CINECA IRIS Institutional Research Information System

GALLONE, SALVATORE
 Distribuzione geografica
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Continente #
NA - Nord America 1.301
EU - Europa 726
AS - Asia 441
SA - Sud America 20
AF - Africa 16
OC - Oceania 12
Totale 2.516
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Nazione #
US - Stati Uniti d'America 1.289
IT - Italia 248
SG - Singapore 156
CN - Cina 154
IE - Irlanda 90
SE - Svezia 78
AT - Austria 69
DE - Germania 45
FR - Francia 34
GB - Regno Unito 32
FI - Finlandia 29
JP - Giappone 24
TR - Turchia 20
UA - Ucraina 19
BE - Belgio 16
ES - Italia 15
ID - Indonesia 14
IN - India 14
HK - Hong Kong 12
VN - Vietnam 12
AU - Australia 11
BR - Brasile 11
KR - Corea 11
NL - Olanda 11
SN - Senegal 10
PL - Polonia 9
CA - Canada 7
MY - Malesia 7
RU - Federazione Russa 7
CL - Cile 5
DK - Danimarca 5
IR - Iran 5
CO - Colombia 4
GR - Grecia 4
MX - Messico 4
PT - Portogallo 4
CY - Cipro 3
CZ - Repubblica Ceca 3
SI - Slovenia 3
TW - Taiwan 3
IQ - Iraq 2
MA - Marocco 2
TH - Thailandia 2
BG - Bulgaria 1
CH - Svizzera 1
CI - Costa d'Avorio 1
LU - Lussemburgo 1
MD - Moldavia 1
NG - Nigeria 1
NZ - Nuova Zelanda 1
PA - Panama 1
RO - Romania 1
SA - Arabia Saudita 1
TG - Togo 1
UZ - Uzbekistan 1
ZA - Sudafrica 1
Totale 2.516
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Città #
Chandler 176
Singapore 134
Dublin 90
Fairfield 81
Ashburn 71
Vienna 69
Houston 67
Torino 60
Beijing 59
Santa Clara 59
Woodbridge 40
Nyköping 35
Seattle 34
Ann Arbor 33
Wilmington 33
Columbus 31
Turin 31
Jacksonville 28
Redwood City 27
Villeurbanne 23
Cambridge 22
Dearborn 21
Medford 20
Princeton 18
Pisa 16
New York 15
Jakarta 14
Munich 13
Chicago 12
Milan 12
Boston 11
Boardman 10
Brussels 10
Istanbul 10
Fremont 9
Guangzhou 8
Helsinki 8
Tokyo 8
Warsaw 8
Buffalo 7
Blackpool 6
Harbin 6
Hong Kong 6
Jinan 6
Moncalieri 6
Pavia 6
Rome 6
Amsterdam 5
Atlanta 5
Bologna 5
Hefei 5
Ipoh 5
Seongnam-si 5
Silver Spring 5
Ankara 4
Assago 4
Dong Ket 4
Los Angeles 4
Madrid 4
Mumbai 4
Nanjing 4
San Mateo 4
Stockholm 4
Aarhus 3
Antofagasta 3
Bari 3
Central District 3
Chongqing 3
Edinburgh 3
Florence 3
Hamburg 3
Hyderabad 3
Kunming 3
Lappeenranta 3
Larnaca 3
Mississauga 3
Monza 3
Phoenix 3
Plymouth 3
Rochester 3
San Diego 3
Seville 3
Shanghai 3
Southampton 3
Toronto 3
Upper Marlboro 3
Washington 3
Wigan 3
Wuhan 3
Ambivere 2
Amparo 2
Arbil 2
Berlin 2
Bethesda 2
Brno 2
Capannori 2
Chiang Mai 2
Chiba 2
Chiclana de la Frontera 2
Cisternino 2
Totale 1.646
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Nome #
Three novel missense mutations in SLC20A2 associated with idiopathic basal ganglia calcification 274
Chemotherapy-Induced Neurotoxicity: Evidence of a Protective Role of CC Homozygosis in the Interleukin-1β Gene-511 C>T Polymorphism 273
Design of a multiplex ligation-dependent probe amplification assay for SLC20A2: identification of two novel deletions in primary familial brain calcification 240
Late onset bipolar disorder and frontotemporal dementia with mutation in progranulin gene: a case report 223
Novel mutation of SLC20A2 in an Italian patient presenting with migraine. 209
O056. Migraine as presenting symptom of SLC20A2gene mutations 125
Late onset bipolar disorder preceding frontotemporal dementia with mutation in progranulin gene: a case report 102
Progranulin plasma levels in patients with and without TDP-43 pathology. 92
Mutation Screening of Neuromedin B (NMB) gene in behavioral variant Frontotemporal Dementia 89
