Keyword Index

A

  • Agammaglobulinemia Gastrointestinal Manifestations in Patients with Agammaglobulinemia [Volume 2, Issue 3, 2019, Pages 104-113]
  • Associated Unilateral Flaccid Paraplegia Associated with Chronic Granulomatous Disease [Volume 2, Issue 2, 2019, Pages 84-89]
  • Ataxia telangiectasia Anti-peptide Antibody Responses in Patients with Ataxia-telangiectasia [Volume 2, Issue 1, 2019, Pages 28-36]
  • Ataxia telangiectasia Misclassification of Ataxia Telangiectasia with Hyper IgM immune profile [Volume 2, Issue 3, 2019, Pages 147-152]

B

  • Bruton's tyrosine kinase Differential expression and phosphorylation of BTK protein domain in X-linked agammaglobulinemia [Volume 2, Issue 2, 2019, Pages 58-71]

C

  • Chediak-Higashi syndrome Chediak-Higashi Syndrome Presented with Recurrent Episodes of Diarrhea: A Case Report [Volume 1, Issue 1, 2018, Pages 44-51]
  • Chronic Granulomatous Disease Unilateral Flaccid Paraplegia Associated with Chronic Granulomatous Disease [Volume 2, Issue 2, 2019, Pages 84-89]
  • Class Switch Recombination Clinical Outcomes of a Cohort of Patients with CD40L deficiency [Volume 2, Issue 3, 2019, Pages 114-123]
  • Class Switch Recombination Misclassification of Ataxia Telangiectasia with Hyper IgM immune profile [Volume 2, Issue 3, 2019, Pages 147-152]
  • Clinical and immunological characteristics Correlation Analysis of Mutation Severity and BTK-expression by Clinical Manifestations in Patients with X-linked Agammaglobulinemia [Volume 1, Issue 1, 2018, Pages 34-42]
  • Clinical presentation Chediak-Higashi Syndrome Presented with Recurrent Episodes of Diarrhea: A Case Report [Volume 1, Issue 1, 2018, Pages 44-51]
  • CMV retinitis Efficacy of Ganciclovir on CMV Retinitis Complication of Common Variable Immunodeficiency [Volume 1, Issue 2, 2018, Pages 103-107]
  • Common variable immunodeficiency Genetic Association in Familial Common Variable Immunodeficiency (CVID) and IgA Deficiency (IgAD) [Volume 1, Issue 1, 2018, Pages 24-33]
  • Common variable immunodeficiency Unique Presentation of Common Variable Immunodeficiency: Enteropathy Unaccompanied by Infectious Phenotype [Volume 2, Issue 1, 2019, Pages 37-43]
  • Correlation analysis Correlation Analysis of Mutation Severity and BTK-expression by Clinical Manifestations in Patients with X-linked Agammaglobulinemia [Volume 1, Issue 1, 2018, Pages 34-42]
  • CVID Efficacy of Ganciclovir on CMV Retinitis Complication of Common Variable Immunodeficiency [Volume 1, Issue 2, 2018, Pages 103-107]

D

  • Diagnosis Predominantly Antibody Deficiencies [Volume 1, Issue 2, 2018, Pages 52-80]
  • Diagnostic delay Unique Presentation of Common Variable Immunodeficiency: Enteropathy Unaccompanied by Infectious Phenotype [Volume 2, Issue 1, 2019, Pages 37-43]
  • Diarrhea Gastrointestinal Manifestations in Patients with Agammaglobulinemia [Volume 2, Issue 3, 2019, Pages 104-113]
  • Disorder The frequency of Helicobacter pylori infection in patients with primary antibody deficiencies [Volume 2, Issue 2, 2019, Pages 72-83]
  • DOCK8 A Review on Hyper-IgE Syndromes: Clinical Manifestations, Diagnosis and Therapeutic Approaches [Volume 2, Issue 3, 2019, Pages 90-103]

