IRIS UniCatt

Conte, Amelia
 Distribuzione geografica
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Continente #
EU - Europa 4.102
NA - Nord America 4.096
AS - Asia 2.724
SA - Sud America 455
AF - Africa 101
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 4
Totale 11.492
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Nazione #
US - Stati Uniti d'America 4.000
DE - Germania 1.824
SG - Singapore 1.195
CN - Cina 758
SE - Svezia 466
BR - Brasile 366
IT - Italia 348
UA - Ucraina 343
FR - Francia 254
VN - Vietnam 242
PL - Polonia 224
GB - Regno Unito 175
IE - Irlanda 129
FI - Finlandia 102
IN - India 87
ID - Indonesia 86
RU - Federazione Russa 80
JP - Giappone 64
TR - Turchia 56
CA - Canada 55
BE - Belgio 52
HK - Hong Kong 52
BD - Bangladesh 43
CI - Costa d'Avorio 37
NL - Olanda 35
IQ - Iraq 30
AR - Argentina 28
ZA - Sudafrica 22
MX - Messico 20
PK - Pakistan 19
ES - Italia 15
SA - Arabia Saudita 13
AE - Emirati Arabi Uniti 12
CO - Colombia 12
MA - Marocco 12
PY - Paraguay 12
AT - Austria 11
CH - Svizzera 11
CL - Cile 11
AU - Australia 10
EC - Ecuador 10
IL - Israele 8
TN - Tunisia 8
JO - Giordania 7
DO - Repubblica Dominicana 6
IR - Iran 6
PH - Filippine 6
VE - Venezuela 6
HN - Honduras 5
KG - Kirghizistan 5
TH - Thailandia 5
ET - Etiopia 4
KE - Kenya 4
PE - Perù 4
PT - Portogallo 4
RO - Romania 4
SN - Senegal 4
UY - Uruguay 4
UZ - Uzbekistan 4
AZ - Azerbaigian 3
BH - Bahrain 3
DK - Danimarca 3
DZ - Algeria 3
GR - Grecia 3
HR - Croazia 3
JM - Giamaica 3
LK - Sri Lanka 3
AO - Angola 2
BG - Bulgaria 2
BY - Bielorussia 2
CR - Costa Rica 2
CZ - Repubblica Ceca 2
EU - Europa 2
GE - Georgia 2
KR - Corea 2
KZ - Kazakistan 2
LT - Lituania 2
MD - Moldavia 2
MM - Myanmar 2
MN - Mongolia 2
NO - Norvegia 2
NP - Nepal 2
SK - Slovacchia (Repubblica Slovacca) 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AD - Andorra 1
AM - Armenia 1
BB - Barbados 1
BO - Bolivia 1
BZ - Belize 1
CG - Congo 1
EG - Egitto 1
GM - Gambi 1
GT - Guatemala 1
GY - Guiana 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
MT - Malta 1
MU - Mauritius 1
MY - Malesia 1
PA - Panama 1
Totale 11.488
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Città #
Singapore 658
Chandler 520
Ashburn 503
San Jose 297
Warsaw 190
Ann Arbor 171
San Mateo 149
Jacksonville 142
Nürnberg 141
Beijing 128
Dublin 125
Nanjing 121
New York 121
Redmond 117
Wilmington 86
Woodbridge 86
Ho Chi Minh City 78
Jakarta 77
Houston 74
Lauterbourg 73
Boston 72
Los Angeles 65
Seattle 64
Cattolica 63
Fairfield 62
Hanoi 62
Nanchang 58
Dearborn 56
Rome 54
Milan 53
Munich 51
Lawrence 49
Tokyo 49
Frankfurt am Main 47
Moscow 47
Hefei 42
São Paulo 39
Hong Kong 38
Abidjan 37
Izmir 33
Redwood City 33
Brussels 31
Buffalo 31
Shenyang 31
Detroit 30
Kraków 29
Santa Clara 26
Chicago 25
Marseille 25
Cambridge 23
Hebei 23
Dallas 20
Bremen 19
Guangzhou 19
Hangzhou 19
London 19
Changsha 18
Paris 18
Boardman 17
Jiaxing 17
Lappeenranta 17
Stockholm 17
Kunming 16
Norwalk 16
Orem 16
Fremont 15
Kent 15
Montreal 15
Mountain View 15
Princeton 15
University Park 15
Helsinki 14
Shanghai 14
Waanrode 14
Pune 13
Baghdad 12
Johannesburg 12
Ottawa 12
Phoenix 12
Tianjin 12
Zhengzhou 12
Atlanta 11
Chennai 11
Leawood 11
Nuremberg 11
Auburn Hills 10
Council Bluffs 10
Denver 10
Philadelphia 10
Poplar 10
Simi Valley 10
Brooklyn 9
Dhaka 9
Lancaster 9
Rio de Janeiro 9
San Francisco 9
The Dalles 9
Toronto 9
Turku 9
Belo Horizonte 8
Totale 5.854
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Nome #
Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients 417
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 357
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 314
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 267
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 260
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 246
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 242
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 212
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 204
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 195
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS 190
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 186
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 185
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 183
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 182
Matrin 3 variants are frequent in Italian ALS patients 180
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 178
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 166
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 166
New ALS-related genes expand the spectrum paradigm of amyotrophic lateral sclerosis 165
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 161
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 161
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 159
ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis 159
Mechanically assisted cough in amyotrophic lateral sclerosis: Effect on vital capacity decline and timing of non invasive ventilation onset 158
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 157
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 155
A novel L67P SOD1 mutation in an Italian ALS patient. 154
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 154
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 153
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 152
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 149
ATXN2 polyQ intermediate repeats are a modifier of ALS survival 148
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 148
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 147
Is it the use of Non Invasive Ventilation for less than four hours in the day sufficient to prolong survival in patients with Amyotrophic Lateral Sclerosis? 145
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 144
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 144
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 143
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 143
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 141
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 141
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 139
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 133
Sural nerve pathology in ALS patients: a single-centre experience 132
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 127
HFE p.H63D polymorphism does not influence ALS phenotype and survival 126
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 125
Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs. 123
Teaching NeuroImage: MRI of diabetic lumbar plexopathy treated with local steroid injection. 122
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72 122
Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis 120
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 119
A novel GJB1 mutation in an Italian patient with Charcot-Marie-Tooth disease and pyramidal signs 116
Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients 114
Elevated Levels of Selenium Species in Cerebrospinal Fluid of Amyotrophic Lateral Sclerosis Patients with Disease-Associated Gene Mutations 114
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population 112
'White nails'. Skin changes in POEMS syndrome 111
Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity 110
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 110
Gadolinium enhancement of the lumbar leptomeninges and roots in a case of ALS 108
Effect of RNS60 in amyotrophic lateral sclerosis: a phase II multicentre, randomized, double-blind, placebo-controlled trial 106
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 106
Exploring the Role of CCNF Variants in Italian ALS Patients 105
A novel compound heterozygous ALS2 mutation in two Italian siblings with juvenile amyotrophic lateral sclerosis 102
Clinical, electrophysiological and pathological findings in a patient with Charcot-Marie-Tooth disease 4D caused by the NDRG1 Lom mutation 100
Clinical and genetic heterogeneity of amyotrophic lateral sclerosis 97
Factors predicting survival in ALS: a multicenter Italian study 95
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis 88
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis 86
Factors predicting survival in ALS: a multicenter Italian study 86
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis 85
Elevated Levels of Selenium Species in Cerebrospinal Fluid of Amyotrophic Lateral Sclerosis Patients with Disease-Associated Gene Mutations 84
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 83
Posterior ischaemic myelopathy associated with cocaine abuse. 80
FUS mutations in sporadic amyotrophic lateral sclerosis 74
Comorbidity of dementia with amyotrophic lateral sclerosis (ALS): insights from a large multicenter Italian cohort 71
Long-term treatment of SOD1 ALS with tofersen: a multicentre experience in 17 patients 54
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data 22
Burden of pathogenetic and likely pathogenetic variants in SPG7, SPG11 and AP4 genes in Amyotrophic Lateral Sclerosis. A case-control study 21
Totale 11.639
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Categoria #
all - tutte 41.751
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 41.751
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021174 0 0 0 0 0 0 0 0 0 48 112 14
2021/2022709 70 64 17 89 27 25 19 114 39 32 90 123
2022/20231.417 147 219 125 218 100 198 72 102 172 8 32 24
2023/2024619 23 218 18 22 9 113 33 21 3 26 57 76
2024/20251.259 46 42 107 85 107 37 63 43 166 104 235 224
2025/20263.298 519 93 186 379 675 188 620 207 225 206 0 0
Totale 11.639