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P1001: DNMT3A/TET2/ASXL1 MUTATIONS DETERMINE THROMBOTIC RISK IN POLYCYTHAEMIA VERA

HemaSphere, 2022-06, Vol.6 (Suppl), p.891-892

2022

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An IPSS-R Cutoff Point of 3 Stratified Myelodysplastic Syndromes Patients Into Two Risk Groups

Leukemia research, 2017-04, Vol.55, p.S145-S146

2017

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An IPSS-R Cutoff Point of 3 Stratified Chronic Myelomonocytic Leukemia Patients Into Two Risk Groups

Leukemia research, 2017-04, Vol.55, p.S144-S145

2017

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Spanish Guidelines for the use of Targeted Deep Sequencing in MDS and CMML

Leukemia research, 2017-04, Vol.55, p.S16-S16

2017

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Collagen type IV (α3–α4) nephropathy: from isolated haematuria to renal failure

Nephrology, dialysis, transplantation, 2004-10, Vol.19 (10), p.2429-2432

2004

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Topic: AS07-Singular Entities/Subtypes/AS07c-Hereditary MDS including predisposition syndromes: HIGH PREVALENCE OF IDIOPATHIC DYPSLASIA OF UNDETERMINED SIGNIFICANCE (IDUS) AND CLONAL HEMATOPOIESIS OF INDETEMINATE POTENTIAL (CHIP) AMONG RELATIVES OF HEMATOLOGIC NEOPLASMS WITH GERMLINE PREDISPOSITION PATIENTS

Leukemia research, 2023-05, Vol.128, p.107249, Article 107249

2023

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Topic: AS04-MDS Biology and Pathogenesis/AS04h-Immune deregulation/inflammation: BONE MARROW CYTOKINES AND CHEMOKINES CONCENTRATIONS IN MYELODISPLASTIC NEOPLASMS

Leukemia research, 2023-05, Vol.128, p.107210, Article 107210

2023

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Topic: AS04-MDS Biology and Pathogenesis/AS04h-Immune deregulation/inflammation: BONE MARROW MICROENVIRONMENT CHANGES IN MYELODYSPLASTIC NEOPLASMS AND ITS RELATIONSHIP WITH CLONAL HEMATOPOIESIS

Leukemia research, 2023-05, Vol.128, p.107209, Article 107209

2023

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Topic: AS07-Singular Entities/Subtypes/AS07a-ARCH, CCUS, ICUS: PREVALENCE, DYNAMICS AND CLINICAL SIGNIFICANCE OF CLONAL HEMATOPOIESIS OF INDETERMINATE POTENTIAL (CHIP) IN NEWLY DIAGNOSED CANCER PATIENTS

Leukemia research, 2023-05, Vol.128, p.107244, Article 107244

2023

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Topic: AS07-Singular Entities/Subtypes/AS07a-ARCH, CCUS, ICUS: CLINICAL AND CARDIOVASCULAR RISK ASSESSMENT OF SUBJECTS WITH JAK2-V617F CLONAL HEMATOPOIESIS

Leukemia research, 2023-05, Vol.128, p.107240, Article 107240

2023

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Topic: AS04-MDS Biology and Pathogenesis/AS04h-Immune deregulation

Leukemia research, 2021-09, Vol.108, p.106681, Article 106681.31

2021

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P31 - Topic: AS04-MDS Biology and Pathogenesis/AS04h-Immune deregulation: PHENOTYPE AND GENOTYPE OF NATURAL KILLERS IN MYELODISPLASITIC SYNDROME

Leukemia research, 2021-09, Vol.108

2021

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Single human blastomere allele dropout (ADO) and amplification efficiency by PCR

Fertility and sterility, 2010, Vol.94 (4), p.S124-S124

2010

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Topic: AS04-MDS Biology and Pathogenesis/AS04h-Immune deregulation

Leukemia research, 2021-09, Vol.108, p.106681, Article 106681.30

2021

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P30 - Topic: AS04-MDS Biology and Pathogenesis/AS04h-Immune deregulation: RELATION BETWEEN INMUNE CELL POPULATIONS AND MALIGNANT CLONE MUTATIONAL STATUS IN MYELODYSPLASTIC SYNDROMES

Leukemia research, 2021-09, Vol.108

2021

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253 - An IPSS-R Cutoff Point of 3 Stratified Myelodysplastic Syndromes Patients Into Two Risk Groups

Leukemia research, 2017-04, Vol.55, p.S145-S146

2017

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252 - An IPSS-R Cutoff Point of 3 Stratified Chronic Myelomonocytic Leukemia Patients Into Two Risk Groups

Leukemia research, 2017-04, Vol.55, p.S144-S145

2017

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Study of candidate genes affecting the progression of renal disease in autosomal dominant polycystic kidney disease type 1

