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Still’s disease in a patient with common variable immunodeficiency: NFKB1 defect
Roppelt A.A., Nikitaeva Е.A., Andrenova G.V., Markina U.A., Kruglova T.S., Baryakh E.A., Mutovina Z.Y., Mudarisov R.R., Karaulov A.V., Lysenko M.A., Fomina D.S.
Interdisciplinary approach to diagnosis and treatment of primary immunodeficiency
Luntsov A.V., Latysheva E.A., Skorokhodkina O.V., Valeeva A.R., Dvoeglazova N.I.
Delayed allergic reaction to eating lemon
Prilutskiy A.S., Lygina Y.A.
Diagnostics and treatment of urticarial vasculitis associated with COVID-19
Ishchanka A.V., Shchurok I.N., Chernokov O.I., Zakharova V.V., Lesnichaya O.V., Laporevich V.B.
Chronic spontaneous urticaria or urticarial vasculitis?
Dorofeeva I.V., Danilycheva I.V., Shuljenko A.E.
Development of cofactor-dependent anaphylaxis in a patient with cross-reactive food allergy
Smolnikov E.V., Litovkina A.O., Byazrova M.G.
Case of newly diagnosed primary immunodeficiency at age 65
Demko I.V., Sobko E.A., Shestakova N.A., Kraposhina A.Y.
New opportunities of therapy of severe atopic dermatitis
Demko I.v., Sobko E.A., Kraposhina A.Y., Shestakova N.A., Gordeeva N.V., Kasymova K.F.
Use of an extract from a culture of thermophilic strain Staphylococcus aureusin the complex therapy of a patient with atopic dermatitis: a clinical case
Smolnikov E.V., Sklyarova V.O., Shtyrbul T.I., Litovkina A.O., Shtyrbul O.V., Elisyutina O.G., Fedenko E.S.
Eosinophilic esophagitis in children: Experience in diagnosis, clinical observation in a multidisciplinary hospital
Khakimova R.F., Kamalova A.A., Polyakov N.S., Khomyakov A.E., Nizamova R.A., Zaynetdinova M.S., Cheminava L.D.
Vasculitis with nervous system damage in a patient with adenosine deaminase 2 deficiency
Golovina O.A., Roppelt A.A., Markina U.A., Mutovina Z.Y., Shishimorov A.A., Schukin K.A., Karaulov A.V., Lysenko M.A., Fomina D.S.
Clinical and immunological characteristics of sensitization to tropomyosins
Mokronosova M.A., Zheltikova T.M.
EVALI syndrome in a patient with hypersensitivity pneumonitis
Asatryan A.O., Sinelnik E.A., Nedashkovskaya N.G., Kostryukov A.S., Barsukova N.A., Churyukina E.V.
Familial case of hereditary angioneurotic angioedema, caused by deficiency in the C1 inhibitor complement system
Kovzel E.F., Nurpeisov T.T., Gani B., Volodchenko S.A., Zhamanbaeva Z.Z., Syzdykova A.B., Batyrbaeva A.Z.
1 - 14 of 14 Items

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