Investigating involvement of Von Economo neurons in behavioral variant frontotemporal dementia 89
Genetic analysis of TDP-43 gene in blood and tumoral tissue in a group of patients with gliomas 73
Amyotrophic lateral sclerosis with SOD1 mutations shows distinct brain metabolic changes 69
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis 68
Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degeneration 62
GBA variants influence cognitive status in amyotrophic lateral sclerosis 60
Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degeneration 59
A novel splice site FUS mutation in a familial ALS case: effects on protein expression 59
A Schematic Approach to Defining the Prevalence of COL VI Variants in Five Years of Next-Generation Sequencing 45
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study 45
An integrated approach to the evaluation of patients with asymptomatic or minimally symptomatic hyperCKemia 38
Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeats 36
Polymorphisms of the Proinflammatory Cytokine Genes Modulate the Response to NSAIDs but Not to Triptans in Migraine Attacks 34
Brain 18fluorodeoxyglucose-positron emission tomography changes in amyotrophic lateral sclerosis with TARDBP mutations 33
Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral Sclerosis 32
Phenotype Analysis of Fused in Sarcoma Mutations in Amyotrophic Lateral Sclerosis 27
Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis 23
A Novel PSEN1 Variant Leading to Posterior Cortical Atrophy: A Case Report 18
Cognitive and Behavioral Features of Patients With Amyotrophic Lateral Sclerosis Who Are Carriers of the TARDBP Pathogenic Variant 18
High Frequency of Cognitive and Behavioral Impairment in Amyotrophic Lateral Sclerosis Patients with SOD1 Pathogenic Variants 17
Cognitive dysfunction, social behavior disorder, cerebellar ataxia, and atypical brain FDG-PET presentation in spinocerebellar ataxia 17: a case report 15
Adult-onset spastic paraplegia associated with a novel SPTBN2 missense heterozygous variant 14
Hereditary motor sensory neuropathy with proximal involvement (HMSN‐P) associated with TFG p.Pro285Leu variant in an Italian family with a motor neuron disease‐like clinical picture 14
A novel DHTKD1 variant is associated with an atypical form of Charcot-Marie-Tooth disease type 2Q? 13
A mother and her daughter carrying a pathogenic expansion of the HTT gene with a phenotype encompassing motor neuron disease and Huntington's disease 13
A patient with demyelinating CMT carrying the p.Y347C heterozygous variant of the MME gene and the p.L131F heterozygous variant of the HARS1 gene 7
The p.D417N variant of TUBB4A as a possible cause of hereditary spastic paraplegia: a case report 5
EMILIN1 gene variant associated with polyneuropathy, language impairment, and motor dysfunction 4
Totale 2.617
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Categoria #
all - tutte 9.446
article - articoli 0
book - libri 0
conference - conferenze 1.583
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 11.029
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020191 0 0 0 0 15 33 31 37 40 14 10 11
2020/2021270 18 27 32 17 24 43 28 15 21 13 13 19
2021/2022296 11 8 15 34 14 19 15 10 15 19 88 48
2022/2023531 48 51 14 57 38 117 29 51 59 11 37 19
2023/2024353 39 55 13 20 24 46 19 16 12 29 35 45
2024/2025393 14 73 39 104 163 0 0 0 0 0 0 0
Totale 2.617