IRIS UniCatt

Conte, Amelia
 Distribuzione geografica
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Continente #
EU - Europa 3.938
NA - Nord America 3.481
AS - Asia 2.191
SA - Sud America 410
AF - Africa 86
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 4
Totale 10.120
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Nazione #
US - Stati Uniti d'America 3.397
DE - Germania 1.807
SG - Singapore 1.006
CN - Cina 676
SE - Svezia 466
BR - Brasile 342
UA - Ucraina 339
IT - Italia 316
PL - Polonia 223
FR - Francia 169
GB - Regno Unito 168
IE - Irlanda 127
VN - Vietnam 104
FI - Finlandia 100
ID - Indonesia 85
RU - Federazione Russa 78
IN - India 74
CA - Canada 50
BE - Belgio 46
TR - Turchia 44
CI - Costa d'Avorio 37
HK - Hong Kong 37
JP - Giappone 36
NL - Olanda 32
BD - Bangladesh 31
AR - Argentina 23
IQ - Iraq 19
ZA - Sudafrica 19
MX - Messico 18
ES - Italia 14
AE - Emirati Arabi Uniti 11
CH - Svizzera 11
CL - Cile 11
AT - Austria 10
AU - Australia 10
MA - Marocco 10
PY - Paraguay 9
SA - Arabia Saudita 9
EC - Ecuador 8
IL - Israele 7
PK - Pakistan 7
IR - Iran 6
JO - Giordania 5
VE - Venezuela 5
CO - Colombia 4
DO - Repubblica Dominicana 4
RO - Romania 4
UY - Uruguay 4
DK - Danimarca 3
DZ - Algeria 3
ET - Etiopia 3
GR - Grecia 3
HN - Honduras 3
HR - Croazia 3
KE - Kenya 3
LK - Sri Lanka 3
PH - Filippine 3
PT - Portogallo 3
TH - Thailandia 3
UZ - Uzbekistan 3
AO - Angola 2
AZ - Azerbaigian 2
BG - Bulgaria 2
BH - Bahrain 2
BY - Bielorussia 2
CR - Costa Rica 2
CZ - Repubblica Ceca 2
EU - Europa 2
GE - Georgia 2
JM - Giamaica 2
KG - Kirghizistan 2
KR - Corea 2
KZ - Kazakistan 2
LT - Lituania 2
MD - Moldavia 2
MN - Mongolia 2
NO - Norvegia 2
NP - Nepal 2
PE - Perù 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
TN - Tunisia 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
MM - Myanmar 1
MT - Malta 1
MU - Mauritius 1
MY - Malesia 1
PA - Panama 1
Totale 10.116
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Città #
Chandler 520
Singapore 493
Ashburn 338
Warsaw 189
Ann Arbor 171
San Mateo 149
Jacksonville 142
Nürnberg 141
Beijing 125
Dublin 124
Nanjing 121
New York 118
Redmond 117
Wilmington 86
Woodbridge 86
Jakarta 77
Houston 73
Boston 70
Seattle 64
Cattolica 63
Fairfield 62
Los Angeles 59
Nanchang 58
Dearborn 56
Milan 52
Munich 51
Lawrence 49
Moscow 47
Rome 45
Hefei 42
Abidjan 37
São Paulo 37
Frankfurt am Main 35
Hanoi 35
Izmir 33
Redwood City 33
Ho Chi Minh City 32
Brussels 31
Buffalo 31
Detroit 30
Shenyang 30
Kraków 29
Hong Kong 26
Marseille 24
Cambridge 23
Hebei 23
Tokyo 22
Dallas 20
Chicago 19
Guangzhou 19
Bremen 18
Changsha 18
London 18
Boardman 17
Jiaxing 17
Lappeenranta 17
Santa Clara 17
Stockholm 17
Kunming 16
Norwalk 16
Fremont 15
Hangzhou 15
Kent 15
Mountain View 15
Princeton 15
University Park 15
Waanrode 14
Montreal 13
Helsinki 12
Ottawa 12
Pune 12
Zhengzhou 12
Leawood 11
Phoenix 11
Tianjin 11
Auburn Hills 10
Nuremberg 10
Philadelphia 10
Poplar 10
Simi Valley 10
Atlanta 9
Dhaka 9
Johannesburg 9
Lancaster 9
San Francisco 9
The Dalles 9
Toronto 9
Turku 9
Belo Horizonte 8
Brooklyn 8
Denver 8
Monza 8
Rio de Janeiro 8
Baghdad 7
Chennai 7
Curitiba 7
Düsseldorf 7
Falls Church 7
Manchester 7
Santiago 7
Totale 4.937
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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 380
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 334
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 290
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 243
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 239
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 229
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 225
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 189
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 187
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 177
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 175
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 167
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 159
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 159
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 159
Matrin 3 variants are frequent in Italian ALS patients 158
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS 155
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 148
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 147
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 146
New ALS-related genes expand the spectrum paradigm of amyotrophic lateral sclerosis 145
ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis 142
