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Follicular T-helper cell recruitment governed by bystander B cells and ICOS-driven motility

(2013) Heping Xu et al.   NATURE

Mutation of FAS, XIAP, and UNC13D Genes in a Patient With a Complex Lymphoproliferative Phenotype

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Variations of the UNC13D Gene in Patients with Autoimmune Lymphoproliferative Syndrome

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Familial haemophagocytic lymphohistiocytosis: advances in the genetic basis, diagnosis and management

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Revised diagnostic criteria and classification for the autoimmune lymphoproliferative syndrome (ALPS): report from the 2009 NIH International Workshop

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X-linked lymphoproliferative syndrome: a genetic condition typified by the triad of infection, immunodeficiency and lymphoma

(2010) Nima Rezaei et al.   BRITISH JOURNAL OF HAEMATOLOGY

Clinical and immunological overlap between autoimmune lymphoproliferative syndrome and common variable immunodeficiency

(2010) A. Rensing-Ehl et al.   CLINICAL IMMUNOLOGY

The Jekyll and Hyde Functions of Caspases

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Flowcytometric phenotyping of common variable immunodeficiency

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Variations of the Perforin Gene in Patients With Type 1 Diabetes

(2008) E. Orilieri et al.   DIABETES

Common variable immunodeficiency: a new look at an old disease

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Interleukin-32 induces the differentiation of monocytes into macrophage-like cells

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