ESTUDIO OBSERVACIONAL EUROPEO DE DASATINIB (SPRYCEL) EN EL TRATAMIENTO DE PACIENTES CON LEUCEMIA MIELOIDE CRONICA, RESISTENTES E INTOLERANTES A IMATINIB

Dades bàsiques

Protocol:
CA180211
EURDRACT:
NO PROCEDE
NCT:
Centre:
HOSPITAL UNIVERSITARI I POLITÈCNIC LA FE
Any inici:
2009
Any de finalització:
ESTUDIO OBSERVACIONAL INTERNACIONAL

Objectius del projecte

Observaciones: Estado Comité: FINALIZADO

Documents

  • No hi ha documents

Participants

Finançadors - Promotors

BRISTOL-MYERS SQUIBB EMEA SARL

Resultats de l'Assaig Clínic


A NEW INTRONIC MUTATION CAUSES AN ABERRANT SPLICING IN THE ANK1 GENE

Liquori, A.; (...); Cervera, J., V

Meeting Abstract. 2018

  • Open Access.

A novel NUP98/RARG gene fusion in acute myeloid leukemia resembling acute promyelocytic leukemia.

Such E; (...); Sanz MA

Article. 10.1182/blood-2010-06-291658. 2011


A Single-Run Next-Generation Sequencing (NGS) Assay for the Simultaneous Detection of Both Gene Mutations and Large Chromosomal Abnormalities in Patients with Myelodysplastic Syndromes (MDS) and Related Myeloid Neoplasms

Liquori, A; (...); Cervera, J

Article. 10.3390/cancers13081947. 2021

  • Open Access.

Aberrant Alternative Splicing in U2af1/Tet2 Double Mutant Mice Contributes to Major Hematological Phenotypes

Martínez-Valiente C; (...); Sanjuan-Pla A

Article. 10.3390/ijms22136963. 2021

  • Open Access.

Aberrant methylation of tumor suppressor genes in patients with refractory anemia with ring sideroblasts

Valencia, Ana; (...); Sanz, Guillermo F.

Article. 10.1016/j.leukres.2010.08.012. 2011


Absence of mutations in the activation loop and juxtamembrane domains of VEGFR-1 and VEGFR-2 gene in chronic myelomonocytic leukemia (CMML).

Such E; (...); Sanz MA

Letter. 10.1016/j.leukres.2011.10.029. 2012


Absence of mutations in the tyrosine kinase and juxtamembrane domains of C-FMS gene in chronic myelomonocytic leukemia (CMML).

Such, Esperanza; (...); Sanz, Guillermo F

Article. 10.1016/j.leukres.2009.03.018. 2009


Acute Promyelocytic Leukemia: A Constellation of Molecular Events around a Single PML-RARA Fusion Gene

Liquori A; (...); Cervera J

Review. 10.3390/cancers12030624. 2020

  • Open Access.

Acute Promyelocytic Leukemia: A Constellation of Molecular Events around a Single PML-RARA Fusion Gene (vol 12, 624, 2020)

Liquori A; (...); Cervera J

Article. 10.3390/cancers13143440. 2021

  • Open Access.

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

Cervera, Jose; (...); Sanz, Miguel A.

Article. 10.3324/haematol.2009.013243. 2010

  • Open Access.

Adverse prognostic impact of complex karyotype (>= 3 cytogenetic alterations) in adult T-cell acute lymphoblastic leukemia (T-ALL)

Genesca, E; (...); Ribera, JM

Article. 10.1016/j.leukres.2021.106612. 2021

  • Open Access.

Adverse prognostic value of MYBL2 overexpression and association with microRNA-30 family in acute myeloid leukemia patients.

Fuster O; (...); Barragán E

Article. 10.1016/j.leukres.2013.09.015. 2013


Analysis of ASXL1, IDH1, IDH2, c-CBL, and WT1 Mutations in De Novo Acute Myeloid Leukaemia

Ibanez, Mariam; (...); Sanz, Miguel A.

Article. 2011


Analysis of SNP Array Abnormalities in Patients with DE NOVO Acute Myeloid Leukemia with Normal Karyotype

Ibanez, M; (...); Cervera, J

Article. 10.1038/s41598-020-61589-9. 2020

  • Open Access.

Analysis of SNP rs16754 of WT1 gene in a series of de novo acute myeloid leukemia patients.

Luna I; (...); Sanz MA

Article. 10.1007/s00277-012-1596-x. 2012


Analysis of the Possible Persistent Genotoxic Damage in Workers Linked to the Ardystil Syndrome

Montoro, Alegria; (...); Ignacio Villaescusa, Juan

Article. 10.1089/gtmb.2015.0177. 2016


Application of FISH 7q in MDS patients without monosomy 7 or 7q deletion by conventional G-banding cytogenetics: does -7/7q- detection by FISH have prognostic value?

Ademà V; (...); Solé F

Article. 10.1016/j.leukres.2012.12.010. 2013


APPLICATION OF THE MASS SEQUENCING FOR THE STUDY OF MUTATIONS, REORDERINGS AND CHANGES IN GENE EXPRESSION IN THE HEMATOLOGICAL MYELOID NEOPLASIAS

Simarro, CS; (...); Gonzalez, EB

Meeting Abstract. 2018

  • Open Access.

APPROACH TO THE STUDY OF THE ALTERATIONS OF METABOLISM IN THE LMA

Simarro, CS; (...); Gonzalez, EB

Meeting Abstract. 2018

  • Open Access.

Assessing an improved protocol for plasma microRNA extraction.

Moret I; (...); Beltrán B

Article. 10.1371/journal.pone.0082753. 2013

  • Open Access.

Association of MDM2 Gene Polymorphisms SNP285 and 309 with Myelodysplastic Syndromes (MDS) Susceptibility and Outcome.

McGraw, Kathy L.; (...); List, Alan F.

Article. 10.1182/blood.V120.21.2823.2823. 2012


Association of Unbalanced Translocation der(1;7) with Germline GATA2 Mutations.

Kozyra, EJ; (...); Wlodarski, MW

Article. 10.1182/blood.2021012781. 2021

  • Open Access.

Atypical B-Cell Acute Lymphoblastic Leukemia with iAMP21 in the Context of Constitutional Ring Chromosome 21: A Case Report and Review of the Genetic Insights.

Gil, Jose Vicente; (...); Llop, Marta

Article. 10.3390/ijms26010357. 2025

  • Open Access.

Author Correction: Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes.

Bernard E; (...); Papaemmanuil E

Correction. 10.1038/s41591-021-01253-5. 2021

  • Open Access.

Better prognosis for patients with del(7q) than for patients with monosomy 7 in myelodysplastic syndrome.

Cordoba I; (...); Spanish Myelodysplastic Syndrome Registry

Article. 10.1002/cncr.26279. 2012


Biallelic losses of 13q do not confer a poorer outcome in chronic lymphocytic leukemia: analysis of 627 patients with isolated 13q deletion

Puiggros, Anna; (...); Espinet, Blanca

Article. 2013


Bloodstream Infections in Adult Patients Undergoing Cord Blood Transplantation from Unrelated Donors after Myeloablative Conditioning Regimen

Sanz J; (...); Sanz GF

Article. 10.1016/j.bbmt.2014.12.038. 2015


BONE BIOPSY AGAINST PET/CT IN THE DETERMINATION OF MEDULAR INFILTRATION IN INITIAL STATISTICS IN FOLLICULAR LYMPHOMA: DIAGNOSTIC PRECISION AND PRONOSTIC IMPACT

Reguilon Gallego, L.; (...); Jerez Cayuela, A.

