HLH/FEL/FHL

Proteolytic Maturation of Perforin: Determining the Requirements for Cytotoxic Function in Patients with Hemophagocytic Lymphohistiocytosis

The Pathogenesis of XLP Due to XIAP Deficiency

Mechanisms of Interferon Gamma-Induced Hemophagocytosis

Interrogating Disease Mechanisms in a Novel Mouse Model of Hemophagocytosis

Investigations into the Clinical and Molecular Pathogenesis of XIAP Deficiency

Ganglioside-Induced Defective Granule Exocytosis-Mediated Cytotoxicity in Hemophagocytic Lymphohistiocytosis

Structure/Function Relationships in the MUNC13-4 Protein: Molecular Consequences of Familial Hemophagocytic Lymphohistiocytosis Associated Mutations

Homozygosity Mapping to Reveal Novel Genetic Defects in Patients with Familial Hemophagocytic Lymphohistiocytosis

Homozygozity Mapping for Identification of a Novel Genetic Defect in Patients with Familial Hemphogocytic Lymphohistiocytosis

Genetic Studies on the Pathogenesis of FHL