IRIS - Res&Arch Institutional Research Information System - Research & Archive

DONTI, Emilio
 Distribuzione geografica
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Continente #
NA - Nord America 4.741
EU - Europa 3.852
AS - Asia 3.037
SA - Sud America 469
AF - Africa 61
Continente sconosciuto - Info sul continente non disponibili 8
OC - Oceania 8
Totale 12.176
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Nazione #
US - Stati Uniti d'America 4.659
SG - Singapore 1.309
UA - Ucraina 973
SE - Svezia 577
RU - Federazione Russa 570
IE - Irlanda 565
CN - Cina 432
HK - Hong Kong 408
BR - Brasile 354
VN - Vietnam 352
DE - Germania 260
IT - Italia 228
KR - Corea 212
FI - Finlandia 210
FR - Francia 194
GB - Regno Unito 90
IN - India 53
CA - Canada 42
BD - Bangladesh 39
TR - Turchia 39
PL - Polonia 35
AR - Argentina 34
IQ - Iraq 28
AT - Austria 27
CH - Svizzera 27
MX - Messico 21
UZ - Uzbekistan 21
ZA - Sudafrica 21
JP - Giappone 20
CO - Colombia 18
ID - Indonesia 17
PK - Pakistan 17
BE - Belgio 16
SA - Arabia Saudita 16
CL - Cile 15
VE - Venezuela 15
RO - Romania 13
PH - Filippine 12
ES - Italia 11
LB - Libano 11
NL - Olanda 11
EC - Ecuador 10
PY - Paraguay 10
CZ - Repubblica Ceca 9
GR - Grecia 9
EU - Europa 8
LT - Lituania 8
KE - Kenya 7
MA - Marocco 7
MY - Malesia 7
PE - Perù 7
JM - Giamaica 6
PS - Palestinian Territory 6
TN - Tunisia 6
BY - Bielorussia 5
NZ - Nuova Zelanda 5
AE - Emirati Arabi Uniti 4
DZ - Algeria 4
EG - Egitto 4
IL - Israele 4
JO - Giordania 4
KZ - Kazakistan 4
NP - Nepal 4
OM - Oman 4
UY - Uruguay 4
AU - Australia 3
BG - Bulgaria 3
CR - Costa Rica 3
KG - Kirghizistan 3
NG - Nigeria 3
AM - Armenia 2
AZ - Azerbaigian 2
BB - Barbados 2
BH - Bahrain 2
ET - Etiopia 2
NI - Nicaragua 2
RS - Serbia 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
TT - Trinidad e Tobago 2
AD - Andorra 1
AL - Albania 1
BA - Bosnia-Erzegovina 1
BJ - Benin 1
BN - Brunei Darussalam 1
BO - Bolivia 1
BW - Botswana 1
CI - Costa d'Avorio 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
GA - Gabon 1
GT - Guatemala 1
GY - Guiana 1
HN - Honduras 1
HU - Ungheria 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
LY - Libia 1
MK - Macedonia 1
PA - Panama 1
Totale 12.173
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Città #
Singapore 860
Chandler 749
Dublin 563
Jacksonville 533
Hong Kong 407
San Mateo 332
Boardman 281
San Jose 255
Dong Ket 227
Seoul 212
Ashburn 178
Santa Clara 171
Moscow 158
Medford 154
Princeton 153
Lauterbourg 127
Andover 121
Wilmington 121
Beijing 103
Ann Arbor 102
Piscataway 94
Los Angeles 62
Saint Petersburg 61
Altamura 56
The Dalles 53
Munich 49
New York 47
Perugia 47
Ho Chi Minh City 45
Lawrence 43
São Paulo 37
Des Moines 33
Helsinki 32
Hanoi 25
Norwalk 25
Turku 24
Auburn Hills 21
Woodbridge 21
Falls Church 20
Izmir 19
Frankfurt am Main 17
Nuremberg 17
Tokyo 17
Brussels 16
Orem 16
Shanghai 15
Warsaw 15
London 14
Stockholm 14
Denver 13
San Paolo di Civitate 13
Boston 12
Montreal 12
Chennai 11
Houston 11
Brooklyn 10
Johannesburg 10
Licata 10
Poplar 10
Santiago 10
Tashkent 10
Vienna 10
Baghdad 9
Belo Horizonte 9
Jeddah 9
Redwood City 9
Seattle 9
Chicago 8
Dallas 8
Rio de Janeiro 8
Toronto 8
Buenos Aires 7
Curitiba 7
Dearborn 7
Guangzhou 7
Lahore 7
Nanjing 7
Secaucus 7
Venice 7
Brasília 6
Caracas 6
Changsha 6
Frankfurt Am Main 6
Fremont 6
Istanbul 6
Lima 6
Medellín 6
Mexico City 6
Nairobi 6
Ottawa 6
Phoenix 6
Piediluco 6
Quito 6
Ribeirão Preto 6
Roubaix 6
Tianjin 6
Timisoara 6
Asunción 5
Charlotte 5
Columbus 5
Totale 7.160
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Nome #
2q31.22q32.3 deletion syndrome: report of an adult patient 179
Comparative proteomic analysis of two distinct stem-cell populations from human amniotic fluid 155
ISOLAMENTO E CARATTERIZZAZIONE MOLECOLARE DI CELLULE STAMINALI MESENCHIMALI UMANE DA LIQUIDO AMNIOTICO 150
Occurrence of the same chromosome abnormalities in Ph+ and Ph- cells in chronic myeloid leukaemia. Evidence of a secondary origin of the Ph chromosome? 143
Adattamento alla crescita in vitro di cellule del Tumore ascite ATPC+. 137
Valutazione anatomo-patologica dell’unità feto-placentare nella morte prenatale. 133
Cleft palate and ADULT phenotype in a patient with a novel TP63 mutation suggests lumping of EEC/LM/ADULT syndromes into a unique entity: ELA syndrome. 130
Acute leukemia complicating Waldenstrom's macro¬globulinemia 127
Prenatal Diagnosis in Italy. 124
Centralized cytogenetic analysis of pediatric acute leucemia: results of an Italian collaborative experience. 123
5q- syndrome termi¬nating in acute myeloid leukemia: karyotype evolution and immunological characterization of blast cells. 123
5q- syndrome in a patient with chronic exposure to ionizing radiation. 121
A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy. 121
Acrofrontofacionasal dysostosis 1 in two sisters of Indian origin. 120
Acute Promyelocytic leukemia: from genetics to treatment. 118
Acute Promyelocytic Leukemia: from genetics to treatment. 117
5q- anomaly in a patient with erythroleukemia (M6 FAB classi¬fication) 116
A case of acute myeloid leukemia with deletion of chromosome 7 following PBSC transplantation. 115
A case of complete testicular feminization and 47, XXY karyotype 114
A new human highly tumorigenic neuroblastoma cell line with undetectable expression of N-myc. 107
5q- in a case of blastic phase of chronic myeloid leukemia. 107
Complex chromosome translocations of standard t(8;21) and t(15;17) arise from a two-step mechanism as evidenced by fluorescence in situ hybridization analysis. 106
Deletion 2p15-16.1 syndrome: Case Report and Review 105
Response to low-dose ARA-C + IFN alpha in advanced and second chronic phase chronic myeloid leukemia 104
Acute myeloblastic leukemia after adjuvant chemo¬therapy with melphalan in breast cancer. Case report with cytogenetic analysis. 104
Adattamento alla crescita in vitro di cellule del tumore ascite ATPC+ 103
Aspetti endocrinologici di un caso di sindrome da femminilizzazione testicolare 103
Effects of steroids on human normal and otosclerotic osteoblastic cells: influence on thymidine and leucine uptake and incorporation. 103
Aspetti del citoscheletro di cellule in coltura di osso umano normale ed otosclerotico 102
L'interferone alfa nella leucemia mieloide cronica 101
Isolamento di cellule staminali pluripotenti da liquido amniotico e loro uso nel trattamento o nella prevenzione di malattie autoimmuni 101
Heterozygous X-linked adrenoleukodystrophy-associated myelopathy mimicking primary progressive multiple sclerosis 100
Complex translocations of the Ph chromosome and Ph-negative CML arise from similar mechanisms as evidenced by FISH analysis. 100
A novel spinocerebellar ataxia type 15 family with involuntary movements and cognitive decline 99
A new case of familial paracentric inversion of chromosome 2. 97
MASA syndrome: ultrasonographic evidence in a male fetus. 95
Recurrent ∼100 Kb microdeletion in the chromosomal region 14q11.2, involving CHD8 gene, is associated with autism and macrocephaly. 95