Meeting Abstract. 2019

  • Open Access.

BONE MARROW BIOPSY SUPERIORITY OVER PET/CT IN PREDICTING PROGRESSION FREE SURVIVAL IN A HOMOGENOUSLY-TREATED COHORT OF DIFFUSE LARGE B-CELL LYMPHOMA

Liang, THC; (...); Ortuno, FJ

Meeting Abstract. 2017

  • Open Access.

Bone marrow biopsy superiority over PET/CT in predicting progression-free survival in a homogeneously-treated cohort of diffuse large B-cell lymphoma

Chen-Liang, TH; (...); Jose Ortuno, Francisco

Article. 10.1002/cam4.1205. 2017

  • Open Access.

BRAF V600E mutation in adult acute lymphoblastic leukemia.

Alonso CM; (...); Sanz Alonso MA

Letter. 10.3109/10428194.2012.733878. 2013


Case report of a trichohepatoenteric syndrome due to heterozygous compound of novel mutations in ttc37 gen

Polo, B.; (...); Cervera, J.

Meeting Abstract. 2019


CASE REPORT OF SHAAF-YANG SYNDROME WITH A DE NOVO MUTATION IN MAGEL2 GEN

Pi, G.; (...); Cervera, J.

Meeting Abstract. 2019


Case Report: Partial Uniparental Disomy Unmasks a Novel Recessive Mutation in the LYST Gene in a Patient With a Severe Phenotype of Chediak-Higashi Syndrome.

Boluda-Navarro, Mireia; (...); Cervera, Jose Vicente

Article. 10.3389/fimmu.2021.625591. 2021

  • Open Access.

Central nervous system involvement at first relapse in patients with acute myeloid leukemia.

Martínez-Cuadrón D; (...); Sanz MA

Article. 10.3324/haematol.2011.042960. 2011

  • Open Access.

CIP2A high expression is a poor prognostic factor in normal karyotype acute myeloid leukemia

Barragán E; (...); Odero MD

Letter. 10.3324/haematol.2014.118117. 2015

  • Open Access.

Circulating megakaryocyte in primary myelofibrosis. An uncommon finding in a myelofibrosis blood smear.

Cantó PA, Peris MLS, Castera EM

Editorial Material. 10.5045/br.2021.2020269. 2021

  • Open Access.

Cis-Acting Splicing-Associated Variants Can Redefine the Molecular Signature of Genes Commonly Mutated in Acute Myeloid Leukemia

Morote-Faubel, Mireya; (...); Cervera, Jose

Meeting Abstract. 10.1182/blood-2023-177571. 2023

  • Open Access.

Clinical and biological significance of isolated Y chromosome loss in myelodysplastic syndromes and chronic myelomonocytic leukemia. A report from the Spanish MDS Group

Nomdedeu, M; (...); Spanish MDS Group

Article. 10.1016/j.leukres.2017.10.011. 2017


Clinical and biological significance of Y chromosome loss in a series of 2,423 male patients with Myelodysplastic syndromes and Chronic Myelomonocytic Leukemia

Costa, D.; (...); Campo, E.

Meeting Abstract. 2018


Clinical and molecular characterization by next generation sequencing of Spanish patients affected by congenital deficiencies of fibrinogen.

Moret, A; (...); Bonanad, S

Letter. 10.1016/j.thromres.2019.06.015. 2019


CLINICAL APPLICATION OF THE MASSIVE SEQUENCING ADDRESSED IN ACUTE MYELOBLASTIC LEUKEMIA

Garcia, ML; (...); Gonzalez, EB

Meeting Abstract. 2017

  • Open Access.

Clinical impact of the clone size in MDS cases with monosomy 7 or 7q deletion, trisomy 8, 20q deletion and loss of Y chromosome

Mallo, Mar; (...); Sole, Francesc

Article. 10.1016/j.leukres.2011.01.003. 2011


Clinical Utility of a Next-Generation Sequencing Panel for Acute Myeloid Leukemia Diagnostics

Alonso, CM; (...); Barragan, E

Article. 10.1016/j.jmoldx.2018.09.009. 2019

  • Open Access.

Clonal architecture in patients with myelodysplastic syndromes and double or minor complex abnormalities: Detailed analysis of clonal composition, involved abnormalities, and prognostic significance

Schanz, J; (...); Haase, D

Article. 10.1002/gcc.22667. 2018


Clonal composition and its prognostic significance in patients with MDS

Schanz, J; (...); Int Working Grp Prognosis MDS

Meeting Abstract. 2018


Clonal Hematopoiesis Landscape in Patients with De Novo Acute Myeloid Leukemia By Deep Sequencing

Ibanez, Mariam; (...); Cervera, Jose

Meeting Abstract. 10.1182/blood.V128.22.598.598. 2016


COMPARISON OF THREE PANELS OF NGS APPLICATION IN ONCOHEMATOLOGY TO DISCARD SOMATIC AND/OR GERMINAL VARIANTS

Guzman-Gimenez, C.; (...); Such, E.

Meeting Abstract. 2021

  • Open Access.

Complex Karyotype with >= 3 Cytogenetic Alterations is a New Marker of Worse Prognosis in Adult T-Cell Acute Lymphoblastic Leukemia (T-ALL)

Genesca, Eulalia; (...); Maria Ribera, Josep

Meeting Abstract. 2020


Complex Variant t(9;22) Chromosome Translocations in Five Cases of Chronic Myeloid Leukemia.

Valencia A; (...); Sanz MA

Article. 10.1155/2009/187125. 2009


CONCORDANCE STUDY ON THE CATEGORIZATION OF NON-CANONICAL VARIANTS OF JAK2 GENE

Guzman-Gimenez, C.; (...); Such, E.

Meeting Abstract. 2021

  • Open Access.

Concurrent Zrsr2 mutation and Tet2 loss promote myelodysplastic neoplasm in mice

Garcia-Ruiz C; (...); Sanjuan-Pla A

Article. 10.1038/s41375-022-01674-2. 2022

  • Open Access.

Considering Bone Marrow Blasts from Nonerythroid Cellularity Improves the Prognostic Evaluation of MDS in the Context of IPSS-R and Permits a Better Risk Assessment of MDS Patients Classified into the Intermediate Risk Category

Calvo, Xavier; (...); Florensa, Lourdes

Meeting Abstract. 10.1182/blood.V128.22.3185.3185. 2016


Considering Bone Marrow Blasts From Nonerythroid Cellularity Improves the Prognostic Evaluation of Myelodysplastic Syndromes

Arenillas L; (...); Florensa L

Article. 10.1200/JCO.2016.66.9705. 2016


Copper deficiency: a cause of misdiagnosis of myelodysplastic syndrome

Villalba, A; (...); Senent, L

Letter. 10.1007/s00277-018-3334-5. 2018


Cord blood transplantation from unrelated donors in adults with high-risk acute myeloid leukemia.

Sanz J; (...); Sanz GF

Article. 10.1016/j.bbmt.2009.09.001. 2010


Correction to: Spanish registry of hemoglobinopathies and rare anemias (REHem- AR): demographics, complications, and management of patients with ß-thalassemia.

Bardón-Cancho EJ; (...); Cela E

Correction. 10.1007/s00277-024-05838-1. 2024

  • Open Access.

Correlation of myelodysplastic syndromes with i(17)(q10) and TP53 and SETBP1 mutations

Adema V; (...); Solé F

Letter. 10.1111/bjh.13355. 2015


CRISPR to fix bad blood: a new tool in basic and clinical hematology

Gonzalez-Romero, E; (...); Sanjuan-Pla, A

Review. 10.3324/haematol.2018.211359. 2019

  • Open Access.

Critical evaluation of ASO RQ-PCR for minimal residual disease evaluation in multiple myeloma. A comparative analysis with flow cytometry

Puig N; (...); García-Sanz R

Article. 10.1038/leu.2013.217. 2014


CYP2C8 gene polymorphism and bisphosphonate-related osteonecrosis of the jaw in patients with multiple myeloma.

Such E; (...); de la Rubia J

Article. 10.3324/haematol.2011.042572. 2011

  • Open Access.

Cytogenetic Assessment and Risk Stratification in Myelofibrosis with Optical Genome Mapping.

Diaz-Gonzalez, Alvaro; (...); Such, Esperanza

Article. 10.3390/cancers15113039. 2023

  • Open Access.

Characteristics and Outcome of Patients with Acute Myeloid Leukemia and Trisomy 4

Kayser, Sabine; (...); Schlenk, Richard F.

Meeting Abstract. 10.1182/blood-2021-150281. 2021

  • Open Access.

Characteristics and outcome of patients with acute myeloid leukemia and trisomy 4.

Kayser, Sabine; (...); Schlenk, Richard F.

Meeting Abstract. 10.3324/haematol.2022.281137. 2022

  • Open Access.

Characterization and prognostic implication of 17 chromosome abnormalities in myelodysplastic syndrome.

Sánchez-Castro J; (...); Solé F

Article. 10.1016/j.leukres.2013.04.010. 2013


CHARACTERIZATION OF CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA BY MEANS OF IMMUNOLOGICAL AND MOLECULAR TECHNIQUES: RESULTS OF THE GEPTT NATIONAL COLLECTION

Liquori, A.; (...); Gomez-Segui, I

Meeting Abstract. 2019

  • Open Access.

CHARACTERIZATION OF MUTATIONS ALTERING THE PROCESS OF SPLICING IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES (MDS)

Boluda-Navarro, M.; (...); Cervera, J.

Meeting Abstract. 2018

  • Open Access.

CHARACTERIZATION OF RECURRENTLY MUTATED GENES IN ACUTE MYELOID LEUKEMIA DE NOVO WITH NORMAL KARPOTYPE BY TARGETED MASSIVE SEQUENCING

Ibanez, M.; (...); Cervera, J.

Article. 2015

  • Open Access.

CHARACTERIZATION OF THE GENOMIC AND TRANSCRIPTOMIC PROFILE OF THE ACUTE MYELOID LEUKEMIA (AML) SUBGROUP "CHROMATIN-SPLICEOSOME"

Alessandro, Liquori; (...); Zamora Jose, Cervera

Meeting Abstract. 2020

  • Open Access.

Chromosome 8 Abnormalities (8p Losses and 8q Gains) in Patients with Chronic Lymphocytic Leukemia (CLL) and Del(17p)

Blanco, Gonzalo; (...); Espinet, Blanca

Article. 2014


Chronic graft-versus-host disease could ameliorate the impact of adverse somatic mutations in patients with myelodysplastic syndromes and hematopoietic stem cell transplantation.

Caballero JC; (...); Díez Campelo M

Article. 10.1007/s00277-019-03751-6. 2019


Chronic Myelomonocytic Leukemia (CMML) with More Than 15% of Ring Sideroblasts in Bone Marrow: An Overlapping Disorder Between CMML and Refractory Anemia with Ring Sideroblasts

Such, Esperanza; (...); Sanz, Guillermo

Article. 2009


DEEP SEQUENCING OF 23 GENES DESIGNATED BY TCGA STUDY IN ACUTE MYELOID LEUKEMIA PATIENTS WITH NORMAL KARYOTYPE

Ibanez, M.; (...); Cervera, J.

Meeting Abstract. 2016

  • Open Access.

Development and validation of a prognostic scoring system for patients with chronic myelomonocytic leukemia.

Such E; (...); Sanz G

Article. 10.1182/blood-2012-08-452938. 2013


DEVELOPMENT OF A CELLULAR MODEL OF ACUTE MYELOID LEUKEMIA THROUGH CRISPR/CAS 9 TECHNOLOGY

Romero, EG; (...); Zamora, JVC

Meeting Abstract. 2017

  • Open Access.

DEVELOPMENT OF A MASSIVE SEQUENCING TEST FOR THE SIMULTANEOUS DETECTION OF POTENTIAL MUTATIONS AND CHROMOSOMAL ALTERATIONS IN PATIENTS WITH MYELODISPLASIC SYNDROMES

Liquori, A.; (...); Zamora, JVC

Meeting Abstract. 2017

  • Open Access.

Dexamethasone does not prevent malignant cell reintroduction in leukemia patients undergoing ovarian transplant: risk assessment of leukemic cell transmission by a xenograft model

Diaz-Garcia, C; (...); Pellicer, A

Article. 10.1093/humrep/dez115. 2019


DIAGNOSIS OF NOONAN SYNDROME AFTER STUDY OF NGS BY ESSENTIAL THROMBOCITEMIA

Marco Ayala, J.; (...); Sanz, M. A.

Meeting Abstract. 2018

  • Open Access.

Differential diagnosis of myelodysplastic syndrome: anemia associated with copper deficiency

Villalba, A, Senent, L

Editorial Material. 10.1182/blood-2017-11-818013. 2018

  • Open Access.

Early-Onset Myelodysplastic Syndromes (MDS) with Ring Sideroblasts (RS) without SF3B1 Mutations in Adults: Enrichment with Germline Variants in Genes Responsible for Congenital Sideroblastic Anemias

Jauregui, Sandra Novoa; (...); Jerez, Andres

Meeting Abstract. 10.1182/blood-2023-185836. 2023

  • Open Access.

EBV-associated post-transplant lymphoproliferative disorder after umbilical cord blood transplantation in adults with hematological diseases

Sanz J; (...); Sanz GF

Article. 10.1038/bmt.2013.190. 2014


Effect of CD8(+) Cell Content on Umbilical Cord Blood Transplantation in Adults with Hematological Malignancies

Moscardó F; (...); Sanz GF

Article. 10.1016/j.bbmt.2014.06.038. 2014


EFFECT OF MISSENSE MUTATIONS IN THE SPLICING OF PATIENTS WITH ACUTE MYELOID LEUKAEMIA

Morote-Faubel, M.; (...); Cervera, J.

Meeting Abstract. 2019

  • Open Access.

EFFECTS OF B-MYB ABERRANT EXPRESSION ON HEMATOPOIETIC PROGENITOR CELL GROWTH AND DETECTION OF GENETIC VARIATIONS THAT MAY MODIFY ITS PROTEIN FUNCTION

Dolz, S.; (...); Sanz, M.

Article. 2013

  • Open Access.

El nuevo reto en oncologia: la secuenciacion NGS y su aplicacion a la medicina de precision.

Calabria I; (...); Castel V

Article. 10.1016/j.anpedi.2016.05.006. 2016


Enhancing Cytogenetic Diagnostics: Incorporating Optical Genome Mapping in the Laboratory Routine

Diaz-Gonzalez, Alvaro; (...); Such, Esperanza

Meeting Abstract. 10.1182/blood-2023-180691. 2023

  • Open Access.

Enumerating bone marrow blasts from nonerythroid cellularity improves outcome prediction in myelodysplastic syndromes and permits a better definition of the intermediate risk category of the Revised International Prognostic Scoring System (IPSS-R)

Calvo, X; (...); Florensa, L

Article. 10.1002/ajh.24732. 2017

  • Open Access.

Epigenome profiling reveals aberrant DNA methylation signature in GATA2 deficiency.

Marin-Bejar, Oskar; (...); Giorgetti, Alessandra

Article. 10.3324/haematol.2022.282305. 2023

  • Open Access.

ERCC6L2 in Early-Onset Adult Myelodysplastic Syndrome without Pre-Existing Disorder

Carrillo-Tornel, Salvador; (...); Jerez, Andres

Meeting Abstract. 10.1182/blood-2022-168759. 2022

  • Open Access.

Erythroleukemia shares biological features and outcome with myelodysplastic syndromes with excess blasts: a rationale for its inclusion into future classifications of myelodysplastic syndromes

Calvo X; (...); Florensa L

Article. 10.1038/modpathol.2016.146. 2016

  • Open Access.

Evaluation of chimerism by quantitative PCR analysis of DNA polymorphism after allogeneic hematopoietic stem cell transplantation in a pediatric population with malignancies

Bautista, F.; (...); Verdeguer, A.

Article. 10.1111/j.1399-3046.2010.01416.x. 2011


EVALUATION OF THE EFFECT OF DIFFERENT LIGANDS OF TLRS IN THE PROLIFERATION AND DIFFERENTIATION OF ACUTE MYELOID LEUKEMIA CELLS

Fernandez, JG; (...); Ribate, EV

Meeting Abstract. 2017

  • Open Access.

Evaluation of the potential therapeutic effects of a double-stranded RNA mimic complexed with polycations in an experimental mouse model of endometriosis

García-Pascual CM; (...); Gómez R

Article. 10.1016/j.fertnstert.2015.07.1147. 2015

  • Open Access.

Exome sequencing reveals novel and recurrent mutations with clinical impact in blastic plasmacytoid dendritic cell neoplasm

Menezes J; (...); Cigudosa JC

Article. 10.1038/leu.2013.283. 2014


Ex-vivo T-cell depleted peripheral blood stem cell transplantation from HLA-matched sibling donors for the treatment of severe aplastic anemia

Cano-Ferri, I.; (...); Sanz, G.

Meeting Abstract. 2015


Factor XIII deficiency in two Spanish families with a novel variant in gene F13A1 detected by next-generation sequencing; symptoms and clinical management.

Moret A; (...); Bonanad S

Article. 10.1007/s11239-020-02065-z. 2020


FRAGMENT LENGTH ANALYSIS SCREENING FOR CEBPA MUTATIONS DETECTION IN ACUTE MYELOID LEUKEMIA

Fuster, O.; (...); Sanz, M. A.

Article. 2009

  • Open Access.

Fragment length analysis screening for detection of CEBPA mutations in intermediate-risk karyotype acute myeloid leukemia.

Fuster O; (...); Sanz MÁ

Article. 10.1007/s00277-011-1234-z. 2012


FREQUENCY AND CLINICAL IMPACT OF CDKN2A/B GENE LOCUS IN AN ADULT T-ALL COHORT OF PATIENTS ENROLLED IN THE SPANISH PETHEMA GROUP PROTOCOLS

Genesca, E; (...); Ribera, JM

Meeting Abstract. 2017

  • Open Access.

Frequency of dicentrics and contamination levels in Ukrainian children and adolescents from areas near Chernobyl 20 years after the nuclear plant accident.

Montoro A; (...); Villaescusa JI

Article. 10.3109/09553002.2013.809172. 2013


FUNCTIONAL CLASSIFICATION OF DEEP INTRONIC VARIANTS IN PATIENTS WITH ACUTE MYELOBLASTIC LEUKEMIA

Liquori, A.; (...); Cervera Zamora, J.

Meeting Abstract. 2019

  • Open Access.

Functional polymorphisms in SOCS1 and PTPN22 genes correlate with the response to imatinib treatment in newly diagnosed chronic-phase chronic myeloid leukemia.

Guillem V; (...); Hernández-Boluda JC

Article. 10.1016/j.leukres.2011.06.011. 2012


FUNCTIONAL RECLASSIFICATION THROUGH MINIGENE TESTS OF MISSENSE VARIANTS WITH EFFECT ON SPLICING IN PATIENTS WITH ACUTE MYELOID LEUKEMIA

Morote-Faubel, Mireya; (...); Cervera, Jose

Meeting Abstract. 2020

  • Open Access.

FUNCTIONAL STUDY OF SILENCED HMGCR GENE IN CELL LINES OF ACUTE MYELOID LEUKEMIA PATIENTS

De Matteo, B; (...); Zamora, JVC

Meeting Abstract. 2017

  • Open Access.

GENOME-WIDE ANALYSIS OF SINGLE NUCLEOTIDE POLYMORPHISM (SNPS) IN PATIENTS WITH DE NOVO ACUTE MYELOID LEUKEMIA WITH NORMAL KARYOTYPE

Ibanez, M.; (...); Cervera, J.

Meeting Abstract. 2016

  • Open Access.

Genome-wide association study identifies susceptibility loci for acute myeloid leukemia (vol 13, 2, 2022)

Lin, Wei-Yu; (...); Allan, James M.

Article. 10.1038/s41467-021-27679-6. 2022

  • Open Access.

GENOMIC AND TRANSCRIPTOMIC CHARACTERIZATION OF MYELODYSPLASTIC SYNDROMES/MYELOPROLIFERATIVE NEOPLASMS

Acha, P.; (...); Sole, F.

Meeting Abstract. 10.1016/j.leukres.2023.107253. 2023


GENOMIC CLASSIFICATION OF MYELODYSPLASTIC SYNDROMES

Bernard, E.; (...); Papaemmanuil, E.

Meeting Abstract. 10.1016/j.leukres.2023.107146. 2023


Genomic characterization of patients with polycythemia vera developing resistance to hydroxyurea.

Alvarez-Larrán A; (...); Hernández-Boluda JC

Letter. 10.1038/s41375-020-0849-2. 2020

  • Open Access.

Genotype FBN1/Phenotype relationship in a cohort of patients with Marfan syndrome.

Hernándiz A; (...); Sepúlveda P

Article. 10.1111/cge.13879. 2020


Germline and Acquired Genetic Variants in Myelodysplastic Syndromes in Young Adults without a Preexisting Disorder or Organ Dysfunction

Chen-Liang, TH; (...); Jerez, A

Meeting Abstract. 10.1182/blood-2018-99-116045. 2018

  • Open Access.

Germline assessment for alloHSCT candidates over 50 years: A 'Fast-Track' screening in myeloid neoplasms.

Torres-Esquius S; (...); Jerez A

Article. 10.1111/bjh.19460. 2024

  • Open Access.

Germline Predisposition in Myeloid Neoplasms Aged =50: A Novel Approach for Allogeneic Stem Cell -Transplantation Decision-Making

Torres-Esquius, Sara; (...); Jerez, Andres

Meeting Abstract. 10.1182/blood-2023-179234. 2023


GERMLINE PREDISPOSITION TO MYELOID MALIGNANCIES IN A CONSECUTIVE COHORT OF 183 PATIENTS

Santiago, M.; (...); Cervera-Zamora, J.

Meeting Abstract. 10.1016/j.leukres.2023.107247. 2023


Healthcare resource utilization in adult patients with relapsed/refractory FLT3 mutated acute myeloid leukemia: A retrospective chart review from Spain.

Solana-Altabella A; (...); Montesinos P

Article. 10.1111/ejh.13604. 2021


Helpful Criteria When Implementing NGS Panels in Childhood Lymphoblastic Leukemia.

