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Detection of minimally disseminated disease in the cerebrospinal fluid of children with high-risk retinoblastoma by reverse transcriptase-polymerase chain reaction for GD2 synthase mRNA

European journal of cancer (1990), 2013-09, Vol.49 (13), p.2892-2899

2013

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Hemoglobin San Martin: A New Unstable Variant Associated with Hemoglobin S in an Argentinean Boy

Blood, 2007-11, Vol.110 (11), p.3806-3806

2007

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Multicenter Study of Pyruvate Kinase Deficiency in Argentina

Journal of Hematology Research, 2022-06, Vol.9, p.4-9

2022

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Metahemoglobinemia recesiva congénita. A propósito de un caso

Hematología (En línea), 2022, Vol.26 (2), p.1-4

2022

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Anemia sideroblástica por una variante en el gen ALAS2

Hematología (En línea), 2024-08, Vol.28 (2), p.6-10

2024

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Vitamina B12 activa (holotranscobalamina)

Hematología (En línea), 2019, Vol.23 (2), p.92-94

2019

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Efecto de la hidroxiurea en hemoglobina S

Medicina (Buenos Aires), 2003-04, Vol.63 (2), p.140-142

2003

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Megaloblastic anemia with homocystinuria type cblE: Atypical presentation in a pediatric patient with high transfusion requirement and autoimmune phenomena

Pediatric blood & cancer, 2024-04, Vol.71 (4), p.e30867-n/a

2024

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Hemoglobin Denver, a cause of desaturated pulse oximetry. A pediatric case report

Archivos argentinos de pediatría, 2023-10, Vol.121 (5), p.e202202801

2023

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Lineage switch in childhood acute leukemia: An unusual event with poor outcome

American journal of hematology, 2012-09, Vol.87 (9), p.890-897

2012

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Corrigendum to ‘Two novel DNA variants associated with glucose-6-phosphate dehydrogenase deficiency found in Argentine pediatric patients’ [Clin. Biochem. 49 (2016) 808–810]

Clinical biochemistry, 2018-08, Vol.58, p.131-131

2018

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Six novel variants in the PKLR gene associated with pyruvate kinase deficiency in Argentinian patients

Clinical biochemistry, 2021-05, Vol.91, p.26-30

2021

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Experience with four consecutive BFM-based protocols for treatment of childhood with non-promyelocytic acute myeloblastic leukemia in Argentina

Leukemia & lymphoma, 2016-09, Vol.57 (9), p.2090-2099

2016

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Glucose 6 phosphate dehydrogenase deficiency: Description of a novel and de novo variant associated with chronic nonspherocytic hemolytic anemia

Clinical biochemistry, 2020-07, Vol.81, p.63-64

2020

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Phenotypic and genotypic characterization of glucose-6-phosphate dehydrogenase deficiency in Argentina. Retrospective and descriptive study

Archivos argentinos de pediatría, 2019-08, Vol.117 (4), p.263-270

2019

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Two novel DNA variants associated with glucose-6-phosphate dehydrogenase deficiency found in Argentine pediatric patients

Clinical biochemistry, 2016-07, Vol.49 (10-11), p.808-810

2016

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Cytogenetic and Molecular Findings in Children with Acute Lymphoblastic Leukemia: Experience of a Single Institution in Argentina

Molecular syndromology, 2015-10, Vol.6 (4), p.193-203

2015

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FLT3, NPM1 and CEBPA Mutations in 195 Children with Acute Myeloid Leukemia in Argentina

Blood, 2014-12, Vol.124 (21), p.5318-5318

2014

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Cytoplasmic CD3 expression in infant acute megakaryoblastic leukemia: A new ambiguous lineage subtype?

