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Ex vivo generation of fully mature human red blood cells from hematopoietic stem cells

Nature biotechnology, 2005-01, Vol.23 (1), p.69-74

2005

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Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A

Blood, 2008-06, Vol.111 (11), p.5380-5389

2008

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Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis

Blood, 2001-01, Vol.97 (2), p.399-403

2001

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Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia

Blood, 2001-11, Vol.98 (10), p.2894-2899

2001

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Effect of subtotal splenectomy for management of hereditary pyropoikilocytosis

British journal of haematology, 2008-07, Vol.142 (2), p.315-317

2008

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Dehydrated hereditary stomatocytosis mimicking familial hyperkalaemic hypertension: clinical and genetic investigation

European journal of haematology, 2007-03, Vol.78 (3), p.253-259

2007

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Antiphospholipid antibodies in a family with dehydrated hereditary stomatocytosis

Thrombosis research, 2008, Vol.122 (4), p.572-575

2008

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INCIDENCE OF HEREDITARY SPHEROCYTOSIS IN A POPULATION OF JAUNDICED NEONATES

Pediatric hematology and oncology, 2006-07, Vol.23 (5), p.387-397

2006

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Band 3 Courcouronne: Homozygous Mutation Ser667Phe Causes Severe Hereditary Spherocytosis and Incomplete Distal Renal Tubular Acidosis

Blood, 2006-11, Vol.108 (11), p.1563-1563

2006

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Oral magnesium supplements reduce erythrocyte dehydration in patients with sickle cell disease

The Journal of clinical investigation, 1997-10, Vol.100 (7), p.1847-1852

1997

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Oral magnesium pidolate: effects of long‐term administration in patients with sickle cell disease

British journal of haematology, 2000-02, Vol.108 (2), p.284-289

2000

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Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects

British journal of haematology, 1997-07, Vol.98 (1), p.32-40

1997

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Usefulness of the eosin‐5′‐maleimide cytometric method as a first‐line screening test for the diagnosis of hereditary spherocytosis: comparison with ektacytometry and protein electrophoresis

British journal of haematology, 2008-02, Vol.140 (4), p.468-470

2008

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Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in a cohort of French children

Journal of pediatric hematology/oncology, 2005-08, Vol.27 (8), p.416-419

2005

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Morphological and functional platelet abnormalities in Berkeley sickle cell mice

Blood cells, molecules, & diseases, 2008-07, Vol.41 (1), p.109-118

2008

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Elliptocytosis in patients with C-terminal domain mutations of protein 4.1 correlates with encoded messenger RNA levels rather than with alterations in primary protein structure

Blood, 2000-03, Vol.95 (5), p.1834-1841

2000

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Red cell abnormalities in hereditary spherocytosis: Relevance to diagnosis and understanding of the variable expression of clinical severity

The Journal of laboratory and clinical medicine, 1996-09, Vol.128 (3), p.259-269

1996

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Massive and Selective Ex Vivo Generation of Matured and Functional Human Red Blood Cells (RBC) from Hematopoietic Stem Cells of Diverse Origins: Towards the New Concept of “Cultured RBC”

Blood, 2004-11, Vol.104 (11), p.379-379

2004

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Automated Pre-Classification of Anemia Based on the Results of a Routine Automated Hematology System

Blood, 2005-11, Vol.106 (11), p.2253-2253

2005

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Congenital dyserythropoietic anemias

The hematology journal : the official journal of the European Haematology Association, 2004, Vol.5 Suppl 3, p.S191-S194

2004

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Infantile pyknocytosis: a cause of haemolytic anaemia of the newborn

British journal of haematology, 2006-05, Vol.133 (4), p.439-442

2006

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Long term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis

Blood, 2000-05, Vol.97 (2)

2000

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Four new cases of stomatin‐deficient hereditary stomatocytosis syndrome: association of the stomatin‐deficient cryohydrocytosis variant with neurological dysfunction

British journal of haematology, 2004-06, Vol.125 (6), p.796-803

2004

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Cas clinique

Bio tribune magazine, 2005-06, Vol.15 (1), p.48-49

2005

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An Extreme Consequence of Splenectomy in Dehydrated Hereditary Stomatocytosis: Gradual Thrombo-embolic Pulmonary Hypertension and Lung-Heart Transplantation

Hemoglobin, 2003-01, Vol.27 (3), p.139-147

2003

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Ex vivo generation of fully mature human red blood cells from hematopoietic stem cells

Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A

Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis

Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia

Effect of subtotal splenectomy for management of hereditary pyropoikilocytosis

Dehydrated hereditary stomatocytosis mimicking familial hyperkalaemic hypertension: clinical and genetic investigation

Antiphospholipid antibodies in a family with dehydrated hereditary stomatocytosis

INCIDENCE OF HEREDITARY SPHEROCYTOSIS IN A POPULATION OF JAUNDICED NEONATES

Band 3 Courcouronne: Homozygous Mutation Ser667Phe Causes Severe Hereditary Spherocytosis and Incomplete Distal Renal Tubular Acidosis

Oral magnesium supplements reduce erythrocyte dehydration in patients with sickle cell disease

Oral magnesium pidolate: effects of long‐term administration in patients with sickle cell disease

Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects

Usefulness of the eosin‐5′‐maleimide cytometric method as a first‐line screening test for the diagnosis of hereditary spherocytosis: comparison with ektacytometry and protein electrophoresis

Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in a cohort of French children

Morphological and functional platelet abnormalities in Berkeley sickle cell mice

Elliptocytosis in patients with C-terminal domain mutations of protein 4.1 correlates with encoded messenger RNA levels rather than with alterations in primary protein structure

Red cell abnormalities in hereditary spherocytosis: Relevance to diagnosis and understanding of the variable expression of clinical severity

Massive and Selective Ex Vivo Generation of Matured and Functional Human Red Blood Cells (RBC) from Hematopoietic Stem Cells of Diverse Origins: Towards the New Concept of “Cultured RBC”

Automated Pre-Classification of Anemia Based on the Results of a Routine Automated Hematology System

Congenital dyserythropoietic anemias

Infantile pyknocytosis: a cause of haemolytic anaemia of the newborn

Long term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis

Four new cases of stomatin‐deficient hereditary stomatocytosis syndrome: association of the stomatin‐deficient cryohydrocytosis variant with neurological dysfunction

Cas clinique

An Extreme Consequence of Splenectomy in Dehydrated Hereditary Stomatocytosis: Gradual Thrombo-embolic Pulmonary Hypertension and Lung-Heart Transplantation

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