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

DONTI, Emilio
 Distribuzione geografica
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Continente #
NA - Nord America 4.258
EU - Europa 3.501
AS - Asia 2.424
SA - Sud America 368
AF - Africa 22
Continente sconosciuto - Info sul continente non disponibili 8
OC - Oceania 7
Totale 10.588
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Nazione #
US - Stati Uniti d'America 4.204
SG - Singapore 994
UA - Ucraina 968
SE - Svezia 576
IE - Irlanda 563
RU - Federazione Russa 420
HK - Hong Kong 401
CN - Cina 362
VN - Vietnam 314
BR - Brasile 308
DE - Germania 246
KR - Corea 212
FI - Finlandia 208
IT - Italia 208
GB - Regno Unito 79
FR - Francia 60
PL - Polonia 33
CA - Canada 32
AT - Austria 27
CH - Svizzera 27
TR - Turchia 24
AR - Argentina 16
BE - Belgio 16
UZ - Uzbekistan 16
JP - Giappone 15
IN - India 13
MX - Messico 13
RO - Romania 13
BD - Bangladesh 11
ES - Italia 10
IQ - Iraq 10
CL - Cile 9
CZ - Repubblica Ceca 9
GR - Grecia 9
LB - Libano 9
NL - Olanda 9
ZA - Sudafrica 9
EU - Europa 8
ID - Indonesia 8
CO - Colombia 7
EC - Ecuador 7
PY - Paraguay 7
LT - Lituania 6
PK - Pakistan 6
PE - Perù 5
SA - Arabia Saudita 5
KE - Kenya 4
NZ - Nuova Zelanda 4
UY - Uruguay 4
VE - Venezuela 4
AU - Australia 3
BG - Bulgaria 3
BY - Bielorussia 3
IL - Israele 3
AZ - Azerbaigian 2
BB - Barbados 2
BH - Bahrain 2
EG - Egitto 2
JM - Giamaica 2
KG - Kirghizistan 2
KZ - Kazakistan 2
MA - Marocco 2
NP - Nepal 2
OM - Oman 2
PS - Palestinian Territory 2
RS - Serbia 2
SK - Slovacchia (Repubblica Slovacca) 2
TT - Trinidad e Tobago 2
AD - Andorra 1
AE - Emirati Arabi Uniti 1
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BN - Brunei Darussalam 1
BW - Botswana 1
CI - Costa d'Avorio 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
GA - Gabon 1
GT - Guatemala 1
GY - Guiana 1
HN - Honduras 1
HU - Ungheria 1
JO - Giordania 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
MK - Macedonia 1
PH - Filippine 1
SN - Senegal 1
Totale 10.588
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Città #
Chandler 749
Singapore 573
Dublin 562
Jacksonville 533
Hong Kong 400
San Mateo 332
Boardman 281
Dong Ket 227
Seoul 212
Santa Clara 167
Medford 154
Princeton 153
Ashburn 122
Andover 121
Wilmington 121
Moscow 109
Ann Arbor 102
Beijing 101
Piscataway 92
Saint Petersburg 61
Altamura 56
Los Angeles 54
Munich 49
Perugia 46
Lawrence 43
Ho Chi Minh City 38
Des Moines 33
New York 33
Helsinki 30
São Paulo 30
Norwalk 25
Turku 24
Auburn Hills 21
Woodbridge 21
Falls Church 20
Hanoi 19
Izmir 18
The Dalles 17
Brussels 16
Nuremberg 15
San Paolo di Civitate 13
Shanghai 13
Stockholm 13
Boston 12
London 12
Montreal 12
Tokyo 12
Warsaw 12
Denver 11
Houston 11
Licata 10
Vienna 10
Brooklyn 9
Redwood City 9
Chicago 8
Seattle 8
Belo Horizonte 7
Dearborn 7
Guangzhou 7
Johannesburg 7
Nanjing 7
Poplar 7
Rio de Janeiro 7
Secaucus 7
Venice 7
Frankfurt Am Main 6
Frankfurt am Main 6
Fremont 6
Ottawa 6
Piediluco 6
Ribeirão Preto 6
Roubaix 6
Santiago 6
Tianjin 6
Timisoara 6
Toronto 6
Changsha 5
Charlotte 5
Columbus 5
Curitiba 5
Dallas 5
Kraków 5
Lausanne 5
Orem 5
Tashkent 5
Asunción 4
Atlanta 4
Baghdad 4
Brasília 4
Brno 4
Buenos Aires 4
Chennai 4
Chongqing 4
Cuiabá 4
Goiânia 4
Lima 4
Montevideo 4
Porto Alegre 4
Quito 4
Redmond 4
Totale 6.189
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Nome #
2q31.22q32.3 deletion syndrome: report of an adult patient 160
ISOLAMENTO E CARATTERIZZAZIONE MOLECOLARE DI CELLULE STAMINALI MESENCHIMALI UMANE DA LIQUIDO AMNIOTICO 144
Comparative proteomic analysis of two distinct stem-cell populations from human amniotic fluid 135
Valutazione anatomo-patologica dell’unità feto-placentare nella morte prenatale. 122
Adattamento alla crescita in vitro di cellule del Tumore ascite ATPC+. 122
Centralized cytogenetic analysis of pediatric acute leucemia: results of an Italian collaborative experience. 113
Acute leukemia complicating Waldenstrom's macro¬globulinemia 112
Prenatal Diagnosis in Italy. 110
Occurrence of the same chromosome abnormalities in Ph+ and Ph- cells in chronic myeloid leukaemia. Evidence of a secondary origin of the Ph chromosome? 109
Acute Promyelocytic leukemia: from genetics to treatment. 107
Acrofrontofacionasal dysostosis 1 in two sisters of Indian origin. 105
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. 105
