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In-vitro and in-silico evidence for oxidative stress as drivers for RDW

Scientific reports, 2023-06, Vol.13 (1), p.9223-9223, Article 9223

2023

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GATA-1 Defects in Diamond-Blackfan Anemia: Phenotypic Characterization Points to a Specific Subset of Disease

Genes, 2022-02, Vol.13 (3), p.447

2022

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Hematological Parameters Improve Prediction of Mortality and Secondary Adverse Events in Coronary Angiography Patients: A Longitudinal Cohort Study

Medicine (Baltimore), 2015-11, Vol.94 (45), p.e1992

2015

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Squeezing for Life - Properties of Red Blood Cell Deformability

Frontiers in physiology, 2018-06, Vol.9, p.656-656

2018

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Hematological Parameters Outperform Plasma Markers in Predicting Long-Term Mortality After Coronary Angiography

Angiology, 2018-08, Vol.69 (7), p.600-608

2018

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Management of Gene Promoter Mutations in Molecular Diagnostics

Clinical chemistry (Baltimore, Md.), 2009-04, Vol.55 (4), p.698-708

2009

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Editorial: New Methods for Red Blood Cell Research and Diagnosis

Frontiers in physiology, 2021-09, Vol.12, p.755664-755664

2021

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Recommendations for diagnosis and treatment of methemoglobinemia

American journal of hematology, 2021-12, Vol.96 (12), p.1666-1678

2021

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Editorial: Pathophysiology of Rare Hemolytic Anemias

Frontiers in physiology, 2020-10, Vol.11, p.601746-601746

2020

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Red Blood Cells: Chasing Interactions

Frontiers in physiology, 2019-07, Vol.10, p.945-945

2019

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Biallelic hexokinase 1 (HK1) variants causative of non‐spherocytic haemolytic anaemia: A case series with emphasis on the HK1 promoter variant and literature review

British journal of haematology, 2024-05, Vol.204 (5), p.2040-2048

2024

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Safety and efficacy of mitapivat, an oral pyruvate kinase activator, in sickle cell disease: A phase 2, open‐label study

American journal of hematology, 2022-07, Vol.97 (7), p.E226-E229

2022

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Comment on: Oxygen gradient ektacytometry does not predict pain in children with sickle cell anaemia

British journal of haematology, 2022-06, Vol.197 (5), p.e61-e62

2022

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The fluid membrane determines mechanics of erythrocyte extracellular vesicles and is softened in hereditary spherocytosis

Nature communications, 2018-11, Vol.9 (1), p.4960-9, Article 4960

2018

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Next-generation osmotic gradient ektacytometry for the diagnosis of hereditary spherocytosis: interlaboratory method validation and experience

Clinical chemistry and laboratory medicine, 2017-03, Vol.55 (3), p.394

2017

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The use of next‐generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper

British journal of haematology, 2022-08, Vol.198 (3), p.459-477

2022

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The variable manifestations of disease in pyruvate kinase deficiency and their management

Haematologica (Roma), 2020-09, Vol.105 (9), p.2229

2020

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The energy-less red blood cell is lost: erythrocyte enzyme abnormalities of glycolysis

Blood, 2005-12, Vol.106 (13), p.4034-4042

2005

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Heterozygosity for bisphosphoglycerate mutase deficiency expressing clinically as congenital erythrocytosis: A case series and literature review

British journal of haematology, 2023-01, Vol.200 (2), p.249-255

2023

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Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations

Haematologica (Roma), 2016-11, Vol.101 (11), p.1306

2016

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Rapid and reproducible characterization of sickling during automated deoxygenation in sickle cell disease patients

American journal of hematology, 2019-05, Vol.94 (5), p.575-584

2019

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Comparisons of oxygen gradient ektacytometry parameters between sickle cell patients with or without α‐thalassaemia

British journal of haematology, 2021-11, Vol.195 (4), p.629-633

2021

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Red blood cell phenotyping from 3D confocal images using artificial neural networks

PLoS computational biology, 2021-05, Vol.17 (5), p.e1008934-e1008934

2021

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Proton pump inhibition for secondary hemochromatosis in hereditary anemia: a phase III placebo‐controlled randomized cross‐over clinical trial

American journal of hematology, 2022-07, Vol.97 (7), p.924-932

2022

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The RoxyScan is a novel measurement of red blood cell deformability under oxidative and shear stress

Scientific reports, 2024-03, Vol.14 (1), p.6344-6344, Article 6344

2024

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In-vitro and in-silico evidence for oxidative stress as drivers for RDW

GATA-1 Defects in Diamond-Blackfan Anemia: Phenotypic Characterization Points to a Specific Subset of Disease

Hematological Parameters Improve Prediction of Mortality and Secondary Adverse Events in Coronary Angiography Patients: A Longitudinal Cohort Study

Squeezing for Life - Properties of Red Blood Cell Deformability

Hematological Parameters Outperform Plasma Markers in Predicting Long-Term Mortality After Coronary Angiography

Management of Gene Promoter Mutations in Molecular Diagnostics

Editorial: New Methods for Red Blood Cell Research and Diagnosis

Recommendations for diagnosis and treatment of methemoglobinemia

Editorial: Pathophysiology of Rare Hemolytic Anemias

Red Blood Cells: Chasing Interactions

Biallelic hexokinase 1 (HK1) variants causative of non‐spherocytic haemolytic anaemia: A case series with emphasis on the HK1 promoter variant and literature review

Safety and efficacy of mitapivat, an oral pyruvate kinase activator, in sickle cell disease: A phase 2, open‐label study

Comment on: Oxygen gradient ektacytometry does not predict pain in children with sickle cell anaemia

The fluid membrane determines mechanics of erythrocyte extracellular vesicles and is softened in hereditary spherocytosis

Next-generation osmotic gradient ektacytometry for the diagnosis of hereditary spherocytosis: interlaboratory method validation and experience

The use of next‐generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper

The variable manifestations of disease in pyruvate kinase deficiency and their management

The energy-less red blood cell is lost: erythrocyte enzyme abnormalities of glycolysis

Heterozygosity for bisphosphoglycerate mutase deficiency expressing clinically as congenital erythrocytosis: A case series and literature review

Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations

Rapid and reproducible characterization of sickling during automated deoxygenation in sickle cell disease patients

Comparisons of oxygen gradient ektacytometry parameters between sickle cell patients with or without α‐thalassaemia

Red blood cell phenotyping from 3D confocal images using artificial neural networks

Proton pump inhibition for secondary hemochromatosis in hereditary anemia: a phase III placebo‐controlled randomized cross‐over clinical trial

The RoxyScan is a novel measurement of red blood cell deformability under oxidative and shear stress

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