Volume 16 (2019)
Volume 15 (2018)
Volume 14 (2017)
Volume 13 (2016)
Volume 12 (2015)
Volume 11 (2014)
Volume 10 (2013)
Volume 9 (2012)
Volume 8 (2011)
Volume 7 (2010)
Volume 6 (2009)
Volume 5 (2008)
Volume 4 (2007)
Volume 3 (2006)
Volume 2 (2005)
Volume 1 (2004)
1. A Case of Probable MHC Class II Deficiency with Disseminated BCGitis

Soheyla Alyasin; Farhad Abolnezhadian; Maryam Khoshkhui

Volume 12, Issue 3 , Summer 2015, , Pages 219-225

Abstract
  Major histocompatibility complex (MHC) class II deficiency is a primary immunodeficiency disease characterized by abnormality of MHC class II molecules surface expression on peripheral blood lymphocytes and monocytes. Clinical manifestations include extreme susceptibility to viral, bacterial, and fungal ...  Read More

2. Autoimmune Hemolytic Anemia in a Patient with Probable Ataxia Telangiectasia: A Case Report

Soheila Alyasin; Maryam Khoshkhui; Farhad Abolnezhadian

Volume 11, Issue 3 , Summer 2014, , Pages 217-220

Abstract
  Background: Ataxia telangiectasia (AT) is one of the combined immunodeficiency syndromes with immunologic, neurologic, endocrinologic, hepatic and cutaneous abnormalities. Regarding the fact that autoimmune disorders; such as autoimmune hemolytic anemia (AIHA), are not generally expected in the course ...  Read More

3. A Case of Bruton’s Disease with Normal Immunoglobulin G Level

Soheila Alyasin; Farhad Abolnezhadian; Amir Rezaei

Volume 11, Issue 1 , Winter 2014, , Pages 59-63

Abstract
  X-linked agamaglobulinemia (XLA) or Bruton’s disease is a genetic disease resulting from a mutation in the Bruton’s tyrosine kinase (Btk) gene. This mutation leads to B cell arrest during differentiation (1). This disease was first described by Ogden Bruton in 1952 (2). Approximately 85% ...  Read More