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Natural history of hereditary spherocytosis during the first year of life

Blood, 2000-01, Vol.95 (2), p.393-397

2000

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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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Congenital dyserythropoietic anaemia, type I, in a Caucasian patient with retinal angioid streaks (homozygous arg1042trp mutation in codanin‐1)

European journal of haematology, 2008-03, Vol.80 (3), p.271-274

2008

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Management of high risk pregnancy in sickle cell disease by a strategy of prophylactic red cell transfusion or automated red cell exchange

Transfusion clinique et biologique : journal de la Société française de transfusion sanguine, 2007-10, Vol.14 (4), p.386-392

2007

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Hereditary spherocytosis: guidelines for the diagnosis and management in children

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2008-09, Vol.15 (9), p.1464-1473

2008

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Quantification of the neurotoxins Annonaceous acetogenins in the edible fruits of several Annona species using 1H NMR

Planta medica, 2016, Vol.81 (S 01), p.S1-S381

2016

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Mild dehydrated hereditary stomatocytosis revealed by marked hepatosiderosis

Clinical and laboratory haematology, 2006-08, Vol.28 (4), p.270-274

2006

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Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24

Blood, 2000-10, Vol.96 (7), p.2599-2605

2000

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Hereditary spherocytosis: guidelines for the diagnosis and management in children

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2009-06, Vol.16 (6), p.556-558

2009

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Sphérocytose héréditaire : diagnostic et prise en charge chez l’enfant

Archives de pédiatrie (Paris), 2009-06, Vol.16 (6), p.556-558

2009

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A genetic syndrome associating dehydrated hereditary stomatocytosis, pseudohyperkalaemia and perinatal oedema

British journal of haematology, 1998-11, Vol.103 (2), p.383-386

1998

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Prise en charge des grossesses à risque chez les femmes drépanocytaires : intérêt d’une stratégie préventive par des transfusions de globules rouges ou des échanges érythrocytaires automatisés

Transfusion clinique et biologique : journal de la Société française de transfusion sanguine, 2007-10, Vol.14 (4), p.386-392

2007

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Sphérocytose héréditaire : recommandations pour le diagnostic et la prise en charge chez l’enfant

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2008-09, Vol.15 (9), p.1464-1473

2008

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Dehydrated hereditary stomatocytosis with transient perinatal ascites

Archives of disease in childhood. Fetal and neonatal edition, 2003-09, Vol.88 (5), p.F438-F439

2003

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Different impacts of alleles αLEPRA and αLELY as assessed versus a novel, virtually null allele of the SPTA1 gene in trans

British journal of haematology, 2004-10, Vol.127 (1), p.118-122

2004

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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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Schizocytes : reproductibilité du diagnostic morphologique et intérêt de méthodes observateur-indépendantes

Annales de biologie clinique (Paris), 2005-05, Vol.63 (3), p.279-289

2005

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Abstract P4-08-25: Decentralized beta testing of MammaPrint and BluePrint NGS kit at University Hospitals Leuven and Curie Institute Paris

Cancer research (Chicago, Ill.), 2019-02, Vol.79 (4_Supplement), p.P4-P4-08-25

2019

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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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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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Coinheritance of two α-spectrin gene defects in a recessive spherocytosis family

Clinical and laboratory haematology, 2000-12, Vol.22 (6), p.329-336

2000

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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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The GEN.S : a fortuitous finding of a routine screening test for hereditary spherocytosis

Hematology and cell therapy, 1999-06, Vol.41 (3), p.113-116

1999

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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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Natural history of hereditary spherocytosis during the first year of life

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

Congenital dyserythropoietic anaemia, type I, in a Caucasian patient with retinal angioid streaks (homozygous arg1042trp mutation in codanin‐1)

Management of high risk pregnancy in sickle cell disease by a strategy of prophylactic red cell transfusion or automated red cell exchange

Hereditary spherocytosis: guidelines for the diagnosis and management in children

Quantification of the neurotoxins Annonaceous acetogenins in the edible fruits of several Annona species using 1H NMR

Mild dehydrated hereditary stomatocytosis revealed by marked hepatosiderosis

Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24

Hereditary spherocytosis: guidelines for the diagnosis and management in children

Sphérocytose héréditaire : diagnostic et prise en charge chez l’enfant

A genetic syndrome associating dehydrated hereditary stomatocytosis, pseudohyperkalaemia and perinatal oedema

Prise en charge des grossesses à risque chez les femmes drépanocytaires : intérêt d’une stratégie préventive par des transfusions de globules rouges ou des échanges érythrocytaires automatisés

Sphérocytose héréditaire : recommandations pour le diagnostic et la prise en charge chez l’enfant

Dehydrated hereditary stomatocytosis with transient perinatal ascites

Different impacts of alleles αLEPRA and αLELY as assessed versus a novel, virtually null allele of the SPTA1 gene in trans

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

Schizocytes : reproductibilité du diagnostic morphologique et intérêt de méthodes observateur-indépendantes

Abstract P4-08-25: Decentralized beta testing of MammaPrint and BluePrint NGS kit at University Hospitals Leuven and Curie Institute Paris

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

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

Coinheritance of two α-spectrin gene defects in a recessive spherocytosis family

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

The GEN.S : a fortuitous finding of a routine screening test for hereditary spherocytosis

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

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