SCHOOL OF IMMUNOLOGY – EXPERT OPINION
| Issue | Title | File | |
| Vol 24, No 1 (2025) | Immune thrombocytopenia as the first symptom of primary immunodeficiency with immune dysregulation: a clinical case report and literature review |
 (Rus) |
|
| Bataev A.S., Bogdanova D.V., Burlakov V.I., Pershin D.E., Deordieva E.A., Suntsova E.V., Pshonkin A.V., Rodina Y.A., Shcherbina A.Y. | |||
| Vol 23, No 2 (2024) | A case of allogeneic hematopoietic stem cell transplantation in a patient with hyper-IgE syndrome |
(Rus) |
|
| Bazaev A.A., Kozlovskaya S.N., Vasilyeva A.P., Skvortsova Y.V., Balashov D.N. | |||
| Vol 21, No 2 (2022) | A familial case of Louis–Bar syndrome |
(Rus) |
|
| Asekretova T.V., Sineokova A.V., Lebedev V.V., Rodina Y.A., Deripapa E.V. | |||
| Vol 19, No 4 (2020) | Immune dysregulation symptoms as a rare manifestation of X-linked lymphoproliferative syndrome type 1 |
(Rus) |
|
| Roppelt A.А., Fadeeva M.S., Pershin D.E., Kieva A.М., Raykina E.M., Gutovskaya E.I., Radygina S.A., Abramov D.S., Shcherbina A.Y. | |||
| Vol 21, No 4 (2022) | A case report of autoinflammation and PLCy2-associated antibody deficiency and immune dysregulation |
(Rus) |
|
| Leontyeva M.E., Bogdanova D.V., Moiseeva A.A., Burlakov V.I., Nesterenko Z.A., Merkushov A.Y., Kan N.Y., Khoreva A.L., Rodina Y.A., Shvets O.A., Deordieva E.A., Kuzmenko N.B., Mukhina A.A., Mersiyanova I.V., Raikina E.V., Kozlova A.L. | |||
| Vol 21, No 3 (2022) | Clinical characteristics of patients with the SAMD9/SAMD9L gene defects |
(Rus) |
|
| Avedova A.Y., Mersiyanova I.V., Pavlova A.V., Sultanova E.R., Petrova U.N., Balashov D.N., Shelikhova L.N., Raykina E.V., Pershin D.E., Pshonkin A.V., Fedorova D.V. | |||
| Vol 21, No 1 (2022) | A case of medulloblastoma in a patient with hereditary angioedema with C1 inhibitor deficiency |
(Rus) |
|
| