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Antiphospholipid antibodies: what dermatologists must know

Annales de dermatologie et de vénéréologie, 2012-05, Vol.139 (5), p.417-420

2012

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Anticorps antiphospholipides : ce que le dermatologue doit savoir

Annales de dermatologie et de vénéréologie, 2012-05, Vol.139 (5), p.417-420

2012

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Anticorps antiphosphotipides: ce que le dermatologue doit savoir

Annales de dermatologie et de vénéréologie, 2012, Vol.139 (5), p.417-420

2012

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Les expressions du collectif dans les écritures juives d'Europe centrale et orientale

2018

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Thrombotic risk according to SERPINC1 genotype in a large cohort of subjects with antithrombin inherited deficiency

Thrombosis and haemostasis, 2017, Vol.117 (6), p.1040-1051

2017

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Genetic modulation of plasma protein S levels by two frequent dimorphisms in the PROS1 gene

Thrombosis and haemostasis, 1999-09, Vol.82 (3), p.1088-1092

1999

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Créer des services innovants : Stratégies et répertoire d'actions pour les bibliothèques

Marie-Christine Jacquinet

2011

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Thrombose d’un circuit de circulation extracorporelle sous danaparoïde sodique à la phase aiguë d’une thrombopénie induite par l’héparine de type II en dépit d’une hypocoagulation recommandée

Annales françaises d'anesthésie et de réanimation, 2006-11, Vol.25 (11), p.1144-1148

2006

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Identification of 15 Different Candidate Causal Point Mutations and Three Polymorphisms in 19 Patients With Protein S Deficiency Using a Scanning Method for the Analysis of the Protein S Active Gene

Blood, 1995-01, Vol.85 (1), p.130-138

1995

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Influence of the nt 2148 A to G substitution (Pro 626 dimorphism) in the PROS1 gene on circulating free protein S levels in healthy volunteers--reappraisal of protein S normal ranges

Thrombosis and haemostasis, 2000-05, Vol.83 (5), p.798-799

2000

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A Mutation of the Active Protein S Gene Leading to an EGF1-Lacking Protein in a Family With Qualitative (Type II) Deficiency

Blood, 1998-06, Vol.91 (12), p.4608-4615

1998

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The Ser 460 to Pro Substitution of the Protein S α (PROS1) Gene Is a Frequent Mutation Associated With Free Protein S (type IIa) Deficiency

Blood, 1995-11, Vol.86 (9), p.3436-3443

1995

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In vivo 23Na nuclear magnetic resonance study of maintenance of a sodium gradient in the ruminal bacterium Fibrobacter succinogenes S85

Applied and environmental microbiology, 2001-09, Vol.67 (9), p.4390-4392

2001

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Protein S inherited qualitative deficiency: novel mutations and phenotypic influence

Journal of thrombosis and haemostasis, 2010-12, Vol.8 (12), p.2718-2726

2010

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Re-investigation of glucose metabolism in Fibrobacter succinogenes, using NMR spectroscopy and enzymatic assays. : Evidence for pentose phosphates phosphoketolase and pyruvate formate lyase activities

Biochimica et biophysica acta, 1997-01, Vol.1355 (1), p.50-60

1997

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Factor V Leiden-dependent APC resistance: Improved sensitivity and specificity of the APC resistance test by plasma dilution in factor V-depleted plasma

Thrombosis research, 1996-05, Vol.82 (3), p.281-283

1996

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Interactions between carbon and nitrogen metabolism in Fibrobacter succinogenes S85 : A 1H and 13C nuclear magnetic resonance and enzymatic study

Applied and environmental microbiology, 1999-05, Vol.65 (5), p.1941-1948

1999

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A Mutation of the Active Protein S Gene Leading to an EGF1-Lacking Protein in a Family With Qualitative (Type II) Deficiency

Blood, 1998-06, Vol.91 (12), p.4608-4615

1998

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Contribution of «in situ» NMR to the study of the glucose metabolism of different strains of Fibrobacter species

Annales de zootechnie, 1996, Vol.45 (Suppl. 1), p.349-349

1996

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13C and 1H nuclear magnetic resonance study of glycogen futile cycling in strains of the genus Fibrobacter

Applied and Environmental Microbiology, 1998, Vol.64 (1), p.74-81

1998

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A new functional assay for human protein S activity using activated factor V as substrate

Thrombosis and haemostasis, 1989-12, Vol.62 (4), p.1144

1989

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An improved electronic microarray-based diagnostic assay for identification of MEFV mutations

Human mutation, 2004-06, Vol.23 (6), p.621-628

2004

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Comment améliorer le suivi des prescriptions d’antivitamine k en hôpital de gériatrie ?

