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]
  • 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]

U

  • Unilateral Flaccid Paraplegia Unilateral Flaccid Paraplegia Associated with Chronic Granulomatous Disease [Volume 2, Issue 2, 2019, Pages 84-89]

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]