IRIS
RAIA, VALERIA
 Distribuzione geografica
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Continente #
NA - Nord America 2.555
EU - Europa 1.502
AS - Asia 355
AF - Africa 35
SA - Sud America 3
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 1
Totale 4.453
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Nazione #
US - Stati Uniti d'America 2.497
IT - Italia 643
CN - Cina 299
UA - Ucraina 235
FI - Finlandia 152
NL - Olanda 152
IE - Irlanda 97
DE - Germania 91
CA - Canada 57
SE - Svezia 53
GB - Regno Unito 49
CI - Costa d'Avorio 32
VN - Vietnam 24
FR - Francia 15
IR - Iran 12
IN - India 10
SG - Singapore 6
EG - Egitto 3
GR - Grecia 3
RO - Romania 3
AR - Argentina 2
BE - Belgio 2
ES - Italia 2
EU - Europa 2
TR - Turchia 2
AU - Australia 1
BG - Bulgaria 1
CO - Colombia 1
CY - Cipro 1
HR - Croazia 1
ID - Indonesia 1
PA - Panama 1
PL - Polonia 1
RS - Serbia 1
SI - Slovenia 1
Totale 4.453
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Città #
Chandler 494
Jacksonville 261
Napoli 207
Millbury 171
Ashburn 164
Princeton 154
Amsterdam 148
Naples 141
Boston 113
Nanjing 91
Wilmington 79
Beijing 62
Ottawa 51
Des Moines 42
Houston 36
Lawrence 29
Nanchang 29
Shenyang 25
Dong Ket 24
Changsha 21
Norwalk 21
Hebei 19
Washington 19
Jiaxing 16
Rome 16
Orange 14
Augusta 12
Boardman 12
Falls Church 12
Mugnano Di Napoli 12
Seattle 12
Tianjin 9
Woodbridge 9
Milan 8
Villaricca 8
Dublin 7
Kronberg 7
Los Angeles 7
Redmond 7
San Mateo 7
Fairfield 6
Lucca 6
Pune 6
Ardabil 5
Bologna 5
Hangzhou 5
Leawood 5
New York 5
Redwood City 5
Walnut 5
Avellino 4
Brierley Hill 4
Indiana 4
Lanzhou 4
Turin 4
Cairo 3
Eboli 3
Fremont 3
Kunming 3
Lappeenranta 3
Marcianise 3
Marsala 3
Mugnano di Napoli 3
Selargius 3
Toronto 3
Zhengzhou 3
Ann Arbor 2
Barcelona 2
Basildon 2
Campofelice di Roccella 2
Cattolica 2
Costa di Mezzate 2
Foggia 2
Frankfurt am Main 2
Kish 2
North York 2
Palermo 2
Poggiomarino 2
Sector 5 2
Shanghai 2
Stockholm 2
Venice 2
Altamura 1
Alzano Lombardo 1
Ancona 1
Andover 1
Beograd 1
Bogotá 1
Bournemouth 1
Brescia 1
Brussels 1
Busto Arsizio 1
Casoria 1
Cerro Maggiore 1
Chaidari 1
Chieti 1
Chiusano di San Domenico 1
Civezzano 1
Como 1
Cormeilles-en-Parisis 1
Totale 2.732
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Nome #
Clinical expression of patients with the D1152H CFTR mutation 77
A novel treatment of cystic fibrosis acting on-target: cysteamine plus epigallocatechin gallate for the autophagy-dependent rescue of class II-mutated CFTR 74
An "ex vivo model" contributing to the diagnosis and evaluation of new drugs in cystic fibrosis 58
Genotype-phenotype correlation and functional studies in patients with cystic fibrosis bearing CFTR complex alleles 53
Normative growth charts for Shwachman-Diamond syndrome from Italian cohort of 0-8 years old. 49
Can glargine reduce the number of lung infections in patients with cystic fibrosis-related diabetes? 48
Intra-individual biological variation in sweat chloride concentrations in CF, CFTR dysfunction, and healthy pediatric subjects 48
Microbiology of airway disease in a cohort of patients with Cystic Fibrosis. 47
Lung structure and function similarities between primary ciliary dyskinesia and mild cystic fibrosis: a pilot study 46
Comprehensive cystic fibrosis mutation epidemiology and haplotype characterization in a southern Italian population. 44
Chryseobacterium respiratory tract infections in patients with cystic fibrosis 44
Alterazioni metaboliche degli acidi grassi nella Fibrosi Cistica 44
Identification of Inquilinus limosus in Cystic Fibrosis: a first report in Italy 43
S737F is a new CFTR mutation typical of patients originally from the Tuscany region in Italy 43
Diabetes in an infant with cystic fibrosis 42
TAS2R38 is a novel modifier gene in patients with cystic fibrosis 42
A complicated association between two different genetic rare disorders: Cystic Fibrosis and Spinal Muscular Atrophy 42
Liver expression in Cystic Fibrosis could be modulated by genetic factors different from the Cystic Fibrosis Transmembrane Regulator genotype. 41
Burkholderia cepacia complex infection in a cohort of Italian patients with cystic fibrosis. 41
Reduced absorption and enhanced synthesis of cholesterol in patients with cystic fibrosis: a preliminary study of plasma sterols 41
An investigation on parenting stress of children with cystic fibrosis 41
