IRIS
NERI, Tauro Maria
 Distribuzione geografica
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Continente #
NA - Nord America 7.151
AS - Asia 6.505
EU - Europa 4.699
SA - Sud America 857
AF - Africa 298
Continente sconosciuto - Info sul continente non disponibili 9
OC - Oceania 7
Totale 19.526
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Nazione #
US - Stati Uniti d'America 6.951
SG - Singapore 2.449
CN - Cina 2.042
VN - Vietnam 970
IE - Irlanda 777
SE - Svezia 701
UA - Ucraina 684
BR - Brasile 679
IT - Italia 669
FI - Finlandia 601
DE - Germania 520
HK - Hong Kong 456
NL - Olanda 213
ZA - Sudafrica 209
FR - Francia 181
TR - Turchia 154
CA - Canada 139
GB - Regno Unito 138
IN - India 75
AR - Argentina 62
RU - Federazione Russa 54
BD - Bangladesh 53
IQ - Iraq 46
BE - Belgio 39
JP - Giappone 38
EC - Ecuador 33
KR - Corea 29
CO - Colombia 28
MX - Messico 28
ID - Indonesia 27
CI - Costa d'Avorio 25
PK - Pakistan 25
AT - Austria 23
PL - Polonia 23
PH - Filippine 21
UZ - Uzbekistan 21
MA - Marocco 20
VE - Venezuela 17
LT - Lituania 16
ES - Italia 15
PY - Paraguay 11
KE - Kenya 10
SA - Arabia Saudita 10
TH - Thailandia 10
TW - Taiwan 10
EG - Egitto 9
MY - Malesia 9
CL - Cile 8
KZ - Kazakistan 8
CZ - Repubblica Ceca 7
ET - Etiopia 7
PE - Perù 7
AU - Australia 6
AZ - Azerbaigian 6
BO - Bolivia 6
EU - Europa 6
HN - Honduras 6
JO - Giordania 6
NP - Nepal 6
OM - Oman 6
PA - Panama 6
AL - Albania 5
DO - Repubblica Dominicana 5
KW - Kuwait 5
RO - Romania 5
TN - Tunisia 5
UY - Uruguay 5
CR - Costa Rica 4
HU - Ungheria 4
IL - Israele 4
IR - Iran 4
LB - Libano 4
NI - Nicaragua 4
DZ - Algeria 3
LU - Lussemburgo 3
SN - Senegal 3
XK - ???statistics.table.value.countryCode.XK??? 3
AE - Emirati Arabi Uniti 2
BB - Barbados 2
BY - Bielorussia 2
GT - Guatemala 2
HR - Croazia 2
MD - Moldavia 2
MU - Mauritius 2
NO - Norvegia 2
PS - Palestinian Territory 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
SY - Repubblica araba siriana 2
TT - Trinidad e Tobago 2
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
CD - Congo 1
CG - Congo 1
CM - Camerun 1
DK - Danimarca 1
GD - Grenada 1
GI - Gibilterra 1
Totale 19.513
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Città #
Singapore 1.208
Jacksonville 800
Dublin 775
Chandler 673
Ashburn 627
Santa Clara 587
Beijing 538
San Jose 529
Dearborn 448
Hong Kong 438
Ho Chi Minh City 303
Boardman 271
Dallas 251
Nanjing 228
Hanoi 219
Johannesburg 195
San Mateo 176
Princeton 174
Lauterbourg 153
Ann Arbor 150
Los Angeles 133
Izmir 125
Wilmington 105
New York 102
Toronto 101
Shenyang 86
Nanchang 75
Helsinki 73
Kunming 71
Jinan 68
Shanghai 68
Hefei 67
Munich 60
Buffalo 58
Hebei 52
São Paulo 50
Jiaxing 49
Columbus 48
Da Nang 47
Parma 47
Milan 42
Haiphong 41
Tito 40
Des Moines 39
Council Bluffs 38
Tianjin 38
Changsha 37
Bremen 36
Guangzhou 36
The Dalles 32
Moscow 31
Woodbridge 31
Rome 29
Genoa 28
Tokyo 28
Brussels 27
Seattle 27
Abidjan 24
Brooklyn 24
Norwalk 23
Taranto 22
Zhengzhou 21
Belo Horizonte 20
Grafing 20
Nardò 20
Frankfurt am Main 19
Warsaw 19
Haikou 18
Houston 18
Rio de Janeiro 18
Curitiba 17
Hải Dương 16
Naples 16
Tashkent 16
Chengdu 15
Chicago 15
Fuzhou 15
London 15
Ningbo 15
Seoul 15
Turku 15
Baghdad 14
Brasília 14
Dong Ket 14
Fremont 14
Taizhou 14
Vienna 14
Atlanta 13
Biên Hòa 13
Guayaquil 13
Montreal 13
Boston 12
Chongqing 12
Denver 12
Kocaeli 12
Nuremberg 12
Quito 12
Auburn Hills 11
Bari 11
Hangzhou 11
Totale 11.485
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Nome #
5 OP Keratin 8 gene mutation in patients with chronic pancreatitis 352
Role of immunoglobulin G fragment C receptor polymorphism-mediatedantibody-dependant1. cellular cytotoxicity in colorectal cancer treated withcetuximab therapy. Pharmacogenomics J. 282
