Introductory Remarks by the President of the Beijing Children’s Hospital of Capital Medical University

Introductory Remarks by Chairperson of the Department of Paediatrics and Adolescent Medicine of The University of Hong Kong

Introductory Remarks by the President of APSID

Mendelian Disease Discovery: From Inherited Skin Conditions to Inborn Errors of Immunity

X-Linked Agammaglobulinemia, the Oldest Primary Immunodeficiency/Inborn Error of Immunity, Yet Still Reluctant to Reveal Its Secrets

Improving Patient Care and Treatment through the Primary Immunodeficiency Registry in Malaysia

Epidemiology of Primary Immunodeficiency Identified from the Korean Immunodeficiency Network (KiNET) and Registry Project

CCL2: Old Molecule as a Novel Candidate for Mendelian Susceptibility to Mycobacterial Disease

Respiratory Syncytial Virus Infection and Immunodeficiency

PTPN2 Deficiency Modulates STAT3 Signaling and Induces Muscle Damage in Juvenile Dermatomyositis

Hematopoietic Stem Cell Transplantation for Children with Leukodystrophy: A Single Center Retrospective Study

Newborn Screening of IEI in China

Mild Wiskott-Aldrich Syndrome: Does It Exist? And How Should We Treat It?

Efficacy Analysis of Hematopoietic Stem Cell Transplantation in 16 Cases of Wiskott-Aldrich Syndrome during Infancy

A New Technique of Manipulation in Haploidentical Transplantation: Report of a Single Center Group of Patients with Primary Immunodeficiencies

Type-1 Interferonopathy

Early Diagnosis through Artificial Intelligence in Inborn Errors of Immunity

The Response to Abatacept Therapy in Children with Immune Dysregulation Syndromes - T-regopathies (LRBA and CTLA4 Deficiencies)

Barriers and Challenges to Healthcare Access in Patients with Primary Immunodeficiency Diseases: A Phenomenological Qualitative Study

Hyper IgM Syndromes: Whom to Blame, B cells, T cells, or Other Players?

Poliovirus Excretion Among Patients with Primary Immunodeficiency Disorders (Format: Virtual)

Poliovirus Surveillance Among Patients with Primary Immunodeficiency Disorders

The New Generation of "Immunoglobulin G" in Rheumatic Immune Disease

解锁儿童血管炎临床诊疗前沿进展与临床实践

Gene Therapy and Enzyme Replacement Therapy for Inborn Errors of Immunity Around the World and What Lies Ahead for the Asia Pacific?

First Results of Neonatal Screening Utilizing TREC/KREC in Russia: Statistics and Treatment Outcomes

Two Cases of Combined Immunodeficiency with ITPR3 Mutations Presenting with Life-Threatening Severe EBV-Associated Hemophagocytic Lymphohistiocytosis

Novel Gene Causing Severe Congenital Neutropenia

A Girl with Ipsilateral Temporal Atrophy - A Case of Parry-Romberg Syndrome in Korea

Homozygous p.Arg90His of NCF1 in a Twin-Sister Presenting as Mixed Connective Tissue Disease

Clinical Study Driven by the Diagnosis and Treatment of Patients with Rheumatic Diseases

A Rare Case of Combined Immunodeficiency with Immune Dysregulation in a 4-Month-Old Infant (Cancelled: Speaker unable to attend)

Severe COVID-19 Infections in Three SAMD9 (MIRAGE) Patients

Crescentic Glomerulonephritis in a 6-Year-Old Boy Leading to the Diagnosis of X-Linked Agammaglobulinaemia

Encephalitis due to Enterovirus in XLA Patients: Challenges in Diagnosis and Treatment