Vega-Garcia N; (...); Camós M

Article. 10.3390/jpm10040244. 2020

  • Open Access.

HIDDEN MDS: A PROSPECTIVE STUDY TO CONFIRM OR EXCLUDE MDS IN PATIENTS WITH ANEMIA OF UNCERTAIN ETIOLOGY

Bastida Bermejo, J. M.; (...); Diez-Campelo, M.

Meeting Abstract. 2016

  • Open Access.

Hidden myelodysplastic syndrome (MDS): A prospective study to confirm or exclude MDS in patients with anemia of uncertain etiology

Bastida, JM; (...); Diez-Campelo, M

Article. 10.1111/ijlh.12933. 2019


Human Mesenchymal Stem Cells Growth and Osteogenic Differentiation on Piezoelectric Poly(vinylidene fluoride) Microsphere Substrates

Sobreiro-Almeida, R.; (...); Sempere, A.

Article. 10.3390/ijms18112391. 2017

  • Open Access.

Imiquimod inhibits growth and induces differentiation of myeloid leukemia cell lines

Villamon, E; (...); Gil, ML

Article. 10.1186/s12935-018-0515-1. 2018

  • Open Access.

Impact of ABC single nucleotide polymorphisms upon the efficacy and toxicity of induction chemotherapy in acute myeloid leukemia

Megias-Vericat, JE; (...); Aliño SF

Article. 10.1080/10428194.2016.1231405. 2017


Impact of adjunct cytogenetic abnormalities for prognostic stratification in patients with myelodysplastic syndrome and deletion 5q

Mallo, M.; (...); Sole, F.

Article. 10.1038/leu.2010.231. 2011


IMPACT OF ALLELIC STATUS OF TP53 MUTATIONS IN ACUTE MYELOID LEUKEMIA (AML)

Ibanez, Mariam; (...); Sanz, Guillermo

Meeting Abstract. 2020

  • Open Access.

Impact of combinations of single-nucleotide polymorphisms of anthracycline transporter genes upon the efficacy and toxicity of induction chemotherapy in acute myeloid leukemia.

Megías-Vericat JE; (...); Montesinos P

Article. 10.1080/10428194.2020.1839650. 2020


IMPACT OF CYTOGENETICS ON THE OUTCOME OF ADULT ACUTE LYMPHOBLASTIC LEUKEMIA: RESULTS FROM A SINGLE INSTITUTION

Gomez, I.; (...); Sanz, M.

Article. 2009

  • Open Access.

Impact of NADPH oxidase functional polymorphisms in acute myeloid leukemia induction chemotherapy

Megias-Vericat, JE; (...); Aliño SF

Article. 10.1038/tpj.2017.19. 2018


Impact of SNP array karyotyping on the diagnosis and the outcome of chronic myelomonocytic leukemia with low risk cytogenetic features or no metaphases

Palomo L; (...); Zamora L

Article. 10.1002/ajh.24227. 2016

  • Open Access.

Impact of somatic mutations in myelodysplastic patients with isolated partial or total loss of chromosome 7.

Crisà E; (...); Mufti GJ

Article. 10.1038/s41375-020-0728-x. 2020

  • Open Access.

Impact of Transporter Genes Polymorphisms in Standard Induction of Acute Myeloid Leukemia

Eduardo Megias, Juan; (...); Angel Sanz, Miguel

Meeting Abstract. 2015


Impact on Outcomes of Human Leukocyte Antigen Matching by Allele-Level Typing in Adults with Acute Myeloid Leukemia Undergoing Umbilical Cord Blood Transplantation

Sanz J; (...); Sanz GF

Article. 10.1016/j.bbmt.2013.10.016. 2014


IMPLEMENTATION OF MASSIVE SEQUENCING TECHNOLOGIES TO THE DETECTION OF MUTATIONS IN THE ABL KINASE DOMAIN OF BCR-ABL REORDERING

Simarro, CS; (...); Gonzalez, EB

Meeting Abstract. 2017

  • Open Access.

Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes (vol 26, pg 1549, 2020)

Bernard, Elsa; (...); Elias, Harold K

Article. 10.1038/s41591-021-01367-w. 2021

  • Open Access.

Implications ofTP53allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes

Bernard, E; (...); Papaemmanuil, E

Article. 10.1038/s41591-020-1008-z. 2020

  • Open Access.

In vitro all-trans retinoic acid sensitivity of acute myeloid leukemia blasts with NUP98/RARG fusion gene

Such E; (...); Sanz MA

Letter. 10.1007/s00277-014-2073-5. 2014


In vitro cytogenetic and genotoxic effects of curcumin on human peripheral blood lymphocytes.

Sebastià N; (...); Montoro A

Article. 10.1016/j.fct.2012.06.012. 2012


IN VIVO MODELS FOR THE FUNCTIONAL STUDY OF CO-OCCURRING GENETIC AND EPIGENETIC MUTATIONS IN MYELODYSPLASTIC SYNDROMES

Martinez-Valiente, C.; (...); Sanjuan-Pla, A.

Meeting Abstract. 2018

  • Open Access.

IN VIVO MODELS TO STUDY THE COOPERATION BETWEEN SPLICING AND DNA METHYLATION IN MYELODYSPLASTIC SYNDROMES

Martinez-Valiente, Cristina; (...); Sanjuan-Pla, Alejandra

Meeting Abstract. 2020

  • Open Access.

Incidence and outcome of invasive fungal disease after front-line intensive chemotherapy in patients with acute myeloid leukemia: impact of antifungal prophylaxis.

Rodríguez-Veiga R; (...); Sanz GF

Article. 10.1007/s00277-019-03744-5. 2019


Incidence and risk factors of post-engraftment invasive fungal disease in adult allogeneic hematopoietic stem cell transplant recipients receiving oral azoles prophylaxis

Montesinos P; (...); Sanz MA

Article. 10.1038/bmt.2015.181. 2015


Incidence, Clinical Associations, and Co-Mutation Patterns of UBA1 Mutations in MDS

Sirenko, Maria; (...); Papaemmanuil, Elli

Meeting Abstract. 10.1182/blood-2022-162397. 2022

  • Open Access.

Incidence, Risk Factors, and Outcome of Cytomegalovirus Infection and Disease in Patients Receiving Prophylaxis with Oral Valganciclovir or Intravenous Ganciclovir after Umbilical Cord Blood Transplantation

Montesinos, Pau; (...); Sanz, Guillermo F.

Article. 10.1016/j.bbmt.2009.03.002. 2009

  • Open Access.

Influence of cytarabine metabolic pathway polymorphisms in acute myeloid leukemia induction treatment

Megias-Vericat, JE; (...); Aliño SF

Article. 10.1080/10428194.2017.1323267. 2017


Influence of polymorphisms in anthracyclines metabolism genes in the standard induction chemotherapy of acute myeloid leukemia.

Megías-Vericat JE; (...); Montesinos P

Article. 10.1097/FPC.0000000000000431. 2021


Influence of Single Nucleotide Polymorphisms in Anthracycline Metabolism Pathway in Standard Induction of Acute Myeloid Leukemia

Eduardo Megias, Juan; (...); Angel Sanz, Miguel

Meeting Abstract. 2015


Infusion of Haploidentical Stem Cell after Consolidation in Younger Patients with Acute Myeloid Leukemia: Preliminary Results of a Phase I-II Study

Boluda, Blanca; (...); Sanz, Miguel A.

Meeting Abstract. 10.1182/blood.V128.22.1614.1614. 2016


IN-SILICO AND IN VITRO STUDY OF MUTATIONS THAT ALTER THE SPLICING PROCESS IN PATIENTS WITH MYELODISPLASIC SYNDROMES

Boluda-Navarro, M.; (...); Cervera, J.

