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Journal Articles

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

C. Leroy-Matheron, M. Gouault-Heilmann, M. Aiach, S. Gandrille

Blood (1998) 91 (12): 4608–4615.

https://doi.org/10.1182/blood.V91.12.4608

Published: 1998

Journal Articles

The Ser 460 to Pro substitution of the protein S alpha (PROS1) gene is a frequent mutation associated with free protein S (type IIa) deficiency

J Duchemin, S Gandrille, D Borgel, P Feurgard, M Alhenc-Gelas, C Matheron, M Dreyfus, E Dupuy, I Juhan-Vague, M Aiach

Blood (1995) 86 (9): 3436–3443.

https://doi.org/10.1182/blood.V86.9.3436.bloodjournal8693436

Published: 1995

Journal Articles

Identification of mutations in 90 of 121 consecutive symptomatic French patients with a type I protein C deficiency. The French INSERM Network on Molecular Abnormalities Responsible for Protein C and Protein S deficiencies

S Gandrille, M Aiach

Blood (1995) 86 (7): 2598–2605.

https://doi.org/10.1182/blood.V86.7.2598.2598

Published: 1995

Journal Articles

Incidence of activated protein C resistance caused by the ARG 506 GLN mutation in factor V in 113 unrelated symptomatic protein C-deficient patients. The French Network on the behalf of INSERM

S Gandrille, JS Greengard, M Alhenc-Gelas, I Juhan-Vague, JF Abgrall, B Jude, JH Griffin, M Aiach

Blood (1995) 86 (1): 219–224.

https://doi.org/10.1182/blood.V86.1.219.bloodjournal861219

Published: 1995

Journal Articles

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

S Gandrille, D Borgel, V Eschwege-Gufflet, M Aillaud, M Dreyfus, C Matheron, P Gaussem, JF Abgrall, B Jude, P Sie

Blood (1995) 85 (1): 130–138.

https://doi.org/10.1182/blood.V85.1.130.bloodjournal851130

Published: 1995

Journal Articles

First de novo mutations in the protein C gene of two patients with type I deficiency: a missense mutation and a splice site deletion

S Gandrille, B Jude, M Alhenc-Gelas, J Emmerich, M Aiach

Blood (1994) 84 (8): 2566–2570.

https://doi.org/10.1182/blood.V84.8.2566.2566

Published: 1994

Journal Articles

Five novel mutations located in exons III and IX of the protein C gene in patients presenting with defective protein C anticoagulant activity

S Gandrille, M Alhenc-Gelas, P Gaussem, MF Aillaud, E Dupuy, I Juhan-Vague, M Aiach

Blood (1993) 82 (1): 159–168.

https://doi.org/10.1182/blood.V82.1.159.bloodjournal821159

Published: 1993

NARROW

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 alpha (PROS1) gene is a frequent mutation associated with free protein S (type IIa) deficiency

Identification of mutations in 90 of 121 consecutive symptomatic French patients with a type I protein C deficiency. The French INSERM Network on Molecular Abnormalities Responsible for Protein C and Protein S deficiencies

Incidence of activated protein C resistance caused by the ARG 506 GLN mutation in factor V in 113 unrelated symptomatic protein C-deficient patients. The French Network on the behalf of INSERM

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

First de novo mutations in the protein C gene of two patients with type I deficiency: a missense mutation and a splice site deletion

Five novel mutations located in exons III and IX of the protein C gene in patients presenting with defective protein C anticoagulant activity

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ASH Publications

American Society of Hematology

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 alpha (PROS1) gene is a frequent mutation associated with free protein S (type IIa) deficiency

Identification of mutations in 90 of 121 consecutive symptomatic French patients with a type I protein C deficiency. The French INSERM Network on Molecular Abnormalities Responsible for Protein C and Protein S deficiencies

Incidence of activated protein C resistance caused by the ARG 506 GLN mutation in factor V in 113 unrelated symptomatic protein C-deficient patients. The French Network on the behalf of INSERM

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

First de novo mutations in the protein C gene of two patients with type I deficiency: a missense mutation and a splice site deletion

Five novel mutations located in exons III and IX of the protein C gene in patients presenting with defective protein C anticoagulant activity

Email alerts

ASH Publications

American Society of Hematology

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