IRIS
MONSURRO', Maria Rosaria
 Distribuzione geografica
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Continente #
EU - Europa 3.149
NA - Nord America 2.714
AS - Asia 1.876
SA - Sud America 354
AF - Africa 25
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 8.124
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Nazione #
US - Stati Uniti d'America 2.693
RU - Federazione Russa 973
SG - Singapore 677
IE - Irlanda 650
CN - Cina 506
UA - Ucraina 346
BR - Brasile 300
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
KR - Corea 82
VN - Vietnam 69
GR - Grecia 65
IN - India 57
JP - Giappone 29
BE - Belgio 22
AR - Argentina 19
BD - Bangladesh 12
CA - Canada 10
CO - Colombia 9
EC - Ecuador 8
ID - Indonesia 8
IQ - Iraq 7
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
BG - Bulgaria 3
CL - Cile 3
JM - Giamaica 3
MA - Marocco 3
PY - Paraguay 3
AL - Albania 2
AM - Armenia 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
IR - Iran 2
JO - Giordania 2
KE - Kenya 2
KZ - Kazakistan 2
LB - Libano 2
LT - Lituania 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
IL - Israele 1
KG - Kirghizistan 1
LK - Sri Lanka 1
LV - Lettonia 1
MY - Malesia 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
PS - Palestinian Territory 1
Totale 8.124
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Città #
Dublin 650
Jacksonville 526
Chandler 404
Santa Clara 346
Moscow 303
Hong Kong 284
Singapore 228
Beijing 117
Dallas 103
Ann Arbor 99
Princeton 95
Medford 87
Seoul 80
Roxbury 58
Boardman 52
New York 51
Woodbridge 50
Wilmington 46
Bengaluru 41
San Mateo 41
The Dalles 41
Ashburn 40
Hefei 38
Nanjing 37
Caserta 36
São Paulo 28
Ho Chi Minh City 26
Mountain View 24
Bremen 23
Brussels 21
Dearborn 20
Des Moines 18
Jinan 18
Los Angeles 18
Lappeenranta 14
Nanchang 13
Norwalk 13
Guangzhou 12
Cambridge 10
Düsseldorf 10
Hanoi 10
London 10
Munich 10
Napoli 10
Naples 9
Rome 9
Shenyang 9
Auburn Hills 8
Helsinki 8
San Francisco 8
Zhengzhou 8
Belo Horizonte 7
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
Quito 4
Ribeirão Preto 4
Tokyo 4
Venice 4
Augusta 3
Belém 3
Cotia 3
Johannesburg 3
João Pessoa 3
Lanzhou 3
Londrina 3
Marília 3
Monte Grande 3
Montreal 3
Ottawa 3
Salvador 3
Santiago de Cali 3
Taiyuan 3
Thái Bình 3
Tunis 3
Totale 4.434
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Nome #
Edinburgh Cognitive and Behavioural ALS Screen (ECAS)-Italian version: regression based norms and equivalent scores 198
Beyond motor neurons: new insights on amyotrophic lateral sclerosis neurodegeneration provided by advanced MRI technique 141
Blood Lead, Manganese, and Aluminum Levels in a Regional Italian Cohort of ALS Patients: Does Aluminum Have an Influence? 132
Advantages of QBI in TBSS analyses. 130
Interaction between aging and neurodegeneration in amyotrophic lateral sclerosis 128
Apathy in amyotrophic lateral sclerosis: insights from Dimensional Apathy Scale 126
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. 123
Widespread Microstructural White Matter Involvement in Amyotrophic Lateral Sclerosis: A Whole-Brain DTI Study. 121
Distributed corpus callosum involvement in amyotrophic lateral sclerosis: a deterministic tractography study using q-ball imaging. 118
Frontotemporal cortical thinning in amyotrophic lateral sclerosis. 114
Vitamin D supplementation has no effects on progression of motor dysfunction in amyotrophic lateral sclerosis (ALS) 114
Amyotrophic lateral sclerosis and multiple sclerosis overlap: a case report. 111
Apathy Is Correlated with Widespread Diffusion Tensor Imaging (DTI) Impairment in Amyotrophic Lateral Sclerosis 111
A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy 110
Preliminary results of isolation and identification of rat sarcolemma and the effect of denervation on membrane-bound neuraminidase activity 109
Accumulation of altered aspartyl residues in erythrocyte membrane proteins from patients with sporadic amyotrophic lateral sclerosis. 108
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 108
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis 107
A case of probable autosomal recessive ectodermal dysplasia with corkscrew hairs and menial retardation in a family with tuberous sclerosis 107
Assessing Anxiety and its correlates in Amyotrophic Lateral Sclerosis: the State-Trait Anxiety Inventory 107
Subcortical motor plasticity in patients with sporadic ALS: An fMRI study 105
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. 105
Whole-brain DTI pattern of white matter damage in Amyotrophic lateral sclerosis: further evidences of a multisystem disorder 101
Accuracy of death certificates for amyotrophic lateral sclerosis varies significantly from north to south of Italy: implications for mortality studies 100
Amyotrophic lateral sclerosis and multiple sclerosis overlap: A case report 100
Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy 99
INFRATENTORIAL PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY IN A PATIENT TREATED WITH FLUDARABINE AND RITUXIMAB 97
An Italian kindred with FALS due to c.149T>C mutation in the SOD1 gene: case report of an affected family member 96
Sistema nervoso 95
Beyond motor neurons: new insights on amyotrophic lateral sclerosis neurodegeneration provided by advanced MRI tecnique 94
Dysfunctions within limbic-motor networks in amyotrophic lateral sclerosis. 94
A case of probable autosomal recessive ectodermal dysplasia with corkscrew hairs and mental retardation in a family with tuberous sclerosis 93
Retrospective epidemiology of Duchenne muscular dystrophy in Molise 92
Whole-brain DTI pattern of white metter damage in amyotrophic lateral sclerosis: further evidences of a multisystem disorder 92
Coping strategies and psychological distress in caregivers of patients with Amyotrophic Lateral Sclerosis (ALS) 92
Microstructural Changes across Different Clinical Milestones of Disease in Amyotrophic Lateral Sclerosis. 91
