Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jean-Laurent eCasanova"'
Publikováno v:
Frontiers in Immunology, Vol 6 (2015)
Herpes Simplex Virus-1 (HSV-1) is a common virus that can rarely invade the human central nervous system (CNS), causing devastating encephalitis. The permissiveness to HSV-1 of the various relevant cell types involved in the disease, neurons, astrocy
Externí odkaz:
https://doaj.org/article/cb1a5c71e93240ad96f1453a3864c940
Autor:
Yuval eItan, Jean-Laurent eCasanova
Publikováno v:
Frontiers in Immunology, Vol 6 (2015)
Germline genetic mutations underlie various primary immunodeficiency (PID) diseases. Patients with rare PID diseases (like most non-PID patients and healthy individuals) carry, on average, 20,000 rare and common coding variants detected by high throu
Externí odkaz:
https://doaj.org/article/7a0a4cd88b364301a2ccfdda0ef1bdae
Autor:
Nicholas L Rider, Bertrand eBoisson, Soma eJyonouchi, Eric eHanson, Sergio eRosenzweig, Jean-Laurent eCasanova, Jordan eOrange
Publikováno v:
Frontiers in Pediatrics, Vol 3 (2015)
Unbiased genetic diagnosis has increasingly associated seemingly unrelated somatic and immunological phenotypes. We report a male infant who presented within the first year of life with physical growth impairment, feeding difficulties, hyperemesis wi
Externí odkaz:
https://doaj.org/article/e51c8612b8ed4c2cb07b311ad2640ddf
Autor:
Hubert Bobby Gaspar, Waleed eAl-Herz, Aziz eBousfiha, Jean-Laurent eCasanova, Talal eChatila, Mary Ellen eConley, Charlotte eCunningham-Rundles, Amos eEtzioni, Jose Luis Franco, Steven eHolland, Christoph eKlein, SHIGEAKI eNONOYAMA, Hans eOchs, Eric eOksenhendler, Capucine ePicard, Jennifer ePuck, Kathleen eSullivan, Mimi eTang
Publikováno v:
Frontiers in Immunology, Vol 5 (2014)
Externí odkaz:
https://doaj.org/article/e7ae0a50131c40a981bbe1db30fa7419
Autor:
Waleed eAl-Herz, Aziz eBousfiha, Jean-Laurent eCasanova, Talal eChatila, Mary Ellen eConley, Charlotte eCunningham-Rundles, Amos eEtzioni, Jose Luis Franco, Hubert Bobby Gaspar, Steven eHolland, Christoph eKlein, Shigeaki eNonoyama, Hans eOchs, Eric eOksenhendler, Capucine ePicard, Jennifer ePuck, Kathleen eSullivan, Mimi eTang
Publikováno v:
Frontiers in Immunology, Vol 5 (2014)
We report the updated classification of primary immunodeficiencies compiled by the Expert Committee of the International Union of Immunological Societies. In comparison to the previous version, more than 30 new gene defects are reported in this updat
Externí odkaz:
https://doaj.org/article/9d2ea0303d5a402ebca3134c83051a8f
Autor:
Waleed eAl-Herz, Aziz eBousfiha, jean-laurent eCasanova, Helen eChapel, Mary Ellen eConley, Charlotte eCunningham-Rundles, Amos eEtzioni, Alain eFischer, Jose Luis Franco, Raif eGeha, Lennart eHammarstrom, Shigeaki eNonoyama, Luigi Daniele Notarangelo, Hans Dieter Ochs, Jennifer ePuck, Chaim M Roifman, Reinhard eSeger, Mimi eTang
Publikováno v:
Frontiers in Immunology, Vol 2 (2011)
We report the updated classification of primary immunodeficiency diseases, compiled by the ad-hoc Expert Committee of the International Union of Immunological Societies (IUIS). As compared to the previous edition, more than 15 novel disease entities
Externí odkaz:
https://doaj.org/article/de0526929203419586a7194d802c4fea
Autor:
Nicholas L Rider, Bertrand eBoisson, Soma eJyonouchi, Eric eHanson, Sergio eRosenzweig, Jean-Laurent eCasanova, Jordan eOrange
Publikováno v:
Frontiers in Pediatrics
Frontiers in Pediatrics, Vol 3 (2015)
Frontiers in Pediatrics, Vol 3 (2015)
Unbiased genetic diagnosis has increasingly associated seemingly unrelated somatic and immunological phenotypes. We report a male infant who presented within the first year of life with physical growth impairment, feeding difficulties, hyperemesis wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23c40a17018968ef11999f0e0bb03ddd
https://doi.org/10.3389/fped.2015.00028
https://doi.org/10.3389/fped.2015.00028
Autor:
Yuval eItan, Jean-Laurent eCasanova
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 6 (2015)
Frontiers in Immunology, Vol 6 (2015)
Germline genetic mutations underlie various primary immunodeficiency (PID) diseases. Patients with rare PID diseases (like most non-PID patients and healthy individuals) carry, on average, 20,000 rare and common coding variants detected by high-throu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36dfd0643e2663e811286efcd9f24313
https://pubmed.ncbi.nlm.nih.gov/25883595
https://pubmed.ncbi.nlm.nih.gov/25883595