Sebastian Ginzel

Regulatory T cells in autoimmune kidney diseases and transplantation

Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee

Transcriptional and epigenetic basis of Treg cell development and function: its genetic anomalies or variations in autoimmune diseases

Tregopathies: Monogenic diseases resulting in regulatory T-cell deficiency

Hemophagocytic lymphohistiocytosis and primary immune deficiency disorders

The genetics of macrophage activation syndrome

Regulatory T Cells and Human Disease

The 2021 WHO Classification of Tumors of the Central Nervous System: a summary

Medulloblastoma genomics in the modern molecular era

Cytokine Storm

Concomitant PIK3CD and TNFRSF9 deficiencies cause chronic active Epstein-Barr virus infection of T cells

Combined immunodeficiency with life-threatening EBV-associated lymphoproliferative disorder in patients lacking functional CD27

Diagnostic challenges in a child with early onset desmoplastic medulloblastoma and homozygous variants in MSH2 and MSH6

STAT3 gain-of-function mutations associated with autoimmune lymphoproliferative syndrome like disease deregulate lymphocyte apoptosis and can be targeted by BH3 mimetic compounds