Structure of msj-1 gene: a comparative analysis 91
Extra-motor involvement in ALS patients: a cortical thickeness 3T MRI study 90
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? 89
Towards genetic prevention of Adrenoleukodystrophy through early biochemical diagnosis of hemizygotes and heterozygotes in families at risk 89
[Determination of alimentary value of buffalo muscle proteins using enzymatic methods] 88
Cardiovascular diseases may play a negative role in the prognosis of ALS 88
ALS and CHARGE syndrome: a clinical and genetic study 88
Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophy 87
Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis. 86
Widespread Structural and Functional Connectivity Changes in Amyotrophic Lateral Sclerosis: Insights from Advanced Neuroimaging Research 86
Brain functional networks become more connected as amyotrophic lateral sclerosis progresses: a source level magnetoencephalographic study 86
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 83
Sporadic ALS is not associated with VAPB gene mutations in Southern Italy 83
Factors predicting survival in ALS: a multicenter Italian study 83
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation 82
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis. 80
Earliest videofluoromanometric pharyngeal signs of dysphagia in ALS patients. 79
Motor and extramotor neurodegeneration in amyotrophic lateral sclerosis: a 3T high angular resolution diffusion imaging (HARDI) study 79
Reversible mielopathy due to deficiency of vitamin B12 in patient with associated syringomyelia: a case report 79
Functional overlap and divergence between ALS and bvFTD 78
HFE p.H63D polymorphism does not influence ALS phenotype and survival 78
Theory of Mind and Its Neuropsychological and Quality of Life Correlates in the Early Stages of Amyotrophic Lateral Sclerosis 78
The GH-IGF system in amyotrophic lateral sclerosis: correlations between pituitary GH secretion capacity, insulin-like growth factors and clinical features 77
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 77
FUS mutations in sporadic amyotrophic lateral sclerosis. 76
Microstructural correlates of Edinburgh Cognitive and Behavioural ALS Screen (ECAS) changes in amyotrophic lateral sclerosis 76
Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomized, double blind, placebo controlled, phase III study. 74
Toward genetic prevention of adrenoleukodystrophy trough early biochemical diagnosis of hemizygotes and heterozygotes in families at risk. 74
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population. 74
Neuropsychological assessment in different King's clinical stages of amyotrophic lateral sclerosis 74
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 73
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 73
The application of recently developed methods to investigate glycoconjugate composition of sarcolemma: some preliminary results on Duchenne muscular dystrophy 72
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. 72
Establishment and characterization of a human neuroectodermal cell line (TB) from a cerebrospinal fluid specimen 71
Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis 71
Targeting extracellular cyclophilin A reduces neuroinflammation and extends survival in a mouse model of amyotrophic lateral sclerosis 70
Lithium carbonate in amyotrophic lateral sclerosis Lack of efficacy in a dose-finding trial 69
The neural control of skeletal muscle sarcolemma: preliminary results of different approaches to the study of a possible control of membrane-bound glycoconjugates 69
Clinical features and lifestyle of patients with amyotrophic lateral sclerosis in Campania: brief overview of an Italian database. 68
Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS 68
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 67
Membrane depolarization in LA-N-1 cells. The effect of maitotoxin is Ca(2+)- and Na(+)-dependent 67
Direct inhibition of choline acetyltransferase activity by a monoclonal antibody raised against the plasma membrane of cholinergic nerve terminals 66
The effects of denervation on sarcolemmal glycoconjugates of type skeletal muscle fibres of rat. Su: Synaptic Constituents in Health and Disease 66
FUS mutations in sporadic amyotrophic lateral sclerosis: Clinical and genetic analysis. 66
Isolation and identification of rat's sarcolemma: preliminary results on the effects of denervation on "in vitro" activity of membrane-bound neuraminidase 65
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 63
Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene 63
Neural control of gene expression of skeletal muscle fibers 60
Exposure to environmental toxicants and pathogenesis of amyotrophic lateral sclerosis: state of the art and research perspectives. 59
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 59
Casi clinici 58
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. 58
Myasthenia gravis in a patient affected by glycogen storage disease type Ib: A further manifestation of an increased risk for autoimmune disorders? 57
The effects of denervation on sarcolemmal glycoconjugates of type skeletal muscle fibres of rat 57
Erythropoietin in amyotrophic lateral sclerosis: A multicentre, randomised, double blind, placebo controlled, phase III study 54
The MITOS system predicts long-term survival in amyotrophic lateral sclerosis 50
Impact on children of a parent with ALS: A case-control study 48
Totale 8.280
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Categoria #
all - tutte 32.482
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 32.482
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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
2025/20262.161 153 190 306 265 472 775 0 0 0 0 0 0
Totale 8.280