IRIS
MONSURRO', Maria Rosaria
 Distribuzione geografica
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Continente #
EU - Europa 5.485
NA - Nord America 2.719
AS - Asia 1.917
SA - Sud America 360
AF - Africa 25
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 10.512
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Nazione #
RU - Federazione Russa 3.307
US - Stati Uniti d'America 2.697
SG - Singapore 693
IE - Irlanda 650
CN - Cina 510
UA - Ucraina 347
BR - Brasile 305
GB - Regno Unito 295
HK - Hong Kong 285
IT - Italia 242
DE - Germania 173
FR - Francia 129
TR - Turchia 119
FI - Finlandia 112
SE - Svezia 111
VN - Vietnam 83
KR - Corea 82
GR - Grecia 65
IN - India 58
JP - Giappone 29
BE - Belgio 22
AR - Argentina 20
BD - Bangladesh 13
CA - Canada 11
CO - Colombia 9
ID - Indonesia 9
EC - Ecuador 8
IQ - Iraq 8
ZA - Sudafrica 7
AT - Austria 6
ES - Italia 6
EG - Egitto 5
MX - Messico 5
PE - Perù 5
PL - Polonia 5
VE - Venezuela 5
EU - Europa 4
NL - Olanda 4
PK - Pakistan 4
TN - Tunisia 4
AM - Armenia 3
BG - Bulgaria 3
CL - Cile 3
JM - Giamaica 3
MA - Marocco 3
PY - Paraguay 3
AL - Albania 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
IL - Israele 2
IR - Iran 2
JO - Giordania 2
KE - Kenya 2
KG - Kirghizistan 2
KZ - Kazakistan 2
LB - Libano 2
LT - Lituania 2
LV - Lettonia 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
BW - Botswana 1
GA - Gabon 1
LK - Sri Lanka 1
MY - Malesia 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
PS - Palestinian Territory 1
Totale 10.512
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Città #
Moscow 1.150
Dublin 650
Jacksonville 526
Chandler 404
Santa Clara 346
Hong Kong 284
Singapore 244
Beijing 117
Dallas 103
Ann Arbor 99
Princeton 95
Medford 87
Seoul 80
Roxbury 58
Boardman 52
New York 51
Woodbridge 50
Wilmington 46
Ashburn 42
Bengaluru 41
San Mateo 41
The Dalles 41
Hefei 38
Nanjing 37
Caserta 36
Ho Chi Minh City 31
São Paulo 28
Mountain View 24
Bremen 23
Brussels 21
Dearborn 20
Des Moines 18
Jinan 18
Los Angeles 18
Hanoi 14
Lappeenranta 14
Nanchang 13
Norwalk 13
Guangzhou 12
Cambridge 10
Düsseldorf 10
London 10
Munich 10
Napoli 10
Naples 9
Rome 9
Shenyang 9
Auburn Hills 8
Belo Horizonte 8
Helsinki 8
San Francisco 8
Zhengzhou 8
Changsha 7
Guarulhos 7
Houston 7
Porto Alegre 7
Brasília 6
Kunming 6
Luzzano 6
Stockholm 6
Baghdad 5
Campinas 5
Curitiba 5
Genova 5
Haiphong 5
Ningbo 5
Nuremberg 5
Rio de Janeiro 5
Shanghai 5
Tianjin 5
Turku 5
Biên Hòa 4
Brooklyn 4
Cava De' Tirreni 4
Chicago 4
Dhaka 4
Frankfurt am Main 4
Haikou 4
Hebei 4
Milan 4
Montreal 4
Quito 4
Ribeirão Preto 4
Tokyo 4
Venice 4
Augusta 3
Belém 3
Cotia 3
Dnipro 3
Johannesburg 3
João Pessoa 3
Lanzhou 3
Londrina 3
Marília 3
Monte Grande 3
Ninh Bình 3
Ottawa 3
Phủ Lý 3
Salvador 3
Santiago de Cali 3
Totale 5.310
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Nome #
Edinburgh Cognitive and Behavioural ALS Screen (ECAS)-Italian version: regression based norms and equivalent scores 235
Beyond motor neurons: new insights on amyotrophic lateral sclerosis neurodegeneration provided by advanced MRI technique 179
Advantages of QBI in TBSS analyses. 170
Blood Lead, Manganese, and Aluminum Levels in a Regional Italian Cohort of ALS Patients: Does Aluminum Have an Influence? 167
Apathy in amyotrophic lateral sclerosis: insights from Dimensional Apathy Scale 163
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. 161
Interaction between aging and neurodegeneration in amyotrophic lateral sclerosis 155
Apathy Is Correlated with Widespread Diffusion Tensor Imaging (DTI) Impairment in Amyotrophic Lateral Sclerosis 153
A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy 149
Amyotrophic lateral sclerosis and multiple sclerosis overlap: a case report. 149
A case of probable autosomal recessive ectodermal dysplasia with corkscrew hairs and menial retardation in a family with tuberous sclerosis 147
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis 146
Widespread Microstructural White Matter Involvement in Amyotrophic Lateral Sclerosis: A Whole-Brain DTI Study. 146
Frontotemporal cortical thinning in amyotrophic lateral sclerosis. 143
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 143
Amyotrophic lateral sclerosis and multiple sclerosis overlap: A case report 143
Vitamin D supplementation has no effects on progression of motor dysfunction in amyotrophic lateral sclerosis (ALS) 141
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. 138
Distributed corpus callosum involvement in amyotrophic lateral sclerosis: a deterministic tractography study using q-ball imaging. 137
Preliminary results of isolation and identification of rat sarcolemma and the effect of denervation on membrane-bound neuraminidase activity 137
Accumulation of altered aspartyl residues in erythrocyte membrane proteins from patients with sporadic amyotrophic lateral sclerosis. 137
Assessing Anxiety and its correlates in Amyotrophic Lateral Sclerosis: the State-Trait Anxiety Inventory 137
Accuracy of death certificates for amyotrophic lateral sclerosis varies significantly from north to south of Italy: implications for mortality studies 132
Whole-brain DTI pattern of white matter damage in Amyotrophic lateral sclerosis: further evidences of a multisystem disorder 129
INFRATENTORIAL PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY IN A PATIENT TREATED WITH FLUDARABINE AND RITUXIMAB 128
Subcortical motor plasticity in patients with sporadic ALS: An fMRI study 128
A case of probable autosomal recessive ectodermal dysplasia with corkscrew hairs and mental retardation in a family with tuberous sclerosis 128
[Determination of alimentary value of buffalo muscle proteins using enzymatic methods] 125
Beyond motor neurons: new insights on amyotrophic lateral sclerosis neurodegeneration provided by advanced MRI tecnique 125
An Italian kindred with FALS due to c.149T>C mutation in the SOD1 gene: case report of an affected family member 125
ALS and CHARGE syndrome: a clinical and genetic study 125
Extra-motor involvement in ALS patients: a cortical thickeness 3T MRI study 124
Whole-brain DTI pattern of white metter damage in amyotrophic lateral sclerosis: further evidences of a multisystem disorder 120
Sistema nervoso 118
Dysfunctions within limbic-motor networks in amyotrophic lateral sclerosis. 117
Brain functional networks become more connected as amyotrophic lateral sclerosis progresses: a source level magnetoencephalographic study 117
Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy 116
Retrospective epidemiology of Duchenne muscular dystrophy in Molise 115
Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis. 113
Structure of msj-1 gene: a comparative analysis 113
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? 112
Coping strategies and psychological distress in caregivers of patients with Amyotrophic Lateral Sclerosis (ALS) 112
Towards genetic prevention of Adrenoleukodystrophy through early biochemical diagnosis of hemizygotes and heterozygotes in families at risk 111
Microstructural Changes across Different Clinical Milestones of Disease in Amyotrophic Lateral Sclerosis. 109
Widespread Structural and Functional Connectivity Changes in Amyotrophic Lateral Sclerosis: Insights from Advanced Neuroimaging Research 109
Cardiovascular diseases may play a negative role in the prognosis of ALS 108
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation 107
Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophy 106
Sporadic ALS is not associated with VAPB gene mutations in Southern Italy 105
Factors predicting survival in ALS: a multicenter Italian study 105
Reversible mielopathy due to deficiency of vitamin B12 in patient with associated syringomyelia: a case report 103
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis. 102
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 102
Earliest videofluoromanometric pharyngeal signs of dysphagia in ALS patients. 100
Theory of Mind and Its Neuropsychological and Quality of Life Correlates in the Early Stages of Amyotrophic Lateral Sclerosis 100
HFE p.H63D polymorphism does not influence ALS phenotype and survival 99
Microstructural correlates of Edinburgh Cognitive and Behavioural ALS Screen (ECAS) changes in amyotrophic lateral sclerosis 99
