations in 18 patients with normal tension glaucoma 193
Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias. 192
Vertical supranuclear gaze palsy in Niemann-Pick type C disease 191
Clinical and MRI improvement in a case of progressive multifocal leukoencephalopathy 191
Typical pathological changes of CADASIL in the optic nerve 190
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene. 190
A case of ethambutol-induced optic neuropathy harbouring the primary mitochondrial LHON mutation at nt 11778 190
AARS2-related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases 190
Sixth nerve and superior division of third nerve palsy due to intracranial extension of multiple myeloma. A diagnostic challenge and differential diagnosis 189
A case of bilateral facial palsy with detection of herpes simplex virus type 1 DNA in the cerebrospinal fluid and serum anti-gm1 antibodies. 188
Sindrome di Goldman-Favre: descrizione di un caso 186
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation 185
Spatial ranking strategy and enhanced peripheral vision discrimination optimize performance and efficiency of visual sequential search. 184
Using a simplified trail making test B to assess visuo-spatial and sequencing abilities in hereditary spinocerebellar ataxias (SCA) 181
Ocular-motor profile and effects of memantine in a familial form of adult cerebellar ataxia with slow saccades and square wave saccadic intrusions. 181
null 178
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy. 178
Trigeminal-Nociceptive Activation And Pupillary Changes In Two Patients With Wernicke’s Encephalopathy 178
null 177
Evaluating gaze control on a multi-target sequencing task: The distribution of fixations is evidence of exploration optimisation. 175
Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 174
GABAAergic dysfunction in the olivary-cerebellar-brainstem network may cause eye oscillations and body tremor 174
Vitamin-E serum level in LHON patients 172
A new family with CADASIL: presentation of an homozygous patient and comparison with heterozigous phenotypes. 171
The first cerebrotendinous xanthomatosis family from Argentina: a new mutation in CYP27A1 gene. 170
Anti-saccades in cerebellar ataxias reveal a contribution of the cerebellum in executive functions 170
Valutazione delle associazioni tra polimorfismi del gene OPA 1 e glaucoma normotensivo in Italia 169
Acute vestibular syndrome in a patient with cerebral autosomal dominant leukoencephalopathy with subcortical infarcts and leukoencephalopathy (CADASIL) 168
Wernicke Encephalopathy After Gastrointestinal Surgery for Cancer: Causes of Diagnostic Failure or Delay. 168
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telithromycin consumption 168
Pulsating enophthalmos in an adult patient with type 1 neurofibromatosis 168
Photophobia and bilateral pulvinar involvement in non-alcoholic Wernicke's encephalopathy. 167
Transient periodic lateralised epileptiform discharges (PLEDs) following internal carotid artery stenting 166
Fast versus slow: different saccadic behavior in cerebellar ataxias 166
A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case 166
Impairment of vertical saccades from an acute pontine lesion in multiple sclerosis 165
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Clinical Course of Two Italian Siblings with Ataxia-Telangiectasia-Like Disorder. 165
High energy efficiency biped robot controlled by the human brain for people with ALS disease 165
null 165
Velocity profile and trajectory of saccades in different forms of cerebellar ataxia 164
Alu-element insertion in the OPA1 intron sequence associated with ADOA. 163
Wernicke Syndrome: Seven case reports. 160
Automatic eye fixations identification based on analysis of variance and covariance, 160
CADASIL and cerebrovascular diseases 160
A novel point mutation in the mitochondrial tRNA((Trp)) gene produces late-onset encephalomyopathy, plus additional features 160
Characteristic eye movements in ataxia-telangiectasia-like disorder: An explanatory hypothesis 160
Evaluating the human ongoing visual search performance by eye tracking application and sequencing tests 159
Alu-Element Insertion In The Opa1 Intron Sequence Associated With ADOA 157
Video-Based Eye-Tracking: one year of experience with astidet 157
Four novel CYP27A1 mutations in seven Italian patients with CTX 156
Idiopathic bilateral facial palsy: is a causative role of anti-GM1 ganglioside and herpes simplex type 1 possible? 155
Retinochoroidal atrophy in two adult patients with Angelman syndrome 154
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 154
Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiency 154
Increased QT variability in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. 154
Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). 152
Molecular genetic study of Leber’s hereditary optic neurophaty (LHON): mutation screening by sequencing of ND1, ND4, ND%, ND6 genes 152
null 152
Neuro-Ophthalmological findings in two adult siblings with ataxiatelangiectasia– like disorder 151
Adult-onset phenylketonuria revealed by acute reversible dementia, prosopagnosia and parkinsonism. 151
Lateral Medullary Ischemia Presenting with Persistent Hiccups and Vertigo 150
High frequency of exon 10 mutations in the NOTCH3 gene in Italian CADASIL families: phenotypic peculiarities. 148
Retinal nerve fiber layer thinning in CADASIL: an optical coherence tomography and MRI study. 147
Wernicke's encelophaty after gastro-intestinal surgery for cancer: a retrospective clinical study 146
Evaluating human visual search performance by Monte Carlo methods and heuristic model 146
Lithium neurotoxicity mimicking rapidly progressive dementia 145
Genetic leukoencephalopaties with unknown metabolic pathogenesis 144
Leber hereditary optic neuropathy in 2 of 4 siblings with 11778 mtDNA mutation: clinical variability or effect of toxic exposure? 143
Spike removal through multiscale wavelet and entropy analysis of ocular motor noise: a case study in patients with cerebellar disease. 142
The spectrum of NOTCH3 mutation and phonotype variability in fourteen Italian families with CADASIL. 141
Hemodynamic evaluation at the papilla in CADASIL 141
Plasma levels of asymmetric dimethylarginine (ADMA) in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarct and Leukoencephalopathy (CADASIL) 141
The Primrose syndrome with progressive neurological involvement and cerebral calcification. 141
Assessment of cognitive profile and visual spatial attention in autosomal dominant cerebellar ataxia type 2 (SCA2). Correlation Between eye-tracking and neuropsychological studies. 140
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Totale 17.748
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Categoria #
all - tutte 87.176
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 87.176
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020747 0 0 0 0 0 0 0 0 0 351 126 270
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
2024/20253.246 92 350 451 305 745 275 192 334 413 89 0 0
Totale 29.985