IRIS
RINALDI, Carmela
 Distribuzione geografica
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Continente #
EU - Europa 3.690
NA - Nord America 2.907
AS - Asia 1.800
SA - Sud America 628
AF - Africa 51
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 2
Totale 9.084
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Nazione #
US - Stati Uniti d'America 2.850
RU - Federazione Russa 1.740
SG - Singapore 730
CN - Cina 553
BR - Brasile 534
IE - Irlanda 399
IT - Italia 392
SE - Svezia 377
HK - Hong Kong 178
DE - Germania 173
PL - Polonia 145
UA - Ucraina 116
VN - Vietnam 104
FR - Francia 88
GB - Regno Unito 87
FI - Finlandia 76
IN - India 42
BD - Bangladesh 36
AR - Argentina 28
TR - Turchia 25
CA - Canada 23
BE - Belgio 21
ID - Indonesia 20
EC - Ecuador 19
MX - Messico 18
UZ - Uzbekistan 18
NL - Olanda 17
ZA - Sudafrica 14
CO - Colombia 13
CZ - Repubblica Ceca 13
MA - Marocco 13
AT - Austria 12
IQ - Iraq 11
PK - Pakistan 11
VE - Venezuela 11
JP - Giappone 10
CL - Cile 8
PH - Filippine 8
PY - Paraguay 8
IL - Israele 6
ES - Italia 5
LT - Lituania 5
NP - Nepal 5
OM - Oman 5
AZ - Azerbaigian 4
ET - Etiopia 4
GR - Grecia 4
JM - Giamaica 4
KE - Kenya 4
PE - Perù 4
RO - Romania 4
TH - Thailandia 4
AE - Emirati Arabi Uniti 3
BG - Bulgaria 3
CR - Costa Rica 3
DO - Repubblica Dominicana 3
EG - Egitto 3
IR - Iran 3
KH - Cambogia 3
MY - Malesia 3
NZ - Nuova Zelanda 3
PT - Portogallo 3
SA - Arabia Saudita 3
TN - Tunisia 3
AU - Australia 2
CI - Costa d'Avorio 2
DZ - Algeria 2
EU - Europa 2
GT - Guatemala 2
JO - Giordania 2
MD - Moldavia 2
MT - Malta 2
MU - Mauritius 2
PS - Palestinian Territory 2
RS - Serbia 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
UY - Uruguay 2
AL - Albania 1
AO - Angola 1
BH - Bahrain 1
BO - Bolivia 1
CH - Svizzera 1
GA - Gabon 1
GE - Georgia 1
HR - Croazia 1
KG - Kirghizistan 1
KR - Corea 1
KW - Kuwait 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
LV - Lettonia 1
LY - Libia 1
MN - Mongolia 1
NG - Nigeria 1
NR - Nauru 1
PA - Panama 1
PR - Porto Rico 1
TJ - Tagikistan 1
Totale 9.084
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Città #
Moscow 522
Ashburn 446
Dublin 398
Singapore 395
Dallas 363
Chandler 283
Jacksonville 227
Beijing 209
Nyköping 195
Messina 186
Hong Kong 177
Warsaw 136
San Jose 133
The Dalles 109
Ann Arbor 65
Princeton 65
Medford 62
Lauterbourg 57
New York 54
Los Angeles 53
Munich 51
Cambridge 49
Des Moines 46
Dearborn 43
São Paulo 41
Boardman 39
Bremen 33
Buffalo 30
Ho Chi Minh City 29
Lancaster 29
Council Bluffs 27
Wilmington 21
Brussels 20
Redondo Beach 20
Woodbridge 20
Hanoi 19
Tianjin 19
Orem 17
Jinan 16
Rio de Janeiro 16
Tashkent 16
Belo Horizonte 15
Rome 15
Turku 15
Brasília 14
Catania 13
Santa Clara 13
Seattle 13
Brooklyn 12
Frankfurt am Main 12
Houston 12
Jakarta 12
Ningbo 12
Dong Ket 11
Milan 11
Helsinki 10
Manchester 10
San Mateo 10
Shanghai 10
Shenyang 10
Shenzhen 10
Amsterdam 9
Boston 9
Chennai 9
Chicago 9
Phoenix 9
Pune 9
Tokyo 9
Bologna 8
San Francisco 8
Toronto 8
Düsseldorf 7
Guarulhos 7
Hyderabad 7
Istanbul 7
London 7
Montreal 7
Nanjing 7
Quito 7
São José dos Campos 7
Atlanta 6
Curitiba 6
Guangzhou 6
Johannesburg 6
Lappeenranta 6
Mexico City 6
Stockholm 6
Vienna 6
Baghdad 5
Contagem 5
Da Nang 5
Denver 5
Duque de Caxias 5
Guayaquil 5
Hefei 5
Muscat 5
Naples 5
Olomouc 5
Padova 5
Perugia 5
Totale 5.234
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Nome #
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype 261
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study. 238
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. 234
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens 208
CCR5Δ32 Polymorphism Associated with a Slower Rate DiseaseProgression in a Cohort of RR-MS Sicilian Patients 206
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome 197
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes 194
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa 187
A MOLECULAR- GENETIC ANALYSIS OF FLAVIN-CONTAINING MONOOXYGENASE3 GENE (FMO3) IN AN ITALIAN CHILD WITH A TMAURIA LIKE-PHENOTYPE 186
Age dependent switching role of ciclyn D1 in breast cancer 182
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions 179
FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor 172
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis? 172
Costameric proteins in human skeletal muscle during muscular inactivity. 171
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study 169
An intronic variant in PTEN gene is probably involved in splicing alteration events 167
Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells 163
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies 161
LITHIUM TRANSPORT PATHWAYS IN HUMAN, CHICKEN AND EEL ERYTHROCYTES 160
A rare case of TMAU associated with suspected Currarino triad 155
Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration 153
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study 152
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations 150
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? 147
