IRIS
RINALDI, Carmela
 Distribuzione geografica
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Continente #
NA - Nord America 2.466
EU - Europa 1.904
AS - Asia 1.420
SA - Sud America 585
AF - Africa 41
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 2
Totale 6.423
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Nazione #
US - Stati Uniti d'America 2.418
SG - Singapore 593
BR - Brasile 511
CN - Cina 416
IE - Irlanda 406
SE - Svezia 382
IT - Italia 355
HK - Hong Kong 172
DE - Germania 167
PL - Polonia 144
UA - Ucraina 118
VN - Vietnam 83
GB - Regno Unito 80
FI - Finlandia 77
RU - Federazione Russa 60
AR - Argentina 27
IN - India 27
FR - Francia 26
BE - Belgio 21
MX - Messico 19
TR - Turchia 19
UZ - Uzbekistan 17
CA - Canada 16
EC - Ecuador 15
ID - Indonesia 15
NL - Olanda 14
CZ - Repubblica Ceca 13
MA - Marocco 13
AT - Austria 12
BD - Bangladesh 12
ZA - Sudafrica 12
PK - Pakistan 10
IQ - Iraq 9
JP - Giappone 9
VE - Venezuela 8
CL - Cile 6
CO - Colombia 6
IL - Israele 5
PY - Paraguay 5
ES - Italia 4
GR - Grecia 4
LT - Lituania 4
NP - Nepal 4
PE - Perù 4
RO - Romania 4
AZ - Azerbaigian 3
BG - Bulgaria 3
CR - Costa Rica 3
DO - Repubblica Dominicana 3
EG - Egitto 3
IR - Iran 3
JM - Giamaica 3
KE - Kenya 3
KH - Cambogia 3
NZ - Nuova Zelanda 3
PT - Portogallo 3
TN - Tunisia 3
AE - Emirati Arabi Uniti 2
CI - Costa d'Avorio 2
DZ - Algeria 2
EU - Europa 2
KG - Kirghizistan 2
MD - Moldavia 2
MT - Malta 2
OM - Oman 2
PH - Filippine 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
UY - Uruguay 2
AO - Angola 1
AU - Australia 1
BO - Bolivia 1
CH - Svizzera 1
GE - Georgia 1
JO - Giordania 1
KR - Corea 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LV - Lettonia 1
MU - Mauritius 1
MY - Malesia 1
NG - Nigeria 1
NI - Nicaragua 1
NR - Nauru 1
PA - Panama 1
PS - Palestinian Territory 1
RS - Serbia 1
SA - Arabia Saudita 1
TH - Thailandia 1
TJ - Tagikistan 1
Totale 6.423
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Città #
Dublin 405
Dallas 379
Chandler 290
Singapore 277
Ashburn 259
Jacksonville 229
Beijing 200
Nyköping 200
Messina 185
Hong Kong 171
Warsaw 135
The Dalles 74
Ann Arbor 69
Princeton 66
Medford 63
Munich 51
Cambridge 50
Los Angeles 49
New York 48
Des Moines 45
Dearborn 43
Boardman 40
São Paulo 38
Bremen 33
Lancaster 31
Buffalo 28
Ho Chi Minh City 24
Wilmington 21
Brussels 20
Redondo Beach 20
Woodbridge 20
Moscow 19
Hanoi 16
Jinan 16
Rio de Janeiro 15
Tashkent 15
Turku 15
Belo Horizonte 14
Brasília 14
Seattle 13
Tianjin 13
Catania 12
Ningbo 12
Rome 12
Brooklyn 11
Dong Ket 11
Jakarta 11
Helsinki 10
Milan 10
Shenyang 10
Boston 9
San Mateo 9
Amsterdam 8
Houston 8
Phoenix 8
Pune 8
Santa Clara 8
Tokyo 8
Chicago 7
Düsseldorf 7
Frankfurt am Main 7
Hyderabad 7
London 7
São José dos Campos 7
Toronto 7
Chennai 6
Guarulhos 6
Istanbul 6
Johannesburg 6
Lappeenranta 6
Manchester 6
Mexico City 6
Nanjing 6
San Francisco 6
Stockholm 6
Vienna 6
Atlanta 5
Casablanca 5
Contagem 5
Curitiba 5
Duque de Caxias 5
Guayaquil 5
Hefei 5
Olomouc 5
Padova 5
Porto Alegre 5
Prague 5
Quito 5
Shanghai 5
Taiyuan 5
Taizhou 5
Wroclaw 5
Ancona 4
Ankara 4
Baghdad 4
Changsha 4
Formosa 4
Fuzhou 4
Hortolândia 4
Limeira 4
Totale 4.105
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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 182
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. 171
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study. 159
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome 148
CCR5Δ32 Polymorphism Associated with a Slower Rate DiseaseProgression in a Cohort of RR-MS Sicilian Patients 147
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens 141
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions 137
A MOLECULAR- GENETIC ANALYSIS OF FLAVIN-CONTAINING MONOOXYGENASE3 GENE (FMO3) IN AN ITALIAN CHILD WITH A TMAURIA LIKE-PHENOTYPE 128
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis? 128
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes 127
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study 123
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations 119
LITHIUM TRANSPORT PATHWAYS IN HUMAN, CHICKEN AND EEL ERYTHROCYTES 118
Age dependent switching role of ciclyn D1 in breast cancer 116
An intronic variant in PTEN gene is probably involved in splicing alteration events 116
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa 115
FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor 113
Costameric proteins in human skeletal muscle during muscular inactivity. 113
CCR5Δ32 POLYMORPHISM ASSOCIATED WITH A SLOWER RATE DISEASE PROGRESSION IN A COHORT OF RR-MS SICILIAN PATIENTS 112
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies 111
