IRIS UniCatt

Conte, Amelia
 Distribuzione geografica
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Continente #
NA - Nord America 4.317
EU - Europa 4.157
AS - Asia 2.753
SA - Sud America 462
AF - Africa 101
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 4
Totale 11.804
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Nazione #
US - Stati Uniti d'America 4.207
DE - Germania 1.827
SG - Singapore 1.195
CN - Cina 762
SE - Svezia 466
IT - Italia 391
BR - Brasile 371
UA - Ucraina 343
FR - Francia 256
VN - Vietnam 242
PL - Polonia 226
GB - Regno Unito 175
IE - Irlanda 129
FI - Finlandia 102
IN - India 87
ID - Indonesia 86
RU - Federazione Russa 80
BD - Bangladesh 65
JP - Giappone 64
CA - Canada 63
TR - Turchia 56
HK - Hong Kong 54
BE - Belgio 52
CI - Costa d'Avorio 37
NL - Olanda 36
IQ - Iraq 30
AR - Argentina 28
ZA - Sudafrica 22
MX - Messico 20
PK - Pakistan 19
ES - Italia 15
CH - Svizzera 14
CO - Colombia 13
SA - Arabia Saudita 13
AE - Emirati Arabi Uniti 12
MA - Marocco 12
PY - Paraguay 12
AT - Austria 11
CL - Cile 11
EC - Ecuador 11
AU - Australia 10
IL - Israele 8
TN - Tunisia 8
DO - Repubblica Dominicana 7
JO - Giordania 7
HN - Honduras 6
IR - Iran 6
PH - Filippine 6
VE - Venezuela 6
JM - Giamaica 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
CR - Costa Rica 3
DK - Danimarca 3
DZ - Algeria 3
GR - Grecia 3
HR - Croazia 3
LK - Sri Lanka 3
AO - Angola 2
BG - Bulgaria 2
BY - Bielorussia 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
MY - Malesia 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
PA - Panama 1
Totale 11.798
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Città #
Singapore 658
Chandler 520
Ashburn 516
San Jose 355
Warsaw 190
Ann Arbor 171
San Mateo 149
Jacksonville 142
Nürnberg 141
New York 132
Beijing 130
Dublin 125
Nanjing 121
Redmond 117
Wilmington 86
Woodbridge 86
Ho Chi Minh City 78
Jakarta 77
Houston 75
Lauterbourg 73
Boston 72
Los Angeles 70
Seattle 64
Cattolica 63
Rome 63
Fairfield 62
Hanoi 62
Nanchang 58
Milan 57
Dearborn 56
Munich 51
Lawrence 49
Tokyo 49
Frankfurt am Main 47
Moscow 47
Hefei 42
Hong Kong 40
São Paulo 39
Abidjan 37
Izmir 33
Redwood City 33
Brussels 31
Buffalo 31
Shenyang 31
Detroit 30
Santa Clara 30
Kraków 29
Chicago 25
Marseille 25
Cambridge 23
Dallas 23
Hebei 23
Bremen 19
Guangzhou 19
Hangzhou 19
London 19
Boardman 18
Changsha 18
Montreal 18
Paris 18
Jiaxing 17
Lappeenranta 17
Stockholm 17
Kunming 16
Norwalk 16
Orem 16
Fremont 15
Kent 15
Mountain View 15
Princeton 15
Shanghai 15
University Park 15
Atlanta 14
Helsinki 14
Waanrode 14
Pune 13
Baghdad 12
Johannesburg 12
Ottawa 12
Phoenix 12
The Dalles 12
Tianjin 12
Zhengzhou 12
Chennai 11
Leawood 11
Nuremberg 11
Philadelphia 11
Auburn Hills 10
Brooklyn 10
Council Bluffs 10
Denver 10
Poplar 10
Rio de Janeiro 10
San Francisco 10
Simi Valley 10
Toronto 10
Belo Horizonte 9
Dhaka 9
Lancaster 9
Turku 9
Totale 5.983
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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 422
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 361
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 318
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 270
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 264
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 251
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 246
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 214
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 208
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 198
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS 195
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 192
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 189
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 185
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 184
Matrin 3 variants are frequent in Italian ALS patients 183
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 182
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 176
ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis 176
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 170
New ALS-related genes expand the spectrum paradigm of amyotrophic lateral sclerosis 166
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 164
Mechanically assisted cough in amyotrophic lateral sclerosis: Effect on vital capacity decline and timing of non invasive ventilation onset 163
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
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 160
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 159
A novel L67P SOD1 mutation in an Italian ALS patient. 158
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 158
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 154
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 153
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 152
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 151
ATXN2 polyQ intermediate repeats are a modifier of ALS survival 151
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 150
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 148
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 148
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? 147
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 146
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 146
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 146
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 144
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 144
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 137
Effect of RNS60 in amyotrophic lateral sclerosis: a phase II multicentre, randomized, double-blind, placebo-controlled trial 135
Sural nerve pathology in ALS patients: a single-centre experience 134
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 133
HFE p.H63D polymorphism does not influence ALS phenotype and survival 130
Exploring the Role of CCNF Variants in Italian ALS Patients 129
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72 127
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 127
Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs. 125
Teaching NeuroImage: MRI of diabetic lumbar plexopathy treated with local steroid injection. 124
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 124
Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis 123
A novel GJB1 mutation in an Italian patient with Charcot-Marie-Tooth disease and pyramidal signs 118
Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients 117
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population 114
Elevated Levels of Selenium Species in Cerebrospinal Fluid of Amyotrophic Lateral Sclerosis Patients with Disease-Associated Gene Mutations 114
'White nails'. Skin changes in POEMS syndrome 113
Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity 112
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 112
Gadolinium enhancement of the lumbar leptomeninges and roots in a case of ALS 109
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 107
A novel compound heterozygous ALS2 mutation in two Italian siblings with juvenile amyotrophic lateral sclerosis 104
Clinical, electrophysiological and pathological findings in a patient with Charcot-Marie-Tooth disease 4D caused by the NDRG1 Lom mutation 104
Factors predicting survival in ALS: a multicenter Italian study 100
Clinical and genetic heterogeneity of amyotrophic lateral sclerosis 99
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis 96
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis 91
Posterior ischaemic myelopathy associated with cocaine abuse. 89
Factors predicting survival in ALS: a multicenter Italian study 87
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis 86
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
FUS mutations in sporadic amyotrophic lateral sclerosis 75
Comorbidity of dementia with amyotrophic lateral sclerosis (ALS): insights from a large multicenter Italian cohort 72
Long-term treatment of SOD1 ALS with tofersen: a multicentre experience in 17 patients 55
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data 24
Burden of pathogenetic and likely pathogenetic variants in SPG7, SPG11 and AP4 genes in Amyotrophic Lateral Sclerosis. A case-control study 24
Totale 11.951
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Categoria #
all - tutte 44.397
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 44.397
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20263.574 519 93 186 379 675 188 620 207 225 273 119 90
2026/202736 36 0 0 0 0 0 0 0 0 0 0 0
Totale 11.951