Ataxia, Infections, Autoimmunity, Neoplasms - Varied Clinical Manifestations of Patients With Ataxia Telangiectasia from a Center in Western India

Clinical and Genetic Features of UNC13D Deficiency with Hypogammaglobulinemia

A Clinico-Molecular Profile of Patients with X-Linked Chronic Granulomatous Disease: Our Experience At Chandigarh, North India

A Novel CEBPE Variant Associated with Severe Infections and Profound Neutropenia

The Clinical and Immunological Characterization of Three Patients with NFKBIA Mutations

Clinical and Immunological Profile of patients with Mendelian Susceptibility to Mycobacterial Diseases: Our Experience from North-West India

Development of Thymic Output Assay Using Flow Cytometry

Immunological characteristics of children who suffered community-acquired necrotizing pneumonia

Estimation of Anticytokine Antibodies in Patients with Recurrent, Severe or Atypical Infections

Immunogenicity of a Fourth Dose of COVID-19 Vaccine in Individuals with Inborn Errors of Immunity

Novel Compound Heterozygous Mutations in CARD11 Underlie Primary Immunodeficiency with Atopy

Immunoglobulin Replacement or Vaccination? Management of IGLL1-Defects in A Large Paediatric Cohort Detected Via Newborn Screening (NBS) Using TREC/KREC Testing

Development and Validation of SYBR Green-Based qPCR Assay in STAT3 Mutation Screening: A Diagnostic Accuracy Study

STAT3 Loss of Function in Hyper IgE Syndrome: Molecular Insight into Bone Dysregulation

Determining the Digenic Effects of STAT1 and STAT5B Variants on Immune Function and Skin Disorders

Immunophenotype of IKZF1 Haplodeficiency Patient Presenting as Systemic Lupus Erythematosus

RasGRP1 Mutation Cause Lupus-like Autoimmune Features

Characterisation and Diagnostic Model of Monogenic Lupus

Understanding the Molecular and Immune Mechanisms Underlying Deficiency of Adenosine Deaminase Type 2 (DADA2) Using RNA Sequencing

Bidirectional Causal Relationships Between Intestinal Microbiota and Juvenile Idiopathic Arthritis: Insights from Mendelian Randomization

Efficacy and Safety of Bisphosphonates in Pediatric Glucocorticoid- Induced Osteoporosis: A Meta-Analysis and Pharmacovigilance Study

Clinical Features and Novel Pathogenic Variants of Patients with Behçet’s Disease-like Trisomy 8

Severe Phenotype of Wiskott-Aldrich Syndrome Due to C-terminal Variant in WASP

Recurrent Perianal Ulceration in Siblings with CD40LG Mutation: Case Report

T-cell Deficiency in a Wolf-Hirschhorn Syndrome Baby, Presenting with HSV Encephalitis

The First Case of MHC Class II Deficiency Treated with Unrelated Mismatched Cord Blood Transplantation In Vietnam

Clinical and Immunological Analysis of a Novel BCL10 Protein S/T Domain Truncation Mutation in a Patient with Partial Combined Immunodeficiency

A Heavy Heart: Delayed Diagnosis of X-linked Agammaglobulinaemia with Porcelain Aorta

Differential Responses to Sirolimus and Leniolisib in an APDS Patient: Clinical and Transcriptomic Insights

BCGitis and Atypical Salmonella Infection in Four Patients with Mendelian Susceptibility to Mycobacterial Disease: Case Reports

First Case of STAT3 Mutation-Associated Hyper-IgE Syndrome in an Infant from Central Vietnam: Diagnosis and Management

A Case of Immunodysregulatory Disease due to Functional Acquired Mutation in STAT3 Gene

The Imbroglio of Immune Thrombocytopenia in a Challenging Case of Chronic Granulomatous Disease

A Case Study of a Baby Girl with Chronic Granulomatous Disease Due to NCF1 Mutation: Treatment Outcome with Pioglitazone

Ecthyma Gangrenosum in a Previously Healthy Boy Disclosing an Underlying Cyclic Neutropenia

Complex Inflammatory Bowel Disease in a Child with Leukocyte Adhesion Deficiency Type 1: A Case Report

Eleven Cases of Autoinflammatory Recurrent Fevers

Infant with Autoimmunity, Recurrent Infections and Hypotonia - An Interesting Case of A PID with Channelopathy

A Novel TRNT1 Gene Variant Causing SIFD Syndrome in a Child

IL12RB1 with ALPS-like Phenotype

ADA1 Deficiency: A New Genetic Cause of Monogenic Lupus

Effective Treatment of Intractable Diarrhea and Alopecia in Two Cytotoxic T Lymphocyte Antigen-4 Haploinsufficiency Patients with Abatacept Therapy

Pediatric Case of Immune-mediated Necrotizing Myopathy Associated with Anti-HMGCR Antibodies: Multi-target Therapy and Long-term Follow-up

Report of 3 Cases of Dyskeratosis Congenita and Literature Review