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 142
Distribuzione dell'allele mutato Δ32 del gene CCR5 nella popolazione sana del bacino del mediterraneo. 141
Distribution of the mutated delta32 allele of the CCR5 gene in a Sicilian population 141
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations 140
Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. 135
Effetti contrastanti di alcuni ossidanti sul trasporto di litio in globuli rossi umani 134
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function? 130
The interaction of haemoglobin, magnesium, organic phosphates and band 3 protein in nucleated and anucleated erythrocytes 128
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS 125
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations 124
Oxidative Stress and the Neurovascular Unit 124
Sarcoglycan complex in human normal and pathological prostatic tissue: An immunohistochemical and RT-PCR study 121
GENETICS OF CAVERNOMAS: A CASE REPORT 117
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 116
Molecular analysis of CCM genes promoter regions 116
INFLUSSO DELLO IONE SOLFATO NEI GLOBULI ROSSI IN SOGGETTI SANI,IPERTESI E DIABETICI 111
IL SUBCOMPLESSO DEI SARCOGLICANI NEL MUSCOLO LISCIO UMANO 109
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation 109
The biological pathways of Alzheimer disease: a review 109
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling 109
Screening genetico dei geni CCM in pazienti italiani affetti da angioma cavernoso cerebrale: un caso familiare 108
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa 106
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation 104
PON I and GLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy 102
Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? 100
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report 100
The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment 99
Sarcoglycans in muscolar diseases of ureters: an immunohistochemical study. 98
POLIMORFISMI DELLA GLIOSSALASI I E DELLA PARAOXONASI I IN INDIVIDUI SANI ED INDIVIDUI AFFETTI DA SCLEROSI MULTIPLA.FATTORI DI SUSCETTIBILITA'? 95
Sarcoglycans and integrins in muscular inactivity 94
IMMUNOHISTOCHEMICAL AND NUCLEOTIDE SEQUENCING ANALYSIS OF SARCOGLYCANS IN EPITHELIUM 90
EXPRESSION OF SARCOGLYCANS IN THE HUMAN CEREBRAL CORTEX: AN IMMUNOHISTOCHEMICAL AND MOLECULAR STUDY 90
Quantification of trimethylamine (TMA) and trimethylamine oxide (TMAO) for diagnostic and targeted diet purposes. 87
New evaluation methods of read mapping by 17 aligners on simulated and empirical NGS data: an updated comparison of DNA- and RNA-Seq data from Illumina and Ion Torrent technologies 86
interazioni farmaco-cinetiche sul trasporto di litio nei globuli rossi umani 85
Decoding pediatric inherited retinal dystrophies: Bridging genetic complexity and clinical heterogeneity 80
Genetic and functional study of CCR5 gene in HIV-1 infection 80
IS α SARCOGLYCAN A MEMBER OF SARCOGLYCAN COMPLEX IN HUMAN SMOOTH MUSCLE ? 80
LITHIUM TRANSPORT PATHWAYS IN HUMAN CHICKEN AND EEL ERYTHROCYTES 79
IMMUNOISTOCHEMICAL AND NUCLEOTIDE SEQUENCING ANALYSIS OF SARCOGLYCANS IN EPITHELIUM 77
OSMOREGULATION IN NORMAL AND ABNORMAL HUMAN ERYTHROCYTES 74
Sarcoglycan subcomplex expression in normal human smooth muscle 67
Further data on a 9.1-kb insertion-deletion polymorphism: Survey of Mediterranean populations 64
Investigating G-quadruplex structures in RPGR gene: Implications for understanding X-linked retinal degeneration 62
Human retinal secretome: A cross-link between mesenchymal and retinal cells 62
Multifaceted disruption of AMPA receptor signaling by CACNG8 variants: Integrated evidence from human genetics and molecular simulation 47
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Nel labirinto delle distrofie retiniche ereditarie: alla scoperta delle Terapie innovative e delle visioni del futuro 36
Mechanotransduction in development: a focus on angiogenesis 31
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Circulating lncRNAs Remark Expression Profile of Cerebrovascular Malformation Endothelial Cells 16
Oxidative Stress Signaling and Regenerative Responses in a Larval Zebrafish Model of Retinal Light Damage 8
The Italian validation of the Watson Caritas Co-Worker Score for nurses and health care professionals Italian validation of the WCCS 6
Comprehensive transcriptomic analysis reveals canonical and novel pathways modulated by nanoceria in mammalian retinal degeneration 2
Totale 9.312
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Categoria #
all - tutte 30.179
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 30.179
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202119 0 0 0 0 0 0 0 0 0 0 0 19
2021/2022535 3 74 17 13 6 6 29 28 8 152 46 153
2022/20231.196 81 89 58 101 109 108 17 80 503 5 39 6
2023/2024337 32 57 7 31 29 63 0 15 2 17 11 73
2024/20251.477 29 10 41 104 43 59 45 331 355 89 133 238
2025/20264.403 176 337 397 302 377 885 517 512 522 216 83 79
Totale 9.312