IgG4-related disease in autoimmune lymphoproliferative syndrome.
van de Ven, Annick A J M; Seidl, Maximilian; Drendel, Vanessa; Schmitt-Graeff, Annette; Voll, Reinhard E; Rensing-Ehl, Anne; Speckmann, Carsten; Ehl, Stephan; Warnatz, Klaus; Kollert, Florian.
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Artigo em Inglês | MEDLINE | ID: mdl-28478106
ALPS-ten lessons from an international workshop on a genetic disease of apoptosis.
Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation.
Pearls and pitfalls: Autoimmune lymphoproliferative syndrome and autoimmune lymphoproliferative syndrome-like disease.
Revised diagnostic criteria and classification for the autoimmune lymphoproliferative syndrome (ALPS): report from the 2009 NIH International Workshop.
Natural history of autoimmune lymphoproliferative syndrome associated with FAS gene mutations.
Why do T cells cause so much trouble?
Haploinsufficiency of TNFAIP3 (A20) by germline mutation is involved in autoimmune lymphoproliferative syndrome.
Autoimmune and Lymphoproliferative Complications of Common Variable Immunodeficiency.
Autoimmune lymphoproliferative syndrome-like disease with somatic KRAS mutation.
Caspase-8 Deficiency Presenting as Late-Onset Multi-Organ Lymphocytic Infiltration with Granulomas in two Adult Siblings.