Volume 2, Issue 2


ارسال های اخیر

  • The frequency of Helicobacter pylori infection in patients with primary antibody deficiencies 

    Kiaee, Fatemeh؛ Tavakolinia, Naiimeh؛ Moradi, Leila؛ Delavari, Samaneh؛ Abouhamzeh, Kosar؛ Bayat, Shiva؛ Anvari, Pardis؛ Mahdaviani, Seyed Alireza؛ Nabavi, Mohammad؛ Merat, Shahin؛ Zandieh, Fariborz؛ Parvaneh, Nima؛ Malekzadeh, Reza (Research Center For Immunodeficiencies, 2019-06-01)
    Introduction: Primary antibody deficiencies (PADs) are the most common inherited immunodeficiencies, which can present wide clinical presentation including susceptibility to bacterial infections and gastric adenocarcinoma. ...

  • Differential expression and phosphorylation of BTK protein domain in X-linked agammaglobulinemia 

    Sohani, Mahsa؛ Delavari, Samaneh؛ Zarnani, Hassan؛ Parvaneh, Leila؛ Rasouli, Shima؛ Shahkarami, Sepideh؛ Babaie, Sepideh؛ Kiaee, Fatemeh (Research Center For Immunodeficiencies, 2019-06-01)
    Background: X-linked (Bruton's) agammaglobulinemia (XLA) is a rare congenital disorder with defects in early B cell development caused by mutations in the gene encoding BTK (Bruton tyrosine kinase). The aim of this study ...

  • Unilateral Flaccid Paraplegia Associated with Chronic Granulomatous Disease 

    Pourhamdi, Shabnam؛ Mohammadinejad, Payam (Research Center For Immunodeficiencies, 2019-06-01)
    Chronic Granulomatous Disease (CGD) can be associated with several neurological complications. Abscess in the brain in patients diagnosed with CGD has been reported in several publications. Different pathogens have been ...

  • Primary Immunodeficiency Disorders: Awareness Survey of Physicians in Iran 

    Asgardoon, Mohammad Hossein؛ Rezwanifar, Mohamad Mehdi؛ Ataeinia, Bahar؛ Bagheri, Yasser (Research Center For Immunodeficiencies, 2019-06-01)
    Background: Primary immunodeficiency disorders (PID) are a group of hereditary disorders characterized by various complications. Many patients with PID are undiagnosed, underdiagnosed, or misdiagnosed due to lack of ...