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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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Association between myeloid malignancies and acquired deficit in protein 4.1R: A retrospective analysis of six patients

American journal of hematology, 2008-04, Vol.83 (4), p.275-278

2008

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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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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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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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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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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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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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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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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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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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Sub-lethal hydrops as a manifestation of dehydrated hereditary stomatocytosis in two consecutive pregnancies

Prenatal diagnosis, 2003-05, Vol.23 (5), p.380-384

2003

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Red blood cell abnormalities in hereditary elliptocytosis and their relevance to variable clinical expression

American journal of clinical pathology, 1997-10, Vol.108 (4), p.391-399

1997

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Dehydrated hereditary stomatocytosis: a cause of prenatal ascites

Prenatal diagnosis, 2001-12, Vol.21 (13), p.1114-1118

2001

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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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Coinheritance of alpha-and beta-spectrin gene mutations in a case of hereditary elliptocytosis

Blood, 1998-12, Vol.92 (11), p.4481-4482

1998

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Cas clinique

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

2005

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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

Association between myeloid malignancies and acquired deficit in protein 4.1R: A retrospective analysis of six patients

Effect of subtotal splenectomy for management of hereditary pyropoikilocytosis

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

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

Antiphospholipid antibodies in a family with dehydrated hereditary stomatocytosis

INCIDENCE OF HEREDITARY SPHEROCYTOSIS IN A POPULATION OF JAUNDICED NEONATES

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

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

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

Congenital dyserythropoietic anemias

Infantile pyknocytosis: a cause of haemolytic anaemia of the newborn

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

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

Sub-lethal hydrops as a manifestation of dehydrated hereditary stomatocytosis in two consecutive pregnancies

Red blood cell abnormalities in hereditary elliptocytosis and their relevance to variable clinical expression

Dehydrated hereditary stomatocytosis: a cause of prenatal ascites

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

Coinheritance of alpha-and beta-spectrin gene mutations in a case of hereditary elliptocytosis

Cas clinique

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