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 141
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 139
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 137
Mechanically assisted cough in amyotrophic lateral sclerosis: Effect on vital capacity decline and timing of non invasive ventilation onset 137
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 137
A novel L67P SOD1 mutation in an Italian ALS patient. 136
ATXN2 polyQ intermediate repeats are a modifier of ALS survival 136
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 134
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 134
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 133
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? 131
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 129
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 128
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 128
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 126
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 126
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 126
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 126
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 125
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 121
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 121
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 116
Sural nerve pathology in ALS patients: a single-centre experience 115
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 114
HFE p.H63D polymorphism does not influence ALS phenotype and survival 112
Teaching NeuroImage: MRI of diabetic lumbar plexopathy treated with local steroid injection. 110
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 109
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 108
A novel GJB1 mutation in an Italian patient with Charcot-Marie-Tooth disease and pyramidal signs 107
Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity 106
Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients 104
Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs. 103
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72 101
Gadolinium enhancement of the lumbar leptomeninges and roots in a case of ALS 101
Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis 100
'White nails'. Skin changes in POEMS syndrome 99
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 96
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 96
Clinical, electrophysiological and pathological findings in a patient with Charcot-Marie-Tooth disease 4D caused by the NDRG1 Lom mutation 94
Elevated Levels of Selenium Species in Cerebrospinal Fluid of Amyotrophic Lateral Sclerosis Patients with Disease-Associated Gene Mutations 93
A novel compound heterozygous ALS2 mutation in two Italian siblings with juvenile amyotrophic lateral sclerosis 91
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population 90
Clinical and genetic heterogeneity of amyotrophic lateral sclerosis 83
Effect of RNS60 in amyotrophic lateral sclerosis: a phase II multicentre, randomized, double-blind, placebo-controlled trial 76
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis 76
Factors predicting survival in ALS: a multicenter Italian study 76
Elevated Levels of Selenium Species in Cerebrospinal Fluid of Amyotrophic Lateral Sclerosis Patients with Disease-Associated Gene Mutations 75
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis 74
Factors predicting survival in ALS: a multicenter Italian study 73
Posterior ischaemic myelopathy associated with cocaine abuse. 70
Exploring the Role of CCNF Variants in Italian ALS Patients 69
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 68
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis 63
Comorbidity of dementia with amyotrophic lateral sclerosis (ALS): insights from a large multicenter Italian cohort 63
FUS mutations in sporadic amyotrophic lateral sclerosis 56
Long-term treatment of SOD1 ALS with tofersen: a multicentre experience in 17 patients 40
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data 3
Burden of pathogenetic and likely pathogenetic variants in SPG7, SPG11 and AP4 genes in Amyotrophic Lateral Sclerosis. A case-control study 2
null 2
Totale 10.238
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Categoria #
all - tutte 38.826
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 38.826
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021375 0 0 0 0 0 26 68 21 86 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
2025/20261.897 519 93 186 379 676 44 0 0 0 0 0 0
Totale 10.238