IRIS
MONSURRO', Maria Rosaria
 Distribuzione geografica
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Continente #
EU - Europa 5.633
NA - Nord America 3.440
AS - Asia 2.232
SA - Sud America 377
Continente sconosciuto - Info sul continente non disponibili 160
AF - Africa 32
OC - Oceania 2
Totale 11.876
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Nazione #
US - Stati Uniti d'America 3.400
RU - Federazione Russa 3.385
SG - Singapore 774
IE - Irlanda 650
CN - Cina 585
UA - Ucraina 347
BR - Brasile 314
GB - Regno Unito 305
HK - Hong Kong 302
IT - Italia 278
VN - Vietnam 200
DE - Germania 174
FR - Francia 138
TR - Turchia 120
FI - Finlandia 112
SE - Svezia 111
KR - Corea 83
IN - India 67
GR - Grecia 65
JP - Giappone 30
BE - Belgio 22
AR - Argentina 21
CA - Canada 18
BD - Bangladesh 16
NL - Olanda 11
ZA - Sudafrica 11
CO - Colombia 10
EC - Ecuador 9
ID - Indonesia 9
ES - Italia 8
IQ - Iraq 8
MX - Messico 8
PL - Polonia 8
AT - Austria 6
CL - Cile 6
VE - Venezuela 6
EG - Egitto 5
PE - Perù 5
PK - Pakistan 5
TH - Thailandia 5
TN - Tunisia 5
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
CR - Costa Rica 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
AW - Aruba 1
AZ - Azerbaigian 1
BB - Barbados 1
BO - Bolivia 1
BW - Botswana 1
CH - Svizzera 1
GA - Gabon 1
GT - Guatemala 1
LK - Sri Lanka 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
PR - Porto Rico 1
PT - Portogallo 1
TT - Trinidad e Tobago 1
Totale 11.720
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Città #
Moscow 1.194
Dublin 650
Jacksonville 527
Chandler 404
Santa Clara 373
San Jose 304
Singapore 303
Hong Kong 298
Beijing 133
Ashburn 118
Dallas 114
Ann Arbor 99
Princeton 95
Medford 87
Seoul 81
Ho Chi Minh City 66
New York 66
Roxbury 58
Boardman 52
Woodbridge 50
Hanoi 47
Wilmington 46
Bengaluru 41
San Mateo 41
The Dalles 41
Hefei 38
Nanjing 37
Caserta 36
São Paulo 31
Los Angeles 25
Mountain View 24
Bremen 23
Brussels 21
Dearborn 20
Des Moines 18
Jinan 18
Lappeenranta 14
Haiphong 13
Nanchang 13
Norwalk 13
Shanghai 13
Guangzhou 12
Da Nang 11
London 11
Cambridge 10
Düsseldorf 10
Munich 10
Napoli 10
Houston 9
Naples 9
Rome 9
San Francisco 9
Shenyang 9
Auburn Hills 8
Belo Horizonte 8
Chicago 8
Helsinki 8
Porto Alegre 8
Zhengzhou 8
Changsha 7
Guarulhos 7
Amsterdam 6
Atlanta 6
Brasília 6
Johannesburg 6
Kunming 6
Luzzano 6
Memphis 6
Milan 6
Montevecchia 6
Orem 6
Stockholm 6
Baghdad 5
Biên Hòa 5
Brooklyn 5
Buffalo 5
Campinas 5
Curitiba 5
Frankfurt am Main 5
Genova 5
Montreal 5
Ningbo 5
Nuremberg 5
Rio de Janeiro 5
Tianjin 5
Tokyo 5
Turku 5
Cava De' Tirreni 4
Chennai 4
Denver 4
Dhaka 4
Haikou 4
Hebei 4
Phoenix 4
Piscataway 4
Quito 4
Ribeirão Preto 4
Venice 4
Augusta 3
Bangkok 3
Totale 6.017
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Nome #
Blood Lead, Manganese, and Aluminum Levels in a Regional Italian Cohort of ALS Patients: Does Aluminum Have an Influence? 303
Edinburgh Cognitive and Behavioural ALS Screen (ECAS)-Italian version: regression based norms and equivalent scores 267
Beyond motor neurons: new insights on amyotrophic lateral sclerosis neurodegeneration provided by advanced MRI technique 203
Advantages of QBI in TBSS analyses. 187
Apathy in amyotrophic lateral sclerosis: insights from Dimensional Apathy Scale 184
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. 178
Apathy Is Correlated with Widespread Diffusion Tensor Imaging (DTI) Impairment in Amyotrophic Lateral Sclerosis 176
Amyotrophic lateral sclerosis and multiple sclerosis overlap: A case report 170
A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy 166
Amyotrophic lateral sclerosis and multiple sclerosis overlap: a case report. 166
Frontotemporal cortical thinning in amyotrophic lateral sclerosis. 164
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis 162
Interaction between aging and neurodegeneration in amyotrophic lateral sclerosis 162
The GH-IGF system in amyotrophic lateral sclerosis: correlations between pituitary GH secretion capacity, insulin-like growth factors and clinical features 162