Le pharmacien hospitalier & clinicien, 2012-12, Vol.47 (4), p.281-282

2012

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In vivo 13C NMR study of glucose and cellobiose metabolism by four cellulolytic strains of the genus Fibrobacter

Biodegradation (Dordrecht), 1998, Vol.9 (6), p.451-461

1998

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Massive thrombosis of venous cerebral sinuses in a 2-year-old boy with a combined inherited deficiency of antithrombin III and protein C

Thrombosis and haemostasis, 1994, Vol.72 (5), p.782-783

1994

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Antiphospholipid antibodies: what dermatologists must know

Anticorps antiphospholipides : ce que le dermatologue doit savoir

Anticorps antiphosphotipides: ce que le dermatologue doit savoir

Les expressions du collectif dans les écritures juives d'Europe centrale et orientale

Thrombotic risk according to SERPINC1 genotype in a large cohort of subjects with antithrombin inherited deficiency

Genetic modulation of plasma protein S levels by two frequent dimorphisms in the PROS1 gene

Créer des services innovants : Stratégies et répertoire d'actions pour les bibliothèques

Thrombose d’un circuit de circulation extracorporelle sous danaparoïde sodique à la phase aiguë d’une thrombopénie induite par l’héparine de type II en dépit d’une hypocoagulation recommandée

Identification of 15 Different Candidate Causal Point Mutations and Three Polymorphisms in 19 Patients With Protein S Deficiency Using a Scanning Method for the Analysis of the Protein S Active Gene

Influence of the nt 2148 A to G substitution (Pro 626 dimorphism) in the PROS1 gene on circulating free protein S levels in healthy volunteers--reappraisal of protein S normal ranges

A Mutation of the Active Protein S Gene Leading to an EGF1-Lacking Protein in a Family With Qualitative (Type II) Deficiency

The Ser 460 to Pro Substitution of the Protein S α (PROS1) Gene Is a Frequent Mutation Associated With Free Protein S (type IIa) Deficiency

In vivo 23Na nuclear magnetic resonance study of maintenance of a sodium gradient in the ruminal bacterium Fibrobacter succinogenes S85

Protein S inherited qualitative deficiency: novel mutations and phenotypic influence

Re-investigation of glucose metabolism in Fibrobacter succinogenes, using NMR spectroscopy and enzymatic assays. : Evidence for pentose phosphates phosphoketolase and pyruvate formate lyase activities

Factor V Leiden-dependent APC resistance: Improved sensitivity and specificity of the APC resistance test by plasma dilution in factor V-depleted plasma

Interactions between carbon and nitrogen metabolism in Fibrobacter succinogenes S85 : A 1H and 13C nuclear magnetic resonance and enzymatic study

A Mutation of the Active Protein S Gene Leading to an EGF1-Lacking Protein in a Family With Qualitative (Type II) Deficiency

Contribution of «in situ» NMR to the study of the glucose metabolism of different strains of Fibrobacter species

13C and 1H nuclear magnetic resonance study of glycogen futile cycling in strains of the genus Fibrobacter

A new functional assay for human protein S activity using activated factor V as substrate

An improved electronic microarray-based diagnostic assay for identification of MEFV mutations

Comment améliorer le suivi des prescriptions d’antivitamine k en hôpital de gériatrie ?

In vivo 13C NMR study of glucose and cellobiose metabolism by four cellulolytic strains of the genus Fibrobacter

Massive thrombosis of venous cerebral sinuses in a 2-year-old boy with a combined inherited deficiency of antithrombin III and protein C

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