IRIS
MIGNARRI, ANDREA
 Distribuzione geografica
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Continente #
NA - Nord America 6.413
EU - Europa 4.031
AS - Asia 1.969
SA - Sud America 334
AF - Africa 132
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 3
Totale 12.888
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Nazione #
US - Stati Uniti d'America 6.344
GB - Regno Unito 1.273
RU - Federazione Russa 777
CN - Cina 684
SG - Singapore 624
IE - Irlanda 477
IT - Italia 292
BR - Brasile 284
UA - Ucraina 278
SE - Svezia 239
DE - Germania 213
FR - Francia 196
VN - Vietnam 176
HK - Hong Kong 154
FI - Finlandia 100
ZA - Sudafrica 81
KR - Corea 73
ES - Italia 58
BD - Bangladesh 54
TR - Turchia 53
CA - Canada 36
IN - India 34
NL - Olanda 27
PL - Polonia 26
BE - Belgio 23
PK - Pakistan 20
IQ - Iraq 19
MX - Messico 19
JP - Giappone 15
AR - Argentina 13
LT - Lituania 11
MA - Marocco 10
SA - Arabia Saudita 10
IL - Israele 9
CO - Colombia 8
DZ - Algeria 8
EG - Egitto 8
ID - Indonesia 8
NG - Nigeria 7
VE - Venezuela 7
EC - Ecuador 6
EU - Europa 6
PE - Perù 6
SK - Slovacchia (Repubblica Slovacca) 6
CI - Costa d'Avorio 5
CZ - Repubblica Ceca 5
GR - Grecia 5
KE - Kenya 4
KZ - Kazakistan 4
PT - Portogallo 4
TN - Tunisia 4
AT - Austria 3
AZ - Azerbaigian 3
BG - Bulgaria 3
BO - Bolivia 3
IR - Iran 3
MD - Moldavia 3
PH - Filippine 3
SV - El Salvador 3
UY - Uruguay 3
UZ - Uzbekistan 3
AE - Emirati Arabi Uniti 2
AL - Albania 2
AU - Australia 2
CL - Cile 2
ET - Etiopia 2
HN - Honduras 2
JM - Giamaica 2
JO - Giordania 2
KW - Kuwait 2
LB - Libano 2
MK - Macedonia 2
MY - Malesia 2
NP - Nepal 2
PA - Panama 2
PY - Paraguay 2
RO - Romania 2
SI - Slovenia 2
AM - Armenia 1
AO - Angola 1
BB - Barbados 1
BH - Bahrain 1
CG - Congo 1
CR - Costa Rica 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
GD - Grenada 1
HU - Ungheria 1
KG - Kirghizistan 1
LV - Lettonia 1
LY - Libia 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
OM - Oman 1
PS - Palestinian Territory 1
RS - Serbia 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
TJ - Tagikistan 1
Totale 12.888
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Città #
Southend 1.131
Dallas 1.092
Fairfield 675
Menlo Park 504
Dublin 475
Ashburn 411
Woodbridge 337
Singapore 328
Chandler 273
Wilmington 253
Seattle 249
Houston 246
Jacksonville 243
Moscow 241
Cambridge 228
Santa Clara 223
Beijing 197
Ann Arbor 190
San Jose 189
Hong Kong 150
Siena 95
Princeton 93
Hefei 79
Johannesburg 79
Los Angeles 74
Seoul 71
Nanjing 70
New York 62
The Dalles 60
Ho Chi Minh City 55
Munich 54
Málaga 52
Helsinki 44
Lauterbourg 44
Boardman 42
Lancaster 42
San Diego 40
Council Bluffs 34
Izmir 33
Hanoi 31
Buffalo 29
Dong Ket 29
San Mateo 26
Orem 24
Changsha 22
London 22
Nanchang 22
Warsaw 22
Hebei 20
Tianjin 19
Shenyang 18
São Paulo 17
Brussels 16
Shanghai 16
Dearborn 15
Florence 14
Jiaxing 14
Milan 14
San Francisco 14
Tokyo 14
Turku 14
Columbus 13
Redondo Beach 13
Düsseldorf 12
Montreal 12
Norwalk 12
Toronto 12
Chicago 11
Frankfurt am Main 11
Brooklyn 10
Kunming 10
Belo Horizonte 9
Stockholm 9
Atlanta 8
Guangzhou 8
Hangzhou 8
Jinan 8
Rome 8
Bengaluru 7
Bologna 7
Da Nang 7
Denver 7
Waanrode 7
Washington 7
Abuja 6
Baghdad 6
Boston 6
Brasília 6
Bratislava 6
Lahore 6
Manchester 6
Mestre 6
Mumbai 6
Nuremberg 6
Phoenix 6
Richland 6
Rio de Janeiro 6
Abidjan 5
Amsterdam 5
Andover 5
Totale 9.499
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Nome #
An atypical case of Creutzfeldt-Jakob disease mimicking frontotemporal dementia: genotypic influence and clinical implications 476
A CASE OF CEREBROTENDINOUS XANTHOMATOSIS PRESENTING WITH PARKINSONISM IN THE SEVENTH DECADE 395
Cerebellum and neuropsychiatric disorders: insights from ARSACS 315
A mimic of first dorsal interosseus atrophy revealed by ultrasound study 313
Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia 312
Eye movement abnormalities in a patient with Zellweger spectrum disorder 289
Zellweger Spectrum Disorder with Mild Phenotype Caused by PEX2 Gene Mutations 285
Cerebellar hypometabolism with normal structural findings in Cerebrotendinous xanthomatosis. A case report 282
Clinical relevance of brain volume changes in patients with cerebrotendinous xanthomatosis 281
The role of dentate nuclei in human oculomotor control: Insights from cerebrotendinous xanthomatosis 278
Mitochondrial dysfunction in hereditary spastic paraparesis with mutations in DDHD1/SPG28 276
Demyelinating polyneuropathy in a case of anti-LGI1 encephalitis 266
Narcolepsy is a common phenotype in HSAN IE and ADCA-DN 262
Cerebrotendinous xanthomatosis with progressive cerebellar vacuolation. Six-year MRI follow-up 258
Temporal lobe abnormalities in neurosyphilis 253
Two-year follow-up after chelating therapy in a patient with adult-onset parkinsonism and hypermanganesaemia due to SLC30A10 mutations 252
The first Italian patient with oculopharyngodistal myopathy: Case report and considerations on differential diagnosis. 245
