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Standardization of molecular monitoring for chronic myeloid leukemia in Latin America using locally produced secondary cellular calibrators

Leukemia, 2016-11, Vol.30 (11), p.2258-2260

2016

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Genotoxicity of AMPA, the environmental metabolite of glyphosate, assessed by the Comet assay and cytogenetic tests

Ecotoxicology and environmental safety, 2009-03, Vol.72 (3), p.834-837

2009

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Developing a new generation of tests for genotyping hemophilia‐causative rearrangements involving int22h and int1h hotspots in the factor VIII gene

Journal of thrombosis and haemostasis, 2008-05, Vol.6 (5), p.830-836

2008

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Single nucleotide polymorphism in PTEN-Long gene: A risk factor in chronic myeloid leukemia

Gene, 2019-04, Vol.694, p.71-75

2019

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Phenotype–genotype correlations in hemophilia A carriers are consistent with the binary role of the phase between F8 and X‐chromosome inactivation

Journal of thrombosis and haemostasis, 2015-04, Vol.13 (4), p.530-539

2015

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Transforming growth factor-β1 functional polymorphisms in myeloablative sibling hematopoietic stem cell transplantation

Bone marrow transplantation (Basingstoke), 2017-05, Vol.52 (5), p.739-744

2017

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Transforming growth factor- beta 1 functional polymorphisms in myeloablative sibling hematopoietic stem cell transplantation

Bone marrow transplantation (Basingstoke), 2017-05, Vol.52 (5), p.739-744

2017

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Identification of driver and subclonal mutations in ASXL1 and IDH1/IDH2 genes in an Argentine series of patients with myelofibrosis

International journal of laboratory hematology, 2018-08, Vol.40 (4), p.e82-e86

2018

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Clinical and Prognostic Features in a Series of 277 Patients with Chronic Myelomonocytic Leukemia (CMML) from South America: A Multicenter Study

Leukemia research, 2017-04, Vol.55, p.S141-S141

2017

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Polymorphic variants of GSTM1, GSTT1, and GSTP1 genes in childhood acute leukemias: A preliminary study in Argentina

Hematology (Luxembourg), 2015-10, Vol.20 (9), p.511-516

2015

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Reliable and cost-effective approach for diagnosis of heterozygous F8/F9 large deletions by quantitative real-time PCR

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-05, Vol.21 (3), p.e247-e251

2015

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Factor VIII genotype characterization of haemophilia A affected patients with transient and permanent inhibitors: a comprehensive Argentine study of inhibitor risks

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-07, Vol.19 (4), p.511-518

2013

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P-108 Application of the revised International Prognostic Scoring System for myelodysplastic syndromes in 470 Argentinean patients

Leukemia research, 2013-05, Vol.37, p.S71-S72

2013

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Novel Variant Ph Translocation t(9;22;11)(q34;q11.2;p15)inv(9)(p13q34) in Chronic Myeloid Leukemia Involving a One-Step Mechanism

Cytogenetic and genome research, 2011-02, Vol.132 (4), p.304-308

2011

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Cryptic t(4;11) encoding MLL-AF4 due to insertion of 5' MLL sequences in chromosome 4

Leukemia, 2001-04, Vol.15 (4), p.595-600

2001

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Genotoxicity of glyphosate assessed by the comet assay and cytogenetic tests

Environmental toxicology and pharmacology, 2009-07, Vol.28 (1), p.37-41

2009

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Recovery course of foveal microstructure in the nonsurgical resolution of full-thickness macular hole

Graefe's archive for clinical and experimental ophthalmology, 2022-10, Vol.260 (10), p.3173-3183

2022

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Chromosomal aberrations in human lymphocytes exposed in vitro to enrofloxacin and ciprofloxacin

Toxicology letters, 1999-01, Vol.104 (1), p.43-48

1999

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A New Animal Model for Human Undifferentiated Thyroid Carcinoma

Thyroid (New York, N.Y.), 2003-06, Vol.13 (6), p.529-536

2003

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PS1169 CYTOKINE AND ARGINASE‐1 EXPRESSION DYNAMICS IN PATIENTS WITH CHRONIC MYELOID LEUKEMIA REVEALS EARLY MOLECULAR RESPONSE TO IMATINIB

