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]
-
Agammaglobulinemia
Gastrointestinal Manifestations in Patients with Agammaglobulinemia [Volume 2, Issue 3, 2019, Pages 104-113]
-
Allergy
Allergy in Patients with Selective IgA Deficiency [Volume 3, Issue 1, 2020, Pages 54-63]
-
Asghar Aghamohammadi
Obituary of Professor Asghar Aghamohammadi [(Articles in Press)]
-
Associated
Unilateral Flaccid Paraplegia Associated with Chronic Granulomatous Disease [Volume 2, Issue 2, 2019, Pages 84-89]
-
Asthma
Cytokine Patterns in Iranian Patients with Asthma: A Narrative Review of Qualified Studies [(Articles in Press)]
-
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]
-
Ataxia telangiectasia
Clinical manifestations in Iranian Ataxia Telangiectasia Patients [Volume 3, Issue 1, 2020, Pages 29-40]
-
Atherosclerosis
Evaluation of Serum Level of Interleukin 1 in Patients Suffered from Acute Coronary Syndrome Admitted to the CCU Ward of Amir-Almomenin Hospital of Zahedan City [(Articles in Press)]
-
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]
B
-
Biomarker
Cytokine Patterns in Iranian Patients with Asthma: A Narrative Review of Qualified Studies [(Articles in Press)]
-
B lymphocyte
Evaluation of B Cell and T Cell Phenotypes in CVID Patients and its Correlation with the Clinical Phenotype of the Disease: Study Protocol [(Articles in Press)]
-
Bruton's tyrosine kinase
Differential expression and phosphorylation of BTK protein domain in X-linked agammaglobulinemia [Volume 2, Issue 2, 2019, Pages 58-71]
-
Bruton’ s tyrosine kinase
The Evaluation of Neutropenia in X-linked Agammaglobulinemia Patients [(Articles in Press)]
-
BTK
The Evaluation of Neutropenia in X-linked Agammaglobulinemia Patients [(Articles in Press)]
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 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
Unilateral Flaccid Paraplegia Associated with Chronic Granulomatous Disease [Volume 2, Issue 2, 2019, Pages 84-89]
-
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]
-
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 phenotype
Evaluation of B Cell and T Cell Phenotypes in CVID Patients and its Correlation with the Clinical Phenotype of the Disease: Study Protocol [(Articles in Press)]
-
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 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
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]
-
Common variable immunodeficiency
Gastrointestinal Manifestations in Patients with Common Variable Immunodeficiency [Volume 2, Issue 4, 2019, Pages 185-195]
-
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
Evaluation of B Cell and T Cell Phenotypes in CVID Patients and its Correlation with the Clinical Phenotype of the Disease: Study Protocol [(Articles in Press)]
-
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]
-
Consanguinity
The Origin of First Reported Cases of Primary Immunodeficiency Diseases [(Articles in Press)]
-
Coronary Artery Disease
Evaluation of Serum Level of Interleukin 1 in Patients Suffered from Acute Coronary Syndrome Admitted to the CCU Ward of Amir-Almomenin Hospital of Zahedan City [(Articles in Press)]
-
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]
-
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]
-
CVID
Efficacy of Ganciclovir on CMV Retinitis Complication of Common Variable Immunodeficiency [Volume 1, Issue 2, 2018, Pages 103-107]
D
-
Diabetes Mellitus
Toll-like Receptor 3 Deficiency in a Child with Recurrent Infections and Diabetes Mellitus [(Articles in Press)]
-
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]
-
Diarrhea
Gastrointestinal Manifestations in Patients with Common Variable Immunodeficiency [Volume 2, Issue 4, 2019, Pages 185-195]
-
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]
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]
-
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]
-
Gastrointestinal manifestations
Gastrointestinal Manifestations in Patients with Common Variable Immunodeficiency [Volume 2, Issue 4, 2019, Pages 185-195]
-
Genetic diagnosis
Clinical Outcomes of a Cohort of Patients with CD40L deficiency [Volume 2, Issue 3, 2019, Pages 114-123]
-
Grisel’s Syndrome
A Griscelli Syndrome, with Retropharyngeal Abscess, as First Clinical [Volume 3, Issue 2, 2020, Pages 51-55]
-
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
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]
-
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 IgM Syndrome
Autoimmunity in Patients with Hyper IgM Syndrome [Volume 2, Issue 4, 2019, Pages 196-206]
-
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]
-
IL-1
Evaluation of Serum Level of Interleukin 1 in Patients Suffered from Acute Coronary Syndrome Admitted to the CCU Ward of Amir-Almomenin Hospital of Zahedan City [(Articles in Press)]
-
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]
-
Immune deficiency
Anti-peptide Antibody Responses in Patients with Ataxia-telangiectasia [Volume 2, Issue 1, 2019, Pages 28-36]
-
Immune trobocytopenia purpura
Autoimmunity in Patients with Hyper IgM Syndrome [Volume 2, Issue 4, 2019, Pages 196-206]
-
Immunodeficiency