Imaging of the thymus in myotonic dystrophy type 1 245
Brain metabolism changes after therapy with chenodeoxycholic acid in a case of cerebrotendinous xanthomatosis. 234
Polyneuropathy with demyelinating changes in Churg–Strauss syndrome: an unusual association 234
The spectrum of magnetic resonance findings in cerebrotendinous xanthomatosis: redefinition and evidence of new markers of disease progression 233
Primary familial brain calcification: Genetic analysis and clinical spectrum. 231
A suspicion index for early diagnosis and treatment of cerebrotendinous xanthomatosis. 229
Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease. 224
Hand muscles corticomotor excitability in hereditary spastic paraparesis type 4. 223
Electrodiagnosis in cranial botulism 223
Clinical Features and Outcome of the Guillain–Barre Syndrome: A Single-Center 11-Year Experience 222
Hereditary spastic paraplegia type 5: a potentially treatable disorder of cholesterol metabolism 222
Long-Term Bone Density Evaluation in Cerebrotendinous Xanthomatosis: Evidence of Improvement after Chenodeoxycholic Acid Treatment. 217
First report of an Iraqi Kurdish CADASIL patient. 216
Neuroendocrine lung cancer in a patient with limbic encephalopathy due to anti-Hu antibodies: A rare association not to be missed 215
Myoclonus epilepsy, retinitis pigmentosa, leukoencephalopathy and cerebral calcifications associated with a novel m.5513G>A mutation in the MT-TW gene 215
Parkinsonism as neurological presentation of late-onset cerebrotendinous xanthomatosis 214
Brachial plexopathy due to breast cancer metastases: electrophysiological and imaging findings 211
Lithium neurotoxicity mimicking rapidly progressive dementia 205
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study 204
Discordant manifestations in Italian brothers with GNE myopathy 202
Polyneuropathy in cerebrotendinous xanthomatosis and response to treatment with chenodeoxycholic acid. 201
A Novel CSF1R Mutation in a Patient with Clinical and Neuroradiological Features of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids 200
SPG5 siblings with different phenotypes showing reduction of 27-hydroxycholesterol after simvastatin-ezetimibe treatment 164
From the liver to the brain: manganese matters : Focus on cirrhosis-related Parkinsonism. 159
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Enlarging brain xanthomas in a patient with cerebrotendinous xanthomatosis. 130
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Mitochondrial recessive ataxia syndrome: A neurological rarity not to be missed. 119
Ataxia with oculomotor apraxia type 2: not always an easy diagnosis 119
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Erratum: Validation of plasma microRNAs as biomarkers for myotonic dystrophy type 1 (Scientific Reports (2016) 6 (38174) DOI: 10.1038/srep38174) 116
Evaluation of cholesterol metabolism in cerebrotendinous xanthomatosis 114
Correction to: Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review (Journal of Neurology, (2022), 269, 1, (437-450), 10.1007/s00415-021-10792-3) 110
Correction to: Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review 110
The safety and effectiveness of chenodeoxycholic acid treatment in patients withcerebrotendinous xanthomatosis:two retrospective cohort studies 110
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Familial Alzheimer’s disease associated with heterozygous NPC1 mutation 107
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Oculomotor features in SCA27B patients 101
Primary familiall brain calcification caused by MYORG mutations in an Italian family 101
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Primary familial brain calcification with mild phenotype due to a new PDGFB mutation 87
Neuromuscular excitability changes produced by sustained voluntary contraction and response to mexiletine in myotonia congenita 68
Multiple sclerosis and chronic progressive external ophthalmoplegia associated with a large scale mitochondrial DNA single deletion 67
Treatment of SPG5 with cholesterol-lowering drugs 64
Primary familial brain calcification: update on molecular genetics 61
Syntactic complexity in Mild Cognitive Impairment due to Alzheimer’s disease (MCI-AD): long-distance dependencies and working memory in comprehension of relative clauses 50
Totale 13.061
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Categoria #
all - tutte 35.091
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 35.091
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021107 0 0 0 0 0 0 0 0 0 0 0 107
2021/2022699 33 89 39 41 47 26 49 17 48 85 76 149
2022/2023981 58 66 133 125 106 192 21 77 105 58 22 18
2023/2024677 36 21 58 30 17 192 246 15 3 13 4 42
2024/20251.479 17 73 136 60 227 102 64 66 130 42 153 409
2025/20263.944 283 532 910 434 703 114 316 117 139 206 94 96
Totale 13.061