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  1. Article

    Open Access

    Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome

    Inborn errors of immunity (IEI) and autoantibodies to type I interferons (IFNs) underlie critical COVID-19 pneumonia in at least 15% of the patients, while the causes of multisystem inflammatory syndrome in ch...

    Hassan Abolhassani, Nils Landegren, Paul Bastard in Journal of Clinical Immunology (2022)

  2. Article

    Open Access

    X-Linked TLR7 Deficiency Underlies Critical COVID-19 Pneumonia in a Male Patient with Ataxia-Telangiectasia

    Coronavirus disease 2019 (COVID-19) exhibits a wide spectrum of clinical manifestations, ranging from asymptomatic to critical conditions. Understanding the mechanism underlying life-threatening COVID-19 is in...

    Hassan Abolhassani, Ahmad Vosughimotlagh, Takaki Asano in Journal of Clinical Immunology (2022)

  3. No Access

    Article

    Novel Mutations in TACI (TNFRSF13B) Causing Common Variable Immunodeficiency

    Common variable immunodeficiency (CVID) is a heterogeneous syndrome characterized by impaired immunoglobulin production. The disorder is also characterized by co-occurrence of autoimmune, lymphoproliferative, ...

    Javad Mohammadi, Chonghai Liu, Asghar Aghamohammadi in Journal of Clinical Immunology (2009)

  4. Article

    Open Access

    Screening of functional and positional candidate genes in families with common variable immunodeficiency

    Common variable immunodeficiency (CVID) comprises a heterogeneous group of primary antibody deficiencies with complex clinical and immunological phenotypes. The recent discovery that some CVID patients show mo...

    Ulrich Salzer, Carla Neumann, Jens Thiel, Cristina Woellner in BMC Immunology (2008)