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Page 1
Hemoglobin Denver, a cause of desaturated pulse oximetry. A pediatric case report.
Rossetti E, Eandi Eberle S, Aguirre F, Pepe C, Díaz L, Harris V, Ávalos V. Rossetti E, et al. Among authors: eandi eberle s. Arch Argent Pediatr. 2023 Oct 1;121(5):e202202801. doi: 10.5546/aap.2022-02801.eng. Epub 2023 Mar 9. Arch Argent Pediatr. 2023. PMID: 36857142 Free article. English, Spanish.
Six novel variants in the PKLR gene associated with pyruvate kinase deficiency in Argentinian patients.
Milanesio B, Pepe C, Defelipe LA, Eandi Eberle S, Avalos Gomez V, Chaves A, Albero A, Aguirre F, Fernandez D, Aizpurua L, Paula Dieuzeide M, Turjanski A, Bianchi P, Fermo E, Feliu-Torres A. Milanesio B, et al. Among authors: eandi eberle s. Clin Biochem. 2021 May;91:26-30. doi: 10.1016/j.clinbiochem.2021.02.003. Epub 2021 Feb 23. Clin Biochem. 2021. PMID: 33631127
Glucose 6 phosphate dehydrogenase deficiency: Description of a novel and de novo variant associated with chronic nonspherocytic hemolytic anemia.
Chaves A, Eandi Eberle S, Avalos Gomez V, Milanesio B, Fernandez D, Albero A, Aguirre F, Aizpurua L, Dieuzeide MP, Pepe C, Feliu-Torres A. Chaves A, et al. Among authors: eandi eberle s. Clin Biochem. 2020 Jul;81:63-64. doi: 10.1016/j.clinbiochem.2020.04.007. Epub 2020 May 6. Clin Biochem. 2020. PMID: 32387441 No abstract available.
[Hereditary xerocytosis. Presentation of two pediatric cases].
Eandi Eberle S, Pepe C, Aguirre F, Milanesio B, Fernández D, Ávalos Gómez V, Kinen A, Feliu Torres A. Eandi Eberle S, et al. Arch Argent Pediatr. 2019 Dec 1;117(6):e684-e687. doi: 10.5546/aap.2019.e684. Arch Argent Pediatr. 2019. PMID: 31758911 Free article. Spanish.
Phenotypic and genotypic characterization of glucose-6-phosphate dehydrogenase deficiency in Argentina. Retrospective and descriptive study.
Eandi Eberle S, Pepe C, Chaves A, Aguirre F, Milanesio B, Fernández D, Ávalos Gómez V, Sciuccati G, Díaz LA, Candas A, Cervio C, Bonduel M, Feliu Torres A. Eandi Eberle S, et al. Arch Argent Pediatr. 2019 Aug 1;117(4):263-270. doi: 10.5546/aap.2019.eng.267. Arch Argent Pediatr. 2019. PMID: 31339274 Free article. English, Spanish.
Corrigendum to 'Two novel DNA variants associated with glucose-6-phosphate dehydrogenase deficiency found in Argentine pediatric patients' [Clin. Biochem. 49 (2016) 808-810].
Chaves A, Eandi Eberle S, Defelipe L, Pepe C, Milanesio B, Aguirre F, Fernandez D, Turjanski A, Feliú-Torres A. Chaves A, et al. Among authors: eandi eberle s. Clin Biochem. 2018 Aug;58:131. doi: 10.1016/j.clinbiochem.2018.06.005. Epub 2018 Jun 21. Clin Biochem. 2018. PMID: 29908141 No abstract available.
B-cell acute lymphoblastic leukemia with mature phenotype and MLL rearrangement: report of five new cases and review of the literature.
Sajaroff EO, Mansini A, Rubio P, Alonso CN, Gallego MS, Coccé MC, Eandi-Eberle S, Bernasconi AR, Ampatzidou M, Paterakis G, Papadhimitriou SI, Petrikkos L, Papadakis V, Polychronopoulou S, Rossi JG, Felice MS. Sajaroff EO, et al. Among authors: eandi eberle s. Leuk Lymphoma. 2016 Oct;57(10):2289-97. doi: 10.3109/10428194.2016.1141407. Epub 2016 Feb 8. Leuk Lymphoma. 2016. PMID: 26857438 Review.
16 results