Silvia Eberle-Eandi

Hospital De Pediatría S.A.M.I.C. Prof. Dr. Juan P. Garrahan
B, Argentina

Last Updated: 09/26/2026

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Found 16 publications

Clinical clues to recognizing hereditary dehydrated stomatocytosis (DHSt) in children.

Clinical clues to recognizing hereditary dehydrated stomatocytosis (DHSt) in children.

Journal: Archivos argentinos de pediatria

Published: March 17, 2026

From persistent "hypoxemia" to the diagnosis of an hemoglobinopathy

From persistent "hypoxemia" to the diagnosis of an hemoglobinopathy

Journal: Medicina

Published: February 03, 2025

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

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

Journal: Pediatric blood & cancer

Published: December 21, 2023

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

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

Journal: Archivos argentinos de pediatria

Published: March 01, 2023

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

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

Journal: Clinical biochemistry

Published: December 08, 2020

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

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

Journal: Clinical biochemistry

Published: February 11, 2020

Hereditary xerocytosis. Presentation of two pediatric cases

Hereditary xerocytosis. Presentation of two pediatric cases

Journal: Archivos argentinos de pediatria

Published: March 15, 2019

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

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

Journal: Archivos argentinos de pediatria

Published: September 05, 2018

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

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

Journal: Clinical biochemistry

Published: June 17, 2018

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

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

Journal: Leukemia research

Published: March 21, 2018

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

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

Journal: Leukemia & lymphoma

Published: February 10, 2016

Hemoglobin Woodville associated with double point mutation in the gene of glucose-6-phosphate dehydrogenase

Hemoglobin Woodville associated with double point mutation in the gene of glucose-6-phosphate dehydrogenase

Journal: Medicina

Published: December 29, 2015

Showing 1-12 of 16

Last Updated: 09/26/2026