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

DONTI, Emilio
 Distribuzione geografica
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Continente #
NA - Nord America 3.715
EU - Europa 2.971
AS - Asia 983
Continente sconosciuto - Info sul continente non disponibili 8
OC - Oceania 6
SA - Sud America 4
Totale 7.687
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Nazione #
US - Stati Uniti d'America 3.703
UA - Ucraina 964
SE - Svezia 565
IE - Irlanda 563
SG - Singapore 290
HK - Hong Kong 284
VN - Vietnam 227
IT - Italia 188
DE - Germania 181
FI - Finlandia 171
RU - Federazione Russa 144
CN - Cina 116
GB - Regno Unito 53
FR - Francia 37
CH - Svizzera 27
TR - Turchia 18
KR - Corea 17
PL - Polonia 17
BE - Belgio 14
CA - Canada 11
RO - Romania 11
AT - Austria 10
UZ - Uzbekistan 10
GR - Grecia 9
LB - Libano 9
EU - Europa 8
CZ - Repubblica Ceca 7
NZ - Nuova Zelanda 4
ID - Indonesia 3
IN - India 3
JP - Giappone 3
NL - Olanda 3
AU - Australia 2
BR - Brasile 2
CO - Colombia 2
LT - Lituania 2
RS - Serbia 2
AD - Andorra 1
BD - Bangladesh 1
BG - Bulgaria 1
IL - Israele 1
JM - Giamaica 1
PK - Pakistan 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 7.687
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Città #
Chandler 749
Dublin 562
Jacksonville 533
San Mateo 332
Hong Kong 284
Boardman 281
Dong Ket 227
Singapore 219
Santa Clara 161
Medford 154
Princeton 153
Andover 121
Wilmington 121
Ann Arbor 102
Beijing 61
Saint Petersburg 61
Altamura 56
Lawrence 43
Perugia 43
Des Moines 33
Norwalk 25
Auburn Hills 21
Woodbridge 21
Falls Church 20
Los Angeles 20
Ashburn 19
Izmir 18
Helsinki 17
Seoul 17
Brussels 14
New York 14
San Paolo di Civitate 13
Licata 10
Redwood City 9
Munich 8
Dearborn 7
Houston 7
Moscow 7
Shanghai 7
Frankfurt Am Main 6
Fremont 6
Nanjing 6
Ottawa 6
Piediluco 6
Timisoara 6
Kraków 5
Lausanne 5
Brno 4
Redmond 4
Turin 4
Dallas 3
Ludwigshafen 3
Seattle 3
Tappahannock 3
Toronto 3
Belgrade 2
Cluj-Napoca 2
Enna 2
Fairfield 2
Foligno 2
Frankfurt am Main 2
Guangzhou 2
Kiev 2
Livorno 2
London 2
Osaka 2
Palermo 2
Phoenix 2
Rio de Janeiro 2
Santiago de Cali 2
Stockholm 2
Udine 2
Venice 2
Albizzate 1
Altavilla Irpina 1
Andorra la Vella 1
Arcene 1
Arenzano 1
Auckland 1
Ballwin 1
Bedford 1
Blenheim 1
Bratislava 1
Brisbane 1
Chennai 1
Chicago 1
Cormeilles-en-Parisis 1
Corridonia 1
Den Haag 1
Downers Grove 1
Due West 1
Edinburgh 1
Falkenstein 1
Florence 1
Groningen 1
Gualdo Tadino 1
Hamilton 1
Joliet 1
Karachi 1
Kingston 1
Totale 4.706
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Nome #
ISOLAMENTO E CARATTERIZZAZIONE MOLECOLARE DI CELLULE STAMINALI MESENCHIMALI UMANE DA LIQUIDO AMNIOTICO 121
2q31.22q32.3 deletion syndrome: report of an adult patient 115
Comparative proteomic analysis of two distinct stem-cell populations from human amniotic fluid 106
Valutazione anatomo-patologica dell’unità feto-placentare nella morte prenatale. 100
Centralized cytogenetic analysis of pediatric acute leucemia: results of an Italian collaborative experience. 96
Acute leukemia complicating Waldenstrom's macro¬globulinemia 93
Prenatal Diagnosis in Italy. 85
Occurrence of the same chromosome abnormalities in Ph+ and Ph- cells in chronic myeloid leukaemia. Evidence of a secondary origin of the Ph chromosome? 85
Adattamento alla crescita in vitro di cellule del Tumore ascite ATPC+. 85
Aspetti endocrinologici di un caso di sindrome da femminilizzazione testicolare 82
L'interferone alfa nella leucemia mieloide cronica 80
Acute Promyelocytic leukemia: from genetics to treatment. 79
A new human highly tumorigenic neuroblastoma cell line with undetectable expression of N-myc. 78
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. 78
Response to low-dose ARA-C + IFN alpha in advanced and second chronic phase chronic myeloid leukemia 72
A case of complete testicular feminization and 47, XXY karyotype 72
Loss of amplification and appearance of a novel translocation site of the c-myc oncogene in HL-60 leukemia cells. 71
Le cellule RA (rapidly adhering) nel liquido amniotico di feti anencefali. 70
