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Gastrointestinal Manifestations in Patients with Common Variable Immunodeficiency
This study focuses on endoscopic and pathologic alterations of gastrointestinal (GI) disorders of Iranian patients with common variable immunodeficiency (CVID). Nineteen of 39 CVID patients (48%) hadExpand
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Identification of a novel mutation of MTP gene in a patient with abetalipoproteinemia.
Abetalipoproteinemia (ABL), or Bassen-Kornzweig syndrome, is a rare autosomal recessive disorder of lipoprotein metabolism, characterized by fat malabsorption, hypocholesterolemia retinitisExpand
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Lymphoma of mucosa-associated lymphoid tissue in common variable immunodeficiency
Common variable immunodeficiency (CVID) is the most common symptomatic primary immunodeficiency characterized by reduced levels of all major immunoglobuline classes and recurrent c infections. TheExpand
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VEGF and p53 Biomarkers in Pediatric Patients With Langerhans Cell Histiocytosis
Background: Langerhans cell histiocytosis (LCH) is a rare disease with abnormal accumulation of the dendritic Langerhans cells. In the localized form (single system), the disease is self-limiting butExpand
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An Estimation of Steroid Responsiveness of Idiopathic Nephrotic Syndrome in Iranian Children
Objective Idiopathic Nephrotic syndrome (INS) is the most common form of nephrotic syndrome (NS) in children with the potential of progression to end stage renal disease (ESRD). INS isExpand
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Effect of Age on Stereopsis
Purpose: To evaluate the effect of age on stereopsis. Methods: We evaluated stereoacuity using TNO and titmus test after full correction of refractive errors in 87 randomly selected subjects agedExpand