IRIS
MONSURRO', Maria Rosaria
 Distribuzione geografica
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Continente #
EU - Europa 5.609
NA - Nord America 3.047
AS - Asia 2.170
SA - Sud America 373
AF - Africa 32
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 11.237
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Nazione #
RU - Federazione Russa 3.385
US - Stati Uniti d'America 3.020
SG - Singapore 752
IE - Irlanda 650
CN - Cina 555
UA - Ucraina 347
BR - Brasile 312
GB - Regno Unito 302
HK - Hong Kong 294
IT - Italia 261
VN - Vietnam 200
DE - Germania 174
FR - Francia 137
TR - Turchia 120
FI - Finlandia 112
SE - Svezia 111
KR - Corea 82
IN - India 67
GR - Grecia 65
JP - Giappone 30
BE - Belgio 22
AR - Argentina 21
BD - Bangladesh 15
CA - Canada 13
ZA - Sudafrica 11
CO - Colombia 10
NL - Olanda 10
EC - Ecuador 9
ID - Indonesia 9
IQ - Iraq 8
PL - Polonia 8
ES - Italia 7
MX - Messico 7
AT - Austria 6
VE - Venezuela 6
EG - Egitto 5
PE - Perù 5
PK - Pakistan 5
TH - Thailandia 5
TN - Tunisia 5
CL - Cile 4
EU - Europa 4
AM - Armenia 3
BG - Bulgaria 3
DO - Repubblica Dominicana 3
DZ - Algeria 3
JM - Giamaica 3
KE - Kenya 3
MA - Marocco 3
PY - Paraguay 3
AL - Albania 2
IL - Israele 2
IR - Iran 2
JO - Giordania 2
KG - Kirghizistan 2
KZ - Kazakistan 2
LB - Libano 2
LT - Lituania 2
LV - Lettonia 2
MY - Malesia 2
PH - Filippine 2
PS - Palestinian Territory 2
RO - Romania 2
SA - Arabia Saudita 2
UY - Uruguay 2
UZ - Uzbekistan 2
AE - Emirati Arabi Uniti 1
AU - Australia 1
AZ - Azerbaigian 1
BO - Bolivia 1
BW - Botswana 1
GA - Gabon 1
LK - Sri Lanka 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
Totale 11.237
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Città #
Moscow 1.194
Dublin 650
Jacksonville 527
Chandler 404
Santa Clara 350
Singapore 292
Hong Kong 290
San Jose 184
Beijing 119
Dallas 103
Ann Arbor 99
Princeton 95
Ashburn 87
Medford 87
Seoul 80
Ho Chi Minh City 66
Roxbury 58
New York 57
Boardman 52
Woodbridge 50
Hanoi 47
Wilmington 46
Bengaluru 41
San Mateo 41
The Dalles 41
Hefei 38
Nanjing 37
Caserta 36
São Paulo 30
Mountain View 24
Bremen 23
Brussels 21
Dearborn 20
Los Angeles 20
Des Moines 18
Jinan 18
Lappeenranta 14
Haiphong 13
Nanchang 13
Norwalk 13
Guangzhou 12
Da Nang 11
Cambridge 10
Düsseldorf 10
London 10
Munich 10
Napoli 10
Shanghai 10
Naples 9
Rome 9
Shenyang 9
Auburn Hills 8
Belo Horizonte 8
Helsinki 8
Porto Alegre 8
San Francisco 8
Zhengzhou 8
Changsha 7
Guarulhos 7
Houston 7
Amsterdam 6
Brasília 6
Johannesburg 6
Kunming 6
Luzzano 6
Montevecchia 6
Stockholm 6
Atlanta 5
Baghdad 5
Biên Hòa 5
Campinas 5
Curitiba 5
Frankfurt am Main 5
Genova 5
Milan 5
Montreal 5
Ningbo 5
Nuremberg 5
Rio de Janeiro 5
Tianjin 5
Tokyo 5
Turku 5
Brooklyn 4
Cava De' Tirreni 4
Chennai 4
Chicago 4
Dhaka 4
Haikou 4
Hebei 4
Orem 4
Piscataway 4
Quito 4
Ribeirão Preto 4
Venice 4
Augusta 3
Bangkok 3
Belém 3
Columbus 3
Cotia 3
Dnipro 3
Totale 5.760
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Nome #
Edinburgh Cognitive and Behavioural ALS Screen (ECAS)-Italian version: regression based norms and equivalent scores 255
Beyond motor neurons: new insights on amyotrophic lateral sclerosis neurodegeneration provided by advanced MRI technique 195
Advantages of QBI in TBSS analyses. 186
Apathy in amyotrophic lateral sclerosis: insights from Dimensional Apathy Scale 180
Blood Lead, Manganese, and Aluminum Levels in a Regional Italian Cohort of ALS Patients: Does Aluminum Have an Influence? 178
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. 174
Apathy Is Correlated with Widespread Diffusion Tensor Imaging (DTI) Impairment in Amyotrophic Lateral Sclerosis 171
Amyotrophic lateral sclerosis and multiple sclerosis overlap: A case report 165
A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy 163
Interaction between aging and neurodegeneration in amyotrophic lateral sclerosis 161
Amyotrophic lateral sclerosis and multiple sclerosis overlap: a case report. 161
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis 159
Frontotemporal cortical thinning in amyotrophic lateral sclerosis. 158
Assessing Anxiety and its correlates in Amyotrophic Lateral Sclerosis: the State-Trait Anxiety Inventory 158
A case of probable autosomal recessive ectodermal dysplasia with corkscrew hairs and menial retardation in a family with tuberous sclerosis 157
