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Genetic bases and modifiers of β-thalassemia in Argentina

Human gene (Amsterdam, Netherlands), 2022-09, Vol.33, p.201071, Article 201071

2022

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Two novel unstable hemoglobin variants due to in‐frame deletions of key amino acids in the β‐globin chain

European journal of haematology, 2018-06, Vol.100 (6), p.529-535

2018

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Preferences and limitations of hematologists to address the complexity of myelodysplastic syndromes

Medicina, 2019, Vol.79 (3), p.174

2019

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Influence of Acute Myeloid Leukemia Progression on the Prognosis of 831 Patients With Myelodysplastic Syndromes From the Argentine Database

Clinical lymphoma, myeloma and leukemia, 2017-11, Vol.17 (11), p.743-752.e5

2017

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Hereditary spherocytosis. Review. Part II. Symptomatology, outcome, complications, and treatment

Archivos argentinos de pediatría, 2015-04, Vol.113 (2), p.168-176

2015

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Oxidative stress due to aluminum exposure induces eryptosis which is prevented by erythropoietin

Journal of cellular biochemistry, 2012-05, Vol.113 (5), p.1581-1589

2012

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Myelodysplastic syndromes in Latin America: state of the art

Blood advances, 2018-11, Vol.2 (Suppl 1), p.60-62

2018

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Red blood cell aquaporin-1 expression is decreased in hereditary spherocytosis

Annals of hematology, 2016-10, Vol.95 (10), p.1595-1601

2016

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Venetoclax and Azacytidine Therapy in High-Risk Myelodysplastic Syndromes: A Retrospective Evaluation of a Real-World Experience. Latin-American MDS Group - Glam

Blood, 2022-11, Vol.140 (Supplement 1), p.12329-12330

2022

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Eryptosis is induced by hyperthermia in hereditary spherocytosis red blood cells

Clinical chemistry and laboratory medicine, 2016-05, Vol.54 (5), p.e165

2016

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Use of capillary blood to diagnose hereditary spherocytosis

Pediatric blood & cancer, 2012-12, Vol.59 (7), p.1299-1301

2012

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A prospective study to assess the predictive value for hereditary spherocytosis using five laboratory tests (cryohemolysis test, eosin-5′-maleimide flow cytometry, osmotic fragility test, autohemolysis test, and SDS-PAGE) on 50 hereditary spherocytosis families in Argentina

Annals of hematology, 2011-06, Vol.90 (6), p.625-634

2011

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Comparison of the Revised 4 Th (2016) and 5 Th (2022) Editions of the World Health Organization (WHO) Classification in a Cohort of Patients with Lower-Risk Myelodysplastic Syndromes/Neoplasms (MDS) - a Glam Registry (REGLAM) Analysis

Blood, 2023-11, Vol.142 (Supplement 1), p.5179-5179

2023

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Secondary Acute Myeloid Leukemia: Demographic, Physiopathogenic, Clinical and Therapeutic Comparative Study

Blood, 2019-11, Vol.134 (Supplement_1), p.5096-5096

2019

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Flow cytometry “Ogata score” for the diagnosis of myelodysplastic syndromes in a real‐life setting. A Latin American experience

International journal of laboratory hematology, 2019-08, Vol.41 (4), p.536-541

2019

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Argentine Registry of Hematologic Disease (RAEH) Chronics Myeloid Leukemia

Blood, 2011-11, Vol.118 (21), p.4455-4455

2011

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Severe thrombocytopenia as a predictor of survival and response to hypomethylating agents in myelodysplastic syndromes: A Latin‐American cohort of 212 patients

American journal of hematology, 2020-12, Vol.95 (12), p.E323-E326

2020

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Esferocitosis hereditaria: Revisión. Parte I. Historia, demografía, etiopatogenia y diagnóstico

Archivos argentinos de pediatría, 2015-01, Vol.113 (1), p.69-80

2015

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Esferocitosis hereditaria: Revisión. Parte II. Manifestaciones clínicas, evolución, complicaciones y tratamiento