Hyaluronic acid improves "pleasantness" and tolerability of nebulized hypertonic saline in a cohort of patients with cystic fibrosis 40
Methicillin-resistant Staphylococcus aureus eradication in cystic fibrosis patients: A randomized multicenter study 40
Intestinal inflammation is a frequent feature of cystic fibrosis and is reduced by probiotic administration 39
7. An overview of international literature from cystic fibrosis registries. Part 4: update 2011 39
Does virtual reality reduce pain in pediatric patients? A systematic review 39
Amines protect in vitro the celiac small intestine from the damaging activity of gliadin peptides. 38
One-year glargine treatment can improve the course of lung disease in children and adolescents with cystic fibrosis and early glucose derangements. 38
Cysteamine re-establishes the clearance of Pseudomonas aeruginosa by macrophages bearing the cystic fibrosis-relevant F508del-CFTR mutation 38
Association between innate response to gliadin and activation of pathogenic T cells in coeliac disease 37
Unexpected role of surface transglutaminase type II in celiac disease 37
Defective CFTR induces aggresome formation and lung inflammation in cystic fibrosis through ROS-mediated autophagy inhibition 37
Effect of an 8-month treatment with omega-3 fatty acid (eicosapentanoic and docosahexaenoic) in patients with cystic fibrosis 36
Amines Protect Invitro the Celiac Small-intestine From the Damaging Activity of Gliadin Peptides 36
Trans-heterozygosity for mutations enhances the risk of recurrent/chronic pancreatitis in patients with Cystic Fibrosis 36
Clinical expression of cystic fibrosis in a large cohort of Italian siblings 36
Salivary cytokines and airways disease severity in patients with cystic fibrosis 36
Metabolic interactions between cysteamine and epigallocatechin gallate 35
A pathogenic role for cystic fibrosis transmembrane conductance regulator in celiac disease 35
Impaired cholesterol metabolism in the mouse model of cystic fibrosis. A preliminary study 35
Aspergillosi broncopolmonare 34
Different mutations in mucA gene of Pseudomonasaeruginosa mucoid strains in cystic fibrosispatients and their effect on algU gene expression 34
Aneuploidy of lymphocytes in familial polyposis coli. 33
A-GLIADIN RELATED SYNTHETIC PEPTIDES AGGLUTINATE UNDIFFERENTIATED K TO 562 S CELLS AND AFFECT IN VITRO DEVELOPING FETAL RAT INTESTINE AND ULTURED ATROPHIC COELIAC MUCOSA 33
FAS engagement driver apoptosis of the enterocytes of coeliac patients 32
Epidemiologia di Burkholderia cepacia in pazienti con fibrosi cistica: primi risultati di uno studio comprendente la tipizzazione genotipica dei ceppi isolati 32
A triphalangeal thumb associated with otological abnormalities. A new syndrome?] 32
Ursodeoxycholic acid treatment in patients with cystic fibrosis at risk for liver disease 32
Nasal polyposis in atypical cystic fibrosis: A case report 32
Disrupted Intestinal Microbiota and Intestinal Inflammation in Children with Cystic Fibrosis and Its Restoration with Lactobacillus GG: A Randomised Clinical Trial. 32
Inhaled medications in cystic fibrosis beyond antibiotics 32
Long-Term Follow-Up in a Girl with Cystic Fibrosis and Diabetes Since the First Year of Life 31
Brand new SPINK1 and CFTR mutations in a child with acute recurrent pancreatitis: a case report. 30
Personalization of therapies in rare diseases: a translational approach for the treatment of cystic fibrosis. 30
Pediatric ultrasonography of the pancreas: normal and abnormal findings 30
Long-term benefits of nusinersen in a child affected by cystic fibrosis and spinal muscular atrophy type 1. 30
Lung involvement, deltaF508 mutation and DNA haplotype analysis in cystic fibrosis. 29
Cystic fibrosis: a disorder with defective autophagy 29
A polymorphism in the 5' UTR of the DEFB1 gene is associated with the lung phenotype in F508del homozygous Italian cystic fibrosis patients. 29
An overview of international literature from cystic fibrosis registries. Part 4: Update 2011. 29
Achromobacter xylosoxidans respiratory tract infection in cystic fibrosis patients. 28
Randomized, single blind, controlled trial of inhaled glutathione vs placebo in patients with cystic fibrosis. 28
Manipulating proteostasis to repair the F508del-CFTR defect in cystic fibrosis 28
