IRIS UniCatt

Conte, Amelia
 Distribuzione geografica
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Continente #
EU - Europa 3.759
NA - Nord America 2.951
AS - Asia 1.084
SA - Sud America 180
AF - Africa 46
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 3
Totale 8.033
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Nazione #
US - Stati Uniti d'America 2.918
DE - Germania 1.777
CN - Cina 491
SE - Svezia 455
SG - Singapore 335
UA - Ucraina 335
IT - Italia 279
PL - Polonia 206
BR - Brasile 165
FR - Francia 158
GB - Regno Unito 130
IE - Irlanda 124
FI - Finlandia 93
ID - Indonesia 78
RU - Federazione Russa 71
IN - India 47
BE - Belgio 46
TR - Turchia 38
CI - Costa d'Avorio 37
NL - Olanda 31
CA - Canada 26
VN - Vietnam 20
HK - Hong Kong 16
JP - Giappone 16
CH - Svizzera 11
AU - Australia 10
AT - Austria 8
ES - Italia 7
AE - Emirati Arabi Uniti 6
CL - Cile 5
AR - Argentina 4
IR - Iran 4
MA - Marocco 4
RO - Romania 4
BD - Bangladesh 3
DK - Danimarca 3
GR - Grecia 3
HR - Croazia 3
IQ - Iraq 3
LK - Sri Lanka 3
SA - Arabia Saudita 3
BG - Bulgaria 2
CZ - Repubblica Ceca 2
EC - Ecuador 2
EU - Europa 2
IL - Israele 2
JO - Giordania 2
KG - Kirghizistan 2
KR - Corea 2
KZ - Kazakistan 2
MD - Moldavia 2
NO - Norvegia 2
PT - Portogallo 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
UZ - Uzbekistan 2
ZA - Sudafrica 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
BZ - Belize 1
CO - Colombia 1
CR - Costa Rica 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
GE - Georgia 1
JM - Giamaica 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LT - Lituania 1
MT - Malta 1
MX - Messico 1
NP - Nepal 1
PA - Panama 1
PE - Perù 1
PH - Filippine 1
PK - Pakistan 1
PY - Paraguay 1
SN - Senegal 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
Totale 8.033
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Città #
Chandler 520
Singapore 219
Ashburn 207
Warsaw 174
Ann Arbor 171
San Mateo 149
Nürnberg 141
Jacksonville 140
Dublin 122
Nanjing 121
Redmond 117
New York 97
Wilmington 86
Woodbridge 86
Jakarta 76
Houston 69
Boston 66
Cattolica 63
Fairfield 62
Seattle 62
Nanchang 58
Dearborn 56
Lawrence 49
Milan 47
Moscow 47
Abidjan 37
Munich 35
Beijing 33
Izmir 33
Redwood City 33
Brussels 31
Detroit 30
Shenyang 30
Kraków 29
Los Angeles 26
Rome 26
Frankfurt am Main 24
Marseille 24
Cambridge 23
Hebei 23
Guangzhou 19
Changsha 18
Jiaxing 17
Bremen 16
Kunming 16
Lappeenranta 16
Norwalk 16
São Paulo 16
Fremont 15
Mountain View 15
Princeton 15
University Park 15
Boardman 14
Hangzhou 14
Waanrode 14
Hanoi 12
Helsinki 12
London 12
Ottawa 12
Zhengzhou 12
Leawood 11
Santa Clara 11
Auburn Hills 10
Chicago 10
Simi Valley 10
Lancaster 9
Nuremberg 9
Philadelphia 9
Pune 9
The Dalles 9
Tianjin 9
Monza 8
Düsseldorf 7
Falls Church 7
Hefei 7
Phoenix 7
San Francisco 7
Shanghai 7
Stockholm 7
Changchun 6
Hong Kong 6
Lauterbourg 6
Portsmouth 6
Toronto 6
Ypsilanti 6
Anzola dell'Emilia 5
Belo Horizonte 5
Central District 5
Fuzhou 5
Vienna 5
Baotou 4
Brooklyn 4
Catania 4
Goiânia 4
Greensboro 4
Hortolândia 4
Indiana 4
Indianapolis 4
Jinan 4
Locarno 4
Totale 4.002
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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 339
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 309
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 270
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 208
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 205
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 203
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 191
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 168
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 168
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 142
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 142
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 137
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 134
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 127
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 125
Matrin 3 variants are frequent in Italian ALS patients 122
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 121
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 119
Mechanically assisted cough in amyotrophic lateral sclerosis: Effect on vital capacity decline and timing of non invasive ventilation onset 118
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 117
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 117
ATXN2 polyQ intermediate repeats are a modifier of ALS survival 115
New ALS-related genes expand the spectrum paradigm of amyotrophic lateral sclerosis 115
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 114
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? 112
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 109
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 109
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 108
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 107
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 107
A novel L67P SOD1 mutation in an Italian ALS patient. 106
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 103
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 101
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 100
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 100
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 99
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 98
ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis 98
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 97
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 96
Teaching NeuroImage: MRI of diabetic lumbar plexopathy treated with local steroid injection. 95
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 94
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS 94
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 92
Sural nerve pathology in ALS patients: a single-centre experience 91
Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients 90
HFE p.H63D polymorphism does not influence ALS phenotype and survival 90
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 89
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 87
Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity 86
Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs. 84
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 84
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72 83
A novel GJB1 mutation in an Italian patient with Charcot-Marie-Tooth disease and pyramidal signs 82
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 82
Gadolinium enhancement of the lumbar leptomeninges and roots in a case of ALS 81
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 81
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 78
Clinical, electrophysiological and pathological findings in a patient with Charcot-Marie-Tooth disease 4D caused by the NDRG1 Lom mutation 75
A novel compound heterozygous ALS2 mutation in two Italian siblings with juvenile amyotrophic lateral sclerosis 72
'White nails'. Skin changes in POEMS syndrome 71
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population 70
Elevated Levels of Selenium Species in Cerebrospinal Fluid of Amyotrophic Lateral Sclerosis Patients with Disease-Associated Gene Mutations 65
Clinical and genetic heterogeneity of amyotrophic lateral sclerosis 64
Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis 64
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis 55
Elevated Levels of Selenium Species in Cerebrospinal Fluid of Amyotrophic Lateral Sclerosis Patients with Disease-Associated Gene Mutations 55
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 53
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis 52
Posterior ischaemic myelopathy associated with cocaine abuse. 50
Factors predicting survival in ALS: a multicenter Italian study 50
Factors predicting survival in ALS: a multicenter Italian study 48
Comorbidity of dementia with amyotrophic lateral sclerosis (ALS): insights from a large multicenter Italian cohort 47
FUS mutations in sporadic amyotrophic lateral sclerosis 38
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis 30
Effect of RNS60 in amyotrophic lateral sclerosis: a phase II multicentre, randomized, double-blind, placebo-controlled trial 26
Exploring the Role of CCNF Variants in Italian ALS Patients 15
Long-term treatment of SOD1 ALS with tofersen: a multicentre experience in 17 patients 10
Totale 8.149
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Categoria #
all - tutte 31.480
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 31.480
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202088 0 0 0 0 0 0 0 0 0 0 0 88
2020/2021675 31 73 25 75 96 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
2024/20251.067 46 42 107 85 107 37 63 43 166 104 235 32
Totale 8.149