IRIS
RINALDI, Carmela
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 3.711
NA - Nord America 3.083
AS - Asia 1.827
SA - Sud America 632
Continente sconosciuto - Info sul continente non disponibili 230
AF - Africa 52
OC - Oceania 6
Totale 9.541
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 3.022
RU - Federazione Russa 1.740
SG - Singapore 732
CN - Cina 566
BR - Brasile 536
IT - Italia 405
IE - Irlanda 399
SE - Svezia 377
HK - Hong Kong 180
DE - Germania 173
PL - Polonia 146
UA - Ucraina 117
VN - Vietnam 106
GB - Regno Unito 90
FR - Francia 88
FI - Finlandia 76
IN - India 42
BD - Bangladesh 40
AR - Argentina 28
TR - Turchia 25
CA - Canada 24
ID - Indonesia 22
BE - Belgio 21
EC - Ecuador 21
MX - Messico 18
NL - Olanda 18
UZ - Uzbekistan 18
CZ - Repubblica Ceca 14
ZA - Sudafrica 14
CO - Colombia 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
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
ET - Etiopia 4
GR - Grecia 4
JM - Giamaica 4
KE - Kenya 4
MY - Malesia 4
PE - Perù 4
RO - Romania 4
TH - Thailandia 4
BG - Bulgaria 3
CR - Costa Rica 3
DO - Repubblica Dominicana 3
EG - Egitto 3
GT - Guatemala 3
IR - Iran 3
KH - Cambogia 3
NZ - Nuova Zelanda 3
PT - Portogallo 3
SA - Arabia Saudita 3
TN - Tunisia 3
TT - Trinidad e Tobago 3
AU - Australia 2
CI - Costa d'Avorio 2
DZ - Algeria 2
EU - Europa 2
JO - Giordania 2
MD - Moldavia 2
MT - Malta 2
MU - Mauritius 2
PS - Palestinian Territory 2
RS - Serbia 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
HN - Honduras 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
NO - Norvegia 1
NR - Nauru 1
PA - Panama 1
PR - Porto Rico 1
Totale 9.311
Salva come PNG Salva come JPEG
Città #
Moscow 522
Ashburn 458
Dublin 398
Singapore 396
Dallas 363
Chandler 283
Jacksonville 228
Beijing 211
Nyköping 195
Messina 186
Hong Kong 179
San Jose 139
Warsaw 137
Council Bluffs 118
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
Lancaster 30
Ho Chi Minh City 29
Wilmington 21
Brussels 20
Hanoi 20
Redondo Beach 20
Santa Clara 20
Woodbridge 20
Tianjin 19
Orem 17
Jinan 16
Rio de Janeiro 16
Tashkent 16
Belo Horizonte 15
Rome 15
Turku 15
Brasília 14
Seattle 14
Catania 13
Houston 13
Brooklyn 12
Frankfurt am Main 12
Jakarta 12
Milan 12
Ningbo 12
Chicago 11
Dong Ket 11
Helsinki 10
Manchester 10
San Mateo 10
Shanghai 10
Shenyang 10
Shenzhen 10
Amsterdam 9
Boston 9
Chennai 9
Columbus 9
Denver 9
Phoenix 9
Pune 9
Tokyo 9
Bologna 8
London 8
Montreal 8
San Francisco 8
Toronto 8
Düsseldorf 7
Guarulhos 7
Guayaquil 7
Hyderabad 7
Istanbul 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
Duque de Caxias 5
Hefei 5
Muscat 5
Naples 5
Olomouc 5
Padova 5
Totale 5.376
Salva come PNG Salva come JPEG
Nome #
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype 266
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study. 243
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. 237
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens 210
CCR5Δ32 Polymorphism Associated with a Slower Rate DiseaseProgression in a Cohort of RR-MS Sicilian Patients 209
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome 204
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa 198
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes 195
A MOLECULAR- GENETIC ANALYSIS OF FLAVIN-CONTAINING MONOOXYGENASE3 GENE (FMO3) IN AN ITALIAN CHILD WITH A TMAURIA LIKE-PHENOTYPE 189
Age dependent switching role of ciclyn D1 in breast cancer 185
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 178
Costameric proteins in human skeletal muscle during muscular inactivity. 178
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study 173
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis? 173
An intronic variant in PTEN gene is probably involved in splicing alteration events 169
LITHIUM TRANSPORT PATHWAYS IN HUMAN, CHICKEN AND EEL ERYTHROCYTES 166
Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells 165
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies 162
A rare case of TMAU associated with suspected Currarino triad 158
Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration 157
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations 155
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study 154
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? 150
Distribuzione dell'allele mutato Δ32 del gene CCR5 nella popolazione sana del bacino del mediterraneo. 145
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 145
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations 144