Cystic fibrosis transmembrane conductance regulator (CFTR) and autophagy: hereditary defects in cystic fibrosis versus gluten-mediated inhibition in celiac disease 28
Positive expiratory pressure treatment: efficacy in pulmonary diseases 27
null 27
Defective proteostasis in celiac disease as a new therapeutic target 27
Diabetes outbreak during COVID19 lock-down in a prediabetic patient with cystic fibrosis long treated with glargine. 27
Detection of rare cystic fibrosis mutations peculiar to Southern Italy: implications in screening for the disease and phenotype charaterization for patients with homozygote mutations. 26
An overview of international literature from cystic fibrosis registries: 1. Mortality and survival studies in cystic fibrosis. J Cyst Fibros. 2009; 8:229-37. 26
Prediction of acute pancreatitis risk based on PIP score in children with cystic fibrosis 26
Autophagy suppresses the pathogenic immune response to dietary antigens in cystic fibrosis. 26
Continuous glucose monitoring system in the screening of early glucose derangements in children and adolescents with cystic fibrosis. 25
Epidemiology and a novel procedure for large scale :analysis of CFTR rearrangements in classic and atypical CF patients: A multicentric Italian study. 25
Italian Cystic Fibrosis Registry: 10 years of activity 25
Burkholderia cepacia complex infection in a cohort of Italian patients with cystic fibrosis. 25
The Italian pilot external quality assessment program for cystic fibrosis sweat test 25
Genistein antagonizes gliadin-induced CFTR malfunction in models of celiac disease. 25
Non-invasive tools for detection of liver disease in children and adolescents with cystic fibrosis. 25
Liver expression in cystic fibrosis could be modulated by genetic factors from the cystic fibrosis transmembrane regulator genotype 24
Comparison of two enteric coated microsphere preparations in the treatment of pancreatic exocrine insufficiency caused by cystic fibrosis 24
Patchy expression of lactase protein in adult rabbit and rat intestine. 24
Mosaic pattern of lactase expression by villous enterocytes in human adult-type hypolactasia 24
Genetic history of cystic fibrosis mutations in Italy. I. Regional distribution 24
Molecular epidemiology of cystic fibrosis mutations and respective haplotypes in southern Italy evaluated with an improved semiautomated robotic procedure. 23
DNA fragmentation is a feature of cystic fibrosis epithelial cells: a disease with inappropriate apoptosis? 23
The epidemiology of Burkholderia cepacia in cystic fibrosis patients: the initial results of a study including the genotypic typing of the strains isolated 23
Mosaic regulation of lactase in human adult-type hypolactasia. 23
Audit of sweat testing: a first report from Italian Cystic Fibrosis Centres 23
Effect of Lactobacillus GG supplementation on pulmonary exacerbations in patients with cystic fibrosis: a pilot study 23
L’intervento nutrizionale in Fibrosi Cistica 23
Rapid identification of Burkholderia cepacia complex species recovered from cystic fibrosis patients using matrix-assisted laser desorption ionization time-of-flight mass spectrometry 23
Towards a rational combination therapy of cystic fibrosis: How cystamine restores the stability of mutant CFTR 23
Clinical features of cystic fibrosis patients bearing rare genotypes. 22
Severe liver impairment in a cystic fibrosis-affected child homozygous for the G542X mutation. 22
First report of three cystic fibrosis patients homozygous for the 1717-1G-->A mutation. 22
Surface staining on the villus of lactase protein and lactase activity in adult-type hypolactasia 22
Positive expiratory pressure treatment: efficacy in pulmonary diseases 22
Lung involvement, the delta F508 mutation and DNA haplotype analysis in cystic fibrosis. 22
CYSTIC FIBROSIS: WHEN SHOULD HIGH-RESOLUTION COMPUTED TOMOGRAPHY OF THE CHEST BE OBTAINED? 22
Totale 3.320
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Categoria #
all - tutte 19.727
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 19.727
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201921 0 0 0 0 0 0 0 0 0 2 8 11
2019/2020542 219 8 45 5 56 3 4 3 9 42 60 88
2020/2021630 17 48 78 64 61 76 54 9 80 12 102 29
2021/20221.023 12 1 5 0 0 156 18 39 108 58 217 409
2022/20231.202 194 120 25 77 137 124 4 118 185 147 54 17
2023/2024640 22 113 162 74 49 98 29 61 13 19 0 0
Totale 4.671