CINECA IRIS Institutional Research Information System

DIANZANI, Irma
 Distribuzione geografica
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Continente #
NA - Nord America 1.979
EU - Europa 1.285
AS - Asia 553
AF - Africa 6
Continente sconosciuto - Info sul continente non disponibili 4
SA - Sud America 4
OC - Oceania 3
Totale 3.834
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Nazione #
US - Stati Uniti d'America 1.931
CN - Cina 336
SE - Svezia 224
IT - Italia 201
IE - Irlanda 177
FR - Francia 151
UA - Ucraina 129
FI - Finlandia 113
DE - Germania 105
KR - Corea 99
SG - Singapore 65
AT - Austria 55
GB - Regno Unito 53
CA - Canada 42
PL - Polonia 39
VN - Vietnam 26
IN - India 10
RU - Federazione Russa 9
BE - Belgio 7
GR - Grecia 6
SN - Senegal 6
MX - Messico 5
NL - Olanda 5
EU - Europa 4
JP - Giappone 4
TW - Taiwan 4
AU - Australia 3
PH - Filippine 3
BR - Brasile 2
CH - Svizzera 2
CO - Colombia 2
HR - Croazia 2
HU - Ungheria 2
ID - Indonesia 2
PT - Portogallo 2
AL - Albania 1
DK - Danimarca 1
IR - Iran 1
KH - Cambogia 1
NI - Nicaragua 1
NP - Nepal 1
RO - Romania 1
TR - Turchia 1
Totale 3.834
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Città #
Chandler 407
Beijing 248
Dublin 177
Ashburn 117
Villeurbanne 96
Dearborn 88
Nyköping 80
Jacksonville 72
Ann Arbor 67
Houston 66
Princeton 63
Medford 61
Vienna 53
Singapore 46
Torino 43
Wilmington 40
Fairfield 38
Warsaw 38
Cambridge 33
Boston 26
Verona 26
Milan 25
Woodbridge 25
Toronto 21
Redwood City 18
Seattle 17
Boardman 16
Guangzhou 14
New York 14
Washington 13
Detroit 12
Fremont 12
Pisa 12
Dong Ket 11
Hefei 10
Lachine 10
Los Angeles 9
Ottawa 9
Norwalk 8
Rome 8
Nanjing 7
Piemonte 7
Düsseldorf 6
Genoa 6
San Mateo 6
Turin 6
Des Moines 5
Hangzhou 5
Ivrea 5
Siena 5
Whitman 5
Brussels 4
Dronten 4
Falls Church 4
Kunming 4
Lexington 4
Mountain View 4
Phoenix 4
Pune 4
San Diego 4
Santa Clara 4
Shenyang 4
Atlanta 3
Fairfax 3
Fuzhou 3
Honolulu 3
Munich 3
Nürnberg 3
Philadelphia 3
Zhengzhou 3
Bangalore 2
Barretos 2
Bucaramanga 2
Budapest 2
Catania 2
Chengdu 2
Chicago 2
Cumiana 2
Harbin 2
Helsinki 2
Jakarta 2
Kharkiv 2
Kwinana 2
Lappeenranta 2
Leicestershire 2
London 2
Monte San Giovanni Campano 2
Newark 2
Ravenna 2
Shanghai 2
Wuhan 2
Xian 2
Zagreb 2
Alghero 1
Amsterdam 1
Ardabil 1
Assèmini 1
Auburn Hills 1
Berlin 1
Bucharest 1
Totale 2.333
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Nome #
DNA methylation profiling of asbestos-treated MeT5A cell line reveals novel pathways implicated in asbestos response 265
Germline mutations in DNA repair genes predispose asbestos-exposed patients to malignant pleural mesothelioma. 212
Analysis of the carbonyl compounds produced in beta thalassaemic erythrocytes by oxidative stress. 108
Whole blood DNA methylation changes are associated to Malignant Pleural Mesothelioma 99
The European Hematology Association roadmap for European Hematology Research: A consensus document 97
WHOLE BLOOD DNA METHYLATION CHANGES ARE ASSOCIATED TO MALIGNANT PLEURAL MESOTHELIOMA 92
Erythrocyte sodium-lithium countertransport in diabetic adolescents. 90
Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation 88
III Italian Consensus Conference on Malignant Mesothelioma of the Pleura. Epidemiology, Public Health and Occupational Medicine related issues 86
High levels of osteopontin associated with polymorphisms in its gene are a risk factor for development of autoimmunity/lymphoproliferation 85
Fifth International Mutation Detection Workshop, May 13-16, 1999, Vicoforte, Italy 84
Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in children. 83
Serum glycoproteins and insulin-dependent juvenile diabetes mellitus. 80
Erythrocyte Na,Li countertransport and arterial pressure in diabetic adolescents. 78