E

  • Education Recent Advances and Current Status of Primary Immunodeficiency Disease in Iran [Volume 1, Issue 1, 2018, Pages 1-23]
  • Enteropathy phenotype Unique Presentation of Common Variable Immunodeficiency: Enteropathy Unaccompanied by Infectious Phenotype [Volume 2, Issue 1, 2019, Pages 37-43]

G

  • Gastric cancer The frequency of Helicobacter pylori infection in patients with primary antibody deficiencies [Volume 2, Issue 2, 2019, Pages 72-83]
  • Gastroenteritis Gastrointestinal Manifestations in Patients with Agammaglobulinemia [Volume 2, Issue 3, 2019, Pages 104-113]
  • Gastrointestinal Gastrointestinal Manifestations in Patients with Agammaglobulinemia [Volume 2, Issue 3, 2019, Pages 104-113]
  • Gastrointestinal manifestation Unique Presentation of Common Variable Immunodeficiency: Enteropathy Unaccompanied by Infectious Phenotype [Volume 2, Issue 1, 2019, Pages 37-43]
  • Genetic diagnosis Clinical Outcomes of a Cohort of Patients with CD40L deficiency [Volume 2, Issue 3, 2019, Pages 114-123]
  • Guillain-barre syndrome Multiple Types of Autoimmunity Resulting from the same CD40 Ligand Mutation [Volume 1, Issue 2, 2018, Pages 81-92]

H

  • Helicopter pylori The frequency of Helicobacter pylori infection in patients with primary antibody deficiencies [Volume 2, Issue 2, 2019, Pages 72-83]
  • Hereditary Angioedema Hereditary Angioedema: A Family with Several Affected Members [Volume 2, Issue 1, 2019, Pages 22-27]
  • Hyper IgE syndromes A Review on Hyper-IgE Syndromes: Clinical Manifestations, Diagnosis and Therapeutic Approaches [Volume 2, Issue 3, 2019, Pages 90-103]
  • Hyper-IgM syndrome Multiple Types of Autoimmunity Resulting from the same CD40 Ligand Mutation [Volume 1, Issue 2, 2018, Pages 81-92]
  • Hyper IgM Syndrome Misclassification of Ataxia Telangiectasia with Hyper IgM immune profile [Volume 2, Issue 3, 2019, Pages 147-152]
  • Hyper-immunoglobulin M syndrome Clinical Outcomes of a Cohort of Patients with CD40L deficiency [Volume 2, Issue 3, 2019, Pages 114-123]

I

  • IgA deficiency HLA Genetic Association in Familial Common Variable Immunodeficiency (CVID) and IgA Deficiency (IgAD) [Volume 1, Issue 1, 2018, Pages 24-33]
  • Immune deficiency Anti-peptide Antibody Responses in Patients with Ataxia-telangiectasia [Volume 2, Issue 1, 2019, Pages 28-36]
  • Immunodeficiency diseases Recent Advances and Current Status of Primary Immunodeficiency Disease in Iran [Volume 1, Issue 1, 2018, Pages 1-23]
  • Iran Recent Advances and Current Status of Primary Immunodeficiency Disease in Iran [Volume 1, Issue 1, 2018, Pages 1-23]

K

L

  • LRBA deficiency Gastrointestinal manifestations of Iranian patients with LRBA deficiency [Volume 1, Issue 2, 2018, Pages 93-102]

M

  • Management Predominantly Antibody Deficiencies [Volume 1, Issue 2, 2018, Pages 52-80]
  • Management National Consensus on Diagnosis and Management Guidelines for Primary Immunodeficiency [Volume 2, Issue 1, 2019, Pages 1-21]
  • Mutation severity Correlation Analysis of Mutation Severity and BTK-expression by Clinical Manifestations in Patients with X-linked Agammaglobulinemia [Volume 1, Issue 1, 2018, Pages 34-42]

N

  • National network Recent Advances and Current Status of Primary Immunodeficiency Disease in Iran [Volume 1, Issue 1, 2018, Pages 1-23]