Oligonucleotide Ligation Assay (OLA) e mutazioni silenti del gene CFTR: una rara causa di parziale fallimento del test 204
Associations between two single nucleotide polymorphisms of the adiponectin gene, its circulating concentrations and cardiometabolic risk factors in prepubertal children with and without abdominal obesity. 196
Evidence fo Epigenetic Abnormalities of the Androgen Receptor Gene in Foreskin from Children with Hypospadias 191
Oligonucleotide Ligation Assay (OLA) e mutazioni silenti del gene CFTR: una rara causa di parziale fallimento del test 190
Alterations of type IV collagen alpha chains in patients with chronic acquired glomerulopathies: analogies with Alport’s syndrome 188
BRCA mutations, molecular markers, and clinical variables in early-onset breast cancer: A population-based study. 184
Analisi dello spettro mutazionale del gene NF1 mediate Protein Truncation Test (PTT) 182
Analysis of HLA-DR and –C in 141 multiple sclerosis patients from Emilia, Northern Italy 174
HLA-DRB4 as a genetic risk factor for Churg-Strauss syndrome 174
Chronic periaortitis and HLA–DRB1*03: Another clue to an autoimmune origin 170
Alterations of type IV collagen alpha chains in patients with chronic acquired glomerulopathies: mRNA levels, protein expression and urinary loss 167
Ruolo dei geni del collagene di tipo IV e dei loro prodotti proteici nelle glomerulopatie umane acquisite 157
Association of HLA-DRB1 *0401 Allele with chronic pancreatitis 157
A novel mutation of the NR0B1 (DAX-1)gene in a family with two monozygotic twin sisters and a congenital adrenal ipoplasia affected child 155
Fluorescent in situ hybridisation on tissue sections: a quantitative approach with confocal laser scanning microscopy 154
Association of keratin 8 gene mutation with chronic pancreatitis 153
Pili canaliculi: a familial study 150
Role of immunoglobulin G fragment C receptor polymorphism-mediated antibody-dependant cellular cytotoxicity in colorectal cancer treated with cetuximab therapy 149
Valutazione del gene COL4A5 e del suo prodotto proteico nelle nefropatie glomerulari acquisite 147
Influence of APOE status on lexical-semantic skills in Mild Cognitive Impairment 147
[Genetic markers in insulin-dependent juvenile diabetes]. 147
A breast cancer patient from Italy with germline mutations in both the BRCA1 and BRCA2 genes 147
PTPN22 R620W polymorphism in the ANCA-associated vasculitides. 144
IL-6, IGFBP-1, IGFBP-2 (mRNA and proteins) and IGF-II are significantly increased in the placenta and correlate with neonatal size in IUGR with altered placental doppler velocimetry 143
BRCA mutations, molecular markers, and clinical variables in early-onset breast cancer: A population-based study 143
Androgen receptor CAG repeats and gene methylation in children with premature pubarche 141
Aromatase is differentially expressed in peripheral blood leukocytes from children, and adult female and male subjects. 141
Correlazione fra HLA-DRB1*03 e periaortite cronica: una ipotesi di origine autoimmune 137
The new tumor suppressor gene inhibitor of growth family member 4 (ING4) regulates the production of pro-angiogenic molecules by myeloma cells and suppresses hypoxia inducible factor (HIF)-1{alpha} activity being involved in myeloma-induced angiogenesis. 137
Ruolo dei geni del collageno di tipo 4 nelle glomerulopatie acquisite 134
BRCA-1 status, molecular markers and clinical viariables in breast cancer (BC) patients with high probability of having an inherited cancer predisposing genetic mutation 132
BRCA1 and BRCA2 status in a sample of italian women with early onset breast cancer (EOBC) 132
