Author Index

A

  • Aghamohamadi, nazanin Activated PI3K-Delta Syndrome: Pathogenesis, Clinical Manifestations, Diagnosis, Classification, and Management [Volume 3, Issue 3, 2020, Pages 8-15]
  • Amirifar, Parisa Clinical manifestations in Iranian Ataxia Telangiectasia Patients [Volume 3, Issue 1, 2020, Pages 29-40]
  • Askarimoghaddam, Forough Chronic granulomatous disease (CGD): Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management [Volume 3, Issue 3, 2020, Pages 16-29]
  • Ataei, Zahra 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]

B

  • Babaha, Fateme Autoimmunity Complications in Common Variable Immunodeficiency Patients; an update from the Iranian registry [Volume 3, Issue 2, 2020, Pages 29-38]

C

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

D

  • Delavari, Samaneh Allergy in Patients with Selective IgA Deficiency [Volume 3, Issue 1, 2020, Pages 54-63]

F

  • Fayyaz, Farimah Chronic granulomatous disease (CGD): Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management [Volume 3, Issue 3, 2020, Pages 16-29]
  • Fekrvand, Saba Infectious Complications in Patients with Common Variable Immunodeficiency (CVID) in Iran [Volume 3, Issue 1, 2020, Pages 41-53]

G

K

  • Keles, Sevgi Past and Future of J Project Meetings in Turkey: Evaluation of Last 10 Years [Volume 3, Issue 2, 2020, Pages 8-11]
  • Khashayar, Kiavash Chronic granulomatous disease (CGD): Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management [Volume 3, Issue 3, 2020, Pages 16-29]

L

  • Lougaris, Vasssilios The genetic heterogeneity of common variable immunodeficiency (CVID) [Volume 3, Issue 1, 2020, Pages 1-14]

M

  • Mehdizadeh, Kasra Comparison of the Familial and Sporadic Forms of Hyper IgM Syndrome in the Iranian Patients [Volume 3, Issue 3, 2020, Pages 39-46]
  • Mehrizi, Reza Infectious Complications in Patients with Common Variable Immunodeficiency (CVID) in Iran [Volume 3, Issue 1, 2020, Pages 41-53]
  • Mirminachi, Babak An Iranian Patient Suffering from Chronic Granulomatous Disease, with Mutation in the NCF1 Gene [Volume 3, Issue 1, 2020, Pages 64-70]
  • Moeini shad, Tannaz Clinical manifestations in Iranian Ataxia Telangiectasia Patients [Volume 3, Issue 1, 2020, Pages 29-40]
  • Moeini shad, Tannaz Allergy in Patients with Selective IgA Deficiency [Volume 3, Issue 1, 2020, Pages 54-63]
  • Moeini shad, Tannaz Case Report: MALT1 Mutation in A Patient with Severe Combined Immunodeficiency [Volume 3, Issue 3, 2020, Pages 47-52]
  • Mozafari Nezhad, Ronak An Iranian Patient Suffering from Chronic Granulomatous Disease, with Mutation in the NCF1 Gene [Volume 3, Issue 1, 2020, Pages 64-70]

N

  • Nazari, Farzad 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]
  • Nirouei, Matineh Chronic granulomatous disease (CGD): Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management [Volume 3, Issue 3, 2020, Pages 16-29]

P

  • Padidar, Kimiya Infectious Complications in Patients with Common Variable Immunodeficiency (CVID) in Iran [Volume 3, Issue 1, 2020, Pages 41-53]
  • Padidar, Kimiya Case Report: MALT1 Mutation in A Patient with Severe Combined Immunodeficiency [Volume 3, Issue 3, 2020, Pages 47-52]
  • Pashangzadeh, Salar Comparison of the Familial and Sporadic Forms of Hyper IgM Syndrome in the Iranian Patients [Volume 3, Issue 3, 2020, Pages 39-46]
  • PashangZadeh, Salar Hematologic problems in Hyper-IgM patients [Volume 3, Issue 1, 2020, Pages 15-28]

R

  • Ramezanzadeh, Reyhaneh A Griscelli Syndrome, with Retropharyngeal Abscess, as First Clinical [Volume 3, Issue 2, 2020, Pages 51-55]
  • Ranjouri, MohammadReza Clinical manifestations in Iranian Ataxia Telangiectasia Patients [Volume 3, Issue 1, 2020, Pages 29-40]
  • Rasouli, Sahar Allergy in Patients with Selective IgA Deficiency [Volume 3, Issue 1, 2020, Pages 54-63]
  • Rezaei, Mahnaz Common Variable Immunodeficiency (CVID) and Autoimmunity [Volume 3, Issue 2, 2020, Pages 12-28]

S

  • Sadeghi Shabestari, Mahnaz 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]
  • Safarirad, Molood A Griscelli Syndrome, with Retropharyngeal Abscess, as First Clinical [Volume 3, Issue 2, 2020, Pages 51-55]
  • Salami, Fereshte Allergy in Patients with Selective IgA Deficiency [Volume 3, Issue 1, 2020, Pages 54-63]
  • Salami, Fereshte An Iranian Patient Suffering from Chronic Granulomatous Disease, with Mutation in the NCF1 Gene [Volume 3, Issue 1, 2020, Pages 64-70]
  • Salami, Fereshte 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]
  • Salami, Fereshte 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]
  • Sanaei, Mohammad Javad Bronchiectasis in Patients with the Common Variable Immunodeficiency (CVID) [Volume 3, Issue 3, 2020, Pages 30-38]
  • Shadani, Shiva A Griscelli Syndrome, with Retropharyngeal Abscess, as First Clinical [Volume 3, Issue 2, 2020, Pages 51-55]
  • Shahrooei, Mohammad 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]
  • Shariati, Sahar Allergy in Patients with Selective IgA Deficiency [Volume 3, Issue 1, 2020, Pages 54-63]
  • Shariati, Sahar An Iranian Patient Suffering from Chronic Granulomatous Disease, with Mutation in the NCF1 Gene [Volume 3, Issue 1, 2020, Pages 64-70]
  • Shirmast, Paniz Case Report: MALT1 Mutation in A Patient with Severe Combined Immunodeficiency [Volume 3, Issue 3, 2020, Pages 47-52]
  • Soltani, Mojde Common Variable Immunodeficiency (CVID) and Autoimmunity [Volume 3, Issue 2, 2020, Pages 12-28]

T

  • Tavakol, Marzieh Chronic granulomatous disease (CGD): Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management [Volume 3, Issue 3, 2020, Pages 16-29]
  • Tavakol, Zahra Chronic granulomatous disease (CGD): Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management [Volume 3, Issue 3, 2020, Pages 16-29]
  • Tavakolifar, Yousef 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]

V

  • Vosughi Motlagh, Ahmad A Griscelli Syndrome, with Retropharyngeal Abscess, as First Clinical [Volume 3, Issue 2, 2020, Pages 51-55]

Y

  • Yousefi, Koroush A Griscelli Syndrome, with Retropharyngeal Abscess, as First Clinical [Volume 3, Issue 2, 2020, Pages 51-55]

Z

  • Zarezadeh mehrabadi, Ali Activated PI3K-Delta Syndrome: Pathogenesis, Clinical Manifestations, Diagnosis, Classification, and Management [Volume 3, Issue 3, 2020, Pages 8-15]