Search Results - Boisson-Dupuis, Stéphanie

Refine Results
  1. 1
    The monogenic basis of human tuberculosis

    The monogenic basis of human tuberculosis by Boisson-Dupuis, Stephanie

    Published 2020
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  2. 2
    Mycobacterial diseases in patients with inborn errors of immunity

    Mycobacterial diseases in patients with inborn errors of immunity by Boisson-Dupuis, Stéphanie, Bustamante, Jacinta

    Published 2021
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  3. 3
    ISG15: leading a double life as a secreted molecule

    ISG15: leading a double life as a secreted molecule by Bogunovic, Dusan, Boisson-Dupuis, Stéphanie, Casanova, Jean-Laurent

    Published 2013
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  4. 4
    Mendelian susceptibility to mycobacterial disease: genetic, immunological, and clinical features of inborn errors of IFN-γ immunity

    Mendelian susceptibility to mycobacterial disease: genetic, immunological, and clinical features of inborn errors of IFN-γ immunity by Bustamante, Jacinta, Boisson-Dupuis, Stéphanie, Abel, Laurent, Casanova, Jean-Laurent

    Published 2014
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  5. 5
    Genetic lessons learnt from X-linked Mendelian susceptibility to mycobacterial diseases

    Genetic lessons learnt from X-linked Mendelian susceptibility to mycobacterial diseases by Bustamante, Jacinta, Picard, Capucine, Boisson-Dupuis, Stéphanie, Abel, Laurent, Casanova, Jean-Laurent

    Published 2011
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  6. 6
    Septins Regulate Bacterial Entry into Host Cells

    Septins Regulate Bacterial Entry into Host Cells by Mostowy, Serge, Nam Tham, To, Danckaert, Anne, Guadagnini, Stéphanie, Boisson-Dupuis, Stéphanie, Pizarro-Cerdá, Javier, Cossart, Pascale

    Published 2009
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  7. 7
    Human STAT1 gain-of-function heterozygous mutations: chronic mucocutaneous candidiasis and type I interferonopathy

    Human STAT1 gain-of-function heterozygous mutations: chronic mucocutaneous candidiasis and type I interferonopathy by Okada, Satoshi, Asano, Takaki, Moriya, Kunihiko, Boisson-Dupuis, Stephanie, Kobayashi, Masao, Casanova, Jean-Laurent, Puel, Anne

    Published 2020
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  8. 8
    Inborn errors of human STAT1: allelic heterogeneity governs the diversity of immunological and infectious phenotypes

    Inborn errors of human STAT1: allelic heterogeneity governs the diversity of immunological and infectious phenotypes by Boisson-Dupuis, Stephanie, Kong, Xiao-Fei, Okada, Satoshi, Cypowyj, Sophie, Puel, Anne, Abel, Laurent, Casanova, Jean-Laurent

    Published 2012
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  9. 9
    Inherited IL-12Rβ1 Deficiency in a Child With BCG Adenitis and Oral Candidiasis: A Case Report

    Inherited IL-12Rβ1 Deficiency in a Child With BCG Adenitis and Oral Candidiasis: A Case Report by Hatipoglu, Nevin, Güvenç, B. Haluk, Deswarte, Caroline, Koksalan, Kaya, Boisson-Dupuis, Stéphanie, Casanova, Jean-Laurent, Bustamante, Jacinta

    Published 2017
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  10. 10
    Human ancient DNA analyses reveal the high burden of tuberculosis in Europeans over the last 2,000 years

    Human ancient DNA analyses reveal the high burden of tuberculosis in Europeans over the last 2,000 years by Kerner, Gaspard, Laval, Guillaume, Patin, Etienne, Boisson-Dupuis, Stéphanie, Abel, Laurent, Casanova, Jean-Laurent, Quintana-Murci, Lluis

    Published 2021
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  11. 11
    A patient with tyrosine kinase 2 deficiency without hyper IgE syndrome

    A patient with tyrosine kinase 2 deficiency without hyper IgE syndrome by Kilic, Sara S., Hacimustafaoglu, Mustafa, Boisson-Dupuis, Stéphanie, Kreins, Alexandra Y., Grant, Audrey V., Abel, Laurent, Casanova, Jean-Laurent

    Published 2012
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  12. 12
    Mendelian Susceptibility to Mycobacterial Disease in Egyptian Children

    Mendelian Susceptibility to Mycobacterial Disease in Egyptian Children by Galal, Nermeen, Boutros, Jeannette, Marsafy, Aisha, Kong, Xiao-Fei, Feinberg, Jacqueline, Casanova, Jean-Laurent, Boisson-Dupuis, Stéphanie, Bustamante, Jacinta

