Natural history of autoimmune lymphoproliferative syndrome associated withFASgene mutations

Assessing Splenomegaly

(2013) Marius George Linguraru et al.   ACADEMIC RADIOLOGY

Splenectomy and the incidence of venous thromboembolism and sepsis in patients with immune thrombocytopenia

(2013) S. Boyle et al.   BLOOD

Somatic loss of heterozygosity, but not haploinsufficiency alone, leads to full-blown autoimmune lymphoproliferative syndrome in 1 of 12 family members with FAS start codon mutation

(2013) Fabian Hauck et al.   CLINICAL IMMUNOLOGY

Sequential decisions on FAS sequencing guided by biomarkers in patients with lymphoproliferation and autoimmune cytopenia

(2013) A. Rensing-Ehl et al.   HAEMATOLOGICA

Investigation of common variable immunodeficiency patients and healthy individuals using autoimmune lymphoproliferative syndrome biomarkers

(2013) C.A. Roberts et al.   HUMAN IMMUNOLOGY

Case 27-2013

(2013) Shuba R. Iyengar et al.   NEW ENGLAND JOURNAL OF MEDICINE

Autoimmune Lymphoproliferative Syndrome Misdiagnosed as Hemophagocytic Lymphohistiocytosis

(2013) A. Rudman Spergel et al.   PEDIATRICS

Elevated vitamin B12 levels in autoimmune lymphoproliferative syndrome attributable to elevated haptocorrin in lymphocytes

(2012) Raffick A.R. Bowen et al.   CLINICAL BIOCHEMISTRY

Helical assembly in the death domain (DD) superfamily

(2012) Ryan Ferrao et al.   CURRENT OPINION IN STRUCTURAL BIOLOGY

Autoimmune lymphoproliferative syndrome due to FAS mutations outside the signal-transducing death domain: molecular mechanisms and clinical penetrance

(2012) Amy P. Hsu et al.   GENETICS IN MEDICINE

A Rapid Ex Vivo Clinical Diagnostic Assay for Fas Receptor-Induced T Lymphocyte Apoptosis

(2012) Bernice Lo et al.   JOURNAL OF CLINICAL IMMUNOLOGY

A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation

(2011) B. Neven et al.   BLOOD

How I treat autoimmune lymphoproliferative syndrome

(2011) V. K. Rao et al.   BLOOD

New advances in the diagnosis and treatment of autoimmune lymphoproliferative syndrome

(2011) David T. Teachey   CURRENT OPINION IN PEDIATRICS

FAS Haploinsufficiency Is a Common Disease Mechanism in the Human Autoimmune Lymphoproliferative Syndrome

(2011) H. S. Kuehn et al.   JOURNAL OF IMMUNOLOGY

Whole-Exome-Sequencing-Based Discovery of Human FADD Deficiency

(2010) Alexandre Bolze et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Development of Disseminated Histiocytic Sarcoma in a Patient With Autoimmune Lymphoproliferative Syndrome and Associated Rosai-Dorfman Disease

(2010) Girish Venkataraman et al.   AMERICAN JOURNAL OF SURGICAL PATHOLOGY

Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome

(2010) K. C. Dowdell et al.   BLOOD

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

(2010) J. B. Oliveira et al.   BLOOD

Somatic KRAS mutations associated with a human nonmalignant syndrome of autoimmunity and abnormal leukocyte homeostasis

(2010) J. E. Niemela et al.   BLOOD

ALPS—Ten Lessons from an International Workshop on a Genetic Disease of Apoptosis

(2010) Michael J. Lenardo et al.   IMMUNITY

Using biomarkers to predict the presence of FAS mutations in patients with features of the autoimmune lymphoproliferative syndrome

(2010) Iusta Caminha et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

The Fas–FADD death domain complex structure reveals the basis of DISC assembly and disease mutations

(2010) Liwei Wang et al.   NATURE STRUCTURAL & MOLECULAR BIOLOGY

FAS-L, IL-10, and double-negative CD4-CD8- TCR  / + T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function

(2009) A. Magerus-Chatinet et al.   BLOOD

Treatment with sirolimus results in complete responses in patients with autoimmune lymphoproliferative syndrome

(2009) David T. Teachey et al.   BRITISH JOURNAL OF HAEMATOLOGY