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Routine use of natriuretic peptides: Lessons from a big data analysis

Annals of clinical biochemistry, 2021-09, Vol.58 (5), p.481-486

2021

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Prognostic Impact of Microsatellite Instability in Colorectal Cancer Patients Treated with Adjuvant FOLFOX

Anticancer research, 2010-10, Vol.30 (10), p.4297-4301

2010

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Microsatellite Instability and Sensitivitiy to FOLFOX Treatment in Metastatic Colorectal Cancer

Anticancer research, 2007-07, Vol.27 (4C), p.2715-2719

2007

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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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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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Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1

American journal of human genetics, 2002-12, Vol.71 (6), p.1467-1474

2002

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Mechanochemistry of Protein 4.1's Spectrin-Actin-Binding Domain: Ternary Complex Interactions, Membrane Binding, Network Integration, Structural Strengthening

The Journal of cell biology, 1995-08, Vol.130 (4), p.897-907

1995

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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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Increasing level of CD56+ T-cells in peripheral blood in sarcoidosis

The European respiratory journal, 2006-03, Vol.27 (3), p.654-654

2006

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Suppression of CDA II expression in a homozygote

British journal of haematology, 1999-09, Vol.106 (4), p.948-953

1999

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Defining of the Minimal Domain of Protein 4.1 Involved in Spectrin-Actin Binding (∗)

The Journal of biological chemistry, 1995-09, Vol.270 (36), p.21243-21250

1995

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Interférences de l'hémolyse et de la lipémie sur trois méthodes de dosage de la bilirubine totale et conjuguée sur ADVIA 1650

Annales de biologie clinique (Paris), 2008-03, Vol.66 (2), p.175-182

2008

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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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Cell Shape-dependent Regulation of Protein 4.1 Alternative Pre-mRNA Splicing in Mammary Epithelial Cells

The Journal of biological chemistry, 1997-04, Vol.272 (15), p.10254-10259

1997

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La périlipine 3 est un nouveau partenaire d’ABHD5 et pourrait être impliquée dans le mécanisme de l’ichtyose du syndrome de Dorfman-Chanarin

Annales de dermatologie et de vénéréologie, 2016-12, Vol.143 (12), p.S435-S435

2016

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Southeast asian ovalocytosis in white persons

Hemoglobin, 1999, Vol.23 (1), p.47-56

1999

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Syndrome de Dorfman-Chanarin : analyse d’une série de 10 patients

Annales de dermatologie et de vénéréologie, 2014-12, Vol.141 (12), p.S370-S371

2014

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Manifestations cutanées chez neuf patients porteurs de mutations bialléliques de MUTYH

Annales de dermatologie et de vénéréologie, 2011-12, Vol.138 (12), p.A71-A72

2011

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Different impacts of alleles Î±^sup LEPRA^ and Î±^sup LELY^ 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

2004

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Novel function of STAT1β in B cells: induction of cell death by a mechanism different from that of STAT1α

Journal of leukocyte biology, 2008-12, Vol.84 (6), p.1604-1612

2008

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Haemolysis and turbidity influence on three analysis methods of quantitative determination of total and conjugated bilirubin on ADVIA 1650

Annales de biologie clinique (Paris), 2008-03, Vol.66 (2), p.175-182

2008

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Different impacts of alleles alphaLEPRA and alphaLELY 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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Abnormal glycosylation of red cell membrane band 3 in the congenital disorder of glycosylation Ig

Pediatric research, 2003-08, Vol.54 (2), p.224-229

2003

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A splicing alteration of 4.1R pre-mRNA generates 2 protein isoforms with distinct assembly to spindle poles in mitotic cells

Blood, 2002-10, Vol.100 (7), p.2629-2636

2002

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Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis

The hematology journal : the official journal of the European Haematology Association, 2000, Vol.1 (3), p.146-152

2000

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Routine use of natriuretic peptides: Lessons from a big data analysis

Prognostic Impact of Microsatellite Instability in Colorectal Cancer Patients Treated with Adjuvant FOLFOX

Microsatellite Instability and Sensitivitiy to FOLFOX Treatment in Metastatic Colorectal Cancer

Natural history of hereditary spherocytosis during the first year of life

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

Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1

Mechanochemistry of Protein 4.1's Spectrin-Actin-Binding Domain: Ternary Complex Interactions, Membrane Binding, Network Integration, Structural Strengthening

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

Increasing level of CD56+ T-cells in peripheral blood in sarcoidosis

Suppression of CDA II expression in a homozygote

Defining of the Minimal Domain of Protein 4.1 Involved in Spectrin-Actin Binding (∗)

Interférences de l'hémolyse et de la lipémie sur trois méthodes de dosage de la bilirubine totale et conjuguée sur ADVIA 1650

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

Cell Shape-dependent Regulation of Protein 4.1 Alternative Pre-mRNA Splicing in Mammary Epithelial Cells

La périlipine 3 est un nouveau partenaire d’ABHD5 et pourrait être impliquée dans le mécanisme de l’ichtyose du syndrome de Dorfman-Chanarin

Southeast asian ovalocytosis in white persons

Syndrome de Dorfman-Chanarin : analyse d’une série de 10 patients

Manifestations cutanées chez neuf patients porteurs de mutations bialléliques de MUTYH

Different impacts of alleles Î±^sup LEPRA^ and Î±^sup LELY^ as assessed versus a novel, virtually null allele of the SPTA1 gene in trans

Novel function of STAT1β in B cells: induction of cell death by a mechanism different from that of STAT1α

Haemolysis and turbidity influence on three analysis methods of quantitative determination of total and conjugated bilirubin on ADVIA 1650

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

Abnormal glycosylation of red cell membrane band 3 in the congenital disorder of glycosylation Ig

A splicing alteration of 4.1R pre-mRNA generates 2 protein isoforms with distinct assembly to spindle poles in mitotic cells

Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis

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