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. 70
Complex translocations of the Ph chromosome and Ph-negative CML arise from similar mechanisms as evidenced by FISH analysis. 69
L'interferone α-2b nel trattamento della leucemia mieloide cronica Ph' positiva. 67
5q- in a case of blastic phase of chronic myeloid leukemia. 66
5q- anomaly in a patient with erythroleukemia (M6 FAB classi¬fication) 66
5q- syndrome in a patient with chronic exposure to ionizing radiation. 66
Deletion 2p15-16.1 syndrome: Case Report and Review 66
Acrofrontofacionasal dysostosis 1 in two sisters of Indian origin. 66
Acute Promyelocytic Leukemia: from genetics to treatment. 65
Aspetti del citoscheletro di cellule in coltura di osso umano normale ed otosclerotico 65
Adattamento alla crescita in vitro di cellule del tumore ascite ATPC+ 64
Mapping of chromosome 17 breakpoint in acute myeloid leukemias 64
Effects of steroids on human normal and otosclerotic osteoblastic cells: influence on thymidine and leucine uptake and incorporation. 64
Localization of the human HF.2 finger gene on the band 1p34p35 deleted in neuroblastoma tumor. 63
Structural and functional organization of the HF.10 human zinc finger gene (ZNF35) located on chromosome 3p21-p22. 63
Acute myeloblastic leukemia after adjuvant chemo¬therapy with melphalan in breast cancer. Case report with cytogenetic analysis. 63
Hormonal receptor site alterations in the ethio-patogenesis of otosclerosis. 62
Piccolo cromosoma metacentrico a mosaico in un bambino con trisomia 21 primaria (47,XY,+21/ 48,XY,+21,+mar). 61
Interferon Alpha-2b as therapy for Ph'-positive chronic myelogenous leukemia. A study of 82 patients treated with intermittent administration. 61
5q- syndrome termi¬nating in acute myeloid leukemia: karyotype evolution and immunological characterization of blast cells. 61
Human bone cell cultures: a new model for studying the mechanism of action of calcitonin. 59
Etiopathogenesis of otosclerosis: cell biology studies. 58
Interferon-alpha-2b as therapy for untreated and pretreated patients with Ph' positive chronic myeloid leukemia 58
A case of acute myeloid leukemia with deletion of chromosome 7 following PBSC transplantation. 57
MASA syndrome: ultrasonographic evidence in a male fetus. 57
Aicardi Syndrome Associated with Autosomal Genomic Imbalance: Coincidence or Evidence for Autosomal Inheritance with Sex-Limited Expression? 57
Effects of steroids on human normal and otosclerotic osteoblastic cells: influence on thymidine and leucine uptake and incorporation. 57
A new case of familial paracentric inversion of chromosome 2. 56
Aspetti morfofunzionali di colture cellulari di tessuto osseo normale e otosclerotico. 56
Coinvolgimento del cromosoma 1 nella mielofibrosi e nelle mielodisplasie. 56
Pluripotent stem cells from human amniotic fluid and their immunomodulatory properties 56
A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy. 56
Immunoregulatory effects of fast human amniotic stem cells on experimental type 1 diabetes 56
In vitro bone-marrow cell cultures and cytogenetic analysis in a case of myelodysplasia. 55
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure. 55
A novel mutation in the SDHD gene responsible for familial paraganglioma. Medical and psychological implications. 54
Isolamento di cellule staminali pluripotenti da liquido amniotico e loro uso nel trattamento o nella prevenzione di malattie autoimmuni 53
L'interferone nel trattamento della leucemia mieloide cronica Philadelphia positiva. 52
ANALYSIS OF ONCOGENE TRANSLOCATIONS BY IN SITU HYBRIDIZATION ON CHROMOSOME PREPARATIONS. 52
De novo balanced chromosome rearrangements in prenatal diagnosis. 51
Characterization of the cytoskeleton in human normal and otosclerotic osteoblastic-like cells. 51
Altered Adenylate Cyclase activity in human otosclerotic bone cell cultures. 51
Glycosaminoglycan metabolism and cytokine release in normal and otosclerotic human bone cells. Interleukin-1 treated. 51
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. 51
