Markina Ua 1

1. GATA2 deficiency: a long way to diagnosis (case report)
2. ASIA syndrome masked as recurrent angioedema: сan development be predicted by genetic screening (pilot study)
3. Vasculitis with nervous system damage in a patient with adenosine deaminase 2 deficiency
4. Recurrent angioedema with normal C1-inhibitor: genetics determine the endotype
5. Clinical and anamnestic analysis of patients with Stevens–Johnson syndrome/toxic epidermal necrolysis hospitalised in Moscow. Development of a prognostic model of unfavourable outcomes
6. Still’s disease in a patient with common variable immunodeficiency: NFKB1 defect
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