IRIS
MELONE, Mariarosa Anna Beatrice
 Distribuzione geografica
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Continente #
EU - Europa 14.697
NA - Nord America 7.088
AS - Asia 5.170
SA - Sud America 904
AF - Africa 72
Continente sconosciuto - Info sul continente non disponibili 16
OC - Oceania 14
Totale 27.961
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Nazione #
RU - Federazione Russa 8.038
US - Stati Uniti d'America 6.951
IT - Italia 2.096
SG - Singapore 1.790
IE - Irlanda 1.499
CN - Cina 1.164
HK - Hong Kong 846
BR - Brasile 739
UA - Ucraina 735
GB - Regno Unito 658
VN - Vietnam 535
DE - Germania 466
FR - Francia 387
KR - Corea 194
FI - Finlandia 191
TR - Turchia 175
SE - Svezia 172
GR - Grecia 160
IN - India 141
NL - Olanda 95
CA - Canada 90
JP - Giappone 68
BD - Bangladesh 62
AR - Argentina 58
BE - Belgio 39
IR - Iran 28
AT - Austria 27
EC - Ecuador 27
ID - Indonesia 24
ES - Italia 23
MX - Messico 23
CO - Colombia 22
PK - Pakistan 21
PL - Polonia 21
CH - Svizzera 18
JO - Giordania 17
IQ - Iraq 15
VE - Venezuela 15
CZ - Repubblica Ceca 14
MA - Marocco 14
ZA - Sudafrica 14
AU - Australia 13
PY - Paraguay 13
EU - Europa 12
CL - Cile 11
RO - Romania 11
DK - Danimarca 10
TH - Thailandia 10
UZ - Uzbekistan 10
MY - Malesia 9
PE - Perù 9
TW - Taiwan 9
UY - Uruguay 9
PT - Portogallo 8
TN - Tunisia 8
EG - Egitto 7
KE - Kenya 7
AE - Emirati Arabi Uniti 6
DZ - Algeria 6
PH - Filippine 6
SA - Arabia Saudita 6
HN - Honduras 5
HU - Ungheria 5
IL - Israele 5
KZ - Kazakistan 5
PA - Panama 5
RS - Serbia 5
BJ - Benin 4
KW - Kuwait 4
LT - Lituania 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AL - Albania 3
CR - Costa Rica 3
NO - Norvegia 3
OM - Oman 3
TT - Trinidad e Tobago 3
AO - Angola 2
AZ - Azerbaigian 2
BB - Barbados 2
BG - Bulgaria 2
CI - Costa d'Avorio 2
DO - Repubblica Dominicana 2
KH - Cambogia 2
LB - Libano 2
LK - Sri Lanka 2
LV - Lettonia 2
MK - Macedonia 2
NG - Nigeria 2
NP - Nepal 2
QA - Qatar 2
SV - El Salvador 2
BH - Bahrain 1
BO - Bolivia 1
BW - Botswana 1
CY - Cipro 1
GA - Gabon 1
GM - Gambi 1
HR - Croazia 1
JM - Giamaica 1
MD - Moldavia 1
Totale 27.951
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Città #
Moscow 2.857
Dublin 1.490
Jacksonville 1.127
Santa Clara 912
Hong Kong 828
Singapore 766
San Jose 676
Chandler 654
Ashburn 290
Princeton 226
Beijing 197
Ann Arbor 184
Ho Chi Minh City 175
Seoul 174
Medford 165
Roxbury 161
Milan 145
Caserta 122
Rome 113
Wilmington 109
Hanoi 108
Boardman 104
New York 101
Dallas 97
Naples 97
Hefei 94
Bremen 90
The Dalles 87
Cambridge 76
San Mateo 76
Woodbridge 73
Mountain View 67
Bengaluru 62
Nanjing 60
Napoli 60
Los Angeles 59
Des Moines 58
São Paulo 47
Houston 40
Jinan 36
Turin 35
Da Nang 33
Brussels 31
Munich 31
Elora 29
Nanchang 29
Redwood City 27
Nuremberg 25
Columbus 24
Dong Ket 24
Palermo 24
Florence 23
Norwalk 23
Guangzhou 22
Rio de Janeiro 22
Shenyang 22
Frankfurt am Main 21
Orem 21
Düsseldorf 20
Tianjin 19
Bologna 18
Changsha 18
Haiphong 17
Kunming 17
Parma 17
Bari 16
Belo Horizonte 16
Brasília 16
Chennai 16
Council Bluffs 16
Hangzhou 16
Porto Alegre 16
Amman 15
Helsinki 15
Montreal 15
Shanghai 15
Tokyo 15
Toronto 15
Genoa 14
Stockholm 14
Varese 14
Zhengzhou 14
Atlanta 13
Catania 13
Chicago 13
Dearborn 13
Manchester 13
Otranto 13
Amsterdam 12
Biên Hòa 12
Jakarta 12
Memphis 12
Padova 12
Salerno 12
Auburn Hills 11
Haikou 11
London 11
Marcianise 11
Quito 11
Trieste 11
Totale 13.929
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Nome #
LO STRESS PROTEOTOSSICO: UN MECCANISMO PATOGENETICO COMUNE ALLA NEURODEGENERAZIONE 879
Aneurisma gigante trombizzato del tratto intracavernoso dell’aci esordito come sindrome di Tolosa - Hunt in un paziente affetto da neurofibromatosi tipo 1 (NF1) portatore di una nuova mutazione genetica: caso clinico e revisione della letteratura 744
Ruta graveolens L. induces death of glioblastoma cells and neural progenitors, but not of neurons, via ERK 1/2 and AKT activation 238
Nano-delivery systems for encapsulation of dietary polyphenols: an experimental approach for neurodegenerative diseases and brain tumors 236
Protective effects of modified Mediterranean diet in patients with Parkinson's disease 230
Nanotechnology-Based Polyphenol Delivery: A Novel Therapeutic Strategy for the Treatment of Age-Related Neurodegenerative Disorder 218
Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry 205
Abnormal accumulation of tTGase products in muscle and erythrocytes of chorea-acanthocytosis patients 201
Modifications moleculaires au cours de la regeneration et reinnervation musculaires in vitro 182
Correlazione Genotipo-Fenotipo nella NF1: Ruolo dell'Imprinting Genomico 181
Alterations in the carnitine cycle in a mouse model of Rett syndrome. 181
Antisense oligonucleotides and myotonin gene expression in C2 mouse cells 178
Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders 176
Changes in autophagy, proteasome activity and metabolism to determine a specific signature for acute and chronic senescent mesenchymal stromal cells 172
DILATAZIONE FUSIFORME ANEURISMATICA DEL SIFONE CAROTIDEO INTRACAVERNOSO IN UN CASO DI NEUROFIBROMATOSI DI TIPO I: UNA SEMPLICE COINCIDENZA? 170
A novel diagnostic method to detect truncated neurofibromin in Neurofibromatosis 1 169
NEUROFIBROMATOSI TIPO 1(NF1): ESISTE UNA CORRELAZIONE TRA UBO ’ S (UNIDENTIFIED BRIGHT OBJECT), IL GLIOMA DELLE VIE OTTICHE E I DISTURBI DELL’ APPRENDIMENTO? 166
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 166
Antisense inhibitory effect: a comparison between 3'-partial and full phosphorothioate antisense oligonucleotides 165
Muscle tissue engineering: Strategies for repair and regeneration in human degenerative muscle diseases 160
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 160
EGF-responsive rat neural stem cells: molecular follow-up of neuron and astrocyte differentiation in vitro 159
Genes involved in regulation of stem cell properties. Studies on their expression in a small cohort of neuroblastoma patients 158
A comparative analysis of different biomaterials in the engineering of skeletal muscle using C2C12 cells in vitro 156
Adherence to anti-Parkinson drug therapy in the "REASON" sample of Italian patients with Parkinson's disease: the linguistic validation of the Italian version of the "Morisky Medical Adherence Scale-8 items" 156
A Biochemical Mechanism for a Transglutaminase-Mediated Cell Death in CAG Triplet Diseases: Tissue Tranglutaminase-Catalyzed Formation of High Molecular Weight Aggregates With Extended Polyglutamine Peptides and Glyceraldehyde 3-Phospate Dehydrogenase 155
Synergistic Interplay between Curcumin and Polyphenol-Rich Foods in the Mediterranean Diet: Therapeutic Prospects for Neurofibromatosis 1 Patients 154
Genotype-Phenotype Correlations in Neurofibromatosis Type 1: Identification of Novel and Recurrent NF1 Gene Variants and Correlations with Neurocognitive Phenotype 154
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort 152
Ruta graveolens aqueous extract inhibits proliferation of undifferentiated neural cells and induces differentiated neurons reentry in cell cycle 152
Metabolic syndrome, Mediterranean diet, and polyphenols: Evidence and perspectives 152
Circulating factors present in the sera of naturally skinny people may influence cell commitment and adipocyte differentiation of mesenchymal stromal cells. 151
Antisense Inhibitory Effect: A Comparison Between 3’-Partial an Full Phosphorothioate Antisense Oligonucleotides 150
A new tRNAHis mutation in the mtDNA results in mitochondrial encephalomyopathy by hampering ATP production 150
Large cardio-embolic ischemic stroke in Kearns-Sayre syndrome 150
Adult-onset brain tumors and neurodegeneration: Are polyphenols protective? 150
Cell-biomaterial interactions: role of transglutaminase enzyme 148