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 155
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. 151
Widespread Microstructural White Matter Involvement in Amyotrophic Lateral Sclerosis: A Whole-Brain DTI Study. 150
Vitamin D supplementation has no effects on progression of motor dysfunction in amyotrophic lateral sclerosis (ALS) 150
Accuracy of death certificates for amyotrophic lateral sclerosis varies significantly from north to south of Italy: implications for mortality studies 146
Distributed corpus callosum involvement in amyotrophic lateral sclerosis: a deterministic tractography study using q-ball imaging. 145
Accumulation of altered aspartyl residues in erythrocyte membrane proteins from patients with sporadic amyotrophic lateral sclerosis. 145
Preliminary results of isolation and identification of rat sarcolemma and the effect of denervation on membrane-bound neuraminidase activity 143
INFRATENTORIAL PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY IN A PATIENT TREATED WITH FLUDARABINE AND RITUXIMAB 138
Extra-motor involvement in ALS patients: a cortical thickeness 3T MRI study 137
Whole-brain DTI pattern of white matter damage in Amyotrophic lateral sclerosis: further evidences of a multisystem disorder 137
An Italian kindred with FALS due to c.149T>C mutation in the SOD1 gene: case report of an affected family member 137
A case of probable autosomal recessive ectodermal dysplasia with corkscrew hairs and mental retardation in a family with tuberous sclerosis 136
[Determination of alimentary value of buffalo muscle proteins using enzymatic methods] 133
Subcortical motor plasticity in patients with sporadic ALS: An fMRI study 132
ALS and CHARGE syndrome: a clinical and genetic study 132
Beyond motor neurons: new insights on amyotrophic lateral sclerosis neurodegeneration provided by advanced MRI tecnique 131
Structure of msj-1 gene: a comparative analysis 128
Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy 126
Whole-brain DTI pattern of white metter damage in amyotrophic lateral sclerosis: further evidences of a multisystem disorder 126
Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis. 125
Sistema nervoso 124
Dysfunctions within limbic-motor networks in amyotrophic lateral sclerosis. 123
Brain functional networks become more connected as amyotrophic lateral sclerosis progresses: a source level magnetoencephalographic study 120
Retrospective epidemiology of Duchenne muscular dystrophy in Molise 119
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? 117
Coping strategies and psychological distress in caregivers of patients with Amyotrophic Lateral Sclerosis (ALS) 117
Microstructural Changes across Different Clinical Milestones of Disease in Amyotrophic Lateral Sclerosis. 115
Towards genetic prevention of Adrenoleukodystrophy through early biochemical diagnosis of hemizygotes and heterozygotes in families at risk 115
Widespread Structural and Functional Connectivity Changes in Amyotrophic Lateral Sclerosis: Insights from Advanced Neuroimaging Research 113
Theory of Mind and Its Neuropsychological and Quality of Life Correlates in the Early Stages of Amyotrophic Lateral Sclerosis 112
Cardiovascular diseases may play a negative role in the prognosis of ALS 112
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis. 111
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation 110
Sporadic ALS is not associated with VAPB gene mutations in Southern Italy 110
Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophy 110
Factors predicting survival in ALS: a multicenter Italian study 109
Reversible mielopathy due to deficiency of vitamin B12 in patient with associated syringomyelia: a case report 108
Microstructural correlates of Edinburgh Cognitive and Behavioural ALS Screen (ECAS) changes in amyotrophic lateral sclerosis 108
Earliest videofluoromanometric pharyngeal signs of dysphagia in ALS patients. 105
HFE p.H63D polymorphism does not influence ALS phenotype and survival 105
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 104
The GH-IGF system in amyotrophic lateral sclerosis: correlations between pituitary GH secretion capacity, insulin-like growth factors and clinical features 104