A case of probable autosomal recessive ectodermal dysplasia with corkscrew hairs and menial retardation in a family with tuberous sclerosis 159
Assessing Anxiety and its correlates in Amyotrophic Lateral Sclerosis: the State-Trait Anxiety Inventory 159
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 157
Vitamin D supplementation has no effects on progression of motor dysfunction in amyotrophic lateral sclerosis (ALS) 156
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. 154
Widespread Microstructural White Matter Involvement in Amyotrophic Lateral Sclerosis: A Whole-Brain DTI Study. 153
Accuracy of death certificates for amyotrophic lateral sclerosis varies significantly from north to south of Italy: implications for mortality studies 148
Preliminary results of isolation and identification of rat sarcolemma and the effect of denervation on membrane-bound neuraminidase activity 148
Distributed corpus callosum involvement in amyotrophic lateral sclerosis: a deterministic tractography study using q-ball imaging. 147
Accumulation of altered aspartyl residues in erythrocyte membrane proteins from patients with sporadic amyotrophic lateral sclerosis. 146
An Italian kindred with FALS due to c.149T>C mutation in the SOD1 gene: case report of an affected family member 142
A case of probable autosomal recessive ectodermal dysplasia with corkscrew hairs and mental retardation in a family with tuberous sclerosis 141
Whole-brain DTI pattern of white matter damage in Amyotrophic lateral sclerosis: further evidences of a multisystem disorder 141
Extra-motor involvement in ALS patients: a cortical thickeness 3T MRI study 140
INFRATENTORIAL PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY IN A PATIENT TREATED WITH FLUDARABINE AND RITUXIMAB 139
Subcortical motor plasticity in patients with sporadic ALS: An fMRI study 137
[Determination of alimentary value of buffalo muscle proteins using enzymatic methods] 137
ALS and CHARGE syndrome: a clinical and genetic study 137
Beyond motor neurons: new insights on amyotrophic lateral sclerosis neurodegeneration provided by advanced MRI tecnique 135
Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy 131
Structure of msj-1 gene: a comparative analysis 131
Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis. 127
Whole-brain DTI pattern of white metter damage in amyotrophic lateral sclerosis: further evidences of a multisystem disorder 127
Sistema nervoso 127
Dysfunctions within limbic-motor networks in amyotrophic lateral sclerosis. 125
Retrospective epidemiology of Duchenne muscular dystrophy in Molise 123
Brain functional networks become more connected as amyotrophic lateral sclerosis progresses: a source level magnetoencephalographic study 122
Towards genetic prevention of Adrenoleukodystrophy through early biochemical diagnosis of hemizygotes and heterozygotes in families at risk 120
Coping strategies and psychological distress in caregivers of patients with Amyotrophic Lateral Sclerosis (ALS) 120
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? 119
Microstructural Changes across Different Clinical Milestones of Disease in Amyotrophic Lateral Sclerosis. 117
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis. 115
Reversible mielopathy due to deficiency of vitamin B12 in patient with associated syringomyelia: a case report 115
Theory of Mind and Its Neuropsychological and Quality of Life Correlates in the Early Stages of Amyotrophic Lateral Sclerosis 115
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation 114
Sporadic ALS is not associated with VAPB gene mutations in Southern Italy 114
Widespread Structural and Functional Connectivity Changes in Amyotrophic Lateral Sclerosis: Insights from Advanced Neuroimaging Research 114
Cardiovascular diseases may play a negative role in the prognosis of ALS 114
Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophy 112
Microstructural correlates of Edinburgh Cognitive and Behavioural ALS Screen (ECAS) changes in amyotrophic lateral sclerosis 111
Factors predicting survival in ALS: a multicenter Italian study 110
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 110
