IRIS
MONSURRO', Maria Rosaria
 Distribuzione geografica
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Continente #
NA - Nord America 2.094
EU - Europa 2.087
AS - Asia 482
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
SA - Sud America 1
Totale 4.670
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Nazione #
US - Stati Uniti d'America 2.090
IE - Irlanda 649
UA - Ucraina 339
GB - Regno Unito 288
CN - Cina 231
IT - Italia 222
DE - Germania 153
FR - Francia 125
TR - Turchia 112
SE - Svezia 109
FI - Finlandia 106
SG - Singapore 84
GR - Grecia 65
KR - Corea 41
BE - Belgio 22
IN - India 6
CA - Canada 4
EU - Europa 4
NL - Olanda 3
PL - Polonia 3
IR - Iran 2
JP - Giappone 2
VN - Vietnam 2
AE - Emirati Arabi Uniti 1
AU - Australia 1
BG - Bulgaria 1
BR - Brasile 1
ES - Italia 1
HK - Hong Kong 1
NZ - Nuova Zelanda 1
RO - Romania 1
Totale 4.670
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Città #
Dublin 649
Jacksonville 525
Chandler 404
Ann Arbor 99
Princeton 95
Medford 87
Beijing 78
Roxbury 58
Boardman 52
Woodbridge 50
New York 48
Singapore 47
Wilmington 46
San Mateo 41
Seoul 39
Caserta 36
Nanjing 35
Mountain View 24
Bremen 23
Brussels 21
Dearborn 20
Des Moines 18
Ashburn 17
Jinan 17
Lappeenranta 13
Nanchang 13
Norwalk 13
Cambridge 10
Düsseldorf 10
Los Angeles 10
Napoli 10
Shenyang 9
Auburn Hills 8
Helsinki 8
London 8
Guangzhou 7
Rome 7
Zhengzhou 7
Houston 6
Kunming 6
Luzzano 6
Changsha 5
Genova 5
Naples 5
Ningbo 5
Cava De' Tirreni 4
Haikou 4
Hebei 4
Hefei 4
Stockholm 4
Tianjin 4
Venice 4
Augusta 3
Lanzhou 3
Ottawa 3
Taiyuan 3
Baotou 2
Berlin 2
Buffalo 2
Capua 2
Dong Ket 2
Frattamaggiore 2
Gavirate 2
Groningen 2
Gunzenhausen 2
Kraków 2
Langfang 2
Limoges 2
Milan 2
Palermo 2
Redwood City 2
San Giovanni Rotondo 2
Scottsdale 2
Selargius 2
Shanghai 2
Siena 2
Abbiategrasso 1
Arienzo 1
Asti 1
Atella 1
Auckland 1
Aversa 1
Bangalore 1
Bari 1
Bologna 1
Bonn 1
Brighton 1
Bucharest 1
Casale Monferrato 1
Central District 1
Chaoyang 1
Clearwater 1
Cornigliano 1
Crotone 1
Cuneo 1
Dubai 1
Elora 1
Fairfield 1
Ferentino 1
Florence 1
Totale 2.804
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Nome #
Edinburgh Cognitive and Behavioural ALS Screen (ECAS)-Italian version: regression based norms and equivalent scores 155
Interaction between aging and neurodegeneration in amyotrophic lateral sclerosis 94
Beyond motor neurons: new insights on amyotrophic lateral sclerosis neurodegeneration provided by advanced MRI technique 89
Distributed corpus callosum involvement in amyotrophic lateral sclerosis: a deterministic tractography study using q-ball imaging. 85
Blood Lead, Manganese, and Aluminum Levels in a Regional Italian Cohort of ALS Patients: Does Aluminum Have an Influence? 84
Advantages of QBI in TBSS analyses. 79
Widespread Microstructural White Matter Involvement in Amyotrophic Lateral Sclerosis: A Whole-Brain DTI Study. 79
Apathy in amyotrophic lateral sclerosis: insights from Dimensional Apathy Scale 79
Frontotemporal cortical thinning in amyotrophic lateral sclerosis. 78
INFRATENTORIAL PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY IN A PATIENT TREATED WITH FLUDARABINE AND RITUXIMAB 69
Whole-brain DTI pattern of white matter damage in Amyotrophic lateral sclerosis: further evidences of a multisystem disorder 69
Preliminary results of isolation and identification of rat sarcolemma and the effect of denervation on membrane-bound neuraminidase activity 67
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. 66
Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy 65
Towards genetic prevention of Adrenoleukodystrophy through early biochemical diagnosis of hemizygotes and heterozygotes in families at risk 65
Subcortical motor plasticity in patients with sporadic ALS: An fMRI study 64
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. 62
Whole-brain DTI pattern of white metter damage in amyotrophic lateral sclerosis: further evidences of a multisystem disorder 62
Amyotrophic lateral sclerosis and multiple sclerosis overlap: a case report. 62
A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy 61
Widespread Structural and Functional Connectivity Changes in Amyotrophic Lateral Sclerosis: Insights from Advanced Neuroimaging Research 61
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 61
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis 60
Apathy Is Correlated with Widespread Diffusion Tensor Imaging (DTI) Impairment in Amyotrophic Lateral Sclerosis 60
Retrospective epidemiology of Duchenne muscular dystrophy in Molise 59
Accumulation of altered aspartyl residues in erythrocyte membrane proteins from patients with sporadic amyotrophic lateral sclerosis. 59
A case of probable autosomal recessive ectodermal dysplasia with corkscrew hairs and menial retardation in a family with tuberous sclerosis 59
Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophy 58
Beyond motor neurons: new insights on amyotrophic lateral sclerosis neurodegeneration provided by advanced MRI tecnique 58
Dysfunctions within limbic-motor networks in amyotrophic lateral sclerosis. 58
Assessing Anxiety and its correlates in Amyotrophic Lateral Sclerosis: the State-Trait Anxiety Inventory 58
Microstructural Changes across Different Clinical Milestones of Disease in Amyotrophic Lateral Sclerosis. 57
Sistema nervoso 57
Vitamin D supplementation has no effects on progression of motor dysfunction in amyotrophic lateral sclerosis (ALS) 56
Reversible mielopathy due to deficiency of vitamin B12 in patient with associated syringomyelia: a case report 54
Sporadic ALS is not associated with VAPB gene mutations in Southern Italy 53
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 52
A case of probable autosomal recessive ectodermal dysplasia with corkscrew hairs and mental retardation in a family with tuberous sclerosis 52