Sustained molecular remissions are achievable with tyrosine kinase inhibitor therapy in patients with chronic myeloid leukemia and additional cytogenetic clonal evolution 51
Characterization of the cytoskeleton in human normal and otosclerotic osteoblast-like cells. 51
The translocation breakpoint of acute promyelocytic leukemia lies within the retonoic acid receptor alpha locus. 50
Chromosome abnormalities in PHA- stimulated and non-stimulated bone marrow coltures from patients with non-Hodgkin lymphoma. 49
Etude d'un sujet avec caryotype 46, XY,22p+. 49
Studio della fragilità cromosomica in linfociti di pazienti con carcinoma mammario 49
Otosclerosis: a disease due to hormonal receptor site alterations? 49
Craniometaphyseal dysplasia with severe craniofacial involvement shows homozygosity at 6q21-22.1 locus. 49
Cytoskeletal characteristics and functional response to PHT stimulation in human normal and otosclerotic bone cell cultures 49
Pluripotent stem cells from human amniotic fluidand their immunomodulatory properties 49
Prenatal diagnosis and molecular characterization of an interstitial 1q24.3-31.3 deletion: case report and review. 48
Pluripotent Stem Cells from Human Amniotic Fluid and their Immunomodulatory Properties 48
Familial pericentric inversion of chromosome 18: intrafamilial variability of the recombinant dup(18q). 48
Genetica Medica 47
Immunological and molecular studies in a case of follicular lymphoma with an extra chromosome 12 and t(2;8) translocation. 47
Cytogenetic and molecular study on two human neuroblastoma cell cultures. 47
t(4;21)(p16;q22) in blastic crisis of a chronic myeloid leukemia with variant Phila¬delphia translocation. 47
Trisomy 4 in acute nonlymphocytic leukemia: Report of two cases and review of the literature. 47
Trisomy 6p22pter due to familial t(6;13)(p22;q34 or 33) translocation 47
Studio citogenetico dei linfomi B-cellulari. 47
Shapiro's syndrome: Defining the clinical spectrum of the spontaneous paroxysmal hypothermia syndrome. 47
Expression of aphidicolin- induced fragile sites in lymphocytes of patients with breast cancer. 46
Neonatal mucolipidosis II (I-cell disease): Clinical, radiological and biochemical studies in a case. 46
cDNA isolation, expression analysis and chromosomal localization of two human zinc finger genes. 46
A novel spinocerebellar ataxia type 15 family with involuntary movements and cognitive decline 46
Evolving modalities of treatment with Interferon alfa-2b for Ph'-positive chronic myelogenous leukaemia. 45
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. 45
Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: cooperative study of 19 Italian laboratories. 45
Heterozygous X-linked adrenoleukodystrophy-associated myelopathy mimicking primary progressive multiple sclerosis 45
X-ring Turner's syndrome with combined immunodeficiency and selective gonadotropin defect. 44
Study on normal and otosclerotic bone cell cultures: an advance in understanding the patho¬genesis of otosclerosis. 44
Spontaneous expression of FRA3P in a patient with Nager Syndrome 44
Myeloperoxidase gene maps to chromosome 17q22-23 and is not rearranged in acute promyelocytic leukemia. 44
Studio citogenetico di un caso di carcinoma a cellule basali e revisione della letteratura. 44
Possible alteration of the catalytic part of the receptor site for calcitonin in otosclerotic bone cell cultures. 44
Morphological and functional characteristics of human temporal bone cell cultures. 44
Trisomy 15 mosaicism owing to familial reciprocaltranslocation t(1;15): implication for prenatal diagnosis 44
Yq- in una famiglia con più casi di femminilizzazione testicolare completa 43
Totale 5.949
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Categoria #
all - tutte 30.626
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 30.626
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020601 0 0 0 0 134 5 144 4 145 48 11 110
2020/20211.719 9 136 56 142 441 109 144 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
2024/2025583 21 246 58 61 197 0 0 0 0 0 0 0
Totale 7.919