RINALDI, Carmela
 Distribuzione geografica
Continente #
EU - Europa 350
NA - Nord America 35
AS - Asia 17
SA - Sud America 4
Totale 406
Nazione #
IT - Italia 272
IE - Irlanda 33
US - Stati Uniti d'America 32
FR - Francia 13
VN - Vietnam 10
PL - Polonia 8
CH - Svizzera 6
DE - Germania 4
CZ - Repubblica Ceca 3
SG - Singapore 3
UA - Ucraina 3
CL - Cile 2
GB - Regno Unito 2
HU - Ungheria 2
KR - Corea 2
MX - Messico 2
NL - Olanda 2
AR - Argentina 1
BE - Belgio 1
BR - Brasile 1
CA - Canada 1
FI - Finlandia 1
IL - Israele 1
IN - India 1
Totale 406
Città #
Messina 169
Dublin 33
Lago 14
Dong Ket 10
Rome 10
Padova 8
Warsaw 8
Zurich 6
Boardman 5
Treviglio 5
Bremen 4
Ashburn 3
Ispica 3
Paris 3
Pozzo Di Gotto 3
Enna 2
Fara in Sabina 2
Francofonte 2
Graneros 2
Houston 2
Lexington 2
Nashville 2
Pécs 2
Ragusa 2
Siracusa 2
Tlalnepantla 2
Adrano 1
Amsterdam 1
Banstead 1
Bay Village 1
Boston 1
Brooklyn 1
Caltagirone 1
Chennai 1
Cleveland 1
Council Bluffs 1
Córdoba 1
Denver 1
Doylestown 1
Duncan 1
Fleming Island 1
Gaffney 1
Genoa 1
Los Angeles 1
Macerata 1
Mineo 1
Mountain View 1
New York 1
Perugia 1
Redmond 1
Santa Venerina 1
Sydney 1
Torregrotta 1
Trieste 1
Turku 1
Totale 335
Nome #
An intronic variant in PTEN gene is probably involved in splicing alteration events, file de3e52b2-c0f0-762d-e053-3705fe0a30e0 58
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions, file de3e52b1-3323-762d-e053-3705fe0a30e0 38
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study., file de3e52b0-639b-762d-e053-3705fe0a30e0 37
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis?, file de3e52b1-3a1b-762d-e053-3705fe0a30e0 32
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations, file de3e52b0-ad20-762d-e053-3705fe0a30e0 25
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study, file de3e52b0-fc5f-762d-e053-3705fe0a30e0 23
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions, file de3e52b1-afa6-762d-e053-3705fe0a30e0 21
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations, file de3e52b2-6a8b-762d-e053-3705fe0a30e0 21
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations, file de3e52b1-c53c-762d-e053-3705fe0a30e0 14
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation, file de3e52ae-c3eb-762d-e053-3705fe0a30e0 13
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens, file de3e52b1-05f7-762d-e053-3705fe0a30e0 13
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype, file de3e52b2-a174-762d-e053-3705fe0a30e0 11
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation, file de3e52b0-9e3f-762d-e053-3705fe0a30e0 10
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype, file de3e52b2-a175-762d-e053-3705fe0a30e0 10
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study., file de3e52ae-d132-762d-e053-3705fe0a30e0 9
FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor, file de3e52ae-e511-762d-e053-3705fe0a30e0 9
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study, file de3e52b3-3687-762d-e053-3705fe0a30e0 6
PON I and GLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy, file de3e52af-06b5-762d-e053-3705fe0a30e0 5
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome, file de3e52b3-97af-762d-e053-3705fe0a30e0 5
null, file de3e52ae-b54f-762d-e053-3705fe0a30e0 4
null, file de3e52ae-bb2e-762d-e053-3705fe0a30e0 4
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis?, file de3e52ae-bc0b-762d-e053-3705fe0a30e0 4
Age dependent switching role of ciclyn D1 in breast cancer, file de3e52ae-d224-762d-e053-3705fe0a30e0 4
EXPRESSION OF SARCOGLYCANS IN THE HUMAN CEREBRAL CORTEX: AN IMMUNOHISTOCHEMICAL AND MOLECULAR STUDY, file de3e52ae-e47e-762d-e053-3705fe0a30e0 4
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report, file de3e52ae-ee7d-762d-e053-3705fe0a30e0 4
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes, file de3e52b4-dfde-762d-e053-3705fe0a30e0 4
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function?, file de3e52af-08b0-762d-e053-3705fe0a30e0 3
null, file de3e52ae-ca3b-762d-e053-3705fe0a30e0 2
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS, file de3e52ae-df17-762d-e053-3705fe0a30e0 2
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling, file de3e52b4-cebe-762d-e053-3705fe0a30e0 2
Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells, file a4316ffd-89d6-45b3-9520-815edc283c8e 1
Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration, file dc7ef7b9-cb3f-40b6-93ee-80051ab30d02 1
IMMUNOHISTOCHEMICAL AND NUCLEOTIDE SEQUENCING ANALYSIS OF SARCOGLYCANS IN EPITHELIUM, file de3e52ae-aea3-762d-e053-3705fe0a30e0 1
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study, file de3e52ae-b20e-762d-e053-3705fe0a30e0 1
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies, file de3e52b3-01ad-762d-e053-3705fe0a30e0 1
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa, file de3e52b3-01af-762d-e053-3705fe0a30e0 1
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa, file de3e52b3-0f4a-762d-e053-3705fe0a30e0 1
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study, file de3e52b3-2463-762d-e053-3705fe0a30e0 1
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, file de3e52b4-e2a5-762d-e053-3705fe0a30e0 1
Oxidative Stress and the Neurovascular Unit, file de3e52b4-ff8b-762d-e053-3705fe0a30e0 1
Totale 407
Categoria #
all - tutte 936
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 936


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20192 0 0 0 0 0 0 0 0 0 0 1 1
2019/202049 2 0 0 0 1 0 1 0 5 9 22 9
2020/2021110 32 9 12 14 0 3 1 0 19 7 2 11
2021/202277 2 0 5 24 5 3 13 8 13 1 2 1
2022/202377 1 1 1 2 8 4 4 3 34 2 14 3
2023/202438 0 5 4 5 3 1 10 2 7 1 0 0
Totale 407