First Case of X-linked Recessive Anhidrotic Ectodermal Dysplasia with Immunodeficiency from Iran with Unusual Aspergillus infection [Volume 2, Issue 4, 2019, Pages 213-220]
-
Immunodeficiency
The Evaluation of Neutropenia in X-linked Agammaglobulinemia Patients [(Articles in Press)]
-
Immunodeficiency
Obituary of Professor Asghar Aghamohammadi [(Articles in Press)]
-
Immunodeficiency diseases
Recent Advances and Current Status of Primary Immunodeficiency Disease in Iran [Volume 1, Issue 1, 2018, Pages 1-23]
-
Infectious complications
Infectious Complications in Patients with Common Variable Immunodeficiency (CVID) in Iran [Volume 3, Issue 1, 2020, Pages 41-53]
-
Iran
Recent Advances and Current Status of Primary Immunodeficiency Disease in Iran [Volume 1, Issue 1, 2018, Pages 1-23]
-
Iran
Cytokine Patterns in Iranian Patients with Asthma: A Narrative Review of Qualified Studies [(Articles in Press)]
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]
K
-
Keywords: Agammaglobulinemia
Evaluating Autoimmunity in Patients with Agammaglobulinemia [Volume 2, Issue 3, 2019, Pages 124-134]
-
KREC
Why should TREC and KREC quantification assay be concerned to screen of newborns in developing countries? [Volume 2, Issue 4, 2019, Pages 173-184]
L
-
Level
Cytokine Patterns in Iranian Patients with Asthma: A Narrative Review of Qualified Studies [(Articles in Press)]
-
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]
-
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]
-
Microbial Agents
Infectious Complications in Patients with Common Variable Immunodeficiency (CVID) in Iran [Volume 3, Issue 1, 2020, Pages 41-53]
-
Mucosa-associated lymphoid lymphoma translocation gene 1
Case Report: MALT1 Mutation in A Patient with Severe Combined Immunodeficiency [Volume 3, Issue 3, 2020, Pages 47-52]
-
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]
-
NCF1 gene
An Iranian Patient Suffering from Chronic Granulomatous Disease, with Mutation in the NCF1 Gene [Volume 3, Issue 1, 2020, Pages 64-70]
-
NFKB2
NFKB2 mutation in a patient with lymphopenia and extreme cold sensitivity (a case report) [Volume 2, Issue 4, 2019, Pages 207-212]
-
NF-κB
NFKB2 mutation in a patient with lymphopenia and extreme cold sensitivity (a case report) [Volume 2, Issue 4, 2019, Pages 207-212]
-
NF-κB essential modulator essential modulator (NEMO)
First Case of X-linked Recessive Anhidrotic Ectodermal Dysplasia with Immunodeficiency from Iran with Unusual Aspergillus infection [Volume 2, Issue 4, 2019, Pages 213-220]
O
-
Obituary
Obituary of Professor Asghar Aghamohammadi [(Articles in Press)]
P
-
Pathogenesis
Predominantly Antibody Deficiencies [Volume 1, Issue 2, 2018, Pages 52-80]
-
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]
-
Pedigree
Hereditary Angioedema: A Family with Several Affected Members [Volume 2, Issue 1, 2019, Pages 22-27]
-
Phosphoinositide-3-kinase δ
Activated PI3K-Delta Syndrome: Pathogenesis, Clinical Manifestations, Diagnosis, Classification, and Management [Volume 3, Issue 3, 2020, Pages 8-15]
-
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
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
Vaccination in Patients with Primary Immunodeficiency Disorders [(Articles in Press)]
-
Primary immunodeficiency disorder
Gastrointestinal Manifestations in Patients with Common Variable Immunodeficiency [Volume 2, Issue 4, 2019, Pages 185-195]
-
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]
-
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]
R
-
RCID
Obituary of Professor Asghar Aghamohammadi [(Articles in Press)]
-
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]
-
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]
-
Skin lesions
Toll-like Receptor 3 Deficiency in a Child with Recurrent Infections and Diabetes Mellitus [(Articles in Press)]
-
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]
-
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]
T
-
TCD4+ lymphocyte
Evaluation of B Cell and T Cell Phenotypes in CVID Patients and its Correlation with the Clinical Phenotype of the Disease: Study Protocol [(Articles in Press)]
-
TCD8+ lymphocyte
Evaluation of B Cell and T Cell Phenotypes in CVID Patients and its Correlation with the Clinical Phenotype of the Disease: Study Protocol [(Articles in Press)]
-
Toll-like receptor 3 deficiency
Toll-like Receptor 3 Deficiency in a Child with Recurrent Infections and Diabetes Mellitus [(Articles in Press)]
-
TREC
Why should TREC and KREC quantification assay be concerned to screen of newborns in developing countries? [Volume 2, Issue 4, 2019, Pages 173-184]
-
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
-
Vaccination
Vaccination in Patients with Primary Immunodeficiency Disorders [(Articles in Press)]
-
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]
-
Vomiting
Gastrointestinal Manifestations in Patients with Agammaglobulinemia [Volume 2, Issue 3, 2019, Pages 104-113]
W
-
Whole exome sequencing
Case Report: MALT1 Mutation in A Patient with Severe Combined Immunodeficiency [Volume 3, Issue 3, 2020, Pages 47-52]
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]
-
XLA
The Evaluation of Neutropenia in X-linked Agammaglobulinemia Patients [(Articles in Press)]
-
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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