Ppw Lee
paed.hku.hk
0000-0002-5934-7338
University of Hong Kong
28 papers found
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Human germline heterozygous gain-of-functionSTAT6variants cause severe allergic disease
Risk factors for drug allergies in Chinese children
Cell Lineage-specific Genome-wide DNA Methylation Analysis of Patients with Paediatric-onset Systemic Lupus Erythematosus
Type I and III Interferon Productions Are Impaired in X-Linked Agammaglobulinemia Patients Toward Poliovirus but Not Influenza Virus
Selective T cell-depleted haploidentical hematopoietic stem cell transplantation for relapsed/refractory neuroblastoma
Molecular diagnosis of severe combined immunodeficiency using whole-exome sequencing.
Paediatric case series of drug reaction with eosinophilia and systemic symptoms (DRESS): 12-year experience at a single referral centre in Hong Kong and the first reported use of infliximab
Wiskott-Aldrich syndrome protein regulates autophagy and inflammasome activity in innate immune cells
Family History of Early Infant Death Correlates with Earlier Age at Diagnosis But Not Shorter Time to Diagnosis for Severe Combined Immunodeficiency
Cellular and Molecular Defects Underlying Invasive Fungal Infections—Revelations from Endemic Mycoses
Donor lymphocyte infusion reversed graft rejection in matched-unrelated donor hematopoietic stem cell transplantation for a child with thalassemia
Genome-Wide DNA Methylation Analysis of Chinese Patients with Systemic Lupus Erythematosus Identified Hypomethylation in Genes Related to the Type I Interferon Pathway
TSG-6 Downregulates IFN-Alpha and TNF-Alpha Expression by Suppressing IRF7 Phosphorylation in Human Plasmacytoid Dendritic Cells
Remission With Donor Lymphocyte Infusion in a Child With Marrow Relapse After Haploidentical Stem Cell Transplantation for Relapsed Stage 4 Neuroblastoma
Cyclosporin A for persistent or chronic immune thrombocytopenia in children
Autologous cord blood transplantation for metastatic neuroblastoma
Genome-wide search followed by replication reveals genetic interaction ofCD80andALOX5APassociated with systemic lupus erythematosus in Asian populations
Meta-analysis of two Chinese populations identifies an autoimmune disease risk allele in 22q11.21 as associated with systemic lupus erythematosus
Compound heterozygous mutations in TTC7A cause familial multiple intestinal atresias and severe combined immunodeficiency
Meta-analysis of GWAS on two Chinese populations followed by replication identifies novel genetic variants on the X chromosome associated with systemic lupus erythematosus
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