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Bone marrow WT1 levels at diagnosis, post-induction and post-intensification in adult de novo AML

Leukemia, 2013-11, Vol.27 (11), p.2157-2164

2013

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Adverse impact of IDH1 and IDH2 mutations in primary AML: Experience of the Spanish CETLAM group

Leukemia research, 2012-08, Vol.36 (8), p.990-997

2012

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Interleukin-3 receptor alpha chain (CD123) is widely expressed in hematologic malignancies

Haematologica (Roma), 2001-12, Vol.86 (12), p.1261

2001

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Immunophenotype of acute myeloid leukemia with NPM mutations: Prognostic impact of the leukemic compartment size

Leukemia research, 2011-02, Vol.35 (2), p.163-168

2011

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MEIS 1 expression is downregulated through promoter hypermethylation in AML1-ETO acute myeloid leukemias

Leukemia, 2004-07, Vol.18 (7), p.1231-1237

2004

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CIZ gene rearrangements in acute leukemia: report of a diagnostic FISH assay and clinical features of nine patients

Leukemia, 2005-09, Vol.19 (9), p.1696-1699

2005

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A case of cryptic acute promyelocytic leukemia

Leukemia, 1998-09, Vol.12 (9), p.1490-1491

1998

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252 NPM1 haploinsufficiency in human myeloid diseases with non-isolated −5/5q

Leukemia research, 2011, Vol.35, p.S99-S99

2011

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253 Insights on centromeric breakpoints of 5q deletions

Leukemia research, 2011, Vol.35, p.S99-S99

2011

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Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia

Leukemia, 2006-06, Vol.20 (6), p.958-964

2006

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Teenage men & unintended pregnancy: acceptability of a film-based prevention program for adolescents

European journal of public health, 2015-10, Vol.25 (suppl_3)

2015

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Loss of heterozygosity of the polymorphic PIG3 microsatellite with low frequency in de novo acute myeloid leukemias

Leukemia, 2004-06, Vol.18 (6), p.1148-1149

2004

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TEL Gene Is Involved in Myelodysplastic Syndromes With Either the Typical t(5;12)(q33;p13) Translocation or its Variant t(10;12)(q24;p13)

Blood, 1995-05, Vol.85 (10), p.2848-2852

1995

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Molecular Delineation of 13q Deletion Boundaries in 20 Patients With Myeloid Malignancies

Blood, 1998-01, Vol.91 (1), p.231-237

1998

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C022 NPM1 monoallelic deletion in a subgroup of MDS/AML with del (5q) or monosomy 5 and complex karyotype

Leukemia research, 2007, Vol.31, p.S34-S35

2007

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Additional chromosome abnormalities in patients with acute promyelocytic leukemia treated with all-trans retinoic acid and chemotherapy

Haematologica (Roma), 2010-03, Vol.95 (3), p.424-431

2010

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AML-1 mutations outside the RUNT domain: description of two cases in myeloid malignancies

Leukemia, 2002-11, Vol.16 (11), p.2329-2332

2002

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NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with t(8;11)(p11.2;p15)

Blood, 2002-05, Vol.99 (10), p.3857-3860

2002

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Usefulness and reproducibility of cytomorphologic evaluations to differentiate myeloma from monoclonal gammopathies of unknown significance

American journal of clinical pathology, 2001, Vol.115 (1), p.127-135

2001

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Clinical utility of bone marrow flow cytometry in B-cell non-Hodgkin lymphomas (B-NHL)

Histopathology, 2004-09, Vol.45 (3), p.268-274

2004

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Recurrent rearrangement of the Ewing's sarcoma gene, EWSR1, or its homologue, TAF15, with the transcription factor CIZ/NMP4 in acute leukemia

Cancer research (Chicago, Ill.), 2002-10, Vol.62 (19), p.5408-5412

2002

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T-cell lymphoblastic lymphoma associated with the t(6;11)(q27;q23)

Haematologica (Roma), 2001-02, Vol.86 (2), p.218

2001

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The hypereosinophilic syndrome: fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinases

Haematologica (Roma), 2005-05, Vol.90 (5), p.596-601

2005

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Occurrence of the JAK2 V617F mutation in the WHO provisional entity: myelodysplastic/myeloproliferative disease, unclassifiable-refractory anemia with ringed sideroblasts associated with marked thrombocytosis

Haematologica (Roma), 2006-05, Vol.91 (5), p.719-720

2006

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Bone marrow WT1 levels at diagnosis, post-induction and post-intensification in adult de novo AML

Adverse impact of IDH1 and IDH2 mutations in primary AML: Experience of the Spanish CETLAM group

Interleukin-3 receptor alpha chain (CD123) is widely expressed in hematologic malignancies

Immunophenotype of acute myeloid leukemia with NPM mutations: Prognostic impact of the leukemic compartment size

MEIS 1 expression is downregulated through promoter hypermethylation in AML1-ETO acute myeloid leukemias

CIZ gene rearrangements in acute leukemia: report of a diagnostic FISH assay and clinical features of nine patients

A case of cryptic acute promyelocytic leukemia

252 NPM1 haploinsufficiency in human myeloid diseases with non-isolated −5/5q

253 Insights on centromeric breakpoints of 5q deletions

Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia

Teenage men & unintended pregnancy: acceptability of a film-based prevention program for adolescents

Loss of heterozygosity of the polymorphic PIG3 microsatellite with low frequency in de novo acute myeloid leukemias

TEL Gene Is Involved in Myelodysplastic Syndromes With Either the Typical t(5;12)(q33;p13) Translocation or its Variant t(10;12)(q24;p13)

Molecular Delineation of 13q Deletion Boundaries in 20 Patients With Myeloid Malignancies

MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene

C022 NPM1 monoallelic deletion in a subgroup of MDS/AML with del (5q) or monosomy 5 and complex karyotype

Additional chromosome abnormalities in patients with acute promyelocytic leukemia treated with all-trans retinoic acid and chemotherapy

AML-1 mutations outside the RUNT domain: description of two cases in myeloid malignancies

NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with t(8;11)(p11.2;p15)

Usefulness and reproducibility of cytomorphologic evaluations to differentiate myeloma from monoclonal gammopathies of unknown significance

Clinical utility of bone marrow flow cytometry in B-cell non-Hodgkin lymphomas (B-NHL)

Recurrent rearrangement of the Ewing's sarcoma gene, EWSR1, or its homologue, TAF15, with the transcription factor CIZ/NMP4 in acute leukemia

T-cell lymphoblastic lymphoma associated with the t(6;11)(q27;q23)

The hypereosinophilic syndrome: fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinases

Occurrence of the JAK2 V617F mutation in the WHO provisional entity: myelodysplastic/myeloproliferative disease, unclassifiable-refractory anemia with ringed sideroblasts associated with marked thrombocytosis

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