IRIS
FUGAZZA, GIUSEPPINA
 Distribuzione geografica
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Continente #
EU - Europa 2.470
Totale 2.470
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Nazione #
IT - Italia 2.470
Totale 2.470
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Città #
Genova 1.916
Rapallo 288
Genoa 261
Bordighera 4
Vado Ligure 1
Totale 2.470
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Nome #
High frequency of trisomy 8 in acute promyelocytic leukemia: a fluorescence in situ hybridization study. 173
A BCR-JAK2 fusion gene as the result of a t(9;22)(p24;q11) in a patient with acute myeloid leukemia 141
Doxorubicin induces senescence or apoptosis in rat neonatal cardiomyocytes by regulating the expression levels of the telomere binding factors 1 and 2 130
High feasibility and antileukemic efficacy of fludarabine, cytarabine, and idarubicin (FLAI) induction followed by risk-oriented consolidation: A critical review of a 10-year, single-center experience in younger, non M3 AML patients 128
Combined assessment of WT1 and BAALC gene expression at diagnosis may improve leukemia-free survival prediction in patients with myelodysplastic syndromes 128
HMGA2 overexpression in plycythemia vera with t(12;21) (q14;q22) 125
Molecular analysis of the Imatinib-induced complete cytogenetic response in chronic myelogenous leukemia 116
CBFA2T2 and C20orf112: two novel fusion partners of RUNX1 in acute myeloid leukemia. 111
Fluorescence in situ hybridization provides evidence for two-step rearrangement in a masked Ph chromosome formation. 107
Masked Philadelphia chromosome due to atypical BCR/ABL localization on the 9q34 band and duplication of the der(9) in a case of chronic myelogenous leukemia 107
Amplified c-MYC sequences localized by fluorescence in-situ hybridization on double minute chromosomes in acute myeloid leukemias. 105
Changes of chromatin condensation in one patient with ataxia telangiectasia disorder: a structural study 103
Complex structural involvement of chromosome 7 in primary myelodysplastic syndromes determined by fluorescence in situ hybridization. 101
A novel mutation of Twinkle in Perrault syndrome: A not rare diagnosis? 95
Variant Philadelphia chromosome translocations are frequently associated with additional structural abnormalities. 94
Normal primitive haemopoietic progenitors are more frequent than their leukaemic counterpart in newly diagnosed patients with chronic myeloid leukaemia but rapidly decline with time 92
Duplication of the der(13)t(12;13)(p13;q14) in chronic myelomonocytic leukemia. 90
Autografting with Ph-negative progenitors in patients at diagnosis of chronic myeloid leukemia induces a prolonged prevalence of Ph-negative hemopoiesis 86
Complex chromosome rearrangements may locate the bcr/abl fusion gene sites other than 22q11 78
Cytogenetic clonality in chronic myelomonocytic leukemia studied with fluorescence in situ hybridization 70
The role of cell shape in control of chromatin structure and organization 69
Cytogenetic and fluorescence in situ hybridization monitoring in Ph+ chronic myeloid leukemia patients treated with Imatinib mesylate. 69
Trisomy 8 detection in Ph+ CML patients using conventional cytogenetic and interphase fluorescence in situ hybridization techniques. 67
Interferon-alpha protects Philadelphia-negative progenitors from exhaustion in chronic myeloid leukemia patients with cytogenetic response. 61
Establishment and characterization of a novel fibroblastic cell line (Sci13d) derived from the broncho-alveolar lavage of a patient with fibrotic hypersensitivity pneumonitis 54
Totale 2.500
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Categoria #
all - tutte 6.812
article - articoli 6.812
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 13.624
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020638 27 18 25 47 53 76 92 41 51 112 70 26
2020/2021198 7 21 8 9 42 7 3 25 23 17 12 24
2021/2022319 5 17 35 23 14 30 8 76 24 37 11 39
2022/2023344 34 28 14 43 53 56 1 26 46 3 39 1
2023/2024202 9 17 4 24 10 71 21 16 7 3 7 13
2024/202512 12 0 0 0 0 0 0 0 0 0 0 0
Totale 2.500