Nephrology, dialysis, transplantation, 2007-06, Vol.22 (6), p.1567-1577

2007

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26 - Spanish Guidelines for the use of Targeted Deep Sequencing in MDS and CMML

Leukemia research, 2017-04, Vol.55, p.S16-S16

2017

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Male-to-male transmission of X-linked Alport syndrome in a boy with a 47,XXY karyotype

European journal of human genetics : EJHG, 2005-09, Vol.13 (9), p.1040-1046

2005

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PS1196 INNOVATIVE DIAGNOSTIC APPROACH FOR RARE ANEMIA

HemaSphere, 2019-06, Vol.3 (S1), p.545-n/a

2019

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Evaluation of genome coverage and fidelity of multiple displacement amplification from single cells by SNP array

Molecular human reproduction, 2009-11, Vol.15 (11), p.739-747

2009

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23 Estudio del gen NPHS2 en el síndrome nefrótico c orticorresistente

Anales de pediatría (Barcelona, Spain : 2003), 2007-11, Vol.67 (5), p.e534

2007

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23 Estudio del gen NPHS2 en el síndrome nefrótico corticorresistente

Anales de pediatría (Barcelona, Spain : 2003), 2007, Vol.67 (5), p.e534-e534

2007

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P-949

Fertility and sterility, 2006-09, Vol.86 (3), p.S485-S486

2006

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P1001: DNMT3A/TET2/ASXL1 MUTATIONS DETERMINE THROMBOTIC RISK IN POLYCYTHAEMIA VERA

An IPSS-R Cutoff Point of 3 Stratified Myelodysplastic Syndromes Patients Into Two Risk Groups

An IPSS-R Cutoff Point of 3 Stratified Chronic Myelomonocytic Leukemia Patients Into Two Risk Groups

Spanish Guidelines for the use of Targeted Deep Sequencing in MDS and CMML

Collagen type IV (α3–α4) nephropathy: from isolated haematuria to renal failure

Topic: AS04-MDS Biology and Pathogenesis/AS04h-Immune deregulation/inflammation: BONE MARROW CYTOKINES AND CHEMOKINES CONCENTRATIONS IN MYELODISPLASTIC NEOPLASMS

Topic: AS04-MDS Biology and Pathogenesis/AS04h-Immune deregulation/inflammation: BONE MARROW MICROENVIRONMENT CHANGES IN MYELODYSPLASTIC NEOPLASMS AND ITS RELATIONSHIP WITH CLONAL HEMATOPOIESIS

Topic: AS07-Singular Entities/Subtypes/AS07a-ARCH, CCUS, ICUS: PREVALENCE, DYNAMICS AND CLINICAL SIGNIFICANCE OF CLONAL HEMATOPOIESIS OF INDETERMINATE POTENTIAL (CHIP) IN NEWLY DIAGNOSED CANCER PATIENTS

Topic: AS07-Singular Entities/Subtypes/AS07a-ARCH, CCUS, ICUS: CLINICAL AND CARDIOVASCULAR RISK ASSESSMENT OF SUBJECTS WITH JAK2-V617F CLONAL HEMATOPOIESIS

Topic: AS04-MDS Biology and Pathogenesis/AS04h-Immune deregulation

P31 - Topic: AS04-MDS Biology and Pathogenesis/AS04h-Immune deregulation: PHENOTYPE AND GENOTYPE OF NATURAL KILLERS IN MYELODISPLASITIC SYNDROME

Single human blastomere allele dropout (ADO) and amplification efficiency by PCR

Topic: AS04-MDS Biology and Pathogenesis/AS04h-Immune deregulation

P30 - Topic: AS04-MDS Biology and Pathogenesis/AS04h-Immune deregulation: RELATION BETWEEN INMUNE CELL POPULATIONS AND MALIGNANT CLONE MUTATIONAL STATUS IN MYELODYSPLASTIC SYNDROMES

253 - An IPSS-R Cutoff Point of 3 Stratified Myelodysplastic Syndromes Patients Into Two Risk Groups

252 - An IPSS-R Cutoff Point of 3 Stratified Chronic Myelomonocytic Leukemia Patients Into Two Risk Groups

Study of candidate genes affecting the progression of renal disease in autosomal dominant polycystic kidney disease type 1

26 - Spanish Guidelines for the use of Targeted Deep Sequencing in MDS and CMML

Male-to-male transmission of X-linked Alport syndrome in a boy with a 47,XXY karyotype

PS1196 INNOVATIVE DIAGNOSTIC APPROACH FOR RARE ANEMIA

Evaluation of genome coverage and fidelity of multiple displacement amplification from single cells by SNP array

23 Estudio del gen NPHS2 en el síndrome nefrótico c orticorresistente

23 Estudio del gen NPHS2 en el síndrome nefrótico corticorresistente

P-949

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