Association beetween fetal Doppler velocimetry abnormalities and confined placental trisomy 22: a case report 132
Rapporti fra citochine infiammatorie e fattori di crescita: meccanismi noti ed ipotizzabili negli IUGR 131
Chronic periaortitis and HLA-DRB1*03: another clue to an autoimmune origin 131
Role of the 4A5 collagen gene and its product in human acquired glomerulopathies 131
Alport syndrome in Italy. A multicenter screening for COL4A5 gene mutations 131
Urinary excretion of brush-border antigen revealed by monoclonal antibody: early indicator of toxic nephropathy. 129
Street ME, Seghini P, Fieni S, Viveri MA, Viani I, Martorana D, Volta C, Neri T M, Granellini D, Bernasconi S 127
A breast cancer patient from Italy with germline mutations in both the BRCA1 and BRCA2 genes 127
BRCA1 and BRCA2 status in a sample of italian women with early onset breast cancer (EOBC) 127
Clinical, histopathological and biochemical findings in Fabry's disease. A case report 127
Studio delle triplette CAG e della metilazione del gene per il recettore degli androgeni in bambini prepuberi, donne e pazienti con pubarca prematuro 126
Riconoscimento in situ di RNA messaggeri umani specifici mediante microscopia confocale in fluorescenza 124
Crescita e disordini puberali nella Neurofibromatosi di tipo 1 123
CORRELAZIONE FRA HLA-DRB1*03 E PERIAORTITE CRONICA: UNA IPOTESI DI ORIGINE AUTOIMMUNE 122
Tipizzazione dei polimorfismi dei geni del locus HLA, delle citochine e dei loro recettori nella Fibrosi Retroperitoneale Idiopatica (FRI) 122
Febbre Mediterranea Familiare (FMF) e sindrome associata a mutazioni del recettore del TNF-alfa (TRAPS): nuove varianti e cross-talk fra i 2 geni 120
BRCA mutations, molecular markers, and clinical variables in early-onset breastcancer: a population-based study. 120
CORRELAZIONE FRA HLA-DRB1*03 E PERIAORTITE CRONICA: UNA IPOTESI DI ORIGINE AUTOIMMUNE 119
Modulazione della riespressione del gene FHIT in cellule di carcinoma polmonare 119
Molecular profile and clinical variables in BRCA1-positive breast cancers. A population-based study 119
Molecular profile and clinical variables in BRCA1-positive breast cancers. A population-based study 118
T-cell receptor beta-chain gene rearrangement and expression during human thymic ontogenesis. 118
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene. 118
Gastrointestinal stromal tumor and other primary metachronous or synchronous neoplasms as a suspicion criterion for syndromic setting 117
Diagnosi di maschio XX nel corso di screening di candidati alla fecondazione assistita mediante ICSI (Intracytoplasmatic Sperm Injection) 116
Comparison of human and porcine insulin therapies in children with newly diagnosed diabetes mellitus. 116
HLA-DRB1 e TNF, ma non CFTR, sono fattori di rischio per la colangite sclerosante 116
Interazioni tra IL-6 e sistema IGF/IGFBP nella placenta e nel siero cordonale di nati IUGR 116
Spectrum of F8 gene mutations in haemophilia A patients from a region of Italy: identification of 23 new mutations. 115
Immunoglobulin G Fragment C Receptor Polymorphisms and Clinical Efficacy of Trastuzumab-Based Therapy in Patients With HER-2/neu-Positive Metastatic Breast Cancer. 115
DUPLICAZIONE DELL DELL’ESONE 13 DEL GENE F8 NEI P ’ESONE PAZIENTI EMOFILICI CON AZIENTI FENO FENOTIPO LIEVE: TIPO LA CASISTICA DELLA REGIONE EMILIA ROMA ROMAGNA GNA 114
Characterization of a novel mutation in the F8 promoter region associated with mild hemophilia A and resistance to DDAVP therapy. 114
T-cell receptor beta-chain gene rearrangement and expression during human thymic ontogenesis. 113
Human T-cell receptor alpha chain gene during ontogeny 113
Serological and molecular study on the HLA phenotype of female breast cancer patients. 113
Mesangio-proliferative glomerulonephritis with prevalent deposits of IgA and histocompatibility antigens 113
Screening mutazionale nel gene BRCA1 in pazienti con tumori al seno e all’ovaio 113
Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome. 113
BRCA1 status. Molecular markers and clinical variables in breast cancer (BC) patients with high probability of having an inherited, cancer-predisposing genetic mutation 112
BRCA STATUS, MOLECULAR PROFILE AND CLINICAL VARIABLES IN PRIMARY BILATERAL BREAST CANCERS: A POPULATION-BASED CANCER REGISTRY STUDY 112
Genetica della Febbre Mediterranea Familiare in Italia 111
HLA ANTIGENS AND INSULIN DEPENDENT DIABETES MELLITUS. A FAMILY STUDY 111
Rapid and sensitive MLPA approach for identification of deletion carriers in haemophilia 111
Polimorfismi di restrizione del gene del recettore dell'insulina ed intolleranza al carico endovenoso di glucosio 110
Keratin 8 mutations in patients with chronic pancreatitis 109
Clinico-pathological and biomolecular findings in Italian patients with multiple cutaneous neurofibromas. 108
Interleukin-6 and Insulin-like growth factor system relationships and differences in the human placenta and fetus from the 35th week of gestation 108
Ulteriori nuove mutazioni sul gene COL4A5 mediante PCR e sequenziamento diretto 108
Sospetta eterogeneità genetica nella Febbre Mediterranea Familiare 106
Coagulation factor genes polymorphisms in primary sporadic focal segmental glomerulosclerosis 106
Polimorfismi dei geni delle citochine e dei loro recettori nella sindrome di Churg-Strauss 106
Meta-analysis of the impact of SPINK1 p.N34S gene variation in Caucasic patients with chronic pancreatitis. An update 105
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene. 105
La tecnica multiplex ligation probe amplification (MLPA) per la determinazione dello stato di portatrice in emofilia. 104
In reply 103
HLA antigens and IgA mesangial glomerulonephritis 103
Expression of TCR beta chain gene N-diversity is not an early event in human thymic ontogeny 102
Screeniong for B cell specific antisera. Results from region Italy 1 102
Familial vasculitides: Churg-Strauss syndrome and Wegener's granulomatosis in 2 first-degree relatives 102
Febbre Mediterranea Familiare (FMF) e sindrome associata a mutazioni del recettore del TNF-alfa (TRAPS): nuove varianti e cross-talk fra i 2 geni. 102
Fine specificity of the human T-cell response to the hepatitis B virus preS1 antigen. 102
Febbre Mediterranea Familiare e Sindrome Associata a mutazioni nel recettore TNF-alfa: nuove varianti ed interazioni fra i due geni 101
Ruolo dei polimorfismi dei geni dei fattori della coagulazione nella glomerulosclerosi focale e segmentaria 101
Fabry's Disease with Familial Lymphedema of the Lower Limbs. Case Report and Family Study 101
Premature pubarche as epiphenomenon of non-random androgen receptor gene methylation 100
T-cell receptor beta chain gene rearrangement and expression during human thymic ontogenesis. 99
Totale 13.229
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Categoria #
all - tutte 62.136
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 62.136
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021293 0 0 0 0 0 0 0 0 0 24 247 22
2021/2022798 9 6 12 29 21 25 106 154 32 69 83 252
2022/20232.770 338 264 175 178 250 317 20 144 958 13 88 25
2023/2024823 36 118 21 18 78 222 34 40 15 54 67 120
2024/20253.407 101 196 238 171 426 474 58 145 417 336 235 610
2025/20266.480 587 687 776 635 1.066 424 902 186 787 430 0 0
Totale 19.552