17-β estradiol elicits an autocrine leiomyoma cell proliferation: Evidence for a stimulation of protein kinase-dependent pathway 148
Biochemical and morphological evidences supporting the hypothesis of a role of Tgase in the pathogeneisi of Chorea-Acanthocytosis 148
Neural stem cells from a mouse model of Rett syndrome are prone to senescence, show reduced capacity to cope with genotoxic stress, and are impaired in the differentiation process 148
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy 146
A rapid, safe, and quantitative in vitro assay for measurement of uracil-DNA glycosylase activity. 146
Differential carnitine/acylcarnitine translocase expression defines distinct metabolic signatures in skeletal muscle cells 145
Preliminary results of isolation and identification of rat sarcolemma and the effect of denervation on membrane-bound neuraminidase activity 145
Differentiation and apoptosis of neuroblastoma cells: role of N-myc gene product 144
A novel KIF5A/SPG10 mutation in spastic paraplegia associated with axonal neuropathy 143
Filamin B and CD13 are components of senescent secretomes that may be involved in primary (stress induced) and paracrine senescence of mesenchymal stromal cells 143
Myotonic dystrophy: antisense oligonucleotide inhibition of DMPK gene expression in vitro 141
Is it Possible to Improve the Success Rate of Cellular Therapy Based on Mesenchymal Stem Cells? 141
Neuroblastoma in a pediatric era: Specific gene expression of staminality 141
Rasagiline improves sleep disorders in Parkinson's disease 141
A novel and rapid method of determining truncated neurofibromin 1 to rapidly screen for neurofibromatosis type 1 (NF1) 140
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 140
Multiple spinal nerve enlargement and SOS1 mutation: further evidence of overlap between Neurofibromatosis type 1 and Noonan phenotype 139
High grade glioblastoma is associated with aberrant expression of ZFP57, a protein involved in gene imprinting, and of CPT1A and CPT1C that regulate fatty acid metabolism. 138
Neurofibromatosis type 1 in children: 10 years of experience 138
Neuro-Behçet’s Disease presenting as an isolated progressive cognitive and behavioral syndrome 138
In vitro studies suggest reduced expression of methyl cytosine protein binding 2 (MECP2) affects cell commitment and maintenance in neurons by triggering senescence, new perspective for Rett syndrome 137
Defective growth in vitro of Duchenne Muscular Dystrophy myoblasts: the molecular and biochemical basis 136
Myotonic dystrophy: antisense oligonucleotides inhibition of DMPK gene expression in vitro 136
A synthetic amino acid substitution of Tyr10 in Aβ peptide sequence yields a dominant negative variant in amyloidogenesis 136
An unusual case of poisoning due to dithiocarbamates with serious neurological symptoms. Analogy with poisoning due to organo-phosphate substances 136
Silencing of RB1 and RB2/P130 during adipogenesis of bone marrow stromal cells results in dysregulated differentiation. 135
Cellular localization of ERK in the R6/2 mouse model of Huntington’s disease 135
Changes in the expression of extracellular regulated kinase (ERK 1/2) in the R6/2 mouse model of Huntington's disease after phosphodiesterase IV inhibition 134
Carnitine protects the molecular chaperone activity of lens alpha-crystallin and decreases the post-translational protein modifications induced by oxidative stress 134
RB and RB2/p130 genes demonstrate both specific and overlapping functions during the early steps of in vitro neural differentiation of marrow stromal stem cells 134
[Phosphorus NMR spectroscopy. Its value in the diagnosis of metabolic myopathies. A case of Mac Ardle's disease] 133
Myoplasticity and myoregeneration; from molecular aspects to clinical perspectives 133
Acetylcholinesterase in neuroblastoma and neuroblastoma x glioma hybrid cells: cellular localization and molecular forms 131