Neuropsychological assessment in different King's clinical stages of amyotrophic lateral sclerosis 104
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 104
Motor and extramotor neurodegeneration in amyotrophic lateral sclerosis: a 3T high angular resolution diffusion imaging (HARDI) study 103
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. 103
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 103
Functional overlap and divergence between ALS and bvFTD 102
Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomized, double blind, placebo controlled, phase III study. 101
FUS mutations in sporadic amyotrophic lateral sclerosis. 100
Establishment and characterization of a human neuroectodermal cell line (TB) from a cerebrospinal fluid specimen 100
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population. 100
Toward genetic prevention of adrenoleukodystrophy trough early biochemical diagnosis of hemizygotes and heterozygotes in families at risk. 99
Targeting extracellular cyclophilin A reduces neuroinflammation and extends survival in a mouse model of amyotrophic lateral sclerosis 98
The application of recently developed methods to investigate glycoconjugate composition of sarcolemma: some preliminary results on Duchenne muscular dystrophy 97
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 97
The neural control of skeletal muscle sarcolemma: preliminary results of different approaches to the study of a possible control of membrane-bound glycoconjugates 95
Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis 93
Membrane depolarization in LA-N-1 cells. The effect of maitotoxin is Ca(2+)- and Na(+)-dependent 93
FUS mutations in sporadic amyotrophic lateral sclerosis: Clinical and genetic analysis. 93
Lithium carbonate in amyotrophic lateral sclerosis Lack of efficacy in a dose-finding trial 92
Direct inhibition of choline acetyltransferase activity by a monoclonal antibody raised against the plasma membrane of cholinergic nerve terminals 92
The effects of denervation on sarcolemmal glycoconjugates of type skeletal muscle fibres of rat. Su: Synaptic Constituents in Health and Disease 91
Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS 91
LAN-1: a human neuroblastoma cell line with M1 and M3 muscarinic receptor subtypes coupled to intracellular Ca2+ elevation and lacking Ca2+ channels activated by membrane depolarization 90
Clinical features and lifestyle of patients with amyotrophic lateral sclerosis in Campania: brief overview of an Italian database. 89
Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene 87
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 87
High sensitivity method for fluorofore detection in gradient polyacrylamide slab gels through excitation by laser light: application to glycoproteins stained with concanavalin A-fluorescein isothiocyanate 86
Exposure to environmental toxicants and pathogenesis of amyotrophic lateral sclerosis: state of the art and research perspectives. 86
Myasthenia gravis in a patient affected by glycogen storage disease type Ib: A further manifestation of an increased risk for autoimmune disorders? 84
Neural control of gene expression of skeletal muscle fibers 84
Isolation and identification of rat's sarcolemma: preliminary results on the effects of denervation on "in vitro" activity of membrane-bound neuraminidase 84
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. 84
Casi clinici 82
The effects of denervation on sarcolemmal glycoconjugates of type skeletal muscle fibres of rat 82
Erythropoietin in amyotrophic lateral sclerosis: A multicentre, randomised, double blind, placebo controlled, phase III study 75
Impact on children of a parent with ALS: A case-control study 75
The MITOS system predicts long-term survival in amyotrophic lateral sclerosis 72
Totale 11.393
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Categoria #
all - tutte 37.175
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 37.175
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021220 0 0 0 0 0 0 0 0 0 100 96 24
2021/2022606 44 10 11 14 221 4 11 14 22 53 39 163
2022/20231.385 136 36 17 135 142 116 0 87 654 5 29 28
2023/2024443 44 9 22 31 158 57 7 3 1 7 43 61
2024/20251.341 2 46 12 20 222 173 195 103 233 179 100 56
2025/20265.274 153 190 306 265 472 3.183 271 159 183 92 0 0
Totale 11.393