IRIS PubliCatt

Conte, Amelia
 Distribuzione geografica
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Continente #
EU - Europa 3.601
NA - Nord America 2.827
AS - Asia 903
AF - Africa 41
SA - Sud America 8
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 3
Totale 7.390
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Nazione #
US - Stati Uniti d'America 2.802
DE - Germania 1.738
CN - Cina 469
SE - Svezia 453
UA - Ucraina 335
IT - Italia 245
SG - Singapore 212
PL - Polonia 202
FR - Francia 128
IE - Irlanda 123
GB - Regno Unito 115
FI - Finlandia 89
ID - Indonesia 78
RU - Federazione Russa 65
BE - Belgio 46
IN - India 44
CI - Costa d'Avorio 37
TR - Turchia 37
NL - Olanda 26
CA - Canada 24
JP - Giappone 15
VN - Vietnam 14
HK - Hong Kong 13
CH - Svizzera 10
AU - Australia 7
ES - Italia 6
CL - Cile 4
IR - Iran 4
RO - Romania 4
AE - Emirati Arabi Uniti 3
GR - Grecia 3
HR - Croazia 3
SA - Arabia Saudita 3
BR - Brasile 2
DK - Danimarca 2
EU - Europa 2
IL - Israele 2
KZ - Kazakistan 2
LK - Sri Lanka 2
NO - Norvegia 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AR - Argentina 1
AT - Austria 1
BZ - Belize 1
CZ - Repubblica Ceca 1
DZ - Algeria 1
JO - Giordania 1
KG - Kirghizistan 1
LA - Repubblica Popolare Democratica del Laos 1
MA - Marocco 1
MD - Moldavia 1
MT - Malta 1
PE - Perù 1
TN - Tunisia 1
ZA - Sudafrica 1
Totale 7.390
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Città #
Chandler 520
Ashburn 204
Singapore 177
Ann Arbor 171
Warsaw 170
San Mateo 149
Nürnberg 141
Jacksonville 140
Dublin 121
Nanjing 121
Redmond 117
New York 93
Wilmington 86
Woodbridge 86
Jakarta 76
Houston 69
Boston 65
Cattolica 63
Fairfield 62
Nanchang 58
Dearborn 56
Seattle 56
Lawrence 49
Moscow 46
Abidjan 37
Munich 34
Beijing 33
Izmir 33
Redwood City 33
Milan 32
Brussels 31
Detroit 30
Shenyang 30
Kraków 29
Marseille 24
Cambridge 23
Hebei 23
Changsha 18
Guangzhou 18
Jiaxing 17
Rome 17
Bremen 16
Kunming 16
Lappeenranta 16
Norwalk 16
Fremont 15
Mountain View 15
Princeton 15
University Park 15
Boardman 14
Hangzhou 14
Los Angeles 14
Waanrode 14
Ottawa 12
Zhengzhou 12
Helsinki 11
Leawood 11
Auburn Hills 10
Chicago 10
London 10
Simi Valley 10
Hanoi 9
Lancaster 9
Philadelphia 9
Pune 9
Tianjin 9
Monza 8
Falls Church 7
Shanghai 7
Changchun 6
Phoenix 6
Santa Clara 6
Stockholm 6
Toronto 6
Ypsilanti 6
Anzola dell'Emilia 5
Central District 5
Fuzhou 5
Baotou 4
Catania 4
Greensboro 4
Hefei 4
Hong Kong 4
Indiana 4
Jinan 4
Locarno 4
Paris 4
San Jose 4
Tower Hamlets 4
Bologna 3
Brugherio 3
Buffalo 3
Clearwater 3
Costa Mesa 3
Fairport 3
Ningbo 3
Almaty 2
Amsterdam 2
Ardabil 2
Augusta 2
Totale 3.815
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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 323
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 303
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 264
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 198
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 197
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 193
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 181
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 165
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 163
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 137
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 134
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 132
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 130
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 116
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 116
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 114
Mechanically assisted cough in amyotrophic lateral sclerosis: Effect on vital capacity decline and timing of non invasive ventilation onset 114
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 114
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 108
New ALS-related genes expand the spectrum paradigm of amyotrophic lateral sclerosis 108
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 107
Matrin 3 variants are frequent in Italian ALS patients 106
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 104
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? 103
ATXN2 polyQ intermediate repeats are a modifier of ALS survival 103
A novel L67P SOD1 mutation in an Italian ALS patient. 102
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 100
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 100
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 99
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 97
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 96
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 95
ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis 93
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 92
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 92
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 91
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 91
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 91
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 90
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 90
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 88
Teaching NeuroImage: MRI of diabetic lumbar plexopathy treated with local steroid injection. 88
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 86
Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients 86
HFE p.H63D polymorphism does not influence ALS phenotype and survival 84
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 84
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS 84
Sural nerve pathology in ALS patients: a single-centre experience 83
Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs. 78
Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity 76
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 76
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 76
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72 74
Gadolinium enhancement of the lumbar leptomeninges and roots in a case of ALS 74
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 74
A novel GJB1 mutation in an Italian patient with Charcot-Marie-Tooth disease and pyramidal signs 72
Clinical, electrophysiological and pathological findings in a patient with Charcot-Marie-Tooth disease 4D caused by the NDRG1 Lom mutation 69
A novel compound heterozygous ALS2 mutation in two Italian siblings with juvenile amyotrophic lateral sclerosis 68
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 67
'White nails'. Skin changes in POEMS syndrome 66
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 65
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population 59
Clinical and genetic heterogeneity of amyotrophic lateral sclerosis 59
Cardiovascular diseases may play a negative role in the prognosis of 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 48
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis 47
Posterior ischaemic myelopathy associated with cocaine abuse. 46
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis 45
Elevated Levels of Selenium Species in Cerebrospinal Fluid of Amyotrophic Lateral Sclerosis Patients with Disease-Associated Gene Mutations 45
Comorbidity of dementia with amyotrophic lateral sclerosis (ALS): insights from a large multicenter Italian cohort 42
Factors predicting survival in ALS: a multicenter Italian study 42
Factors predicting survival in ALS: a multicenter Italian study 41
FUS mutations in sporadic amyotrophic lateral sclerosis 36
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis 12
Totale 7.502
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Categoria #
all - tutte 27.112
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 27.112
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020645 0 0 0 0 0 126 131 47 58 84 111 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
2024/2025420 46 42 107 85 107 33 0 0 0 0 0 0
Totale 7.502