Aicardi Syndrome Associated with Autosomal Genomic Imbalance: Coincidence or Evidence for Autosomal Inheritance with Sex-Limited Expression? 95
A novel mutation in the SDHD gene responsible for familial paraganglioma. Medical and psychological implications. 94
Characterization of the cytoskeleton in human normal and otosclerotic osteoblast-like cells. 92
Hormonal receptor site alterations in the ethio-patogenesis of otosclerosis. 91
Shapiro's syndrome: Defining the clinical spectrum of the spontaneous paroxysmal hypothermia syndrome. 91
Coinvolgimento del cromosoma 1 nella mielofibrosi e nelle mielodisplasie. 90
Pluripotent stem cells from human amniotic fluid and their immunomodulatory properties 90
Interferon Alpha-2b as therapy for Ph'-positive chronic myelogenous leukemia. A study of 82 patients treated with intermittent administration. 89
Cytoskeletal characteristics and functional response to PHT stimulation in human normal and otosclerotic bone cell cultures 89
Pluripotent Stem Cells from Human Amniotic Fluid and their Immunomodulatory Properties 89
Mapping of chromosome 17 breakpoint in acute myeloid leukemias 88
Etiopathogenesis of otosclerosis: cell biology studies. 88
Interferon-alpha-2b as therapy for untreated and pretreated patients with Ph' positive chronic myeloid leukemia 88
Piccolo cromosoma metacentrico a mosaico in un bambino con trisomia 21 primaria (47,XY,+21/ 48,XY,+21,+mar). 87
ANALYSIS OF ONCOGENE TRANSLOCATIONS BY IN SITU HYBRIDIZATION ON CHROMOSOME PREPARATIONS. 87
Nablus mask-like facial syndrome: deletion of chromosome 8q22.1 is necessary but not sufficient to cause the phenotype. 87
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure. 87
Structural and functional organization of the HF.10 human zinc finger gene (ZNF35) located on chromosome 3p21-p22. 86
Le cellule RA (rapidly adhering) nel liquido amniotico di feti anencefali. 86
Genetica Medica 85
Effects of steroids on human normal and otosclerotic osteoblastic cells: influence on thymidine and leucine uptake and incorporation. 85
Immunoregulatory effects of fast human amniotic stem cells on experimental type 1 diabetes 85
FMR1, FMR2, and SLITRK2 deletion inside a paracentric inversion involving bands Xq27.3-q28 in a male and his mother. 84
Sustained molecular remissions are achievable with tyrosine kinase inhibitor therapy in patients with chronic myeloid leukemia and additional cytogenetic clonal evolution 84
Familial pericentric inversion of chromosome 18: intrafamilial variability of the recombinant dup(18q). 84
Brief Report: Functional MRI of a Patient with 7q11.23 Duplication Syndrome and Autism Spectrum Disorder. 84
Loss of amplification and appearance of a novel translocation site of the c-myc oncogene in HL-60 leukemia cells. 83
Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: cooperative study of 19 Italian laboratories. 82
L'interferone α-2b nel trattamento della leucemia mieloide cronica Ph' positiva. 81
DHT-receptor in cultured human fibroblasts: binding study in a family with androgen insensitivity (complete testicular feminization) 81
Localization of the human HF.2 finger gene on the band 1p34p35 deleted in neuroblastoma tumor. 80
Human bone cell cultures: a new model for studying the mechanism of action of calcitonin. 79
Craniometaphyseal dysplasia with severe craniofacial involvement shows homozygosity at 6q21-22.1 locus. 79
Prenatal diagnosis and molecular characterization of an interstitial 1q24.3-31.3 deletion: case report and review. 78
Trisomy 6p22pter due to familial t(6;13)(p22;q34 or 33) translocation 77
Pluripotent stem cells from human amniotic fluidand their immunomodulatory properties 77
In vitro bone-marrow cell cultures and cytogenetic analysis in a case of myelodysplasia. 76
Etude d'un sujet avec caryotype 46, XY,22p+. 76
The translocation breakpoint of acute promyelocytic leukemia lies within the retonoic acid receptor alpha locus. 76
Blood cell mitochondrial DNA content and premature ovarian aging 76
L'interferone nel trattamento della leucemia mieloide cronica Philadelphia positiva. 75
Glycosaminoglycan metabolism and cytokine release in normal and otosclerotic human bone cells. Interleukin-1 treated. 75
Hot water epilepsy and Mccune-Albright syndrome: a case report. 75
Trisomy 2 mosaicism with caudal dysgenesis, Hirschsprung disease, and micro-anophthalmia. 75
Morphological and functional characteristics of human temporal bone cell cultures. 74
Chromosomal localization of four human zinc finger cDNAs. 73
Studio della fragilità cromosomica in linfociti di pazienti con carcinoma mammario 73
DHT-receptor in cultured human fibroblasts: binding study in a family with androgen insensitivity (complete testicular feminisation). 73
X-ring Turner's syndrome with combined immunodeficiency and selective gonadotropin defect. 72
Aspetti morfofunzionali di colture cellulari di tessuto osseo normale e otosclerotico. 72
Trisomy 4 in acute nonlymphocytic leukemia: Report of two cases and review of the literature. 72
Chromosome abnormalities in PHA- stimulated and non-stimulated bone marrow coltures from patients with non-Hodgkin lymphoma. 72
An intermediate phenotype between Hay-Wells and Rapp-Hodgkin syndromes in a patient with a novel P63 mutation: confirmation of a variable phenotypic spectrum with a common aetiology. 72
Trisomy 15 mosaicism owing to familial reciprocaltranslocation t(1;15): implication for prenatal diagnosis 72
t(4;21)(p16;q22) in blastic crisis of a chronic myeloid leukemia with variant Phila¬delphia translocation. 71
De novo balanced chromosome rearrangements in prenatal diagnosis. 70
Neonatal mucolipidosis II (I-cell disease): Clinical, radiological and biochemical studies in a case. 69
THE ITALIAN CO-OPERATIVE STUDY GROUP ON CHRONIC MYELOID LEUKEMIA. A prospective study of alfa-interferon and autologous bene marrow transplantation in chronic myeloid leukaemia. 69
cDNA isolation, expression analysis and chromosomal localization of two human zinc finger genes. 69
Studio citogenetico dei linfomi B-cellulari. 68
Evolving modalities of treatment with Interferon alfa-2b for Ph'-positive chronic myelogenous leukaemia. 67
Tratment of Ph' positive chronic myelogenous leukemia (Ph'+CML) with Interferon α-2b (INF α-2b). Results with intermittent and daily administration in 82 patients. 66
Cytogenetic and molecular study on two human neuroblastoma cell cultures. 66
Totale 9.324
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Categoria #
all - tutte 52.314
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 52.314
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021252 0 0 0 0 0 0 0 0 0 0 0 252
2021/20221.305 27 201 88 100 41 14 7 461 14 35 144 173
2022/20232.051 160 218 13 198 207 254 3 109 780 3 84 22
2023/2024822 55 113 42 20 17 3 176 7 130 7 110 142
2024/20251.753 21 246 58 61 198 69 44 155 422 114 224 141
2025/20263.319 278 313 151 539 371 303 500 162 379 245 62 16
Totale 12.408