Search Results - "Marzais, François"

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    Dectin-1 Polymorphism: A Genetic Disease Specifier in Autism Spectrum Disorders? by Bennabi, Meriem, Delorme, Richard, Oliveira, José, Fortier, Catherine, Lajnef, Mohamed, Boukouaci, Wahid, Feugeas, Jean-Paul, Marzais, François, Gaman, Alexandru, Charron, Dominique, Ghaleh, Bijan, Krishnamoorthy, Rajagopal, Leboyer, Marion, Tamouza, Ryad

    Published in PloS one (09-09-2015)
    “…In autism spectrum disorders (ASD), complex gene-environment interactions contribute to disease onset and progress. Given that gastro-intestinal dysfunctions…”
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    Journal Article
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    Functional polymorphisms of Monocyte Chemoattractant Protein-1 gene and Pott’s disease risk by Mecabih, Fethi, Sadouki, Fatiha, Bennabi, Meriem, Salah, Sofiane, Boukouaci, Wahid, Amroun, Habiba, Fortier, Catherine, Marzais, François, Charron, Dominique, Djoudi, Hachemi, Abbadi, Mohamed Cherif, Krishnamoorthy, Rajagopal, Tamouza, Ryad

    Published in Immunobiology (1979) (01-03-2016)
    “…Abstract Objective Monocyte Chemoattractant Protein-1 (MCP-1/CCL2), a key player in immune-mediated responses against Mycobacterium tuberculosis , is encoded…”
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    Journal Article
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    Infectious complications in sickle cell disease are influenced by HLA class II alleles by Tamouza, Ryad, Neonato, Maria-Grazia, Busson, Marc, Marzais, François, Girot, Robert, Labie, Dominique, Elion, Jacques, Charron, Dominique

    Published in Human immunology (01-03-2002)
    “…Despite systematic antibiotic therapy, severe infections (septicemia, meningitis, or osteomyelitis) are a major cause of mortality and morbidity in children…”
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    Dectin-1 Polymorphism: A Genetic Disease Specifier in Autism Spectrum Disorders?: e0137339 by Bennabi, Meriem, Delorme, Richard, Oliveira, Jose, tier, Catherine, Lajnef, Mohamed, Boukouaci, Wahid, Feugeas, Jean-Paul, Marzais, Francois, Gaman, Alexandru, Charron, Dominique

    Published in PloS one (01-09-2015)
    “…Introduction In autism spectrum disorders (ASD), complex gene-environment interactions contribute to disease onset and progress. Given that gastro-intestinal…”
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    Journal Article
  12. 12

    A novel HLA-B39 allele (HLA-B3916) due to a rare mutation causing cryptic splice site activation by Tamouza, R, El Kassar, N, Schaeffer, V, Carbonnelle, E, Tatari, Z, Marzais, F, Fortier, C, Poirier, J C, Sadki, K, Bernaudin, F, Toubert, A, Krishnamoorthy, R, Charron, D

    Published in Human immunology (01-05-2000)
    “…A novel HLA-B*39 variant, found in an African patient with sickle cell anemia undergoing bone marrow transplantation is described. Initially suspected by…”
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    Journal Article