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]
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]
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