Accuracy of death certificates for amyotrophic lateral sclerosis varies significantly from north to south of Italy: implications for mortality studies 50
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? 50
The GH-IGF system in amyotrophic lateral sclerosis: correlations between pituitary GH secretion capacity, insulin-like growth factors and clinical features 50
Structure of msj-1 gene: a comparative analysis 50
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis. 48
Extra-motor involvement in ALS patients: a cortical thickeness 3T MRI study 48
The neural control of skeletal muscle sarcolemma: preliminary results of different approaches to the study of a possible control of membrane-bound glycoconjugates 48
Amyotrophic lateral sclerosis and multiple sclerosis overlap: A case report 48
Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis. 47
Motor and extramotor neurodegeneration in amyotrophic lateral sclerosis: a 3T high angular resolution diffusion imaging (HARDI) study 47
[Determination of alimentary value of buffalo muscle proteins using enzymatic methods] 47
Toward genetic prevention of adrenoleukodystrophy trough early biochemical diagnosis of hemizygotes and heterozygotes in families at risk. 47
An Italian kindred with FALS due to c.149T>C mutation in the SOD1 gene: case report of an affected family member 47
HFE p.H63D polymorphism does not influence ALS phenotype and survival 46
Membrane depolarization in LA-N-1 cells. The effect of maitotoxin is Ca(2+)- and Na(+)-dependent 45
ALS and CHARGE syndrome: a clinical and genetic study 45
Functional overlap and divergence between ALS and bvFTD 44
FUS mutations in sporadic amyotrophic lateral sclerosis. 44
Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomized, double blind, placebo controlled, phase III study. 43
Establishment and characterization of a human neuroectodermal cell line (TB) from a cerebrospinal fluid specimen 43
Neuropsychological assessment in different King's clinical stages of amyotrophic lateral sclerosis 43
Theory of Mind and Its Neuropsychological and Quality of Life Correlates in the Early Stages of Amyotrophic Lateral Sclerosis 43
Lithium carbonate in amyotrophic lateral sclerosis Lack of efficacy in a dose-finding trial 42
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation 42
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population. 42
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 42
Earliest videofluoromanometric pharyngeal signs of dysphagia in ALS patients. 41
The application of recently developed methods to investigate glycoconjugate composition of sarcolemma: some preliminary results on Duchenne muscular dystrophy 41
Targeting extracellular cyclophilin A reduces neuroinflammation and extends survival in a mouse model of amyotrophic lateral sclerosis 41
Brain functional networks become more connected as amyotrophic lateral sclerosis progresses: a source level magnetoencephalographic study 41
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 40
FUS mutations in sporadic amyotrophic lateral sclerosis: Clinical and genetic analysis. 40
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 40
Direct inhibition of choline acetyltransferase activity by a monoclonal antibody raised against the plasma membrane of cholinergic nerve terminals 39
Neural control of gene expression of skeletal muscle fibers 39
Isolation and identification of rat's sarcolemma: preliminary results on the effects of denervation on "in vitro" activity of membrane-bound neuraminidase 39
Clinical features and lifestyle of patients with amyotrophic lateral sclerosis in Campania: brief overview of an Italian database. 39
Coping strategies and psychological distress in caregivers of patients with Amyotrophic Lateral Sclerosis (ALS) 39
Microstructural correlates of Edinburgh Cognitive and Behavioural ALS Screen (ECAS) changes in amyotrophic lateral sclerosis 39
The effects of denervation on sarcolemmal glycoconjugates of type skeletal muscle fibres of rat. Su: Synaptic Constituents in Health and Disease 38
Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis 37
Factors predicting survival in ALS: a multicenter Italian study 37
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 34
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. 33
Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS 33
Cardiovascular diseases may play a negative role in the prognosis of ALS 32
Exposure to environmental toxicants and pathogenesis of amyotrophic lateral sclerosis: state of the art and research perspectives. 31
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 30
The effects of denervation on sarcolemmal glycoconjugates of type skeletal muscle fibres of rat 30
Myasthenia gravis in a patient affected by glycogen storage disease type Ib: A further manifestation of an increased risk for autoimmune disorders? 29
Erythropoietin in amyotrophic lateral sclerosis: A multicentre, randomised, double blind, placebo controlled, phase III study 29
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 29
Impact on children of a parent with ALS: A case-control study 27
Casi clinici 26
Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene 26
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. 26
The MITOS system predicts long-term survival in amyotrophic lateral sclerosis 24
Totale 4.826
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Categoria #
all - tutte 18.530
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 18.530
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020594 0 111 18 11 90 39 132 39 64 51 34 5
2020/2021781 69 10 88 43 139 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
2024/202548 2 46 0 0 0 0 0 0 0 0 0 0
Totale 4.826