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Glucose‐6‐phosphate dehydrogenase deficiency‐associated hemolysis and methemoglobinemia in a COVID‐19 patient treated with chloroquine

American journal of hematology, 2020-08, Vol.95 (8), p.E194-E196

2020

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Analysis of a cohort of 101 CDAII patients: description of 24 new molecular variants and genotype‐phenotype correlations

British journal of haematology, 2016-11, Vol.175 (4), p.696-704

2016

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Rapid diagnosis of hereditary haemolytic anaemias using automated rheoscopy and supervised machine learning

British journal of haematology, 2020-08, Vol.190 (4), p.e250-e255

2020

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P1450: VOXELOTOR TREATMENT LEADS TO IMPROVED VIABILITY OF SICKLE ERYTHROCYTES

HemaSphere, 2023-08, Vol.7 (S3), p.e0036284-n/a

2023

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The cholesterol content of the erythrocyte membrane is an important determinant of phosphatidylserine exposure

Biochimica et biophysica acta, 2012-12, Vol.1821 (12), p.1493-1500

2012

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Mild dyserythropoiesis and β-like globin gene expression imbalance due to the loss of histone chaperone ASF1B

Human genomics, 2020-10, Vol.14 (1), p.39-39, Article 39

2020

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Two novel haemoglobin variants that affect haemoglobin A1c measurement by ion-exchange chromatography

Clinical chemistry and laboratory medicine, 2015-08, Vol.53 (9), p.1465

2015

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Inherited glutathione reductase deficiency and Plasmodium falciparum malaria--a case study

PloS one, 2009-10, Vol.4 (10), p.e7303

2009

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Inborn defects in the antioxidant systems of human red blood cells

Free radical biology & medicine, 2014-02, Vol.67, p.377-386

2014

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Hemolysis in the spleen drives erythrocyte turnover

Blood, 2020-10, Vol.136 (14), p.1579-1589

2020

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Neutrophil FcγRIIIb Deficiency, Nature, and Clinical Consequences: A Study of 21 Individuals From 14 Families

Blood, 1995-09, Vol.86 (6), p.2403-2413

1995

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Voxelotor Treatment Leads to Improved Viability of Sickle Erythrocytes and Altered Neutrophil Phenotype

Blood, 2022-11, Vol.140 (Supplement 1), p.11114-11115

2022

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The Rh complex exports ammonium from human red blood cells

British journal of haematology, 2003-07, Vol.122 (2), p.333-340

2003

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Pleiotropic Effects of Hydroxyurea on Red Blood Cell and Neutrophil Phenotype in Patients with Sickle Cell Disease; Data from the Notice Study

Blood, 2022-11, Vol.140 (Supplement 1), p.2551-2553

2022

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Hemolysis in the Spleen Drives Erythrocyte Turnover

Blood, 2019-11, Vol.134 (Supplement_1), p.946-946

2019

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β-globin mutation detection by tagged single-base extension and hybridization to universal glass and flow-through microarrays

European journal of human genetics : EJHG, 2004-07, Vol.12 (7), p.567-573

2004

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Comparison of Spectrophotometry, Chromate Inhibition, and Cytofluorometry Versus Gene Sequencing for Detection of Heterozygously Glucose-6-Phosphate Dehydrogenase-Deficient Females

The journal of histochemistry and cytochemistry, 2017-11, Vol.65 (11), p.627-636

2017

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Partial pyruvate kinase deficiency aggravates the phenotypic expression of band 3 deficiency in a family with hereditary spherocytosis

American journal of hematology, 2015-03, Vol.90 (3), p.E35-E39

2015

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RBC Adhesive Capacity Is Essential for Efficient 'Immune Adherence Clearance' and Provide a Generic Target to Deplete Pathogens from Septic Patients

Blood, 2016-12, Vol.128 (22), p.1031-1031

2016

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Residual pyruvate kinase activity in PKLR‐deficient erythroid precursors of a patient suffering from severe haemolytic anaemia

