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B07 HIGH EXPRESSION OF NUCLEAR CEREBLON IS ASSOCIATED WITH LONGER SURVIVAL IN PATIENTS WITH MULTIPLE MYELOMA TREATED WITH IMIDS

HemaSphere, 2023-05, Vol.7 (S2), p.7-7

2023

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Hypereosinophilic syndrome in children

Leukemia research, 2012-10, Vol.36 (10), p.1249-1254

2012

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T1768 Generation of a Tightly Regulated Doxycycline-Inducible Model for Studying Mouse Intestinal Biology

Gastroenterology (New York, N.Y. 1943), 2009, Vol.136 (5), p.A-575-A-576

2009

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Comparative therapeutic value of post-remission approaches in patients with acute myeloid leukemia aged 40-60 years

Leukemia, 2015-05, Vol.29 (5), p.1041-1050

2015

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Outcome in children with Down's syndrome and acute lymphoblastic leukemia: role of IKZF1 deletions and CRLF2 aberrations

Leukemia, 2012-10, Vol.26 (10), p.2204-2211

2012

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Clinically and genetically atypical T-cell prolymphocytic leukemia underlines the relevance of a multidisciplinary diagnostic approach

Haematologica (Roma), 2007-03, Vol.92 (3), p.e34-e36

2007

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MicroRNA signatures characterize multiple myeloma patients

Leukemia, 2011-11, Vol.25 (11), p.1784-1789

2011

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Prognostic significance of molecular-cytogenetic abnormalities in pediatric T-ALL is not explained by immunophenotypic differences

Leukemia, 2008-01, Vol.22 (1), p.124-131

2008

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Rapid complete cytogenetic remission after upfront dasatinib monotherapy in a patient with a NUP214-ABL1-positive T-cell acute lymphoblastic leukemia

Leukemia, 2009-03, Vol.23 (3), p.627-629

2009

Volltextzugriff (PDF)

B07 HIGH EXPRESSION OF NUCLEAR CEREBLON IS ASSOCIATED WITH LONGER SURVIVAL IN PATIENTS WITH MULTIPLE MYELOMA TREATED WITH IMIDS

HemaSphere, 2023-05, Vol.7, p.7-7

2023

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EVI1 overexpression in distinct subtypes of pediatric acute myeloid leukemia

Leukemia, 2010-05, Vol.24 (5), p.942-949

2010

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The clinical relevance of minor paroxysmal nocturnal hemoglobinuria clones in refractory cytopenia of childhood: a prospective study by EWOG-MDS

Leukemia, 2014-01, Vol.28 (1), p.189-192

2014

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Cooperative genetic defects in TLX3 rearranged pediatric T-ALL

Leukemia, 2008-04, Vol.22 (4), p.762-770

2008

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PS1374 PROGNOSIS IN ELDERLY MULTIPLE MYELOMA PATIENTS IN THE HOVON‐87/NMSG‐18 STUDY BASED ON REVISED ISS AND SKY92‐ISS

HemaSphere, 2019-06, Vol.3 (S1), p.628-629

2019

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Monoallelic or biallelic LMO2 expression in relation to the LMO2 rearrangement status in pediatric T-cell acute lymphoblastic leukemia

Leukemia, 2008-07, Vol.22 (7), p.1434-1437

2008

Volltextzugriff (PDF)

Segmental uniparental disomy as a recurrent mechanism for homozygous CEBPA mutations in acute myeloid leukemia

Leukemia, 2007-11, Vol.21 (11), p.2382-2384

2007

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BMI1 as oncogenic candidate in a novel TCRB-associated chromosomal aberration in a patient with TCRγ[δ.sup.+] T-cell acute lymphoblastic leukemia

Leukemia, 2008-06, Vol.22 (6), p.1266

2008

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Megalobastic anemia, infantile leukemia, and immunodeficiency caused by a novel homozygous mutation in the DHFR gene

Blood advances, 2022-11, Vol.6 (22), p.5829-5834

2022

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Chromosomal Localization of Three Repair Genes: The Xeroderma Pigmentosum Group C Gene and Two Human Homologs of Yeast RAD23

Genomics (San Diego, Calif.), 1994-10, Vol.23 (3), p.651-658

1994

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The t(10;11) Translocation in Acute Myeloid Leukemia (M5) Consistently Fuses the Leucine Zipper Motif of AF10 Onto the HRX Gene

Blood, 1995-09, Vol.86 (6), p.2073-2076

1995

Volltextzugriff (PDF)

