IRIS
NERI, Tauro Maria
 Distribuzione geografica
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Continente #
EU - Europa 3771
NA - Nord America 3666
AS - Asia 1504
Continente sconosciuto - Info sul continente non disponibili 6
AF - Africa 1
Totale 8948
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Nazione #
US - Stati Uniti d'America 3568
CN - Cina 1310
IE - Irlanda 897
SE - Svezia 690
UA - Ucraina 672
FI - Finlandia 580
DE - Germania 417
IT - Italia 287
TR - Turchia 137
CA - Canada 98
GB - Regno Unito 88
AT - Austria 46
BE - Belgio 43
IN - India 26
NL - Olanda 21
VN - Vietnam 14
FR - Francia 11
KR - Corea 7
EU - Europa 6
JP - Giappone 5
IR - Iran 3
LT - Lituania 3
LU - Lussemburgo 3
RO - Romania 2
SI - Slovenia 2
CM - Camerun 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
ES - Italia 1
GR - Grecia 1
HR - Croazia 1
IL - Israele 1
MD - Moldavia 1
MK - Macedonia 1
PL - Polonia 1
PT - Portogallo 1
SG - Singapore 1
Totale 8948
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Città #
Dublin 897
Jacksonville 800
Chandler 673
Dearborn 448
Beijing 355
Nanjing 225
San Mateo 176
Princeton 174
Ann Arbor 150
Izmir 125
Wilmington 105
Toronto 93
Shenyang 85
Boardman 84
Nanchang 74
Kunming 68
Helsinki 67
Jinan 63
Hebei 52
Hefei 52
Jiaxing 49
Des Moines 39
Bremen 36
Parma 34
Vienna 34
Brussels 33
Woodbridge 31
Changsha 30
Tianjin 30
Norwalk 23
Guangzhou 22
Grafing 20
Haikou 18
Los Angeles 17
Zhengzhou 17
Chengdu 15
Ningbo 15
Dong Ket 14
Fremont 14
Rome 14
Taizhou 14
Fuzhou 12
Kocaeli 12
Auburn Hills 11
Leawood 11
Milan 11
Monmouth Junction 11
Hangzhou 10
Chongqing 9
Waanrode 9
Ashburn 8
Houston 8
Napoli 8
Rockville 8
Taiyuan 8
Seattle 7
Augusta 6
Falls Church 6
Shaoxing 6
Wellesley 6
Wenzhou 6
Rio Saliceto 5
Seongnam 5
Wuhan 5
Ardea 4
Baotou 4
Borås 4
Genova 4
Mestre 4
Mumbai 4
Quzhou 4
Aversa 3
Düsseldorf 3
Florence 3
Huizen 3
Lanzhou 3
Luxembourg 3
Mountain View 3
Pavia 3
Regensburg 3
Vilnius 3
Abbiategrasso 2
Andretta 2
Ardabil 2
Bacoli 2
Bastiglia 2
Bologna 2
Chaoyang 2
Cutrofiano 2
Edinburgh 2
Fairfield 2
Focsani 2
Jinhua 2
Nanning 2
Nantong 2
Perugia 2
Ponte A Moriano 2
Rottofreno 2
San Giorgio Ionico 2
Sassuolo 2
Totale 5569
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Nome #
Role of immunoglobulin G fragment C receptor polymorphism-mediatedantibody-dependant1. cellular cytotoxicity in colorectal cancer treated withcetuximab therapy. Pharmacogenomics J. 131
Analisi dello spettro mutazionale del gene NF1 mediate Protein Truncation Test (PTT) 112
Evidence fo Epigenetic Abnormalities of the Androgen Receptor Gene in Foreskin from Children with Hypospadias 111
Oligonucleotide Ligation Assay (OLA) e mutazioni silenti del gene CFTR: una rara causa di parziale fallimento del test 109
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. 98
Analysis of HLA-DR and –C in 141 multiple sclerosis patients from Emilia, Northern Italy 87
5 OP Keratin 8 gene mutation in patients with chronic pancreatitis 80
Urinary excretion of brush-border antigen revealed by monoclonal antibody: early indicator of toxic nephropathy. 75
BRCA mutations, molecular markers, and clinical variables in early-onset breast cancer: A population-based study. 73
Influence of APOE status on lexical-semantic skills in Mild Cognitive Impairment 72
HLA-DRB4 as a genetic risk factor for Churg-Strauss syndrome 72
Alterations of type IV collagen alpha chains in patients with chronic acquired glomerulopathies: analogies with Alport’s syndrome 72
Rapporti fra citochine infiammatorie e fattori di crescita: meccanismi noti ed ipotizzabili negli IUGR 71
Fluorescent in situ hybridisation on tissue sections: a quantitative approach with confocal laser scanning microscopy 71
Diagnosi di maschio XX nel corso di screening di candidati alla fecondazione assistita mediante ICSI (Intracytoplasmatic Sperm Injection) 71
Street ME, Seghini P, Fieni S, Viveri MA, Viani I, Martorana D, Volta C, Neri T M, Granellini D, Bernasconi S 70
Ruolo dei geni del collagene di tipo IV e dei loro prodotti proteici nelle glomerulopatie umane acquisite 70
Febbre Mediterranea Familiare (FMF) e sindrome associata a mutazioni del recettore del TNF-alfa (TRAPS): nuove varianti e cross-talk fra i 2 geni 69
BRCA-1 status, molecular markers and clinical viariables in breast cancer (BC) patients with high probability of having an inherited cancer predisposing genetic mutation 69
Alterations of type IV collagen alpha chains in patients with chronic acquired glomerulopathies: mRNA levels, protein expression and urinary loss 68
Association of keratin 8 gene mutation with chronic pancreatitis 67
Screening mutazionale nel gene BRCA1 in pazienti con tumori al seno e all’ovaio 67
Polimorfismi dei geni delle citochine e dei loro recettori nella sindrome di Churg-Strauss 65
Correlazione fra HLA-DRB1*03 e periaortite cronica: una ipotesi di origine autoimmune 65
Association of HLA-DRB1 *0401 Allele with chronic pancreatitis 65
PTPN22 R620W polymorphism in the ANCA-associated vasculitides. 65
Oligonucleotide Ligation Assay (OLA) e mutazioni silenti del gene CFTR: una rara causa di parziale fallimento del test 64
Valutazione del gene COL4A5 e del suo prodotto proteico nelle nefropatie glomerulari acquisite 64
BRCA1 and BRCA2 status in a sample of italian women with early onset breast cancer (EOBC) 64
Interazioni tra IL-6 e sistema IGF/IGFBP nella placenta e nel siero cordonale di nati IUGR 64
Clinico-pathological and biomolecular findings in Italian patients with multiple cutaneous neurofibromas. 63
Molecular profile and clinical variables in BRCA1-positive breast cancers. A population-based study 63
Tipizzazione dei polimorfismi dei geni del locus HLA, delle citochine e dei loro recettori nella Fibrosi Retroperitoneale Idiopatica (FRI) 63
Chronic periaortitis and HLA-DRB1*03: another clue to an autoimmune origin 62
Studio delle triplette CAG e della metilazione del gene per il recettore degli androgeni in bambini prepuberi, donne e pazienti con pubarca prematuro 62
Pili canaliculi: a familial study 62
Characterization of a novel mutation in the F8 promoter region associated with mild hemophilia A and resistance to DDAVP therapy. 61
A novel mutation of the NR0B1 (DAX-1)gene in a family with two monozygotic twin sisters and a congenital adrenal ipoplasia affected child 61
BRCA1 and BRCA2 status in a sample of italian women with early onset breast cancer (EOBC) 60
Serological and molecular study on the HLA phenotype of female breast cancer patients. 60
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 60
Aromatase is differentially expressed in peripheral blood leukocytes from children, and adult female and male subjects. 60
Keratin 8 mutations in patients with chronic pancreatitis 59
Androgen receptor CAG repeats and gene methylation in children with premature pubarche 59
Modulazione della riespressione del gene FHIT in cellule di carcinoma polmonare 59
Human T-cell receptor alpha chain gene during ontogeny 59
Chronic periaortitis and HLA–DRB1*03: Another clue to an autoimmune origin 59
Malattia di Fabry e linfedema familiare. Descrizione di due casi 58
Crescita e disordini puberali nella Neurofibromatosi di tipo 1 57
Riconoscimento in situ di RNA messaggeri umani specifici mediante microscopia confocale in fluorescenza 57
T-cell receptor beta-chain gene rearrangement and expression during human thymic ontogenesis. 57
T-cell receptor beta-chain gene rearrangement and expression during human thymic ontogenesis. 57
Alport syndrome in Italy. A multicenter screening for COL4A5 gene mutations 57
Mesangio-proliferative glomerulonephritis with prevalent deposits of IgA and histocompatibility antigens 56
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 56
A breast cancer patient from Italy with germline mutations in both the BRCA1 and BRCA2 genes 56
Novel association of HLA-haplotypes with primary sclerosing cholangitis (PSC) in a southern European population 56
Febbre Mediterranea Familiare e Sindrome Associata a mutazioni nel recettore TNF-alfa: nuove varianti ed interazioni fra i due geni 55
Interleukin-6 and Insulin-like growth factor system relationships and differences in the human placenta and fetus from the 35th week of gestation 55
Expression of TCR beta chain gene N-diversity is not an early event in human thymic ontogeny 55
Ruolo dei geni del collageno di tipo 4 nelle glomerulopatie acquisite 55
Clinical, histopathological and biochemical findings in Fabry's disease. A case report 55
Fabry's Disease with Familial Lymphedema of the Lower Limbs. Case Report and Family Study 55
Premature pubarche as epiphenomenon of non-random androgen receptor gene methylation 54
Genetica della Febbre Mediterranea Familiare in Italia 54
