DIANZANI, Irma
 Distribuzione geografica
Continente #
NA - Nord America 1600
EU - Europa 1209
AS - Asia 457
AF - Africa 5
Continente sconosciuto - Info sul continente non disponibili 4
SA - Sud America 2
Totale 3277
Nazione #
US - Stati Uniti d'America 1554
CN - Cina 316
SE - Svezia 205
IT - Italia 182
IE - Irlanda 173
FR - Francia 147
UA - Ucraina 123
FI - Finlandia 107
DE - Germania 100
KR - Corea 97
AT - Austria 55
GB - Regno Unito 49
CA - Canada 40
PL - Polonia 39
VN - Vietnam 26
BE - Belgio 9
GR - Grecia 6
IN - India 6
RU - Federazione Russa 6
MX - Messico 5
SN - Senegal 5
EU - Europa 4
JP - Giappone 4
PH - Filippine 3
CH - Svizzera 2
CO - Colombia 2
PT - Portogallo 2
AL - Albania 1
DK - Danimarca 1
HU - Ungheria 1
IR - Iran 1
KH - Cambogia 1
NI - Nicaragua 1
NP - Nepal 1
RO - Romania 1
SG - Singapore 1
TW - Taiwan 1
Totale 3277
Città #
Chandler 400
Beijing 242
Dublin 173
Villeurbanne 94
Dearborn 87
Jacksonville 68
Ann Arbor 67
Houston 66
Nyköping 63
Princeton 62
Medford 61
Vienna 53
Torino 43
Wilmington 39
Fairfield 38
Warsaw 38
Cambridge 33
Boston 25
Verona 25
Woodbridge 25
Milan 21
Toronto 21
Ashburn 20
Redwood City 18
Boardman 15
Seattle 13
Detroit 12
Fremont 12
Pisa 12
Dong Ket 11
Guangzhou 10
Hefei 10
Lachine 9
Ottawa 9
New York 8
Norwalk 8
Nanjing 7
Piemonte 7
Rome 7
Brussels 6
Düsseldorf 6
Genoa 6
San Mateo 6
Des Moines 5
Siena 5
Falls Church 4
Kunming 4
Lexington 4
Mountain View 4
San Diego 4
Shenyang 4
Fuzhou 3
Hangzhou 3
Honolulu 3
Munich 3
Nürnberg 3
Philadelphia 3
Zhengzhou 3
Bangalore 2
Bucaramanga 2
Catania 2
Chengdu 2
Chicago 2
Cumiana 2
Kharkiv 2
London 2
Phoenix 2
Ravenna 2
Shanghai 2
Turin 2
Wuhan 2
Xian 2
Alghero 1
Ardabil 1
Assèmini 1
Auburn Hills 1
Berlin 1
Bucharest 1
Budapest 1
Buffalo 1
Carate 1
Centro 1
Chiusi 1
Dallas 1
Dalmine 1
Duarte 1
Durham 1
Edmonton 1
Gießen 1
Graz 1
Grugliasco 1
Gualdo Tadino 1
Hebei 1
Hyderabad 1
Jawalakhel 1
Jinan 1
Kurashiki 1
Leuven 1
Levittown 1
Livorno 1
Totale 2067
Nome #
DNA methylation profiling of asbestos-treated MeT5A cell line reveals novel pathways implicated in asbestos response 225
Germline mutations in DNA repair genes predispose asbestos-exposed patients to malignant pleural mesothelioma. 186
Analysis of the carbonyl compounds produced in beta thalassaemic erythrocytes by oxidative stress. 95
Whole blood DNA methylation changes are associated to Malignant Pleural Mesothelioma 91
The European Hematology Association roadmap for European Hematology Research: A consensus document 85
WHOLE BLOOD DNA METHYLATION CHANGES ARE ASSOCIATED TO MALIGNANT PLEURAL MESOTHELIOMA 83
Erythrocyte sodium-lithium countertransport in diabetic adolescents. 82
Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation 80
III Italian Consensus Conference on Malignant Mesothelioma of the Pleura. Epidemiology, Public Health and Occupational Medicine related issues 78
Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in children. 75
High levels of osteopontin associated with polymorphisms in its gene are a risk factor for development of autoimmunity/lymphoproliferation 75
Fifth International Mutation Detection Workshop, May 13-16, 1999, Vicoforte, Italy 75
Defective function of Fas in T cells from paediatric patients with autoimmune thyroid diseases. 73
Serum glycoproteins and insulin-dependent juvenile diabetes mellitus. 69
La scelta vita/morte del linfocita.112: 297-309, 1998. 68
Erythrocyte Na,Li countertransport and arterial pressure in diabetic adolescents. 67
EPIGENETIC PROFILES IN RELATION TO ASBESTOS EXPOSURE IN MALIGNANT PLEURAL MESOTHELIOMA 67
Diamond Blackfan anaemia in the Italian population 65
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. 65
Whole blood DNA methylation changes are associated to Malignant Pleural Mesothelioma 65
Construction of a genetic map telomeric to HAL-A by microsatellite analysis 65
Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancer. 65
Alteration of heme metabolism in a cellular model of Diamond-Blackfan anemia 64
Diamond-Blackfan Anemia: an Overview 61
Catalytic activity of tetrahydrobiopterin in dihydropteridine reductase deficiency and indications for treatment. 59
Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy. 59
Abnormalities of sodium transport by sodium, potassium-activated adenosine triphosphatase in erythrocytes from obese children. 57
Evaluation of ouabain-insensitive red blood cell cation transport in obese children. 56
HUMAN PHERIPHERAL BLOOD GRANULOCYTES AND MYELOID LEUKEMIC CELL LINES EXPRESS BOTH TRANSCRIPTS ENCODING FOR STEM CELL FACTOR 56
Whole blood DNA methylation changes are associated to Malignant Pleural Mesothelioma 56
Exploiting pre-rRNA processing in Diamond Blackfan anemia gene discovery and diagnosis. 56
Diamond-Blackfan anemia: a congenital defect in erythropoiesis 56
Course of retinopathy in children and adolescents with insulin-dependent diabetes mellitus: a ten-year study. 55
Molecular basis of Dihydropterine Reductase Deficiency. 54
Genetic history of hyperphenylalaninemias in Italy 53
Inborn errors of neurotransmitter metabolism: from Phenotype to Genotype 52
Prenatal diagnosis in primary hyperphenylalaninemias. 51
Wolfram's syndrome. Presentation of a case. 50
Identification of microdeletions spanning the Diamond-Blackfan anemia locus on 19q13 and evidence for genetic heterogeneity. 49
Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemia. 47
Progression of 6-pyruvoyl-tetrahydropterin synthase deficiency from a peripheral into a central phenotype. 47
Molecular basis of Phenylketonuria. 47
Ipoplasie midollari congenite 46
Basi molecolari delle aplasie ereditarie 46
Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression 42
Insulin-dependent diabetes mellitus and maternal age. 42
Nonsense-mediated and nonstop decay of ribosomal protein S19 mRNA in Diamond-Blackfan anemia 40
Variations of the perforin gene in patients with autoimmunity/lymphoproliferation and defective Fas function 39
Phenotyping of phenylketonuric patients by oral phenylalanine loading. 39
Genotype-phenotype correlation in phenylketonuria. 39
Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-F 36
Haplotype distribution and molecular defects of PKU in Italy. 34
Tetrahydrobiopterin loading test in hyperphenylalaninemia. 29
Totale 3416
Categoria #
all - tutte 6088
article - articoli 0
book - libri 0
conference - conferenze 1108
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 7196


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/2018337 0000 00 00 21711046
2018/2019237 731811 426 1341 16235124
2019/2020419 1572634 3483 6429 38511721
2020/2021377 39163614 3832 2921 55312541
2021/2022529 57848 1621 3931 938156151
2022/2023897 958017114 91252 5957 132000
Totale 3416