Archivos argentinos de pediatría, 2015-04, Vol.113 (2), p.168-176

2015

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Hereditary spherocytosis: Review. Part I. History, demographics, pathogenesis, and diagnosis

Archivos argentinos de pediatría, 2015-01, Vol.113 (1), p.69-80

2015

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Homenaje a la trayectoria de la Dra. Nilda Ester Fink

Acta bioquímica clínica latinoamericana, 2017-09, Vol.51 (3), p.277-277

Crisp, Renée Leonor

2017

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Preferencias y limitaciones de los hematólogos para afrontar la complejidad de los síndromes mielodisplásicos

Medicina (Buenos Aires), 2019-06, Vol.79 (3), p.174-184

2019

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Esferocitosis hereditaria: experiencia clínica y diagnóstica en Argentina

Acta bioquímica clínica latinoamericana, 2017-09, Vol.51 (3), p.307-318

2017

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Early Cold Stored Platelet Transfusion Following Severe Injury: A Randomized Clinical Trial

Annals of surgery, 2024-08, Vol.280 (2), p.212-221

2024

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Genetic bases and modifiers of β-thalassemia in Argentina

Two novel unstable hemoglobin variants due to in‐frame deletions of key amino acids in the β‐globin chain

Preferences and limitations of hematologists to address the complexity of myelodysplastic syndromes

Influence of Acute Myeloid Leukemia Progression on the Prognosis of 831 Patients With Myelodysplastic Syndromes From the Argentine Database

Active Surveillance of Asymptomatic, Presymptomatic, and Oligosymptomatic SARS-CoV-2-Infected Individuals in Communities Inhabiting Closed or Semi-closed Institutions

Hereditary spherocytosis. Review. Part II. Symptomatology, outcome, complications, and treatment

Oxidative stress due to aluminum exposure induces eryptosis which is prevented by erythropoietin

Myelodysplastic syndromes in Latin America: state of the art

Red blood cell aquaporin-1 expression is decreased in hereditary spherocytosis

Venetoclax and Azacytidine Therapy in High-Risk Myelodysplastic Syndromes: A Retrospective Evaluation of a Real-World Experience. Latin-American MDS Group - Glam

Eryptosis is induced by hyperthermia in hereditary spherocytosis red blood cells

Use of capillary blood to diagnose hereditary spherocytosis

A prospective study to assess the predictive value for hereditary spherocytosis using five laboratory tests (cryohemolysis test, eosin-5′-maleimide flow cytometry, osmotic fragility test, autohemolysis test, and SDS-PAGE) on 50 hereditary spherocytosis families in Argentina

Comparison of the Revised 4 Th (2016) and 5 Th (2022) Editions of the World Health Organization (WHO) Classification in a Cohort of Patients with Lower-Risk Myelodysplastic Syndromes/Neoplasms (MDS) - a Glam Registry (REGLAM) Analysis

Secondary Acute Myeloid Leukemia: Demographic, Physiopathogenic, Clinical and Therapeutic Comparative Study

Flow cytometry “Ogata score” for the diagnosis of myelodysplastic syndromes in a real‐life setting. A Latin American experience

Argentine Registry of Hematologic Disease (RAEH) Chronics Myeloid Leukemia

Severe thrombocytopenia as a predictor of survival and response to hypomethylating agents in myelodysplastic syndromes: A Latin‐American cohort of 212 patients

Esferocitosis hereditaria: Revisión. Parte I. Historia, demografía, etiopatogenia y diagnóstico

Esferocitosis hereditaria: Revisión. Parte II. Manifestaciones clínicas, evolución, complicaciones y tratamiento

Hereditary spherocytosis: Review. Part I. History, demographics, pathogenesis, and diagnosis

Homenaje a la trayectoria de la Dra. Nilda Ester Fink

Preferencias y limitaciones de los hematólogos para afrontar la complejidad de los síndromes mielodisplásicos

Esferocitosis hereditaria: experiencia clínica y diagnóstica en Argentina

Early Cold Stored Platelet Transfusion Following Severe Injury: A Randomized Clinical Trial

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