HemaSphere, 2019-06, Vol.3 (S1), p.531-532

2019

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PB1425 High Cell-free (cf)DNA in Patients with Myelofibrosis (MF) is Associated with Adverse Clinical Outcomes, Activation of the AIM2 Inflammasome and Elevated Levels of Inflammasome-Related Cytokine IL-18

Research and practice in thrombosis and haemostasis, 2023-10, Vol.7, p.101694, Article 101694

2023

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Specific analysis of the intron 22 XbaI polymorphism of the human factor VIII gene using long‐distance PCR

British journal of haematology, 1999-12, Vol.107 (3), p.566-568

1999

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The CpG island in intron 22 of the factor VIII gene is predominantly methylated on the X chromosome of human males

Journal of human genetics, 2002-05, Vol.47 (5), p.239-242

2002

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Transforming growth factor-[beta]1 functional polymorphisms in myeloablative sibling hematopoietic stem cell transplantation

Bone marrow transplantation (Basingstoke), 2017-05, Vol.52 (5), p.739

2017

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246 - Clinical and Prognostic Features in a Series of 277 Patients with Chronic Myelomonocytic Leukemia (CMML) from South America: A Multicenter Study

Leukemia research, 2017-04, Vol.55, p.S141-S141

2017

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Standardization of molecular monitoring for chronic myeloid leukemia in Latin America using locally produced secondary cellular calibrators

Genotoxicity of AMPA, the environmental metabolite of glyphosate, assessed by the Comet assay and cytogenetic tests

Developing a new generation of tests for genotyping hemophilia‐causative rearrangements involving int22h and int1h hotspots in the factor VIII gene

Single nucleotide polymorphism in PTEN-Long gene: A risk factor in chronic myeloid leukemia

Phenotype–genotype correlations in hemophilia A carriers are consistent with the binary role of the phase between F8 and X‐chromosome inactivation

Transforming growth factor-β1 functional polymorphisms in myeloablative sibling hematopoietic stem cell transplantation

Transforming growth factor- beta 1 functional polymorphisms in myeloablative sibling hematopoietic stem cell transplantation

Identification of driver and subclonal mutations in ASXL1 and IDH1/IDH2 genes in an Argentine series of patients with myelofibrosis

Clinical and Prognostic Features in a Series of 277 Patients with Chronic Myelomonocytic Leukemia (CMML) from South America: A Multicenter Study

Polymorphic variants of GSTM1, GSTT1, and GSTP1 genes in childhood acute leukemias: A preliminary study in Argentina

Reliable and cost-effective approach for diagnosis of heterozygous F8/F9 large deletions by quantitative real-time PCR

Factor VIII genotype characterization of haemophilia A affected patients with transient and permanent inhibitors: a comprehensive Argentine study of inhibitor risks

P-108 Application of the revised International Prognostic Scoring System for myelodysplastic syndromes in 470 Argentinean patients

Novel Variant Ph Translocation t(9;22;11)(q34;q11.2;p15)inv(9)(p13q34) in Chronic Myeloid Leukemia Involving a One-Step Mechanism

Cryptic t(4;11) encoding MLL-AF4 due to insertion of 5' MLL sequences in chromosome 4

Genotoxicity of glyphosate assessed by the comet assay and cytogenetic tests

Recovery course of foveal microstructure in the nonsurgical resolution of full-thickness macular hole

Chromosomal aberrations in human lymphocytes exposed in vitro to enrofloxacin and ciprofloxacin

A New Animal Model for Human Undifferentiated Thyroid Carcinoma

PS1169 CYTOKINE AND ARGINASE‐1 EXPRESSION DYNAMICS IN PATIENTS WITH CHRONIC MYELOID LEUKEMIA REVEALS EARLY MOLECULAR RESPONSE TO IMATINIB

PB1425 High Cell-free (cf)DNA in Patients with Myelofibrosis (MF) is Associated with Adverse Clinical Outcomes, Activation of the AIM2 Inflammasome and Elevated Levels of Inflammasome-Related Cytokine IL-18

Specific analysis of the intron 22 XbaI polymorphism of the human factor VIII gene using long‐distance PCR

The CpG island in intron 22 of the factor VIII gene is predominantly methylated on the X chromosome of human males

Transforming growth factor-[beta]1 functional polymorphisms in myeloablative sibling hematopoietic stem cell transplantation

246 - Clinical and Prognostic Features in a Series of 277 Patients with Chronic Myelomonocytic Leukemia (CMML) from South America: A Multicenter Study

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