Keyword Index

A

  • Activated phosphoinositide 3- kinase d syndrome (APDS) Activated PI3K-Delta Syndrome: Pathogenesis, Clinical Manifestations, Diagnosis, Classification, and Management [Volume 3, Issue 3, 2020, Pages 8-15]
  • Allergy Allergy in Patients with Selective IgA Deficiency [Volume 3, Issue 1, 2020, Pages 54-63]
  • Ataxia telangiectasia Clinical manifestations in Iranian Ataxia Telangiectasia Patients [Volume 3, Issue 1, 2020, Pages 29-40]
  • ATM Clinical manifestations in Iranian Ataxia Telangiectasia Patients [Volume 3, Issue 1, 2020, Pages 29-40]
  • Autoimmune complications Autoimmunity Complications in Common Variable Immunodeficiency Patients; an update from the Iranian registry [Volume 3, Issue 2, 2020, Pages 29-38]

C

  • Chronic diarrhea Atrophic Thymus in the First Case of the Interleukin 10 Receptor Beta Deficiency due to the Homozygous Large Deletion [Volume 3, Issue 2, 2020, Pages 46-50]
  • Chronic Granulomatous Disease Chronic granulomatous disease (CGD): Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management [Volume 3, Issue 3, 2020, Pages 16-29]
  • Chronic granulomatous disease (CGD) An Iranian Patient Suffering from Chronic Granulomatous Disease, with Mutation in the NCF1 Gene [Volume 3, Issue 1, 2020, Pages 64-70]
  • Common variable immune deficiency (CVID) Infectious Complications in Patients with Common Variable Immunodeficiency (CVID) in Iran [Volume 3, Issue 1, 2020, Pages 41-53]
  • Common variable immunodeficiency Autoimmunity Complications in Common Variable Immunodeficiency Patients; an update from the Iranian registry [Volume 3, Issue 2, 2020, Pages 29-38]
  • Common variable immunodeficiency Common Variable Immunodeficiency (CVID) and Autoimmunity [Volume 3, Issue 2, 2020, Pages 12-28]
  • Common variable immunodeficiency Bronchiectasis in Patients with the Common Variable Immunodeficiency (CVID) [Volume 3, Issue 3, 2020, Pages 30-38]
  • Common Variable Immunodeficiency (CVID) The genetic heterogeneity of common variable immunodeficiency (CVID) [Volume 3, Issue 1, 2020, Pages 1-14]
  • Consanguinity Past and Future of J Project Meetings in Turkey: Evaluation of Last 10 Years [Volume 3, Issue 2, 2020, Pages 8-11]
  • CTLA4 Normal Expression of cytotoxic T-lymphocyte-associated protein 4 (CTLA4) in LPS-responsive and beige-like anchor protein (LRBA) Patient [Volume 3, Issue 3, 2020, Pages 53-58]

F

  • Familial HIGM Comparison of the Familial and Sporadic Forms of Hyper IgM Syndrome in the Iranian Patients [Volume 3, Issue 3, 2020, Pages 39-46]
  • FANCA A New Missense Mutation in FANCA Gene Detected by Whole Exome Sequencing in a Case with Fanconi Anemia (a case report) [Volume 3, Issue 2, 2020, Pages 39-45]
  • Fanconi anemia A New Missense Mutation in FANCA Gene Detected by Whole Exome Sequencing in a Case with Fanconi Anemia (a case report) [Volume 3, Issue 2, 2020, Pages 39-45]

G

  • Gain of function Activated PI3K-Delta Syndrome: Pathogenesis, Clinical Manifestations, Diagnosis, Classification, and Management [Volume 3, Issue 3, 2020, Pages 8-15]
  • Grisel’s Syndrome A Griscelli Syndrome, with Retropharyngeal Abscess, as First Clinical [Volume 3, Issue 2, 2020, Pages 51-55]

