Alesa Kristan
Ljubljana, Slovenia
Last Updated: 09/26/2026
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Found 9 publications
Targeted Next-Generation Sequencing in Rare Diseases.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: November 15, 2024
Integration and Visualization of Regulatory Elements and Variations of the EPAS1 Gene in Human.
Journal: Genes
Published: October 25, 2021
Congenital erythrocytosis - A condition behind recurrent thromboses: A case report and literature review.
Journal: Clinical hemorheology and microcirculation
Published: June 07, 2021
Identification of Variants Associated With Rare Hematological Disorder Erythrocytosis Using Targeted Next-Generation Sequencing Analysis.
Journal: Frontiers in genetics
Published: April 01, 2021
Diagnosis and management of non-clonal erythrocytosis remains challenging: a single centre clinical experience.
Journal: Annals of hematology
Published: February 19, 2021
Genetic analysis of 39 erythrocytosis and hereditary hemochromatosis-associated genes in the Slovenian family with idiopathic erythrocytosis.
Journal: Journal of clinical laboratory analysis
Published: August 31, 2020
Erythrocytosis: genes and pathways involved in disease development.
Journal: Blood transfusion = Trasfusione del sangue
Published: June 17, 2020
Genetic variability of hypoxia-inducible factor alpha (HIFA) genes in familial erythrocytosis: Analysis of the literature and genome databases.
Journal: European journal of haematology
Published: June 22, 2019
Showing 1-9 of 9
Last Updated: 09/26/2026