Distribution of the mutated delta32 allele of the CCR5 gene in a Sicilian population 143
Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. 138
Effetti contrastanti di alcuni ossidanti sul trasporto di litio in globuli rossi umani 137
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function? 135
The interaction of haemoglobin, magnesium, organic phosphates and band 3 protein in nucleated and anucleated erythrocytes 131
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS 127
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations 127
Sarcoglycan complex in human normal and pathological prostatic tissue: An immunohistochemical and RT-PCR study 127
Oxidative Stress and the Neurovascular Unit 127
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 118
GENETICS OF CAVERNOMAS: A CASE REPORT 118
Molecular analysis of CCM genes promoter regions 118
The biological pathways of Alzheimer disease: a review 115
INFLUSSO DELLO IONE SOLFATO NEI GLOBULI ROSSI IN SOGGETTI SANI,IPERTESI E DIABETICI 113
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation 112
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling 111
IL SUBCOMPLESSO DEI SARCOGLICANI NEL MUSCOLO LISCIO UMANO 110
Screening genetico dei geni CCM in pazienti italiani affetti da angioma cavernoso cerebrale: un caso familiare 109
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation 107
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa 107
PON I and GLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy 106
The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment 102
Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? 101
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report 101
Sarcoglycans in muscolar diseases of ureters: an immunohistochemical study. 99
Sarcoglycans and integrins in muscular inactivity 98
POLIMORFISMI DELLA GLIOSSALASI I E DELLA PARAOXONASI I IN INDIVIDUI SANI ED INDIVIDUI AFFETTI DA SCLEROSI MULTIPLA.FATTORI DI SUSCETTIBILITA'? 96
IMMUNOHISTOCHEMICAL AND NUCLEOTIDE SEQUENCING ANALYSIS OF SARCOGLYCANS IN EPITHELIUM 93
EXPRESSION OF SARCOGLYCANS IN THE HUMAN CEREBRAL CORTEX: AN IMMUNOHISTOCHEMICAL AND MOLECULAR STUDY 93
Quantification of trimethylamine (TMA) and trimethylamine oxide (TMAO) for diagnostic and targeted diet purposes. 89
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 88
interazioni farmaco-cinetiche sul trasporto di litio nei globuli rossi umani 87
Genetic and functional study of CCR5 gene in HIV-1 infection 85
Decoding pediatric inherited retinal dystrophies: Bridging genetic complexity and clinical heterogeneity 83
LITHIUM TRANSPORT PATHWAYS IN HUMAN CHICKEN AND EEL ERYTHROCYTES 83
IS α SARCOGLYCAN A MEMBER OF SARCOGLYCAN COMPLEX IN HUMAN SMOOTH MUSCLE ? 81
IMMUNOISTOCHEMICAL AND NUCLEOTIDE SEQUENCING ANALYSIS OF SARCOGLYCANS IN EPITHELIUM 79
OSMOREGULATION IN NORMAL AND ABNORMAL HUMAN ERYTHROCYTES 76
Sarcoglycan subcomplex expression in normal human smooth muscle 71
Further data on a 9.1-kb insertion-deletion polymorphism: Survey of Mediterranean populations 66
Investigating G-quadruplex structures in RPGR gene: Implications for understanding X-linked retinal degeneration 65
Human retinal secretome: A cross-link between mesenchymal and retinal cells 65
Multifaceted disruption of AMPA receptor signaling by CACNG8 variants: Integrated evidence from human genetics and molecular simulation 51
Nel labirinto delle distrofie retiniche ereditarie: alla scoperta delle Terapie innovative e delle visioni del futuro 38
null 38
Mechanotransduction in development: a focus on angiogenesis 33
null 31
null 31
null 29
null 23
Circulating lncRNAs Remark Expression Profile of Cerebrovascular Malformation Endothelial Cells 18
Oxidative Stress Signaling and Regenerative Responses in a Larval Zebrafish Model of Retinal Light Damage 11
The Italian validation of the Watson Caritas Co-Worker Score for nurses and health care professionals Italian validation of the WCCS 9
Comprehensive transcriptomic analysis reveals canonical and novel pathways modulated by nanoceria in mammalian retinal degeneration 5
Totale 9.541
Salva come PNG Salva come JPEG
Categoria #
all - tutte 31.626
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 31.626
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022532 0 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
2025/20264.414 176 337 397 302 377 885 517 512 522 216 83 90
2026/2027218 89 129 0 0 0 0 0 0 0 0 0 0
Totale 9.541