Meeting Abstract. 2019

  • Open Access.

JUVENILE MYELOMONOCITIC LEUKEMIA IN PATIENTS WITH NOONAN SYNDROME AND NOONAN-LIKE SYNDROMES: EXPERIENCE OF THE SPANISH YOUTH MYELOMONOCITIC LEUKEMIA REGISTRATION

Arques Martinez, L.; (...); Catala Temprano, A.

Meeting Abstract. 2019

  • Open Access.

Karyotypic complexity rather than chromosome 8 abnormalities aggravates the outcome of chronic lymphocytic leukemia patients with TP53 aberrations

Blanco, G; (...); Espinet, B

Article. 10.18632/oncotarget.13106. 2016

  • Open Access.

K-Means Clustering Identifies Diverse Clinical Phenotypes in COVID-19 Patients: Implications for Mortality Risks and Remdesivir Impact.

Garcia-Vidal C; (...); Soriano A

Article. 10.1007/s40121-024-00938-x. 2024

  • Open Access.

Lineage switch from B lymphoblastic leukemia with KMT2A-rearranged to mixed-phenotype acute leukemia under daratumumab

Marco-Ayala, J; (...); Peris, MLS

Editorial Material. 10.5045/br.2020.2020059. 2020

  • Open Access.

Los elementos decorativos ambientales en el Area de Imagen Medica mejoran la percepcion de agradabilidad del paciente.

Garcia Marcos R; (...); Diaz Dho R

Abstract of Published Item. 10.1016/j.rx.2012.07.006. 2014


MASS SEQUENCING DIRECTED TO THE STUDY OF REARRANGEMENTS AND CHANGES IN GENIC EXPRESSION IN ACUTE MYELOID LEUKEMIA

Sargas Simarro, C.; (...); Barragan Gonzalez, E.

Meeting Abstract. 2019

  • Open Access.

MODELING OF IDH2 GENE MUTATIONS IN THE CAENORHABDITIS ELEGANS ORGANISM. DEVELOPMENT OF A NEW STUDY MODEL

Gonzalez-Romero, E.; (...); Cervera-Zamora, J.

Meeting Abstract. 2021

  • Open Access.

Molecular and clinical presentation of UBA1-mutated myelodysplastic syndromes.

Sirenko, Maria; (...); Papaemmanuil, Elli

Article. 10.1182/blood.2023023723. 2024


MOLECULAR CHARACTERIZATION OF CELLULAR MODELS OF ACUTE MYELOBLASTIC LEUKEMIA (AML) BY MASS SEQUENCING

Navarro, MB; (...); Cervera, J

Meeting Abstract. 2017

  • Open Access.

MOLECULAR CHARACTERIZATION OF PATIENTS WITH HEREDITARY MYELOID NEOPLASIAS THROUGH MASS SEQUENCING

Pardo-Lorente, N.; (...); Cervera, J.

Meeting Abstract. 2018

  • Open Access.

MOLECULAR CHARACTERIZATION OF VARIANTS THAT ALTER SPLICING (VAS) IN PATIENTS WITH MYELODYSPLASIC SYNDROMES

Boluda-Navarro, M.; (...); Cervera, J.

Meeting Abstract. 2020

  • Open Access.

Molecular Taxonomy of Myelodysplastic Syndromes and Its Clinical Implications

Bernard, Elsa; (...); Papaemmanuil, Elli

Meeting Abstract. 10.1182/blood-2023-186863. 2023

  • Open Access.

Molecular Taxonomy of Myelodysplastic Syndromes and its Clinical Implications.

Bernard, Elsa; (...); Papaemmanuil, Elli

Article. 10.1182/blood.2023023727. 2024


Monosomal karyotype in MDS: explaining the poor prognosis?

Schanz J; (...); Haase D

Article. 10.1038/leu.2013.187. 2013


Multiple phenotypes and epigenetic profiles in a three-generation family history with GATA2 deficiency.

Romero-Moya, Damia; (...); Giorgetti, Alessandra

Article. 10.1038/s41375-025-02519-4. 2025


Mutations in the DNA methylation pathway and number of driver mutations predict response to azacitidine in myelodysplastic syndromes

Cedena, MT; (...); Martinez-Lopez, J

Article. 10.18632/oncotarget.22157. 2017

  • Open Access.

Negative impact on clinical outcome of the mutational co-occurrence of SF3B1 and DNMT3A in refractory anemia with ring sideroblasts (RARS)

Martin, I; (...); Sanz, G

Article. 10.1080/10428194.2016.1246725. 2017


New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II.

Musri, Melina Mara; (...); Sanchez, Mayka

Article. 10.3390/ijms24129935. 2023

  • Open Access.

New comprehensive cytogenetic scoring system for primary myelodysplastic syndromes (MDS) and oligoblastic acute myeloid leukemia after MDS derived from an international database merge.

Schanz J; (...); Haase D

Article. 10.1200/JCO.2011.35.6394. 2012


New mutations found by Next-Generation Sequencing screening of Spanish patients with Nemaline Myopathy

Moreau-Le Lan, S; (...); Pedrola, L

Article. 10.1371/journal.pone.0207296. 2018

  • Open Access.

Next generation sequencing in bleeding disorders: two novel variants in the F5 gene (Valencia-1 and Valencia-2) associated with mild factor V deficiency.

Moret, A; (...); Bonanad, S

Article. 10.1007/s11239-019-01911-z. 2019


Novel real-time polymerase chain reaction assay for simultaneous detection of recurrent fusion genes in acute myeloid leukemia.

Dolz S; (...); Sanz MA

Article. 10.1016/j.jmoldx.2013.04.003. 2013


Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies.

Bogliolo M; (...); Surralles J

Article. 10.1136/jmedgenet-2019-106249. 2020


OPTIMIZATION OF THE EFFICIENCY OF GENETIC EDITING OF HEMAPOYETIC PROGENITOR CELLS USING CRISPR/CAS9 RIBONUCLEOPROTEINS

Martinez-Valiente, C.; (...); Sanjuan-Pla, A.

Meeting Abstract. 2019

  • Open Access.

Panel Sequencing for Clinically Oriented Variant Screening and Copy Number Detection in Chronic Lymphocytic Leukemia Patients

Ibanez, Mariam; (...); Luna I

Article. 10.3390/diagnostics12040953. 2022

  • Open Access.

Partial T Cell-Depleted Peripheral Blood Stem Cell Transplantation from HLA-Identical Sibling Donors for Patients with Severe Aplastic Anemia.

Sanz J; (...); Piñana JL

Article. 10.1016/j.bbmt.2019.08.020. 2020

  • Open Access.

PCR-Based Strategy for Introducing CRISPR/Cas9 Machinery into Hematopoietic Cell Lines.

González-Romero E; (...); Vázquez-Manrique RP

Article. 10.3390/cancers15174263. 2023

  • Open Access.

Personalized Medicine: Learning to Walk

Gargallo, P.; (...); Canete, A.

