Concepedia

Author

Lavergne Jm

Inserm

Also Known As

J M Lavergne, JM Lavergne, Lavergne Jm

11

Publications

411

Citations

7

H-Index

19

Concepts

All Affiliations

InsermBicêtre HospitalScripps Clinic
LJ

About

Lavergne Jm is an author at Inserm specializing in medicine, pathogenesis, and molecular genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

3

3

131

2

Molecular Genetics

2

2

106

3

Pathology

2

2

106

4

Public Health

1

1

96

5

Immunology

1

1

25

Lavergne Jm

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7

Publications

402

Citations

7

H-Index

YearCitations

Multimeric structure of factor VIII/von Willebrand factor in von Willebrand's disease.

Dominique Meyer, Bernadette Obert, Geneviève Piétu,

PubMed

1980

129

Gene defects in 150 unrelated French cases with type 2 von Willebrand disease: from the patient to the gene. INSERM Network on Molecular Abnormalities in von Willebrand Disease.

Dominique Meyer, E Fressinaud, Céline Gaucher,

PubMed

1997

96

Mapping of distinct von Willebrand factor domains interacting with platelet GPIb and GPIIb/IIIa and with collagen using monoclonal antibodies

JP Girma, M Kalafatis, Geneviève Piétu,

Blood

1986

91

Duplication of a methionine within the glycoprotein Ib binding domain of von Willebrand factor detected by denaturing gradient gel electrophoresis in a patient with type IIB von Willebrand disease

Lavergne Jm, BR Bahnak, A Derlon,

Blood

1991

36

[Various molecular states of factor II (prothrombin). Their study by means of staphylocoagulase and anti-factor II antibodies. I. Factor II in patients treated with vitamin K antagonists].

F Josso, Lavergne Jm, M Gouault,

PubMed

1968

25

Fluid-phase immunoradiometric assay for the detection of qualitative abnormalities of factor VIII/von Willebrand factor in variants of von Willebrand's disease.

Girma Jp, N Ardaillou, Dominique Meyer,

PubMed

1979

15

A directed search for mutations in hemophilia A using restriction enzyme analysis and denaturing gradient gel electrophoresis. A study of seven exons in the factor VIII gene of 170 cases.

Lavergne Jm, Bahnak Br, Michel Vidaud,

PubMed

1992

10

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