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]
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]
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]
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