Beatrice Gulbis

Brussels, BRU, Belgium

Last Updated: 09/26/2026

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Found 57 publications

EHA Recommendations for preconceptual and antenatal screening and prenatal diagnosis for hemoglobinopathies.

EHA Recommendations for preconceptual and antenatal screening and prenatal diagnosis for hemoglobinopathies.

Journal: HemaSphere

Published: December 21, 2025

Osmotic Gradient Ektacytometry in the Diagnosis of Hereditary Red Blood Cell Membrane Disorders: A Need for Standardisation.

Osmotic Gradient Ektacytometry in the Diagnosis of Hereditary Red Blood Cell Membrane Disorders: A Need for Standardisation.

Journal: International journal of laboratory hematology

Published: October 31, 2025

Role of Additional Erythrocyte and Reticulocyte Parameters Offered by Sysmex XN-9000 in the Diagnostic Workup of Hereditary Spherocytosis: A New Screening Algorithm According to Age.

Role of Additional Erythrocyte and Reticulocyte Parameters Offered by Sysmex XN-9000 in the Diagnostic Workup of Hereditary Spherocytosis: A New Screening Algorithm According to Age.

Journal: International journal of laboratory hematology

Published: July 01, 2025

COVID- 19 in patients affected by red blood cell disorders, results from the European registry ERN-EuroBloodNet.

COVID- 19 in patients affected by red blood cell disorders, results from the European registry ERN-EuroBloodNet.

Journal: Orphanet journal of rare diseases

Published: January 04, 2025

Sickle cell disease landscape and challenges in the EU: the ERN-EuroBloodNet perspective.

Sickle cell disease landscape and challenges in the EU: the ERN-EuroBloodNet perspective.

Journal: The Lancet. Haematology

Published: May 31, 2023

Newborn screening for sickle cell disease in Kisangani, Democratic Republic of the Congo: an update.

Newborn screening for sickle cell disease in Kisangani, Democratic Republic of the Congo: an update.

Journal: Hematology (Amsterdam, Netherlands)

Published: May 15, 2023

Sickle cell disease: embedding patient participation into an international conference can transform the role of lived experience.

Sickle cell disease: embedding patient participation into an international conference can transform the role of lived experience.

Journal: Orphanet journal of rare diseases

Published: March 13, 2023

Differential diagnosis of lymphocytosis in routine laboratory practice: Contribution of lymphocyte parameters using the Sysmex-XN9000 haematology analyzer.

Differential diagnosis of lymphocytosis in routine laboratory practice: Contribution of lymphocyte parameters using the Sysmex-XN9000 haematology analyzer.

Journal: International journal of laboratory hematology

Published: January 16, 2023

Osmotic gradient ektacytometry: A tool for more than just hereditary haemolytic anaemia.

Osmotic gradient ektacytometry: A tool for more than just hereditary haemolytic anaemia.

Journal: International journal of laboratory hematology

Published: August 23, 2022

Rare unstable and low oxygen affinity haemoglobin variant, Hb Hazebrouck, detected on Sysmex XN-9000.

Rare unstable and low oxygen affinity haemoglobin variant, Hb Hazebrouck, detected on Sysmex XN-9000.

Journal: Clinical chemistry and laboratory medicine

Published: December 16, 2021

Diagnosis and clinical relevance of co-inheritance of haemoglobin D-Punjab/β+-thalassemia traits in an immigrant Afghan family.

Diagnosis and clinical relevance of co-inheritance of haemoglobin D-Punjab/β+-thalassemia traits in an immigrant Afghan family.

Journal: Journal of clinical pathology

Published: October 26, 2021

Influence of diabetes and hypercholesterolemia on laboratory methods for hereditary spherocytosis diagnosis.

Influence of diabetes and hypercholesterolemia on laboratory methods for hereditary spherocytosis diagnosis.

Journal: Journal of clinical laboratory analysis

Published: June 28, 2021

Showing 1-12 of 57

Last Updated: 09/26/2026