Meeting Abstract. 2018


Pharmacological Profiles of Acute Myeloid Leukemia Treatments in Patient Samples by Automated Flow Cytometry: A Bridge to Individualized Medicine

Bennett TA; (...); Ballesteros J

Article. 10.1016/j.clml.2013.11.006. 2014


Prognostic Impact of Anthracycline Metabolism Gene Polymorphisms in Newly Diagnosed Acute Myeloid Leukemia Adults

Eduardo Megias, Juan; (...); Angel Sanz, Miguel

Article. 2014


Prognostic Impact of Cytarabine Pathway Gene Polymorphisms in Acute Myeloid Leukemia Adults Undergoing Induction Chemotherapy

Eduardo Megias, Juan; (...); Angel Sanz, Miguel

Article. 2014


Prognostic impact of chromosomal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemia patients. A study by the spanish group of myelodysplastic syndromes

Nomdedeu, M; (...); Costa, D

Article. 10.1002/gcc.22333. 2016


Prognostic impact of gene mutations in myelodysplastic syndromes with ring sideroblasts

Martin, I; (...); Sanz, G

Article. 10.1038/s41408-017-0016-9. 2017

  • Open Access.

PROGNOSTIC IMPACT OF TRANSPORTER GENE POLYMORPHISMS IN NEWLY DIAGNOSED ACUTE MYELOID LEUKEMIA ADULTS

Megias Vericat, J. E.; (...); Sanz, M. A.

Article. 2015

  • Open Access.

Prognostic Significance of Complex Karyotype and Monosomal Karyotype in Adult Patients With Acute Lymphoblastic Leukemia Treated With Risk-Adapted Protocols

Motlló C; (...); Feliu E

Article. 10.1002/cncr.28950. 2014


PROGNOSTIC VALUE OF B-MYB AND ITS REGULATION BY MIRNAS IN ACUTE MYELOID LEUKEMIA

LLop, M.; (...); Angel Sanz, M.

Article. 2013

  • Open Access.

Prognostic value of cytogenetics in adult patients with Philadelphia-negative acute lymphoblastic leukemia.

Gómez-Seguí I; (...); Sanz MA

Article. 10.1007/s00277-011-1331-z. 2012


Prognostic Value of Chromosome 1 Abnormalities in Myelodysplastic Syndrome

Ibarrondo, Paloma; (...); Batlle-Lopez, Ana

Article. 2014


Prognostic value of trisomy 8 as a single anomaly and the influence of additional cytogenetic aberrations in primary myelodysplastic syndromes.

Saumell S; (...); Solé F

Article. 10.1111/bjh.12035. 2012


Proposed global prognostic score for systemic mastocytosis: a retrospective prognostic modelling study.

Muñoz-González JI; (...); Orfao A

Article. 10.1016/S2352-3026(20)30400-2. 2021


PROPOSED MOLECULAR CLASSIFICATION OF ACUTE MYELOBLASTIC LEUKEMIA (AML) BASED ON SPLICING EVENTS

Liquori, A.; (...); Cervera Zamora, J.

Meeting Abstract. 2021

  • Open Access.

Purtscher-like retinopathy associated with dermatomyositis and hemophagocytic lymphohistiocytosis.

Barreiro-González A; (...); Azorín Villena I

Article. 10.1016/j.oftal.2017.03.009. 2018


Quantitative Expression Analysis of WT1 Main Isoforms in AML

Luna, Irene; (...); Sanz, Miguel A.

Article. 2011


Radioprotective activity and cytogenetic effect of resveratrol in human lymphocytes: an in vitro evaluation.

Sebastià N; (...); Montoro A

Article. 10.1016/j.fct.2012.10.013. 2013


Rapid Detection of KIT Mutations in Core-Binding Factor Acute Myeloid Leukemia Using High-Resolution Melting Analysis

Fuster, Oscar; (...); Angel Sanz, Miguel

Article. 10.2353/jmoldx.2009.090043. 2009

  • Open Access.

Rapid screening of ASXL1, IDH1, IDH2, and c-CBL mutations in de novo acute myeloid leukemia by high-resolution melting.

Ibáñez M; (...); Sanz MA

Article. 10.1016/j.jmoldx.2012.06.006. 2012


Reciprocal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemias: review of 5,654 patients with an evaluable karyotype.

Costa D; (...); Nomdedeu B

Article. 10.1002/gcc.22071. 2013


Regions of homozygosity confer a worse prognostic impact in myelodysplastic syndrome with normal karyotype.

Mallo, Mar; (...); Sole, Francesc

Article. 10.1002/jha2.651. 2023

  • Open Access.

REMOVAL OF GERMINAL LINE MUTATIONS IN PATIENTS WITH MDS AND AML: WHO SHOULD BE PERFORMED?

Santiago, Marta; (...); Cervera, Jose

Meeting Abstract. 2020


Reproducibility of the World Health Organization 2008 criteria for myelodysplastic syndromes.

Senent L; (...); Florensa L

Article. 10.3324/haematol.2012.071449. 2013

  • Open Access.

Response to lenalidomide in myelodysplastic syndromes with del(5q): influence of cytogenetics and mutations.

Mallo M; (...); Solé F

Article. 10.1111/bjh.12354. 2013


Revealing the mutational landscape of acute promyelocytic leukemia

Cervera, J, Sanz, MA

Editorial Material. 10.21037/tcr.2017.02.47. 2017


RNA Sequencing Analysis for the Identification of a PCM1/PDGFRB Fusion Gene Responsive to Imatinib

Such, E; (...); Cervera, J

Article. 10.1159/000497348. 2019


Screening for IDH mutations in chronic myelomonocytic leukemia.

Ibañez M; (...); Sanz MA

Letter. 10.3109/10428194.2012.701295. 2013


Significance of increased blastic-appearing cells in bone marrow following myeloablative unrelated cord blood transplantation in adult patients.

Montesinos P; (...); Sanz GF

Article. 10.1016/j.bbmt.2011.11.008. 2012


SIGNIFICANCE OF INCREASED BONE MARROW BLASTS AFTER MYELOID ENGRAFTMENT IN ADULT PATIENTS UNDERGOING UNRELATED CORD BLOOD TRANSPLANTATION

Gascon, A.; (...); Sanz, M.

Article. 2010

  • Open Access.

Simplified in-House Deep Sequencing Method of Inmunoglobulin Genes for Minimal Residual Dissease Quantification and Risk Stratification in Multiple Myeloma

Sanchez-Vega, Beatriz; (...); Martinez Lopez, Joaquin

Article. 2015


Single nucleotide polymorphism array karyotyping: a diagnostic and prognostic tool in myelodysplastic syndromes with unsuccessful conventional cytogenetic testing.

Arenillas L; (...); Solé F

Article. 10.1002/gcc.22112. 2013


Single-Nucleotide Polymorphism Array-Based Karyotyping of Acute Promyelocytic Leukemia

Gómez-Seguí I; (...); Sanz MA

Article. 10.1371/journal.pone.0100245. 2014

  • Open Access.

Sister chromatid exchange, (SCE), High-Frequency Cells (HFCs) and SCE distribution patterns in peripheral blood lymphocytes of Spanish adult smokers compared to non-smokers

Sebastià N; (...); Montoro A

Article. 10.1016/j.fct.2014.01.011. 2014


SJOGREN-LARSSON SYNDROME IN TWO SISTERS WITH AN INTRONIC VARIANT OF ALDH3A2 GENE: CLINICAL FINDINGS

Fernandez, F.; (...); Cervera, J.

Meeting Abstract. 2019


Somatic Genetic and Epigenetic Architecture of Myelodysplastic Syndromes Arising from GATA2 Deficiency

Loyola, Victor Bengt Pastor; (...); Wlodarski, Marcin W.

Article. 2015


Spanish Guidelines for the use of targeted deep sequencing in myelodysplastic syndromes and chronic myelomonocytic leukaemia.

Palomo L; (...); Such E

Article. 10.1111/bjh.16175. 2020

  • Open Access.

Spanish registry of hemoglobinopathies and rare anemias (REHem-AR): demographics, complications, and management of patients with ß-thalassemia.