    Published 2012
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  13. 13
    Induction of MxA Gene Expression by Influenza A Virus Requires Type I or Type III Interferon Signaling

    Induction of MxA Gene Expression by Influenza A Virus Requires Type I or Type III Interferon Signaling by Holzinger, Dirk, Jorns, Carl, Stertz, Silke, Boisson-Dupuis, Stéphanie, Thimme, Robert, Weidmann, Manfred, Casanova, Jean-Laurent, Haller, Otto, Kochs, Georg

    Published 2007
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  14. 14
    Granulomatous skin lesions, severe scrotal and lower limb edema due to mycobacterial infections in a child with complete IFN–γ receptor–1 deficiency

    Granulomatous skin lesions, severe scrotal and lower limb edema due to mycobacterial infections in a child with complete IFN–γ receptor–1 deficiency by Karaca, Neslihan Edeer, Boisson-Dupuis, Stephanie, Aksu, Güzide, Bustamante, Jacinta, Kandiloglu, Gulsen, Ozsan, Nazan, Hekimgil, Mine, Casanova, Jean-Laurent, Kutukculer, Necil

    Published 2012
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  15. 15
    Recurrent Salmonellosis in a Child with Complete IL-12Rβ1 Deficiency

    Recurrent Salmonellosis in a Child with Complete IL-12Rβ1 Deficiency by Zahid, Mohammad Faizan, Ali, Syed Asad, Jehan, Fyezah, Billo, Abdul Gaffar, Casanova, Jean-Laurent, Bustamante, Jacinta, Boisson-Dupuis, Stephanie, Mir, Fatima

    Published 2014
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  16. 16
    A new patient with inherited TYK2 Deficiency

    A new patient with inherited TYK2 Deficiency by Sarrafzadeh, Shokouh Azam, Mahloojirad, Maryam, Casanova, Jean-Laurent, Badalzadeh, Mohsen, Bustamante, Jacinta, Boisson-Dupuis, Stephanie, Pourpak, Zahra, Nourizadeh, Maryam, Moin, Mostafa

    Published 2019
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  17. 17
    Treatment of Disseminated Mycobacterial Infection with High-Dose IFN-γ in a Patient with IL-12Rβ1 Deficiency

    Treatment of Disseminated Mycobacterial Infection with High-Dose IFN-γ in a Patient with IL-12Rβ1 Deficiency by Alangari, Abdullah A., Al-Zamil, Fahad, Al-Mazrou, Abdulrahman, Al-Muhsen, Saleh, Boisson-Dupuis, Stéphanie, Awadallah, Sitalbanat, Kambal, Abdelmageed, Casanova, Jean-Laurent

    Published 2011
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  18. 18
    BCG Lymphadenitis and Recurrent Oral Candidiasis in an Infant with a New Mutation Leading to Interleukin-12 Receptor Beta-1 Deficiency

    BCG Lymphadenitis and Recurrent Oral Candidiasis in an Infant with a New Mutation Leading to Interleukin-12 Receptor Beta-1 Deficiency by Aytekin, Caner, Dogu, Figen, Tuygun, Nilden, Tanir, Gonul, Guloglu, Deniz, Boisson-Dupuis, Stephanie, Bustamante, Jacinta, Feinberg, Jacqueline, Casanova, Jean-Laurent, Ikinciogullari, Aydan

    Published 2011
    Get full text Get full text
    Text
    Save to List
    Saved in:
  19. 19
    Clinical Disease Caused by Klebsiella in 2 Unrelated Patients With Interleukin 12 Receptor β1 Deficiency

    Clinical Disease Caused by Klebsiella in 2 Unrelated Patients With Interleukin 12 Receptor β1 Deficiency by Pedraza, Sigifredo, Lezana, Jose Luis, Samarina, Arina, Aldana, Ruth, Herrera, Maria Teresa, Boisson-Dupuis, Stéphanie, Bustamante, Jacinta, Pages, Perle, Casanova, Jean-Laurent, Picard, Capucine

    Published 2010
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  20. 20
    Heterozygosity for the Y701C STAT1 mutation in a multiplex kindred with multifocal osteomyelitis

    Heterozygosity for the Y701C STAT1 mutation in a multiplex kindred with multifocal osteomyelitis by Hirata, Osamu, Okada, Satoshi, Tsumura, Miyuki, Kagawa, Reiko, Miki, Mizuka, Kawaguchi, Hiroshi, Nakamura, Kazuhiro, Boisson-Dupuis, Stéphanie, Casanova, Jean-Laurent, Takihara, Yoshihiro, Kobayashi, Masao

    Published 2013
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:

Search Tools: