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

DONTI, Emilio
 Distribuzione geografica
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Continente #
NA - Nord America 5.549
EU - Europa 4.037
AS - Asia 3.082
SA - Sud America 489
Continente sconosciuto - Info sul continente non disponibili 245
AF - Africa 62
OC - Oceania 8
Totale 13.472
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Nazione #
US - Stati Uniti d'America 5.388
SG - Singapore 1.336
UA - Ucraina 973
SE - Svezia 577
RU - Federazione Russa 570
IE - Irlanda 565
CN - Cina 434
HK - Hong Kong 410
IT - Italia 402
BR - Brasile 364
VN - Vietnam 353
DE - Germania 260
KR - Corea 212
FI - Finlandia 210
FR - Francia 195
GB - Regno Unito 98
CA - Canada 78
IN - India 54
BD - Bangladesh 44
TR - Turchia 39
AR - Argentina 36
PL - Polonia 35
IQ - Iraq 28
AT - Austria 27
CH - Svizzera 27
MX - Messico 25
CO - Colombia 23
UZ - Uzbekistan 22
ZA - Sudafrica 21
JP - Giappone 20
ID - Indonesia 18
PK - Pakistan 17
SA - Arabia Saudita 17
BE - Belgio 16
VE - Venezuela 16
CL - Cile 15
PH - Filippine 13
RO - Romania 13
ES - Italia 12
JM - Giamaica 12
CR - Costa Rica 11
EC - Ecuador 11
LB - Libano 11
NL - Olanda 11
PY - Paraguay 10
CZ - Repubblica Ceca 9
GR - Grecia 9
MY - Malesia 9
EU - Europa 8
LT - Lituania 8
KE - Kenya 7
MA - Marocco 7
PE - Perù 7
PR - Porto Rico 6
PS - Palestinian Territory 6
TN - Tunisia 6
BY - Bielorussia 5
CW - ???statistics.table.value.countryCode.CW??? 5
NI - Nicaragua 5
NZ - Nuova Zelanda 5
TT - Trinidad e Tobago 5
UY - Uruguay 5
AE - Emirati Arabi Uniti 4
DZ - Algeria 4
EG - Egitto 4
HN - Honduras 4
IL - Israele 4
JO - Giordania 4
KZ - Kazakistan 4
NP - Nepal 4
OM - Oman 4
SV - El Salvador 4
AU - Australia 3
BG - Bulgaria 3
GT - Guatemala 3
KG - Kirghizistan 3
NG - Nigeria 3
AM - Armenia 2
AZ - Azerbaigian 2
BB - Barbados 2
BH - Bahrain 2
ET - Etiopia 2
PA - Panama 2
RS - Serbia 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
AD - Andorra 1
AL - Albania 1
BA - Bosnia-Erzegovina 1
BJ - Benin 1
BN - Brunei Darussalam 1
BO - Bolivia 1
BW - Botswana 1
BZ - Belize 1
CI - Costa d'Avorio 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EE - Estonia 1
GA - Gabon 1
GP - Guadalupe 1
Totale 13.228
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Città #
Singapore 862
Chandler 749
Dublin 563
Jacksonville 533
Hong Kong 408
San Mateo 332
Ashburn 299
San Jose 288
Boardman 281
Dong Ket 227
Seoul 212
Santa Clara 195
Council Bluffs 185
Moscow 158
Medford 154
Princeton 153
Lauterbourg 127
Andover 121
Wilmington 121
Beijing 103
Ann Arbor 102
Piscataway 99
Los Angeles 77
Saint Petersburg 61
New York 59
Altamura 56
The Dalles 53
Munich 49
Perugia 47
Ho Chi Minh City 45
Lawrence 43
São Paulo 43
Des Moines 33
Helsinki 32
Hanoi 25
Norwalk 25
Turku 24
Auburn Hills 21
Rome 21
Woodbridge 21
Falls Church 20
Dallas 19
Izmir 19
Montreal 18
Frankfurt am Main 17
Naples 17
North Bergen 17
Nuremberg 17
Tokyo 17
Brussels 16
London 16
Orem 16
Shanghai 16
Warsaw 15
Milan 14
Phoenix 14
Stockholm 14
Denver 13
San Paolo di Civitate 13
Boston 12
Brooklyn 12
Buffalo 12
Chicago 12
Houston 12
Atlanta 11
Chennai 11
Tashkent 11
Jeddah 10
Johannesburg 10
Licata 10
Poplar 10
Santiago 10
Toronto 10
Turin 10
Vienna 10
Baghdad 9
Belo Horizonte 9
Palermo 9
Redwood City 9
San José 9
Seattle 9
Kingston 8
Mexico City 8
Rio de Janeiro 8
Venice 8
Buenos Aires 7
Caracas 7
Curitiba 7
Dearborn 7
Florence 7
Guangzhou 7
Lahore 7
Medellín 7
Nanjing 7
Quito 7
Secaucus 7
Bologna 6
Brasília 6
Changsha 6
Charlotte 6
Totale 7.675
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Nome #
2q31.22q32.3 deletion syndrome: report of an adult patient 186
Occurrence of the same chromosome abnormalities in Ph+ and Ph- cells in chronic myeloid leukaemia. Evidence of a secondary origin of the Ph chromosome? 161
Comparative proteomic analysis of two distinct stem-cell populations from human amniotic fluid 161
Valutazione anatomo-patologica dell’unità feto-placentare nella morte prenatale. 158
ISOLAMENTO E CARATTERIZZAZIONE MOLECOLARE DI CELLULE STAMINALI MESENCHIMALI UMANE DA LIQUIDO AMNIOTICO 154
Adattamento alla crescita in vitro di cellule del Tumore ascite ATPC+. 147
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. 139
Prenatal Diagnosis in Italy. 132
5q- syndrome termi¬nating in acute myeloid leukemia: karyotype evolution and immunological characterization of blast cells. 132
Acute leukemia complicating Waldenstrom's macro¬globulinemia 131
Centralized cytogenetic analysis of pediatric acute leucemia: results of an Italian collaborative experience. 131
Acute Promyelocytic Leukemia: from genetics to treatment. 129
A case of acute myeloid leukemia with deletion of chromosome 7 following PBSC transplantation. 127
Acute Promyelocytic leukemia: from genetics to treatment. 126
5q- syndrome in a patient with chronic exposure to ionizing radiation. 126
Acrofrontofacionasal dysostosis 1 in two sisters of Indian origin. 126
A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy. 126
A case of complete testicular feminization and 47, XXY karyotype 125
5q- anomaly in a patient with erythroleukemia (M6 FAB classi¬fication) 122
MASA syndrome: ultrasonographic evidence in a male fetus. 118
Deletion 2p15-16.1 syndrome: Case Report and Review 116
5q- in a case of blastic phase of chronic myeloid leukemia. 115
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. 113
Response to low-dose ARA-C + IFN alpha in advanced and second chronic phase chronic myeloid leukemia 112
Effects of steroids on human normal and otosclerotic osteoblastic cells: influence on thymidine and leucine uptake and incorporation. 111
A new human highly tumorigenic neuroblastoma cell line with undetectable expression of N-myc. 110
Acute myeloblastic leukemia after adjuvant chemo¬therapy with melphalan in breast cancer. Case report with cytogenetic analysis. 110
Adattamento alla crescita in vitro di cellule del tumore ascite ATPC+ 109
Aspetti endocrinologici di un caso di sindrome da femminilizzazione testicolare 109
L'interferone alfa nella leucemia mieloide cronica 107
A novel spinocerebellar ataxia type 15 family with involuntary movements and cognitive decline 107
Complex translocations of the Ph chromosome and Ph-negative CML arise from similar mechanisms as evidenced by FISH analysis. 107
Aspetti del citoscheletro di cellule in coltura di osso umano normale ed otosclerotico 106
Heterozygous X-linked adrenoleukodystrophy-associated myelopathy mimicking primary progressive multiple sclerosis 106
Isolamento di cellule staminali pluripotenti da liquido amniotico e loro uso nel trattamento o nella prevenzione di malattie autoimmuni 104
Characterization of the cytoskeleton in human normal and otosclerotic osteoblast-like cells. 103
A new case of familial paracentric inversion of chromosome 2. 102
Recurrent ∼100 Kb microdeletion in the chromosomal region 14q11.2, involving CHD8 gene, is associated with autism and macrocephaly. 101
Coinvolgimento del cromosoma 1 nella mielofibrosi e nelle mielodisplasie. 100
A novel mutation in the SDHD gene responsible for familial paraganglioma. Medical and psychological implications. 100
Piccolo cromosoma metacentrico a mosaico in un bambino con trisomia 21 primaria (47,XY,+21/ 48,XY,+21,+mar). 99
Interferon Alpha-2b as therapy for Ph'-positive chronic myelogenous leukemia. A study of 82 patients treated with intermittent administration. 99
ANALYSIS OF ONCOGENE TRANSLOCATIONS BY IN SITU HYBRIDIZATION ON CHROMOSOME PREPARATIONS. 99
Aicardi Syndrome Associated with Autosomal Genomic Imbalance: Coincidence or Evidence for Autosomal Inheritance with Sex-Limited Expression? 99
Shapiro's syndrome: Defining the clinical spectrum of the spontaneous paroxysmal hypothermia syndrome. 99
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure. 99
Hormonal receptor site alterations in the ethio-patogenesis of otosclerosis. 98
Familial pericentric inversion of chromosome 18: intrafamilial variability of the recombinant dup(18q). 98
Etiopathogenesis of otosclerosis: cell biology studies. 97
Pluripotent Stem Cells from Human Amniotic Fluid and their Immunomodulatory Properties 97
Interferon-alpha-2b as therapy for untreated and pretreated patients with Ph' positive chronic myeloid leukemia 96
Nablus mask-like facial syndrome: deletion of chromosome 8q22.1 is necessary but not sufficient to cause the phenotype. 96
DHT-receptor in cultured human fibroblasts: binding study in a family with androgen insensitivity (complete testicular feminization) 95
Mapping of chromosome 17 breakpoint in acute myeloid leukemias 94
Pluripotent stem cells from human amniotic fluid and their immunomodulatory properties 94
Brief Report: Functional MRI of a Patient with 7q11.23 Duplication Syndrome and Autism Spectrum Disorder. 94
Structural and functional organization of the HF.10 human zinc finger gene (ZNF35) located on chromosome 3p21-p22. 93
Cytoskeletal characteristics and functional response to PHT stimulation in human normal and otosclerotic bone cell cultures 93
Immunoregulatory effects of fast human amniotic stem cells on experimental type 1 diabetes 93
Loss of amplification and appearance of a novel translocation site of the c-myc oncogene in HL-60 leukemia cells. 92
Le cellule RA (rapidly adhering) nel liquido amniotico di feti anencefali. 92
Effects of steroids on human normal and otosclerotic osteoblastic cells: influence on thymidine and leucine uptake and incorporation. 91
FMR1, FMR2, and SLITRK2 deletion inside a paracentric inversion involving bands Xq27.3-q28 in a male and his mother. 91
Genetica Medica 90
Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: cooperative study of 19 Italian laboratories. 90
Chromosomal localization of four human zinc finger cDNAs. 89
Pluripotent stem cells from human amniotic fluidand their immunomodulatory properties 89
Craniometaphyseal dysplasia with severe craniofacial involvement shows homozygosity at 6q21-22.1 locus. 88
Sustained molecular remissions are achievable with tyrosine kinase inhibitor therapy in patients with chronic myeloid leukemia and additional cytogenetic clonal evolution 88
Localization of the human HF.2 finger gene on the band 1p34p35 deleted in neuroblastoma tumor. 87
L'interferone α-2b nel trattamento della leucemia mieloide cronica Ph' positiva. 86
Human bone cell cultures: a new model for studying the mechanism of action of calcitonin. 86
The translocation breakpoint of acute promyelocytic leukemia lies within the retonoic acid receptor alpha locus. 86
Trisomy 15 mosaicism owing to familial reciprocaltranslocation t(1;15): implication for prenatal diagnosis 85
Blood cell mitochondrial DNA content and premature ovarian aging 85
In vitro bone-marrow cell cultures and cytogenetic analysis in a case of myelodysplasia. 84
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. 84
Trisomy 6p22pter due to familial t(6;13)(p22;q34 or 33) translocation 83
De novo balanced chromosome rearrangements in prenatal diagnosis. 82
Trisomy 4 in acute nonlymphocytic leukemia: Report of two cases and review of the literature. 82
Etude d'un sujet avec caryotype 46, XY,22p+. 82
Glycosaminoglycan metabolism and cytokine release in normal and otosclerotic human bone cells. Interleukin-1 treated. 82
Prenatal diagnosis and molecular characterization of an interstitial 1q24.3-31.3 deletion: case report and review. 82
Trisomy 2 mosaicism with caudal dysgenesis, Hirschsprung disease, and micro-anophthalmia. 82
L'interferone nel trattamento della leucemia mieloide cronica Philadelphia positiva. 81
t(4;21)(p16;q22) in blastic crisis of a chronic myeloid leukemia with variant Phila¬delphia translocation. 80
Morphological and functional characteristics of human temporal bone cell cultures. 79
Aspetti morfofunzionali di colture cellulari di tessuto osseo normale e otosclerotico. 78
Chromosome abnormalities in PHA- stimulated and non-stimulated bone marrow coltures from patients with non-Hodgkin lymphoma. 78
DHT-receptor in cultured human fibroblasts: binding study in a family with androgen insensitivity (complete testicular feminisation). 78
X-ring Turner's syndrome with combined immunodeficiency and selective gonadotropin defect. 77
Evolving modalities of treatment with Interferon alfa-2b for Ph'-positive chronic myelogenous leukaemia. 77
Studio della fragilità cromosomica in linfociti di pazienti con carcinoma mammario 77
cDNA isolation, expression analysis and chromosomal localization of two human zinc finger genes. 76
Hot water epilepsy and Mccune-Albright syndrome: a case report. 76
Cytogenetic and molecular study on two human neuroblastoma cell cultures. 74
Neonatal mucolipidosis II (I-cell disease): Clinical, radiological and biochemical studies in a case. 74
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. 74
Studio citogenetico dei linfomi B-cellulari. 74
Characterization of the cytoskeleton in human normal and otosclerotic osteoblastic-like cells. 73
Totale 10.121
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Categoria #
all - tutte 58.279
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 58.279
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022989 0 0 0 100 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
2025/20263.325 278 313 151 539 371 303 500 162 379 245 62 22
2026/20271.058 58 132 220 648 0 0 0 0 0 0 0 0
Totale 13.472