Bardón-Cancho EJ; (...); Cela E

Article. 10.1007/s00277-024-05694-z. 2024

  • Open Access.

STUDY OF CHRONIC ANEMIA IN THE ELDERLY

Villalba, A.; (...); Sanz, M. A.

Meeting Abstract. 2017

  • Open Access.

STUDY OF PRE-EXISTING MUTATIONS IN HEMATOPOYETIC CELLS OF THE BONE MEDULA IN PATIENTS WITH MYELOID NEOPLASIAS RELATED TO THERAPY

Ibanez, M; (...); Sanz, G

Meeting Abstract. 2017

  • Open Access.

Study of the S427G polymorphism and of MYBL2 variants in patients with acute myeloid leukemia

Dolz S; (...); Barragán E

Article. 10.3109/10428194.2015.1049167. 2016


STUDY OF TRANSCRIPTIONAL DIFFERENCES BETWEEN THE IDH2 R140 AND R172 MUTATIONS BY MEANS OF MODELING IN THE ORGANISM CAENORHABDITIS ELEGANS

Gonzalez, Romero Elisa; (...); Cervera, Jose Vicente

Meeting Abstract. 2020

  • Open Access.

Superiority of bortezomib, thalidomide, and dexamethasone (VTD) as induction pretransplantation therapy in multiple myeloma: a randomized phase 3 PETHEMA/GEM study.

Rosiñol L; (...); Programa para el Estudio y la Terapéutica de las Hemopatías Malignas

Article. 10.1182/blood-2012-02-408922. 2012


SUPERIORITY OF THE BIOPSY OF BONE MARROW ON PET/TC IN THE PREDICTION OF THE FREE SURVIVAL OF PROGRESSION IN DIFFUSE LINFOMA B OF BIG CELL

Liang, THC; (...); Ortuno, F.

Meeting Abstract. 2017

  • Open Access.

The Clinical Spectrum, Diagnosis, and Management of GATA2 Deficiency.

Santiago, Marta; (...); Cervera, Jose

Article. 10.3390/cancers15051590. 2023

  • Open Access.

The modular network structure of the mutational landscape of Acute Myeloid Leukemia

Ibanez, M; (...); Cervera, J

Article. 10.1371/journal.pone.0202926. 2018

  • Open Access.

THE MODULAR NETWORK STRUCTURE OF THE MUTATIONAL LANDSCAPE OF ACUTE MYELOID LEUKEMIA

Ibanez, M.; (...); Cervera, J.

Article. 2015

  • Open Access.

The Mutational Landscape of Acute Promyelocytic Leukemia Reveals an Interacting Network of Co-Occurrences and Recurrent Mutations

Ibáñez, M; (...); Cervera, J.

Article. 10.1371/journal.pone.0148346. 2016

  • Open Access.

The relationship of TP53 R72P polymorphism to disease outcome and TP53 mutation in myelodysplastic syndromes

McGraw KL; (...); List AF

Article. 10.1038/bcj.2015.11. 2015

  • Open Access.

The reliability of bone marrow cytology as response criterion in metastatic neuroblastoma.

Schumacher-Kuckelkorn R; (...); Berthold F

Article. 10.1002/pbc.28819. 2021

  • Open Access.

The role of bone marrow biopsy and FDG-PET/CT in identifying bone marrow infiltration in the initial diagnosis of high grade non-Hodgkin B-cell lymphoma and Hodgkin lymphoma. accuracy in a multicenter series of 372 patients

Chen-Liang TH; (...); Ortuño FJ

Article. 10.1002/ajh.24044. 2015


Time and Cost of Hospitalisation for Salvage Therapy in Adults with Philadelphia Chromosome-Negative B Cell Precursor Relapsed or Refractory Acute Lymphoblastic Leukaemia in Spain

Boluda, B; (...); Montesinos, P

Article. 10.1007/s41669-018-0098-8. 2019

  • Open Access.

TP53 State Dictates Genome Stability, Clinical Presentation and Outcomes in Myelodysplastic Syndromes

Bernard, Elsa; (...); Papaemmanuil, Elli

Meeting Abstract. 10.1182/blood-2019-129392. 2019

  • Open Access.

TRANSCRIPTOMICAL ANALYSIS AND MODELING IN C.ELEGANS OF THE IDH2 R140 R172 MUTATION

Gonzalez-Romero, E.; (...); Cervera-Zamora, J., V

Meeting Abstract. 2019

  • Open Access.

TRANSLOCATIONS IN THERAPY-RELATED MYELODYSPLASTIC SYNDROMES: REVIEW OF 69 PATIENTS FROM THE SPANISH SMD GROUP DATABASE WITH AN EVALUABLE KARYOTYPE

Grau, Javier; (...); Granada, Isabel

Meeting Abstract. 2020

  • Open Access.

UBA1 Mutations Identify a Rare but Distinct Subtype of Myelodysplastic Syndromes

Sirenko, Maria; (...); Papaemmanuil, Elli

Meeting Abstract. 10.1182/blood-2023-182949. 2023

  • Open Access.

Untitled

Castel, V; (...); Zuniga, A

Letter. 10.1007/s12094-018-1889-1. 2018


USE OF CRISPR/CAS9 TECHNOLOGY TO MODIFY THE IDH2 GENE IN BOTH IN-VIVO AND IN-VITRO MODELS

Gonzalez Romero, E.; (...); Cervera, J., V

Meeting Abstract. 2018

  • Open Access.

Validation Of a Comprehensive Health Status Assessment Scale In Older Patients (>= 65 years) With Hematological Malignances. Gah Study

Bonanad, Santiago; (...); De La Rubia, Javier

Article. 10.1182/blood.V122.21.2979.2979. 2013


VALIDATION OF A NEW MASSIVE SEQUENCING TECHNIQUE FOR MOLECULAR DIAGNOSIS OF ACUTE MYELOBLASTIC LEUKEMIA

Llop Garcia, M.; (...); Barragan Gonzalez, E.

Meeting Abstract. 2015

  • Open Access.

Validation of a Next-Generation Sequencing Panel for AML Routine Diagnosis

Alonso, Carmen M.; (...); Barragan, Eva

Article. 2015


VALIDATION OF DIFFERENT SYSTEMS OF STRATIFICATION OF PROGNOSIS OF SMD IN AN INDEPENDENT SERIES

Collado Jose, Esteban; (...); Sanz, Guillermo

Meeting Abstract. 2016

  • Open Access.

VALIDATION OF FREQUENT SPLICING EVENTS IN ACUTE MYELOID LEUKEMIA WITH POTENTIAL TO GENERATE NEOANTIGENS

Beatriz, Fernandez-Blanco; (...); Jose Vicente, Cervera Zamora

Meeting Abstract. 2021

  • Open Access.

Visceral leishmaniasis infection during adalimumab therapy: a case report and literature review

Tung Chen Y; (...); Salavert M

Letter. 10.1111/1756-185X.12427. 2014


Vulnerabilities in mIDH2 AML confer sensitivity to APL-like targeted combination therapy

Mugoni, V; (...); Pandolfi, PP

Article. 10.1038/s41422-019-0162-7. 2019

  • Open Access.

Wnt signaling pathway is epigenetically regulated by methylation of Wnt antagonists in acute myeloid leukemia

Valencia, A.; (...); Sanz, M. A.

Article. 10.1038/leu.2009.86. 2009


WT1 isoform expression pattern in acute myeloid leukemia.

Luna I; (...); Sanz MA

Article. 10.1016/j.leukres.2013.10.009. 2013


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