P

  • Pathogenesis Predominantly Antibody Deficiencies [Volume 1, Issue 2, 2018, Pages 52-80]
  • Pedigree Hereditary Angioedema: A Family with Several Affected Members [Volume 2, Issue 1, 2019, Pages 22-27]
  • Pneumonia Clinical Outcomes of a Cohort of Patients with CD40L deficiency [Volume 2, Issue 3, 2019, Pages 114-123]
  • Primary antibody deficiencies Predominantly Antibody Deficiencies [Volume 1, Issue 2, 2018, Pages 52-80]
  • Primary immunodeficiency Chediak-Higashi Syndrome Presented with Recurrent Episodes of Diarrhea: A Case Report [Volume 1, Issue 1, 2018, Pages 44-51]
  • Primary immunodeficiency Gastrointestinal manifestations of Iranian patients with LRBA deficiency [Volume 1, Issue 2, 2018, Pages 93-102]
  • Primary immunodeficiency National Consensus on Diagnosis and Management Guidelines for Primary Immunodeficiency [Volume 2, Issue 1, 2019, Pages 1-21]
  • Primary immunodeficiency The frequency of Helicobacter pylori infection in patients with primary antibody deficiencies [Volume 2, Issue 2, 2019, Pages 72-83]
  • Primary immunodeficiency Primary Immunodeficiency Disorders: Awareness Survey of Physicians in Iran [Volume 2, Issue 2, 2019, Pages 44-57]
  • Primary immunodeficiency Clinical Outcomes of a Cohort of Patients with CD40L deficiency [Volume 2, Issue 3, 2019, Pages 114-123]
  • Primary Immunodeficiency Disorders Evaluating Autoimmunity in Patients with Agammaglobulinemia [Volume 2, Issue 3, 2019, Pages 124-134]
  • Primary Immunodeficiency Disorders Prevalent Autoimmunities in Patients with Selective IgA Deficiency [Volume 2, Issue 3, 2019, Pages 135-146]

R

  • Registry Recent Advances and Current Status of Primary Immunodeficiency Disease in Iran [Volume 1, Issue 1, 2018, Pages 1-23]
  • Research Recent Advances and Current Status of Primary Immunodeficiency Disease in Iran [Volume 1, Issue 1, 2018, Pages 1-23]
  • Rheumatoid arthritis Multiple Types of Autoimmunity Resulting from the same CD40 Ligand Mutation [Volume 1, Issue 2, 2018, Pages 81-92]

S

  • Selective IgA Deficiency Prevalent Autoimmunities in Patients with Selective IgA Deficiency [Volume 2, Issue 3, 2019, Pages 135-146]
  • STAT3 A Review on Hyper-IgE Syndromes: Clinical Manifestations, Diagnosis and Therapeutic Approaches [Volume 2, Issue 3, 2019, Pages 90-103]
  • Survey Primary Immunodeficiency Disorders: Awareness Survey of Physicians in Iran [Volume 2, Issue 2, 2019, Pages 44-57]
  • Symptoms National Consensus on Diagnosis and Management Guidelines for Primary Immunodeficiency [Volume 2, Issue 1, 2019, Pages 1-21]

U

  • Unilateral Flaccid Paraplegia Unilateral Flaccid Paraplegia Associated with Chronic Granulomatous Disease [Volume 2, Issue 2, 2019, Pages 84-89]

V

  • Vomiting Gastrointestinal Manifestations in Patients with Agammaglobulinemia [Volume 2, Issue 3, 2019, Pages 104-113]

X

  • XLA Correlation Analysis of Mutation Severity and BTK-expression by Clinical Manifestations in Patients with X-linked Agammaglobulinemia [Volume 1, Issue 1, 2018, Pages 34-42]
  • X-linked Agammaglobulinemia Differential expression and phosphorylation of BTK protein domain in X-linked agammaglobulinemia [Volume 2, Issue 2, 2019, Pages 58-71]