Volume 2, Issue 1

 

ارسال های اخیر

  • Anti-peptide Antibody Responses in Patients with Ataxia-telangiectasia 

    Jamee, Mahnaz؛ Sharifi, Laleh؛ Ghiasy, Saleh (Research Center For Immunodeficiencies, 2019-03-01)
    Background/Objectives: Ataxia-telangiectasia (AT) is a rare inherited disorder caused by mutations in the ATM (Ataxia Telangiectasia Mutated) gene. Antibody response to diphtheria and tetanus toxoid vaccines ...

  • Unique Presentation of Common Variable Immunodeficiency: Enteropathy Unaccompanied by Infectious Phenotype 

    Ebrahimi Daryani, Nasser؛ Torabi-Sagvand, Babak؛ Panah, Elnaz (Research Center For Immunodeficiencies, 2019-03-01)
    Enteropathy is one of the rare manifestations of common variable immunodeficiency (CVID) as a predominant antibody deficiency. Proper diagnosis of this phenotype in CVID cases is difficult and may result in inaccurate ...

  • Hereditary Angioedema: A Family with Several Affected Members 

    Daneshmandi, Zahra؛ Darougar, Sepideh؛ Akbaroghli, Susan؛ Torabi, Elham؛ Csuka, Dorrotya؛ Farkas, Henriette؛ Varga, Lilian؛ Mesdaghi, Mehrnaz؛ Chavoshzadeh, Zahra (Research Center For Immunodeficiencies, 2019-03-01)
    Hereditary Angioedema (HAE) is a rare, autosomal dominant genetic disease, characterized clinically by episodic non-pruritic swelling of face, limbs and tissue just beneath the skin. Laryngeal edema is the main cause of ...