CORRELAZIONE FRA HLA-DRB1*03 E PERIAORTITE CRONICA: UNA IPOTESI DI ORIGINE AUTOIMMUNE 54
Studio del numero delle triplette CAG e della metilazione del gene per il recettore degli androgeni in bambine prepuberi, donne e pazienti con pubarca prematuro 54
HLA ANTIGENS AND INSULIN DEPENDENT DIABETES MELLITUS. A FAMILY STUDY 54
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene. 54
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene. 54
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. 53
BRCA mutations, molecular markers, and clinical variables in early-onset breast cancer: A population-based study 53
Identification of anchovy (Engraulis encrasicholus L.) and gilt sardine (Sardinella aurita) by polymerase chain reaction, sequence of their mitochondrial cytochrome b gene, and restriction analysis of polymerase chain reaction products in semipreserves 52
HLA-DR antigens and cardiolipin antibodies in northen Italian systemic erythematosus patients. 52
Sospetta eterogeneità genetica nella Febbre Mediterranea Familiare 52
[Genetic markers in insulin-dependent juvenile diabetes]. 52
Febbre Mediterranea Familiare (FMF) e sindrome associata a mutazioni del recettore del TNF-alfa (TRAPS): nuove varianti e cross-talk fra i 2 geni. 52
Inversione dell’introne 1 nel gene del fattore VIII della coagulazione 51
Different expression of BRCA1 status and clinical variables in a sample of Italian women with early onset breast cancer (EOBC) 51
BRCA1 status. Molecular markers and clinical variables in breast cancer (BC) patients with high probability of having an inherited, cancer-predisposing genetic mutation 51
Coagulation factor genes polymorphisms in primary sporadic focal segmental glomerulosclerosis 50
La tecnica multiplex ligation probe amplification (MLPA) per la determinazione dello stato di portatrice in emofilia. 50
Role of the 4A5 collagen gene and its product in human acquired glomerulopathies 50
Ulteriori nuove mutazioni sul gene COL4A5 mediante PCR e sequenziamento diretto 50
L'ANALISI MUTAZIONALE DEL GENE COL4A5 MEDIANTE SEQUENZIAMENTO DIRETTO RENDE POSSIBILE LA DIAGNOSI NELLA QUASI TOTALITA'DEI CASI 50
L’analisi mutazionale del gene COL4A5 mediante sequenziamento diretto rende possibile la diagnosi nella quasi totalità dei casi 49
BRCA mutations, molecular markers, and clinical variables in early-onset breastcancer: a population-based study. 49
Gastrointestinal stromal tumor and other primary metachronous or synchronous neoplasms as a suspicion criterion for syndromic setting 49
Male breast cancer (MBC) in Parma province: descriptive epidemiology, molecular markers and clinical variables. 49
TAP genes, coding for the transporters associated with antigen processing, contribute to the genetic predisposition to primary sclerosing cholangitis (PSC) 49
The contribution of MHC region genes in the genetic predisposition to primary sclerosing cholangitis (PSC) 49
Immunoglobulin G Fragment C Receptor Polymorphisms and Clinical Efficacy of Trastuzumab-Based Therapy in Patients With HER-2/neu-Positive Metastatic Breast Cancer. 49
Selective sensitization of peripheral blood T lymphocytes to hepatitis B core antigen in patients with chronic active hepatitis type B. 49
HLA-DRB1*04 Allele contribute to the genetic susceptibility of chronic pancreatitis 48
Spectrum of F8 gene mutations in haemophilia A patients from a region of Italy: identification of 23 new mutations. 48
Cavallini G. Keratin 8 mutations in patients with chronic pancreatitis 47
Sospetta eterogeneità genetica nella Febbre Mediterranea Familiare 47
Screening del gene COL4A5 mediante sequenziamento diretto in pazienti affetti da sindrome di Alport 47
Familial giant cell arteritis and polymyalgia rheumatica: aggregation in 2 families 47
Diagnosi di mutazioni ignote nella Neurofibromatosi 2 su proteine ricombinanti prodotte in vitro 47
Totale 6100
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Categoria #
all - tutte 17341
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 17341
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/201827 0000 00 00 001710
2018/2019535 2018228 27124 1114 562018530
2019/20202593 38344517655 230300 33947 18021749172
2020/20211264 1617411811 16713 13717 3182424722
2021/2022798 961229 2125 106154 326983252
2022/20232902 338264175178 250317 35153 109921720
Totale 8974