LO CURTO, FRANCESCO
 Distribuzione geografica
Continente #
EU - Europa 6.578
NA - Nord America 6.528
AS - Asia 1.260
SA - Sud America 23
Continente sconosciuto - Info sul continente non disponibili 16
OC - Oceania 3
Totale 14.408
Nazione #
US - Stati Uniti d'America 6.507
IT - Italia 3.678
UA - Ucraina 1.141
TR - Turchia 557
SE - Svezia 430
VN - Vietnam 337
CN - Cina 307
FI - Finlandia 305
IE - Irlanda 270
DE - Germania 225
GB - Regno Unito 216
FR - Francia 193
IN - India 40
PL - Polonia 35
BE - Belgio 26
EU - Europa 16
BR - Brasile 12
CA - Canada 9
MX - Messico 9
NL - Olanda 9
CH - Svizzera 8
ES - Italia 5
AL - Albania 4
AR - Argentina 4
BG - Bulgaria 4
CZ - Repubblica Ceca 4
IL - Israele 4
JP - Giappone 4
AT - Austria 3
AU - Australia 3
DK - Danimarca 3
VE - Venezuela 3
EE - Estonia 2
ID - Indonesia 2
IM - Isola di Man 2
LU - Lussemburgo 2
NO - Norvegia 2
OM - Oman 2
PA - Panama 2
RS - Serbia 2
SG - Singapore 2
SK - Slovacchia (Repubblica Slovacca) 2
AE - Emirati Arabi Uniti 1
BD - Bangladesh 1
BS - Bahamas 1
BY - Bielorussia 1
CL - Cile 1
CO - Colombia 1
EC - Ecuador 1
GR - Grecia 1
HU - Ungheria 1
LT - Lituania 1
MC - Monaco 1
MY - Malesia 1
PK - Pakistan 1
PY - Paraguay 1
RO - Romania 1
RU - Federazione Russa 1
TW - Taiwan 1
Totale 14.408
Città #
Milan 2.298
Chandler 957
Jacksonville 851
Fairfield 599
Woodbridge 368
Ashburn 334
Izmir 293
Princeton 284
Wilmington 282
Dearborn 280
Dublin 270
Houston 263
Ann Arbor 245
Seattle 240
Cambridge 232
Nyköping 229
Rome 200
Dong Ket 188
San Mateo 128
Como 123
Beijing 91
Redwood City 68
San Diego 64
Ogden 61
New York 57
Hefei 32
Nanjing 32
Verona 29
Kunming 28
Brussels 25
Helsinki 23
Radomsko 23
Philadelphia 22
London 19
Norwalk 19
Düsseldorf 17
Nanchang 15
Auburn Hills 14
Jinan 13
Pavia 13
Pune 13
Guangzhou 12
Phoenix 11
Ponte Lambro 11
Washington 11
Los Angeles 10
Catania 9
Piemonte 9
Bangalore 8
Edinburgh 8
Fuzhou 8
Palermo 7
Baotou 6
Boardman 6
Chengdu 6
Frankfurt am Main 6
Kocaeli 6
Quzhou 6
Shanghai 6
Zhengzhou 6
Bari 5
Bologna 5
Brescia 5
Genova 5
Hebei 5
Istanbul 5
Shenyang 5
Toronto 5
Warsaw 5
Amsterdam 4
Berlin 4
Cagliari 4
Dallas 4
Foggia 4
Islington 4
Naples 4
Padova 4
Pescara 4
Prague 4
Sofia 4
Tel Aviv 4
Turin 4
Ancona 3
Atlanta 3
Bergamo 3
Chiswick 3
Chongqing 3
Copenhagen 3
Estrela 3
Genzano Di Roma 3
Kilburn 3
Lissone 3
Mexico 3
Miami 3
Mountain View 3
Napoli 3
Saint Paul 3
Saronno 3
Sassari 3
Stockholm 3
Totale 9.645
Nome #
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia 283
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche 208
Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia 166
Cd bands and centromeric function in dicentric chromosomes 157
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR 155
OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas 155
Le basi genetiche della malattia linfoproliferativa. 151
A new chromosome instability disorder 151
First trimester prenatal diagnosis of Sanfilippo disease (MPS III) type B. 148
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms 148
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis 146
Karyotypic variation in benign pleomorphic adenoma of the parotid and in normal salivary glands. 144
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498) 143
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399) 141
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico 138
The mammary gland and the homeobox gene Otx1 137
Sindrome di Shwachman: isocromosoma i(7)(q10), rischio di MDS/AML ed effetto da dosaggio genico della mutazione c.258+2T→C associata al gene SBDS 137
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi 137
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells 134
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes 134
Chromosome identification in a Chinese hamster pseudodiploid cell line (CHEF-125) 132
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies 132
Nuclear projections in tumour cells 131
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies 130
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning 129
The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome. 128
Chronic Myeloid Leukemia: Molecular Monitoring of Residual Disease by Genomic DNA Compared to Conventional mRNA Analysis in Follow-Ups up to 8 Years 127
Assessing residual disease in imatinib-treated CML patients by DNA compared to MRNA assays 126
Presumptive mosaic origin of an XX/XY female with ambiguous genitalia. 126
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies. 126
The syndrome of partial trisomy 14q. 125
Normal insulin receptors in mitochondrial myopathies with ophthalmoplegia. 125
48,XXXY/49,XXXXY Mosaicism in a month old infant. 122
Studio molecolare del differenziamento da cellule staminali in condrociti in vivo per lo sviluppo di un protocollo di trapianti di cartilagine umana 122
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia 122
Citogenetica Umana: nuove metodiche ed applicazioni in medicina. 121
Indirect immunofluorescence of inactive centromeres as indicator of centromeric function. 121
The role of Yp in sex determination: new evidence from X/Y translocations. 120