Earliest videofluoromanometric pharyngeal signs of dysphagia in ALS patients. 108
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 108
HFE p.H63D polymorphism does not influence ALS phenotype and survival 108
Functional overlap and divergence between ALS and bvFTD 107
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. 107
Neuropsychological assessment in different King's clinical stages of amyotrophic lateral sclerosis 107
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 106
Motor and extramotor neurodegeneration in amyotrophic lateral sclerosis: a 3T high angular resolution diffusion imaging (HARDI) study 106
FUS mutations in sporadic amyotrophic lateral sclerosis. 105
Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomized, double blind, placebo controlled, phase III study. 104
Establishment and characterization of a human neuroectodermal cell line (TB) from a cerebrospinal fluid specimen 102
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 102
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population. 101
Toward genetic prevention of adrenoleukodystrophy trough early biochemical diagnosis of hemizygotes and heterozygotes in families at risk. 100
The application of recently developed methods to investigate glycoconjugate composition of sarcolemma: some preliminary results on Duchenne muscular dystrophy 99
Targeting extracellular cyclophilin A reduces neuroinflammation and extends survival in a mouse model of amyotrophic lateral sclerosis 99
Membrane depolarization in LA-N-1 cells. The effect of maitotoxin is Ca(2+)- and Na(+)-dependent 98
The neural control of skeletal muscle sarcolemma: preliminary results of different approaches to the study of a possible control of membrane-bound glycoconjugates 98
Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis 97
FUS mutations in sporadic amyotrophic lateral sclerosis: Clinical and genetic analysis. 96
Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS 95
Lithium carbonate in amyotrophic lateral sclerosis Lack of efficacy in a dose-finding trial 94
Direct inhibition of choline acetyltransferase activity by a monoclonal antibody raised against the plasma membrane of cholinergic nerve terminals 93
The effects of denervation on sarcolemmal glycoconjugates of type skeletal muscle fibres of rat. Su: Synaptic Constituents in Health and Disease 93
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 92
Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene 92
Clinical features and lifestyle of patients with amyotrophic lateral sclerosis in Campania: brief overview of an Italian database. 91
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 91
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 89
Exposure to environmental toxicants and pathogenesis of amyotrophic lateral sclerosis: state of the art and research perspectives. 89
Myasthenia gravis in a patient affected by glycogen storage disease type Ib: A further manifestation of an increased risk for autoimmune disorders? 88
Neural control of gene expression of skeletal muscle fibers 86
Casi clinici 85
Isolation and identification of rat's sarcolemma: preliminary results on the effects of denervation on "in vitro" activity of membrane-bound neuraminidase 85
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. 85
The effects of denervation on sarcolemmal glycoconjugates of type skeletal muscle fibres of rat 83
Erythropoietin in amyotrophic lateral sclerosis: A multicentre, randomised, double blind, placebo controlled, phase III study 77
Impact on children of a parent with ALS: A case-control study 77
The MITOS system predicts long-term survival in amyotrophic lateral sclerosis 74
Totale 11.876
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Categoria #
all - tutte 40.806
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 40.806
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022562 0 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
2025/20265.481 153 190 306 265 472 3.183 271 159 183 109 84 106
2026/2027276 65 211 0 0 0 0 0 0 0 0 0 0
Totale 11.876