Leukemia research, 2018-08, Vol.71, p.6-12

2018

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Hereditary xerocytosis. Presentation of two pediatric cases

Archivos argentinos de pediatría, 2019-12, Vol.117 (6), p.e684

2019

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B-cell acute lymphoblastic leukemia with mature phenotype and MLL rearrangement: report of five new cases and review of the literature

Leukemia & lymphoma, 2016-10, Vol.57 (10), p.2289-2297

2016

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Acute Megakaryoblastic Leukemia in Childhood: Comparison Between Patients with and without Down Syndrome

Blood, 2014-12, Vol.124 (21), p.952-952

2014

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A new β(0) frameshift mutation, HBB: c.44delT (p.Leu14ArgfsX5), identified in an Argentinean family associated with secondary genetic modifiers of β-thalassemia

Hemoglobin, 2014-01, Vol.38 (6), p.444-446

2014

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A New β 0 Frameshift Mutation, HBB : c.44delT (p.Leu14ArgfsX5), Identified in an Argentinean Family Associated with Secondary Genetic Modifiers of β-Thalassemia

Hemoglobin, 2014-12, Vol.38 (6), p.444-446

2014

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A New β0 Frameshift Mutation, HBB: c.44delT (p.Leu14ArgfsX5), Identified in an Argentinean Family Associated with Secondary Genetic Modifiers of β-Thalassemia

Hemoglobin, 2014-12, Vol.38 (6), p.444-446

2014

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Detection of minimally disseminated disease in the cerebrospinal fluid of children with high-risk retinoblastoma by reverse transcriptase-polymerase chain reaction for GD2 synthase mRNA

Hemoglobin San Martin: A New Unstable Variant Associated with Hemoglobin S in an Argentinean Boy

Multicenter Study of Pyruvate Kinase Deficiency in Argentina

Metahemoglobinemia recesiva congénita. A propósito de un caso

Anemia sideroblástica por una variante en el gen ALAS2

Vitamina B12 activa (holotranscobalamina)

Efecto de la hidroxiurea en hemoglobina S

Megaloblastic anemia with homocystinuria type cblE: Atypical presentation in a pediatric patient with high transfusion requirement and autoimmune phenomena

Hemoglobin Denver, a cause of desaturated pulse oximetry. A pediatric case report

Lineage switch in childhood acute leukemia: An unusual event with poor outcome

Corrigendum to ‘Two novel DNA variants associated with glucose-6-phosphate dehydrogenase deficiency found in Argentine pediatric patients’ [Clin. Biochem. 49 (2016) 808–810]

Six novel variants in the PKLR gene associated with pyruvate kinase deficiency in Argentinian patients

Experience with four consecutive BFM-based protocols for treatment of childhood with non-promyelocytic acute myeloblastic leukemia in Argentina

Glucose 6 phosphate dehydrogenase deficiency: Description of a novel and de novo variant associated with chronic nonspherocytic hemolytic anemia

Phenotypic and genotypic characterization of glucose-6-phosphate dehydrogenase deficiency in Argentina. Retrospective and descriptive study

Two novel DNA variants associated with glucose-6-phosphate dehydrogenase deficiency found in Argentine pediatric patients

Cytogenetic and Molecular Findings in Children with Acute Lymphoblastic Leukemia: Experience of a Single Institution in Argentina

FLT3, NPM1 and CEBPA Mutations in 195 Children with Acute Myeloid Leukemia in Argentina

Cytoplasmic CD3 expression in infant acute megakaryoblastic leukemia: A new ambiguous lineage subtype?

Hereditary xerocytosis. Presentation of two pediatric cases

B-cell acute lymphoblastic leukemia with mature phenotype and MLL rearrangement: report of five new cases and review of the literature

Acute Megakaryoblastic Leukemia in Childhood: Comparison Between Patients with and without Down Syndrome

A new β(0) frameshift mutation, HBB: c.44delT (p.Leu14ArgfsX5), identified in an Argentinean family associated with secondary genetic modifiers of β-thalassemia

A New β 0 Frameshift Mutation, HBB : c.44delT (p.Leu14ArgfsX5), Identified in an Argentinean Family Associated with Secondary Genetic Modifiers of β-Thalassemia

A New β0 Frameshift Mutation, HBB: c.44delT (p.Leu14ArgfsX5), Identified in an Argentinean Family Associated with Secondary Genetic Modifiers of β-Thalassemia

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