H

  • Hyper IgM Comparison of the Familial and Sporadic Forms of Hyper IgM Syndrome in the Iranian Patients [Volume 3, Issue 3, 2020, Pages 39-46]
  • Hyper IgM (HIgM) Hematologic problems in Hyper-IgM patients [Volume 3, Issue 1, 2020, Pages 15-28]

I

  • IL-10R deficiency Atrophic Thymus in the First Case of the Interleukin 10 Receptor Beta Deficiency due to the Homozygous Large Deletion [Volume 3, Issue 2, 2020, Pages 46-50]
  • Infectious complications Infectious Complications in Patients with Common Variable Immunodeficiency (CVID) in Iran [Volume 3, Issue 1, 2020, Pages 41-53]

J

  • J Project Past and Future of J Project Meetings in Turkey: Evaluation of Last 10 Years [Volume 3, Issue 2, 2020, Pages 8-11]

L

  • LRBA Normal Expression of cytotoxic T-lymphocyte-associated protein 4 (CTLA4) in LPS-responsive and beige-like anchor protein (LRBA) Patient [Volume 3, Issue 3, 2020, Pages 53-58]

M

N

  • NCF1 gene An Iranian Patient Suffering from Chronic Granulomatous Disease, with Mutation in the NCF1 Gene [Volume 3, Issue 1, 2020, Pages 64-70]

P

  • Pediatrics Atrophic Thymus in the First Case of the Interleukin 10 Receptor Beta Deficiency due to the Homozygous Large Deletion [Volume 3, Issue 2, 2020, Pages 46-50]
  • Phosphoinositide-3-kinase δ Activated PI3K-Delta Syndrome: Pathogenesis, Clinical Manifestations, Diagnosis, Classification, and Management [Volume 3, Issue 3, 2020, Pages 8-15]
  • Primary immunodeficiency Autoimmunity Complications in Common Variable Immunodeficiency Patients; an update from the Iranian registry [Volume 3, Issue 2, 2020, Pages 29-38]
  • Primary immunodeficiency Past and Future of J Project Meetings in Turkey: Evaluation of Last 10 Years [Volume 3, Issue 2, 2020, Pages 8-11]
  • Primary immunodeficiency Activated PI3K-Delta Syndrome: Pathogenesis, Clinical Manifestations, Diagnosis, Classification, and Management [Volume 3, Issue 3, 2020, Pages 8-15]
  • Primary immunodeficiency Chronic granulomatous disease (CGD): Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management [Volume 3, Issue 3, 2020, Pages 16-29]
  • Primary immunodeficiency Comparison of the Familial and Sporadic Forms of Hyper IgM Syndrome in the Iranian Patients [Volume 3, Issue 3, 2020, Pages 39-46]
  • Primary immunodeficiency disorders (PIDs) Hematologic problems in Hyper-IgM patients [Volume 3, Issue 1, 2020, Pages 15-28]
  • Primary immunodeficiency disorders (PIDs) Allergy in Patients with Selective IgA Deficiency [Volume 3, Issue 1, 2020, Pages 54-63]

S

  • Selective Immunoglobulin A Deficiency Allergy in Patients with Selective IgA Deficiency [Volume 3, Issue 1, 2020, Pages 54-63]
  • Severe Combined Immunodeficiency Case Report: MALT1 Mutation in A Patient with Severe Combined Immunodeficiency [Volume 3, Issue 3, 2020, Pages 47-52]
  • Sporadic HIGM Comparison of the Familial and Sporadic Forms of Hyper IgM Syndrome in the Iranian Patients [Volume 3, Issue 3, 2020, Pages 39-46]

T

  • Turkish experience Past and Future of J Project Meetings in Turkey: Evaluation of Last 10 Years [Volume 3, Issue 2, 2020, Pages 8-11]

V

  • VEO-IBD Atrophic Thymus in the First Case of the Interleukin 10 Receptor Beta Deficiency due to the Homozygous Large Deletion [Volume 3, Issue 2, 2020, Pages 46-50]

W

  • Whole exome sequencing Case Report: MALT1 Mutation in A Patient with Severe Combined Immunodeficiency [Volume 3, Issue 3, 2020, Pages 47-52]