A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy. 105
5q- syndrome in a patient with chronic exposure to ionizing radiation. 103
5q- syndrome termi¬nating in acute myeloid leukemia: karyotype evolution and immunological characterization of blast cells. 101
Acute Promyelocytic Leukemia: from genetics to treatment. 99
A case of acute myeloid leukemia with deletion of chromosome 7 following PBSC transplantation. 98
A case of complete testicular feminization and 47, XXY karyotype 98
5q- anomaly in a patient with erythroleukemia (M6 FAB classi¬fication) 98
A new human highly tumorigenic neuroblastoma cell line with undetectable expression of N-myc. 97
Aspetti endocrinologici di un caso di sindrome da femminilizzazione testicolare 97
L'interferone alfa nella leucemia mieloide cronica 96
Deletion 2p15-16.1 syndrome: Case Report and Review 94
5q- in a case of blastic phase of chronic myeloid leukemia. 93
Adattamento alla crescita in vitro di cellule del tumore ascite ATPC+ 90
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. 90
Aspetti del citoscheletro di cellule in coltura di osso umano normale ed otosclerotico 90
Heterozygous X-linked adrenoleukodystrophy-associated myelopathy mimicking primary progressive multiple sclerosis 89
Effects of steroids on human normal and otosclerotic osteoblastic cells: influence on thymidine and leucine uptake and incorporation. 89
Acute myeloblastic leukemia after adjuvant chemo¬therapy with melphalan in breast cancer. Case report with cytogenetic analysis. 87
A new case of familial paracentric inversion of chromosome 2. 86
Response to low-dose ARA-C + IFN alpha in advanced and second chronic phase chronic myeloid leukemia 86
Complex translocations of the Ph chromosome and Ph-negative CML arise from similar mechanisms as evidenced by FISH analysis. 85
Isolamento di cellule staminali pluripotenti da liquido amniotico e loro uso nel trattamento o nella prevenzione di malattie autoimmuni 84
Pluripotent stem cells from human amniotic fluid and their immunomodulatory properties 82
Recurrent ∼100 Kb microdeletion in the chromosomal region 14q11.2, involving CHD8 gene, is associated with autism and macrocephaly. 81
Loss of amplification and appearance of a novel translocation site of the c-myc oncogene in HL-60 leukemia cells. 80
Le cellule RA (rapidly adhering) nel liquido amniotico di feti anencefali. 80
Hormonal receptor site alterations in the ethio-patogenesis of otosclerosis. 80
Mapping of chromosome 17 breakpoint in acute myeloid leukemias 80
Effects of steroids on human normal and otosclerotic osteoblastic cells: influence on thymidine and leucine uptake and incorporation. 80
L'interferone α-2b nel trattamento della leucemia mieloide cronica Ph' positiva. 79
A novel mutation in the SDHD gene responsible for familial paraganglioma. Medical and psychological implications. 78
Aicardi Syndrome Associated with Autosomal Genomic Imbalance: Coincidence or Evidence for Autosomal Inheritance with Sex-Limited Expression? 78
Interferon Alpha-2b as therapy for Ph'-positive chronic myelogenous leukemia. A study of 82 patients treated with intermittent administration. 77
Etiopathogenesis of otosclerosis: cell biology studies. 77
MASA syndrome: ultrasonographic evidence in a male fetus. 77
A novel spinocerebellar ataxia type 15 family with involuntary movements and cognitive decline 77
Characterization of the cytoskeleton in human normal and otosclerotic osteoblast-like cells. 77
Structural and functional organization of the HF.10 human zinc finger gene (ZNF35) located on chromosome 3p21-p22. 76
Shapiro's syndrome: Defining the clinical spectrum of the spontaneous paroxysmal hypothermia syndrome. 76
Localization of the human HF.2 finger gene on the band 1p34p35 deleted in neuroblastoma tumor. 75
Pluripotent Stem Cells from Human Amniotic Fluid and their Immunomodulatory Properties 75
Immunoregulatory effects of fast human amniotic stem cells on experimental type 1 diabetes 75
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure. 75
Human bone cell cultures: a new model for studying the mechanism of action of calcitonin. 74
Piccolo cromosoma metacentrico a mosaico in un bambino con trisomia 21 primaria (47,XY,+21/ 48,XY,+21,+mar). 73
Coinvolgimento del cromosoma 1 nella mielofibrosi e nelle mielodisplasie. 73
Brief Report: Functional MRI of a Patient with 7q11.23 Duplication Syndrome and Autism Spectrum Disorder. 73
