Fernando M. Aguirre

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 12 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

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

Standards for the Characterization of Endurance in Resistive Switching Devices.

Standards for the Characterization of Endurance in Resistive Switching Devices.

Journal: ACS nano

Published: November 03, 2021

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

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

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

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

Journal: Clinical biochemistry

Published: September 14, 2015

Beta thalassemia intermedia: clinical characteristics and molecular analysis. Case series

Beta thalassemia intermedia: clinical characteristics and molecular analysis. Case series

Journal: Archivos argentinos de pediatria

Published: March 11, 2015

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.

Journal: Hemoglobin

Published: October 01, 2014

Showing 1-12 of 12

Last Updated: 09/26/2026