Lavergne, Jean-Maurice: search on Z-Library

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1

Immunoradiometric Assay of Factor VIII: Coagulant Antigen using Four Human Antibodies. Study of 27 Cases of Haemophilia A

Jean-Pierre Girma, Jean-Maurice Lavergne, Dominique Meyer, Marie-Josea Larrieu

Journal:

British Journal of Haematology

Year:

1981

Language:

english

File:

PDF, 793 KB

english, 1981

2

The arginine-552-cysteine (R1315C) mutation within the A1 loop of von Willebrand factor induces an abnormal folding with a loss of function resulting in type 2Aâlike phenotype of von Willebrand disease: study of 10 patients and mutated recombinant von Willebrand factor

Ribba, Anne-Sophie, Hilbert, Lysiane, Lavergne, Jean-Maurice, Fressinaud, Edith, Boyer-Neumann, Catherine, Ternisien, Catherine, Juhan-Vague, IreÌne, Goudemand, Jenny, Girma, Jean-Pierre, Mazurier, C

Journal:

Year:

2001

File:

PDF, 271 KB

2001

3

Human Gene Mutation

Lavergne, Jean-Maurice, Meyer, Dominique

Journal:

Blood Coagulation & Fibrinolysis

Year:

1994

File:

PDF, 80 KB

1994

4

Precipitating anti-VIII:C antibodies in two patients with haemophilia A

Jean-Maurice Lavergne, Dominique Meyer, Jean-Pierre Girma, Marie-José Larrieu

Journal:

British Journal of Haematology

Year:

1982

Language:

english

File:

PDF, 1.17 MB

english, 1982

5

Immunological Evidence that Human Factor VIII is Composed of Two Linked Moieties

Jerry Koutts, Jean-Maurice Lavergne, Dominique Meyer

Journal:

British Journal of Haematology

Year:

1977

Language:

english

File:

PDF, 1.14 MB

english, 1977

6

Somatic mosaicism and compound heterozygosity in female hemophilia B

Costa, Jean-Marc, Vidaud, Dominique, Laurendeau, Ingrid, Vidaud, Michel, Fressinaud, Edith, Moisan, Jean-Pierre, David, Albert, Meyer, Dominique, Lavergne, Jean-Maurice

Journal:

Year:

2000

File:

PDF, 76 KB

2000

7

Detection of 95 novel mutations in coagulation factor VIII gene F8 responsible for hemophilia A: results from a single institution

Benoît Guillet, Thierry Lambert, Roseline d'Oiron, Valérie Proulle, Jean-Luc Plantier, Anne Rafowicz, Jocelyne Peynet, Jean-Marc Costa, Laurence Bendelac, Yves Laurian, Jean-Maurice Lavergne

Journal:

Year:

2006

Language:

english

File:

PDF, 271 KB

english, 2006

8

Type 2 von Willebrand disease causing defective von Willebrand factor-dependent platelet function

Dominique Meyer, Edith Fressinaud, Lysiane Hilbert, Anne-Sophie Ribba, Jean-Maurice Lavergne, Claudine Mazurier

Journal:

Best Practice & Research Clinical Haematology

Year:

2001

Language:

english

File:

PDF, 160 KB

english, 2001

9

Factor VIII deficiency not induced by FVIII gene mutation in a female first cousin of two brothers with haemophilia A

Claudine Mazurier, Armelle Parquet-Gernez, Christine Gaucher, Jean-Maurice Lavergne, Jenny Goudemand

Journal:

British Journal of Haematology

Year:

2002

Language:

english

File:

PDF, 60 KB

english, 2002

10

Mutations in the catalytic domain of human coagulation factor IX: Rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behavior

Attree, Oliver, Vidaud, Dominique, Vidaud, Michel, Amselem, Serge, Lavergne, Jean-Maurice, Goossens, Michel

Journal:

Year:

1989

Language:

english

File:

PDF, 1.33 MB

english, 1989

11

A novel cause of mild/moderate hemophilia A: mutations scattered in the factor VIII C1 domain reduce factor VIII binding to von Willebrand factor

