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Detection and IgG subclass analysis of antibodies to factor VIII in multitransfused haemophiliacs and healthy individuals

Autor: C. Guerois, F. Meriane, A. Parquet-Gernez, Y. Sultan, A. Derlon, Ph. Gautier

Publikováno v: Haemophilia. 2:88-94

Summary. Using a binding assay to immobilized factor VIII (F VIII) (ELISA) we measured the amount of IgG with binding capacity to FVIII, in the plasma of patients with an inhibitor to F VIII, in multitransfused haemophiliacs without inhibitor and in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9f35d149ddd50927d6fc2a81fa7a50b
https://doi.org/10.1111/j.1365-2516.1996.tb00021.x

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Biological effects of a S/D-treated, very high purity, von Willebrand factor concentrate in five patients with severe von Willebrand disease

Autor: F. Meriane, M Goudemand, N. Djeha, C Mazurier, L. Zerhouni

Publikováno v: Blood Coagulation & Fibrinolysis. 4:1023-1029

A highly purified von Willebrand factor (vWf) concentrate with low factor VIII (FVIII) content was tested to evaluate its biological effects in five patients with severe von Willebrand disease (vWd). The patients were infused with a single dose of th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::16b15025669eb9c2fcac8d812033c6c0
https://doi.org/10.1097/00001721-199304060-00018

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Behçet Syndrome Associated with Protein S Deficiency

Autor: F Otmani, C. Sternberg, Anne-Marie Fischer, F. Meriane, O. Chafa, T. Chellali, M. Benabadji

Publikováno v: Thrombosis and Haemostasis. 67:001-003

SummaryBeçget syndrome is a multisystem disorder characterized by ocular, mucocutaneous, articular, gastrointestinal and neurologic abnormalities. We report here an unusual case of Beçget syndrome, characterized by the importance of the thrombotic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8c2c0b052aecc8ae9183bd5fb3fae3dd
https://doi.org/10.1055/s-0038-1648128

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Behçet syndrome associated with protein S deficiency

Autor: O, Chafa, A M, Fischer, F, Meriane, T, Chellali, C, Sternberg, F, Otmani, M, Benabadji

Publikováno v: Thrombosis and haemostasis. 67(1)

Behçet syndrome is a multisystem disorder characterized by ocular, mucocutaneous, articular, gastrointestinal and neurologic abnormalities. We report here an unusual case of Behçet syndrome, characterized by the importance of the thrombotic events

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d5c887f28ec01e390a014ea3d36eef4c
https://pubmed.ncbi.nlm.nih.gov/1535461

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Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in Algeria

Autor: A. Reghis, Khedoudja Nafa, J. C. Kaplan, Y. Sultan, M. Benabadji, M. Delpech, F. Meriane, Michel Guilloud-Bataille, Florence Demenais

Publikováno v: Human Genetics. 84

The frequency of alleles for intragenic (intron 17 and intron 25) and extragenic (DXS15 and DXS52) F8C RFLPs was investigated in the Algerian population. Altogether 287 X chromosomes (97 males and 95 females) were studied. The allele frequencies foun

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9640f24445d3aebb86a554b228d6153
https://doi.org/10.1007/bf00195808

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