European journal of haematology, 2017-06, Vol.98 (6), p.584-589

2017

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The Gardos effect drives erythrocyte senescence and leads to Lu/BCAM and CD44 adhesion molecule activation

Blood advances, 2020-12, Vol.4 (24), p.6218-6229

2020

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Intrinsic defects in erythroid cells from familial hemophagocytic lymphohistiocytosis type 5 patients identify a role for STXBP2/Munc18-2 in erythropoiesis and phospholipid scrambling

Experimental hematology, 2015-12, Vol.43 (12), p.1072-1076.e2

2015

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Hereditary spherocytosis due to band 3 deficiency: 15 novel mutations in SLC4A1

American journal of hematology, 2013-02, Vol.88 (2), p.159-160

2013

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A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia

Hemoglobin, 2019-03, Vol.43 (2), p.77-82

2019

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Rapid genotyping of blood group antigens by multiplex polymerase chain reaction and DNA microarray hybridization

Transfusion (Philadelphia, Pa.), 2005-05, Vol.45 (5), p.667-679

2005

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Glucose‐6‐phosphate dehydrogenase deficiency‐associated hemolysis and methemoglobinemia in a COVID‐19 patient treated with chloroquine

Analysis of a cohort of 101 CDAII patients: description of 24 new molecular variants and genotype‐phenotype correlations

Rapid diagnosis of hereditary haemolytic anaemias using automated rheoscopy and supervised machine learning

P1450: VOXELOTOR TREATMENT LEADS TO IMPROVED VIABILITY OF SICKLE ERYTHROCYTES

The cholesterol content of the erythrocyte membrane is an important determinant of phosphatidylserine exposure

Mild dyserythropoiesis and β-like globin gene expression imbalance due to the loss of histone chaperone ASF1B

Two novel haemoglobin variants that affect haemoglobin A1c measurement by ion-exchange chromatography

Inherited glutathione reductase deficiency and Plasmodium falciparum malaria--a case study

Inborn defects in the antioxidant systems of human red blood cells

Hemolysis in the spleen drives erythrocyte turnover

Neutrophil FcγRIIIb Deficiency, Nature, and Clinical Consequences: A Study of 21 Individuals From 14 Families

Voxelotor Treatment Leads to Improved Viability of Sickle Erythrocytes and Altered Neutrophil Phenotype

The Rh complex exports ammonium from human red blood cells

Pleiotropic Effects of Hydroxyurea on Red Blood Cell and Neutrophil Phenotype in Patients with Sickle Cell Disease; Data from the Notice Study

Hemolysis in the Spleen Drives Erythrocyte Turnover

β-globin mutation detection by tagged single-base extension and hybridization to universal glass and flow-through microarrays

Comparison of Spectrophotometry, Chromate Inhibition, and Cytofluorometry Versus Gene Sequencing for Detection of Heterozygously Glucose-6-Phosphate Dehydrogenase-Deficient Females

Partial pyruvate kinase deficiency aggravates the phenotypic expression of band 3 deficiency in a family with hereditary spherocytosis

RBC Adhesive Capacity Is Essential for Efficient 'Immune Adherence Clearance' and Provide a Generic Target to Deplete Pathogens from Septic Patients

Residual pyruvate kinase activity in PKLR‐deficient erythroid precursors of a patient suffering from severe haemolytic anaemia

The Gardos effect drives erythrocyte senescence and leads to Lu/BCAM and CD44 adhesion molecule activation

Intrinsic defects in erythroid cells from familial hemophagocytic lymphohistiocytosis type 5 patients identify a role for STXBP2/Munc18-2 in erythropoiesis and phospholipid scrambling

Hereditary spherocytosis due to band 3 deficiency: 15 novel mutations in SLC4A1

A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia

Rapid genotyping of blood group antigens by multiplex polymerase chain reaction and DNA microarray hybridization

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