Rare Variants in Autophagy and Non-Autophagy Genes in Late-Onset Pompe Disease: Suggestions of Their Disease-Modifying Role in Two Italian Families 131
Bioactive Phenolic Compounds in the Modulation of Central and Peripheral Nervous System Cancers: Facts and Misdeeds. 128
Giant thrombosed intracavernous carotid artery aneurysm presenting as Tolosa–Hunt syndrome in a patient harboring a new pathogenic neurofibromatosis type 1 mutation: a case report and review of the literature. 127
Erratum: Correction: Increase of circulating IGFBP-4 following genotoxic stress and its implication for senescence (eLife (2020) 9 PII: e80871) 127
Efficient in vitro delivery of cationic nanoparticles loading siRNA targeting mutant huntingtin 126
Mutant huntingtin regulates EGF receptor fate in non-neuronal cells lacking wild-type protein 124
pRb2/p130 gene overexpression induces astrocyte differentiation 124
Acetylcholinesterase and neuronal differentiation: an ultrastructural and biochemical study in neuroblastoma lines 124
Molecular pathways involved in neural in vitro differentiation of marrow stromal stem cells 123
Brg1 chromatin remodeling factor is involved in cell growth arrest, apoptosis and senescence of rat mesenchymal stem cells. 122
ASSENZA DI PERFUSIONE CEREBELLARE IN UN CASO DI ATASSIA CEREBELLARE PROGRESSIVA PRIMITIVA 122
Atypical Stüve-Wiedemann syndrome (STWS) masquerating as Cold-induced sweating syndrome (CISS): a patient homozygous for a LIFR mutation followed for 30 years 122
Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity 121
LA NEUROMIELITE OTTICA È UN’ ASSOCIAZIONE SINDROMICA COMUNE A PATOLOGIE ETEROGENEE 121
Induction of apoptosis and differentiation in neuroblastoma and astrocytoma cells by the overexpression of Bin1, a novel Myc interacting protein 120
RB2/p130 ectopic gene expression in neuroblastoma stem cells: evidence of cell-fate restriction and induction of differentiation 119
Magnetic Resonance Imaging correlates of benign and malignant alterations of the spinal bone marrow. 119
Long-term effects of asymmetrical posture in boxing assessed by baropodometry 119
Foix-Chavany-Marie syndrome in a 17-year-old female with congenital cytomegalovirus infection. 118
Huntingtin protein: A new option for fixing the Huntington's disease countdown clock 117
Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network 117
Sagittal kinematics and imbalance of the spine and whole body during walking in late-onset Pompe disease 116
Efficient cultivation of neural stem cells with controlled delivery of FGF-2 116
Animal model to study factors influencing regeneration and direct innervation or neurotization of skeletal muscle 116
Towards genetic prevention of Adrenoleukodystrophy through early biochemical diagnosis of hemizygotes and heterozygotes in families at risk 116
LE EMERGENZE NEUROLOGICHE ENCEFALICHE NEI BAMBINI CON NEUROFIBROMATOSI TIPO 1 (NF1). 116
Vacuolated PAS-positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagy. 116
Tissue transglutaminase-catalyzed formation of high-molecular-weight aggregates in vitro is favored with long polyglutamine domains: a possible mechanism contributing to CAG-triplet diseases 115
Effects of glycyl-L-glutamine in vitro on the molecular forms of acetylcholinesterase in the preganglionically denervated superior cervical ganglion of the cat 114
La capacità rigenerativa del muscolo scheletrico danneggiato: studio sperimentale 114
Totale 15.837
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Categoria #
all - tutte 92.728
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 92.728
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202188 0 0 0 0 0 0 0 0 0 0 0 88
2021/20221.594 111 57 27 32 494 19 43 78 75 98 131 429
2022/20232.880 284 48 50 216 277 216 25 169 1.393 39 77 86
2023/20241.434 97 48 96 120 418 147 51 47 22 67 131 190
2024/20253.551 64 95 62 83 565 510 538 286 500 410 260 178
2025/202613.213 429 440 678 799 1.087 7.492 640 563 490 293 226 76
Totale 28.513