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects 118
Le basi genetiche della malattia linfoproliferativa legata al cromosoma X 117
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari 117
Growth Hormone and Estrogens in Patients with Turner Syndrome: in vivo and in vitro studies. 116
Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7. 115
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR 113
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399) 112
Different real time PCR approaches for the fine quantification of SNP's alleles in DNA pools: assays development, characterization and pre-validation. 112
Erratum: OTX1 expression in breast cancer is regulated by p53 (Oncogene (2011) 30 (3096-3103) doi:10.1038/onc.2011.31) 108
Microhomologiee and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia. 107
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa 106
Studio molecolare del differenziamento da cellule staminali in condrociti e osteoblasti in vivo per lo sviluppo di protocolli di trapianto 106
Acquired Chromosome change in Cholesteatoma 105
Myotonic Dystrophy: genetic aspects ; cytochemical findings. 105
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH 105
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare 104
Molecular monitoring of residual disease in chronic myeloid leukemia by genomic DNA compared with conventional mRNA analysis. 104
Anticentromeric antibodies and inactive centromeres. 103
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6 102
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients 102
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome 101
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età 101
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard 100
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula 100
La linea cellulare EUE deriva da una linea HeLa. 99
A woman carrier of two apparently unrelated reciprocal translocations: prenatal diagnosis of normal karyotype in the foetus. 98
Protrusioni nucleari dovute a cromosomi strutturalmente alterati. 98
Danno cromosomico e trattamento della psoriasi. 97
Criobanca automatizzata di materiale biologico: stoccaggio e monitoraggio molecolare di cellule meniscali per il trapianto autologo 97
Distrofia miotonica: genetica e citochimica 96
Chromosomal analysis in cultured lymphocytes and fibroblasts of psoriatic patients before and after treatment. 95
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6 95
Studio dei fibroblasti "in vitro" nella distrofia miotonica. 94
Chromosome identification and karyotypic evolution in a human melanoma cell line. 94
Chromosome size and nuclear projections 94
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells 94
Variabilità cromosomica in linee cellulari derivate da melanomi. 93
Leucemia linfoblastica acuta e traslocazione familiare (15-15) che coinvolge ETV6 93
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge. 93
A liveborn 69,XXX triploid. Origin, X chromosome activity and gene dosage. 92
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George 92
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients 92
Familial partial monosomy 7 and myelodysplasia: different paternal origin of the monosomy 7 suggests action of a mutator gene 91
Correlation between the numbers of sex chromosomes and the H-Y antigen titer. 90
Insulin receptors in psoriasis. 90
Nuclear projections and latent centromeres in primary culture and established cell lines. 90
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale 90
Differente reazione dei centromeri inattivi agli anticorpi anticentromero. 89
Analysis of cross-contamination in established tumour cell lines. 89
Involvement of dendritic cells in juvenile chronic myelomonocytic leukaemia shown by FISH on interphase nuclei 89
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore 89
Insulin receptors in psoriasis. 88
I recettori insulinici nella distrofia miotonica: studio su fibroblasti in coltura. 88
Presenza di anomalie cromosomiche nelle cellule epiteliali della matrice del colesteatoma: studio citogenetico. 88
Nuclear projections and latent centromeres in primary cultures and established cell lines. 88
Diagnostica cromosomica 87
The origin and phenotype of X0 males 86
Insulin receptors in Friedreich's ataxia: studies on cultured fibroblasts. 86
Le basi genetiche della malattia linfoproliferativa legata al cromosoma X 86
Different reaction of inactive centromeres to anticentromeric antibodies. 85
X0 and male phenotype 85
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico. 85
Totale 11.422
Categoria #
all - tutte 39.934
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 39.934


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019717 0 0 0 0 0 0 0 0 0 77 211 429
2019/20202.257 76 72 66 342 80 248 408 324 107 229 44 261
2020/20211.983 22 188 44 191 122 280 64 179 329 63 169 332
2021/20221.265 104 177 137 76 38 26 44 77 70 194 98 224
2022/20232.356 186 143 200 279 156 472 2 336 322 90 101 69
2023/20243.462 594 611 591 636 630 189 23 74 94 20 0 0
Totale 14.451