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HBB loss of heterozygosity in the hemopoietic lineage gives rise to an unusual sickle-cell trait phenotype

Haematologica (Roma), 2013-01, Vol.98 (1), p.e7-e8

2013

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Human B Lymphocytes Synthesize the 92-kDa Gelatinase, Matrix Metalloproteinase-9

The Journal of biological chemistry, 1998-08, Vol.273 (32), p.20677-20684

1998

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Effect of emicizumab on activated clotting time performed on i-STAT Alinity analyzer

International journal of laboratory hematology, 2024-07

2024

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A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease: A New Epidemiologic Picture

Medicine (Baltimore), 2016-03, Vol.95 (11), p.e3038-e3038

2016

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Management of congenital quantitative fibrinogen disorders: a Delphi consensus

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-11, Vol.22 (6), p.898-905

2016

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Compliance with Early Long-Term Prophylaxis Guidelines for Severe Hemophilia A

The Journal of pediatrics, 2021-07, Vol.234, p.212-219.e3

2021

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Compliance with Early Long-Term Prophylaxis Guidelines for Severe Hemophilia A

The Journal of pediatrics, 2021-07, Vol.234, p.212-219.e3

2021

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Xq22.3q23 microdeletion harboring TMEM164 and AMMECR1 genes: Two case reports confirming a recognizable phenotype with short stature, midface hypoplasia, intellectual delay, and elliptocytosis

American journal of medical genetics. Part A, 2019-04, Vol.179 (4), p.650-654

2019

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Les anémies hémolytiques constitutionnelles de causes multiples dévoilées par le séquençage haut-débit

Transfusion clinique et biologique : journal de la Société française de transfusion sanguine, 2021-11, Vol.28 (4), p.S45

2021

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Diagnostic value of serum erythropoietin level in patients with absolute erythrocytosis

Haematologica (Roma), 2004-10, Vol.89 (10), p.1194

2004

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Gelatinase concentration in tears of corneal-grafted patients

Current eye research, 1998-02, Vol.17 (2), p.174-182

1998

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Matrix metalloproteinase expression in rat pancreatic islets

Pancreas, 1998-11, Vol.17 (4), p.378-382

1998

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A New Frameshift Mutation on the α2-Globin Gene Causing α+-Thalassemia: Codon 43 (TTC>-TC or TTC>T-C)

Hemoglobin, 2012-06, Vol.36 (5), p.508-510

2012

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A New Frameshift Mutation on the α 2-Globin Gene Causing α + -Thalassemia: Codon 43 (TTC>–TC or TTC>T–C)

Hemoglobin, 2012-06, Vol.36 (5), p.508-510

2012

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Discordant D‐dimer results of two rapid quantitative automated assays are related to age

Journal of thrombosis and haemostasis, 2008-11, Vol.6 (11), p.1970-1971

2008

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Expansion of cortical interstitium is limited by converting enzyme inhibition in type 2 diabetic patients with glomerulosclerosis

Journal of the American Society of Nephrology, 1999-06, Vol.10 (6), p.1253-1263

1999

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Two New Gγ Chain Variants: Hb F-Saint-Etienne [Gγ79(EF3)Asp→His] and Hb F-Lyon [Gγ97(FG4)His→Arg]

Hemoglobin, 2008, Vol.32 (5), p.491-497

2008

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Should Plasma Homocysteine Be Used as a Biomarker of Venous Thromboembolism? A Case—Control Study

Clinical and applied thrombosis/hemostasis, 2009-10, Vol.15 (5), p.517-522

2009

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Successful use of recombinant factor VIIa for severe surgical liver bleeding in a 5 month‐old baby

Haemophilia : the official journal of the World Federation of Hemophilia, 2004-03, Vol.10 (2), p.183-185

2004

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Two New α-Thalassemia Point Mutations that are Undetectable by Biochemical Techniques

Hemoglobin, 2008-01, Vol.32 (4), p.411-417

2008

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Differential expression and secretion of gelatinases and tissue inhibitor of metalloproteinase-1 during neutrophil adhesion

Biochimica et biophysica acta, 1996-05, Vol.1290 (1), p.101-112

1996

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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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Plasma d-Dimer Testing Improves the Management of Thromboembolic Disease in Hospitalized Patients

Thrombosis research, 1999-09, Vol.95 (5), p.263-269

1999

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The Diamant Alpin Dialysis cohort study: clinico-biological characteristics and cardiovascular genetic risk profile of incident patients

Journal of nephrology, 2004-01, Vol.17 (1), p.66-75

2004

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HBB loss of heterozygosity in the hemopoietic lineage gives rise to an unusual sickle-cell trait phenotype

Clinical and biological features in PIEZO1 -hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients

Human B Lymphocytes Synthesize the 92-kDa Gelatinase, Matrix Metalloproteinase-9

Effect of emicizumab on activated clotting time performed on i-STAT Alinity analyzer

A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease: A New Epidemiologic Picture

Management of congenital quantitative fibrinogen disorders: a Delphi consensus

Compliance with Early Long-Term Prophylaxis Guidelines for Severe Hemophilia A

Compliance with Early Long-Term Prophylaxis Guidelines for Severe Hemophilia A

Xq22.3q23 microdeletion harboring TMEM164 and AMMECR1 genes: Two case reports confirming a recognizable phenotype with short stature, midface hypoplasia, intellectual delay, and elliptocytosis

Les anémies hémolytiques constitutionnelles de causes multiples dévoilées par le séquençage haut-débit

Diagnostic value of serum erythropoietin level in patients with absolute erythrocytosis

Gelatinase concentration in tears of corneal-grafted patients

Matrix metalloproteinase expression in rat pancreatic islets

A New Frameshift Mutation on the α2-Globin Gene Causing α+-Thalassemia: Codon 43 (TTC>-TC or TTC>T-C)

A New Frameshift Mutation on the α 2-Globin Gene Causing α + -Thalassemia: Codon 43 (TTC>–TC or TTC>T–C)

Discordant D‐dimer results of two rapid quantitative automated assays are related to age

Expansion of cortical interstitium is limited by converting enzyme inhibition in type 2 diabetic patients with glomerulosclerosis

Two New Gγ Chain Variants: Hb F-Saint-Etienne [Gγ79(EF3)Asp→His] and Hb F-Lyon [Gγ97(FG4)His→Arg]

Should Plasma Homocysteine Be Used as a Biomarker of Venous Thromboembolism? A Case—Control Study

Successful use of recombinant factor VIIa for severe surgical liver bleeding in a 5 month‐old baby

Two New α-Thalassemia Point Mutations that are Undetectable by Biochemical Techniques

Differential expression and secretion of gelatinases and tissue inhibitor of metalloproteinase-1 during neutrophil adhesion

Dehydrated hereditary stomatocytosis: a cause of prenatal ascites

Plasma d-Dimer Testing Improves the Management of Thromboembolic Disease in Hospitalized Patients

The Diamant Alpin Dialysis cohort study: clinico-biological characteristics and cardiovascular genetic risk profile of incident patients

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