FUS mutations in sporadic amyotrophic lateral sclerosis. 98
Motor and extramotor neurodegeneration in amyotrophic lateral sclerosis: a 3T high angular resolution diffusion imaging (HARDI) study 96
Functional overlap and divergence between ALS and bvFTD 95
The GH-IGF system in amyotrophic lateral sclerosis: correlations between pituitary GH secretion capacity, insulin-like growth factors and clinical features 95
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 95
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 95
Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomized, double blind, placebo controlled, phase III study. 94
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population. 94
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. 94
Neuropsychological assessment in different King's clinical stages of amyotrophic lateral sclerosis 94
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 94
Establishment and characterization of a human neuroectodermal cell line (TB) from a cerebrospinal fluid specimen 93
The application of recently developed methods to investigate glycoconjugate composition of sarcolemma: some preliminary results on Duchenne muscular dystrophy 93
Targeting extracellular cyclophilin A reduces neuroinflammation and extends survival in a mouse model of amyotrophic lateral sclerosis 92
Toward genetic prevention of adrenoleukodystrophy trough early biochemical diagnosis of hemizygotes and heterozygotes in families at risk. 91
The neural control of skeletal muscle sarcolemma: preliminary results of different approaches to the study of a possible control of membrane-bound glycoconjugates 91
Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis 90
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 88
FUS mutations in sporadic amyotrophic lateral sclerosis: Clinical and genetic analysis. 88
Lithium carbonate in amyotrophic lateral sclerosis Lack of efficacy in a dose-finding trial 87
Direct inhibition of choline acetyltransferase activity by a monoclonal antibody raised against the plasma membrane of cholinergic nerve terminals 87
The effects of denervation on sarcolemmal glycoconjugates of type skeletal muscle fibres of rat. Su: Synaptic Constituents in Health and Disease 87
Clinical features and lifestyle of patients with amyotrophic lateral sclerosis in Campania: brief overview of an Italian database. 87
Membrane depolarization in LA-N-1 cells. The effect of maitotoxin is Ca(2+)- and Na(+)-dependent 86
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 84
Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene 84
Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS 84
Isolation and identification of rat's sarcolemma: preliminary results on the effects of denervation on "in vitro" activity of membrane-bound neuraminidase 83
Neural control of gene expression of skeletal muscle fibers 81
Exposure to environmental toxicants and pathogenesis of amyotrophic lateral sclerosis: state of the art and research perspectives. 80
Myasthenia gravis in a patient affected by glycogen storage disease type Ib: A further manifestation of an increased risk for autoimmune disorders? 79
Casi clinici 79
The effects of denervation on sarcolemmal glycoconjugates of type skeletal muscle fibres of rat 79
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. 77
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 77
Erythropoietin in amyotrophic lateral sclerosis: A multicentre, randomised, double blind, placebo controlled, phase III study 73
The MITOS system predicts long-term survival in amyotrophic lateral sclerosis 71
Impact on children of a parent with ALS: A case-control study 70
Totale 10.668
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Categoria #
all - tutte 35.777
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 35.777
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021432 0 0 0 0 0 11 108 87 6 100 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
2025/20264.549 153 190 306 265 472 3.163 0 0 0 0 0 0
Totale 10.668