Chromosome 14 copy number-dependent ICH gene rearrangement patterns in high hyperdiploid childhood B-cell precursor ALL: implications for leukemia biology and minimal residual disease analysis

Leukemia, 2009-05, Vol.23 (5), p.870

2009

Volltextzugriff (PDF)

Dasatinib (SPRYCEL®) in Children and Adolescents with Relapsed or Refractory Leukemia: Preliminary Results of the CA180018 Phase I/II Study from the ITCC Consortium

Blood, 2007-11, Vol.110 (11), p.1049-1049

2007

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Cytogenetics in Pediatric MDS - Data of the EWOG-MDS 98 Study

Blood, 2005-11, Vol.106 (11), p.4914-4914

2005

Volltextzugriff (PDF)

A single split-signal FISH probe set allows detection of TAL1 translocations as well as SIL-TAL1 fusion genes in a single test

Leukemia, 2002-04, Vol.16 (4), p.755-761

2002

Volltextzugriff (PDF)

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B07 HIGH EXPRESSION OF NUCLEAR CEREBLON IS ASSOCIATED WITH LONGER SURVIVAL IN PATIENTS WITH MULTIPLE MYELOMA TREATED WITH IMIDS

Hypereosinophilic syndrome in children

T1768 Generation of a Tightly Regulated Doxycycline-Inducible Model for Studying Mouse Intestinal Biology

Comparative therapeutic value of post-remission approaches in patients with acute myeloid leukemia aged 40-60 years

Outcome in children with Down's syndrome and acute lymphoblastic leukemia: role of IKZF1 deletions and CRLF2 aberrations

Clinically and genetically atypical T-cell prolymphocytic leukemia underlines the relevance of a multidisciplinary diagnostic approach

MicroRNA signatures characterize multiple myeloma patients

Prognostic significance of molecular-cytogenetic abnormalities in pediatric T-ALL is not explained by immunophenotypic differences

Rapid complete cytogenetic remission after upfront dasatinib monotherapy in a patient with a NUP214-ABL1-positive T-cell acute lymphoblastic leukemia

B07 HIGH EXPRESSION OF NUCLEAR CEREBLON IS ASSOCIATED WITH LONGER SURVIVAL IN PATIENTS WITH MULTIPLE MYELOMA TREATED WITH IMIDS

EVI1 overexpression in distinct subtypes of pediatric acute myeloid leukemia

The clinical relevance of minor paroxysmal nocturnal hemoglobinuria clones in refractory cytopenia of childhood: a prospective study by EWOG-MDS

Cooperative genetic defects in TLX3 rearranged pediatric T-ALL

PS1374 PROGNOSIS IN ELDERLY MULTIPLE MYELOMA PATIENTS IN THE HOVON‐87/NMSG‐18 STUDY BASED ON REVISED ISS AND SKY92‐ISS

Monoallelic or biallelic LMO2 expression in relation to the LMO2 rearrangement status in pediatric T-cell acute lymphoblastic leukemia

Clinical Impact of Additional Cytogenetic Aberrations and Treatment in Pediatric t(8;21)-Positive AML: Results from an International Retrospective I-BFM-SG Study

Segmental uniparental disomy as a recurrent mechanism for homozygous CEBPA mutations in acute myeloid leukemia

BMI1 as oncogenic candidate in a novel TCRB-associated chromosomal aberration in a patient with TCRγ[δ.sup.+] T-cell acute lymphoblastic leukemia

Megalobastic anemia, infantile leukemia, and immunodeficiency caused by a novel homozygous mutation in the DHFR gene

Chromosomal Localization of Three Repair Genes: The Xeroderma Pigmentosum Group C Gene and Two Human Homologs of Yeast RAD23

The t(10;11) Translocation in Acute Myeloid Leukemia (M5) Consistently Fuses the Leucine Zipper Motif of AF10 Onto the HRX Gene

Chromosome 14 copy number-dependent ICH gene rearrangement patterns in high hyperdiploid childhood B-cell precursor ALL: implications for leukemia biology and minimal residual disease analysis

Dasatinib (SPRYCEL®) in Children and Adolescents with Relapsed or Refractory Leukemia: Preliminary Results of the CA180018 Phase I/II Study from the ITCC Consortium

Cytogenetics in Pediatric MDS - Data of the EWOG-MDS 98 Study

A single split-signal FISH probe set allows detection of TAL1 translocations as well as SIL-TAL1 fusion genes in a single test

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