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Vol 22, No 2 (2025)
ASIA syndrome masked as recurrent angioedema: сan development be predicted by genetic screening (pilot study)
Fomina D.S., Lebedkina M.S., Nikitina E.A., Kovalkova E.V., Andrenova G.V., Кruglova T.S., Bobrikova E.N., Markina U.A., Abdullaev S.P., Evsegneeva I.V., Karaulov A.V., Lysenko M.A.
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(Rus)
Vol 22, No 1 (2025)
Recurrent angioedema with normal C1-inhibitor: genetics determine the endotype
Lebedkina M.S., Fomina D.S., Bobrikova E.N., Yukhnovskaya Y.D., Roppelt A.A., Kruglova T.S., Mukhina O.A., Mаrkina U.A., Nikitina E.A., Alekseeva Y.G., Karaulov A.V., Lysenko M.A.
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(Rus)
Vol 20, No 2 (2023)
Myoferline gene mutation сan be associated with recurrent angioedema
Fomina D.S., Serdotetskova S.A., Bobrikova E.N., Alekseeva J.G., Roppelt A.A., Lysenko M.A.
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(Rus)
Vol 17, No 1 (2020)
Features of diagnostics and clinical approaches to case management of patients with hereditary angioedema without C1 esterase inhibitor deficiency. Analysis of the clinical case
Fomina D.S., Bobrikova E.N., Serdotetskova S.A.
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(Rus)
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