Defective function of Fas in T cells from paediatric patients with autoimmune thyroid diseases. 78
Diamond Blackfan anaemia in the Italian population 77
La scelta vita/morte del linfocita.112: 297-309, 1998. 77
Whole blood DNA methylation changes are associated to Malignant Pleural Mesothelioma 75
EPIGENETIC PROFILES IN RELATION TO ASBESTOS EXPOSURE IN MALIGNANT PLEURAL MESOTHELIOMA 75
Diamond-Blackfan anemia: expansion of erythroid progenitors in vitro by IL-9, but exclusion of a significant pathogenetic role for the IL-9 gene and the hematopoietic gene cluster on chromosome 5q. 74
HUMAN PHERIPHERAL BLOOD GRANULOCYTES AND MYELOID LEUKEMIC CELL LINES EXPRESS BOTH TRANSCRIPTS ENCODING FOR STEM CELL FACTOR 74
Alteration of heme metabolism in a cellular model of Diamond-Blackfan anemia 74
Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancer. 72
Construction of a genetic map telomeric to HAL-A by microsatellite analysis 71
Diamond-Blackfan Anemia: an Overview 68
Molecular analysis of contiguous exons of the phenylalanine hydroxylase gene: identification of a new PKU mutation. 67
Prenatal diagnosis in primary hyperphenylalaninemias. 67
Whole blood DNA methylation changes are associated to Malignant Pleural Mesothelioma 67
Abnormalities of sodium transport by sodium, potassium-activated adenosine triphosphatase in erythrocytes from obese children. 67
Evaluation of ouabain-insensitive red blood cell cation transport in obese children. 66
Catalytic activity of tetrahydrobiopterin in dihydropteridine reductase deficiency and indications for treatment. 66
Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy. 66
Course of retinopathy in children and adolescents with insulin-dependent diabetes mellitus: a ten-year study. 66
Genetic history of hyperphenylalaninemias in Italy 64
Molecular basis of Dihydropterine Reductase Deficiency. 64
Exploiting pre-rRNA processing in Diamond Blackfan anemia gene discovery and diagnosis. 64
Diamond-Blackfan anemia: a congenital defect in erythropoiesis 62
Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemia. 59
Identification of microdeletions spanning the Diamond-Blackfan anemia locus on 19q13 and evidence for genetic heterogeneity. 58
Inborn errors of neurotransmitter metabolism: from Phenotype to Genotype 56
Molecular basis of Phenylketonuria. 56
Basi molecolari delle aplasie ereditarie 56
Wolfram's syndrome. Presentation of a case. 55
Ipoplasie midollari congenite 52
Genotype-phenotype correlation in phenylketonuria. 51
Insulin-dependent diabetes mellitus and maternal age. 50
Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression 49
Progression of 6-pyruvoyl-tetrahydropterin synthase deficiency from a peripheral into a central phenotype. 48
Nonsense-mediated and nonstop decay of ribosomal protein S19 mRNA in Diamond-Blackfan anemia 46
Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-F 44
Phenotyping of phenylketonuric patients by oral phenylalanine loading. 43
Variations of the perforin gene in patients with autoimmunity/lymphoproliferation and defective Fas function 42
Haplotype distribution and molecular defects of PKU in Italy. 37
Tetrahydrobiopterin loading test in hyperphenylalaninemia. 30
Totale 3.980
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Categoria #
all - tutte 12.430
article - articoli 0
book - libri 0
conference - conferenze 2.049
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 14.479
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020405 0 0 27 34 35 84 66 30 39 51 18 21
2020/2021383 40 16 37 14 38 32 30 21 56 32 26 41
2021/2022538 5 7 8 49 16 21 39 31 9 41 159 153
2022/20231.001 96 81 18 115 91 256 51 62 140 18 43 30
2023/2024364 49 57 28 22 38 67 8 27 1 15 16 36
2024/202553 2 38 13 0 0 0 0 0 0 0 0 0
Totale 3.980