Evans' syndrome (ES) is defined as the concomitant or sequential association of warm auto-
immune haemolytic anaemia (AIHA) with immune thrombocytopenia (ITP), and less …

Primary immunodeficiency disorder (PID) refers to a large heterogeneous group of disorders
that result from defects in immune system development and/or function. PIDs are broadly …

Patients with autoimmune multilineage cytopenias are often refractory to standard therapies
requiring chronic immunosuppression with medications with limited efficacy and high …

Evans syndrome (ES) is a rare and chronic autoimmune disease characterized by
autoimmune hemolytic anemia and immune thrombocytopenic purpura with a positive direct …

Autoimmune hemolytic anemia (AIHA) is a rare and heterogeneous disease that affects 1 to
3/100 000 patients per year. AIHA caused by warm autoantibodies (w-AIHA), ie, antibodies …

Malignancies occur with a higher incidence rate and manifest earlier in life in patients with
primary immunodeficiency disorders (PIDs) than in the general population. However, no …

This is the second report of the United Kingdom Primary Immunodeficiency (UKPID) registry.
The registry will be a decade old in 2018 and, as of August 2017, had recruited 4758 …

Autoimmune lymphoproliferative syndrome (ALPS) is an inherited syndrome characterized
by abnormal lymphocyte survival caused by failure of apoptotic mechanisms to maintain …

Summary The management of Evans Syndrome in children is challenging due to the lack of
evidence‐based data on treatment. Steroids, the first‐choice therapy, are successful in …

Autoimmune lymphoproliferative syndrome (ALPS) is a primary immune regulatory disorder
characterized by benign or malignant lymphoproliferation and autoimmunity. Classically …