FMR1, FMR2, and SLITRK2 deletion inside a paracentric inversion involving bands Xq27.3-q28 in a male and his mother. 72
ANALYSIS OF ONCOGENE TRANSLOCATIONS BY IN SITU HYBRIDIZATION ON CHROMOSOME PREPARATIONS. 71
Sustained molecular remissions are achievable with tyrosine kinase inhibitor therapy in patients with chronic myeloid leukemia and additional cytogenetic clonal evolution 71
Etude d'un sujet avec caryotype 46, XY,22p+. 70
Interferon-alpha-2b as therapy for untreated and pretreated patients with Ph' positive chronic myeloid leukemia 70
Nablus mask-like facial syndrome: deletion of chromosome 8q22.1 is necessary but not sufficient to cause the phenotype. 70
Craniometaphyseal dysplasia with severe craniofacial involvement shows homozygosity at 6q21-22.1 locus. 69
Cytoskeletal characteristics and functional response to PHT stimulation in human normal and otosclerotic bone cell cultures 69
Genetica Medica 68
In vitro bone-marrow cell cultures and cytogenetic analysis in a case of myelodysplasia. 68
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. 68
Familial pericentric inversion of chromosome 18: intrafamilial variability of the recombinant dup(18q). 68
L'interferone nel trattamento della leucemia mieloide cronica Philadelphia positiva. 67
Aspetti morfofunzionali di colture cellulari di tessuto osseo normale e otosclerotico. 67
Chromosomal localization of four human zinc finger cDNAs. 67
The translocation breakpoint of acute promyelocytic leukemia lies within the retonoic acid receptor alpha locus. 67
Trisomy 6p22pter due to familial t(6;13)(p22;q34 or 33) translocation 67
Chromosome abnormalities in PHA- stimulated and non-stimulated bone marrow coltures from patients with non-Hodgkin lymphoma. 66
Hot water epilepsy and Mccune-Albright syndrome: a case report. 66
Prenatal diagnosis and molecular characterization of an interstitial 1q24.3-31.3 deletion: case report and review. 66
Morphological and functional characteristics of human temporal bone cell cultures. 65
Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: cooperative study of 19 Italian laboratories. 64
Glycosaminoglycan metabolism and cytokine release in normal and otosclerotic human bone cells. Interleukin-1 treated. 64
De novo balanced chromosome rearrangements in prenatal diagnosis. 63
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. 63
Studio della fragilità cromosomica in linfociti di pazienti con carcinoma mammario 63
Pluripotent stem cells from human amniotic fluidand their immunomodulatory properties 63
X-ring Turner's syndrome with combined immunodeficiency and selective gonadotropin defect. 62
Cytogenetic and molecular study on two human neuroblastoma cell cultures. 62
Trisomy 4 in acute nonlymphocytic leukemia: Report of two cases and review of the literature. 62
cDNA isolation, expression analysis and chromosomal localization of two human zinc finger genes. 62
Studio citogenetico dei linfomi B-cellulari. 62
Blood cell mitochondrial DNA content and premature ovarian aging 62
Neonatal mucolipidosis II (I-cell disease): Clinical, radiological and biochemical studies in a case. 61
Trisomy 2 mosaicism with caudal dysgenesis, Hirschsprung disease, and micro-anophthalmia. 61
Characterization of the cytoskeleton in human normal and otosclerotic osteoblastic-like cells. 60
Altered Adenylate Cyclase activity in human otosclerotic bone cell cultures. 60
t(4;21)(p16;q22) in blastic crisis of a chronic myeloid leukemia with variant Phila¬delphia translocation. 60
DHT-receptor in cultured human fibroblasts: binding study in a family with androgen insensitivity (complete testicular feminization) 60
Persistence of chromosomal abnormalities additional to the Philadelphia chromosome after Philadelphia chromosome disappearance during imatinib therapy for chronic myeloid leukemia. 60
DHT-receptor in cultured human fibroblasts: binding study in a family with androgen insensitivity (complete testicular feminisation). 60
Totale 8.093
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Categoria #
all - tutte 46.226
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 46.226
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021935 0 0 0 0 0 109 144 2 208 55 165 252
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
2025/20261.731 278 313 151 539 371 79 0 0 0 0 0 0
Totale 10.820