Jacquemin, Marc, Lavend'homme, Renaud, Benhida, Abdellah, Vanzieleghem, Beatrijs, d'Oiron, Roseline, Lavergne, Jean-Maurice, Brackmann, Hans H., Schwaab, Rainer, VandenDriessche, Thierry, Chuah, Marin

Journal:

Year:

2000

File:

PDF, 195 KB

2000

12

A new mutation, S1285F, within the A1 loop of von Willebrand factor induces a conformational change in A1 loop with abnormal binding to platelet GPIb and botrocetin causing type 2M von Willebrand disease

Alain Stepanian, Anne-Sophie Ribba, Jean-Maurice Lavergne, Edith Fressinaud, Irene Juhan-Vague, Claudine Mazurier, Jean-Pierre Girma, Dominique Meyer

Journal:

British Journal of Haematology

Year:

2003

Language:

english

File:

PDF, 414 KB

english, 2003

13

Isolation and partial characterization of a human prothrombin variant: Prothrombin Barcelona

Richard Benarous, Jean-Maurice Lavergne, Dominique Labie, J. Monasterio de Sanchez, François Josso

Journal:

Biochemical and Biophysical Research Communications

Year:

1974

Language:

english

File:

PDF, 2.69 MB

english, 1974

14

Cross-reacting material in congenital factor VIII deficiencies (Haemophilia A and von Willebrand's disease)

Dominique Meyer, Jean-Maurice Lavergne, Marie-José Larrieu, François Josso

Journal:

Thrombosis Research

Year:

1972

Language:

english

File:

PDF, 851 KB

english, 1972

15

Comparison of the primary structure of the functional domains of human and porcine von Willebrand factor that mediate platelet adhesion

Bruce R. Bahnak, Jean-Maurice Lavergne, Valérie Ferreira, Danièle Kerbiriou-Nabias, Dominique Meyer

Journal:

Biochemical and Biophysical Research Communications

Year:

1992

Language:

english

File:

PDF, 583 KB

english, 1992

16

A novel case of compound heterozygosity with “Normandy”/type I von Willebrand disease (vWD). Direct demonstration of the segregation of one allele with a defective expression at the mRNA level causing type I vWD

Virginie Siguret, Jean-Maurice Lavergne, Ghislaine Chérel, Catherine Boyer-Neumann, Anne-Sophie Ribba, Bruce R. Bahnak, Dominique Meyer, Geneviève Piétu

Journal:

Year:

1994

Language:

english

File:

PDF, 1.26 MB

english, 1994

17

Detection of a molecular defect in 40 of 44 patients with haemophilia B by PCR and denaturing gradient gel electrophoresis

Michel Tartary, Dominique Vidaud, Yingchao Piao, Jean-Marc Costa, Bruce R. Bahnak, Edith Fressinaud, Brigitte Congard, Yves Laurian, Dominique Meyer, Jean-Maurice Lavergne, Michel Vidaud

Journal:

British Journal of Haematology

Year:

1993

Language:

english

File:

PDF, 900 KB

english, 1993

18

Somatic Mosaicism in Hemophilia A: A Fairly Common Event

Marco Leuer, Johannes Oldenburg, Jean-Maurice Lavergne, Michael Ludwig, Andreas Fregin, Anton Eigel, Rolf Ljung, Anne Goodeve, Ian Peake, Klaus Olek

Journal:

The American Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 1.73 MB

english, 2001

19

Nucleotide substitutions at the -6 position in the promoter region of the factor IX gene result in different severity of hemophilia B Leyden: consequences for genetic counseling

Dominique Vidaud, Michel Tartary, Jean-Marc Costa, Bruce R. Bahnak, Suzana Gispert-Sanchez, Edith Fressinaud, Claire Gazengel, Dominique Meyer, Michel Goossens, Jean-Maurice Lavergne, Michel Vidaud

Journal:

Year:

1993

Language:

english

File:

PDF, 542 KB

english, 1993

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