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations 110
Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells 108
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study 104
A rare case of TMAU associated with suspected Currarino triad 99
Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration 98
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 98
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations 95
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 94
GENETICS OF CAVERNOMAS: A CASE REPORT 94
Screening genetico dei geni CCM in pazienti italiani affetti da angioma cavernoso cerebrale: un caso familiare 93
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? 92
Molecular analysis of CCM genes promoter regions 92
Distribuzione dell'allele mutato Δ32 del gene CCR5 nella popolazione sana del bacino del mediterraneo. 90
IL SUBCOMPLESSO DEI SARCOGLICANI NEL MUSCOLO LISCIO UMANO 89
Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. 89
Effetti contrastanti di alcuni ossidanti sul trasporto di litio in globuli rossi umani 88
Distribution of the mutated delta32 allele of the CCR5 gene in a Sicilian population 87
The interaction of haemoglobin, magnesium, organic phosphates and band 3 protein in nucleated and anucleated erythrocytes 84
Oxidative Stress and the Neurovascular Unit 84
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation 83
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function? 82
Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? 81
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS 81
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation 81
The biological pathways of Alzheimer disease: a review 81
Sarcoglycans in muscolar diseases of ureters: an immunohistochemical study. 80
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report 78
Sarcoglycans and integrins in muscular inactivity 77
POLIMORFISMI DELLA GLIOSSALASI I E DELLA PARAOXONASI I IN INDIVIDUI SANI ED INDIVIDUI AFFETTI DA SCLEROSI MULTIPLA.FATTORI DI SUSCETTIBILITA'? 76
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa 74
PON I and GLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy 71
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling 71
EXPRESSION OF SARCOGLYCANS IN THE HUMAN CEREBRAL CORTEX: AN IMMUNOHISTOCHEMICAL AND MOLECULAR STUDY 70
Sarcoglycan complex in human normal and pathological prostatic tissue: An immunohistochemical and RT-PCR study 69
IMMUNOHISTOCHEMICAL AND NUCLEOTIDE SEQUENCING ANALYSIS OF SARCOGLYCANS IN EPITHELIUM 67
Quantification of trimethylamine (TMA) and trimethylamine oxide (TMAO) for diagnostic and targeted diet purposes. 65
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 65
interazioni farmaco-cinetiche sul trasporto di litio nei globuli rossi umani 64
INFLUSSO DELLO IONE SOLFATO NEI GLOBULI ROSSI IN SOGGETTI SANI,IPERTESI E DIABETICI 63
IS α SARCOGLYCAN A MEMBER OF SARCOGLYCAN COMPLEX IN HUMAN SMOOTH MUSCLE ? 63
LITHIUM TRANSPORT PATHWAYS IN HUMAN CHICKEN AND EEL ERYTHROCYTES 63
The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment 62
Genetic and functional study of CCR5 gene in HIV-1 infection 58
OSMOREGULATION IN NORMAL AND ABNORMAL HUMAN ERYTHROCYTES 57
IMMUNOISTOCHEMICAL AND NUCLEOTIDE SEQUENCING ANALYSIS OF SARCOGLYCANS IN EPITHELIUM 55
Human retinal secretome: A cross-link between mesenchymal and retinal cells 46
Sarcoglycan subcomplex expression in normal human smooth muscle 43
Further data on a 9.1-kb insertion-deletion polymorphism: Survey of Mediterranean populations 43
Investigating G-quadruplex structures in RPGR gene: Implications for understanding X-linked retinal degeneration 38
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Mechanotransduction in development: a focus on angiogenesis 24
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Decoding pediatric inherited retinal dystrophies: Bridging genetic complexity and clinical heterogeneity 17
Nel labirinto delle distrofie retiniche ereditarie: alla scoperta delle Terapie innovative e delle visioni del futuro 16
Multifaceted disruption of AMPA receptor signaling by CACNG8 variants: Integrated evidence from human genetics and molecular simulation 12
Totale 6.640
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Categoria #
all - tutte 25.060
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 25.060
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021227 0 0 0 0 0 45 26 38 24 54 21 19
2021/2022539 3 74 17 13 6 6 29 28 8 152 47 156
2022/20231.217 83 92 59 104 110 110 17 81 510 5 40 6
2023/2024342 33 57 8 31 29 64 0 15 2 18 11 74
2024/20251.502 29 10 41 111 43 60 45 334 361 94 134 240
2025/20261.660 181 344 409 310 385 31 0 0 0 0 0 0
Totale 6.640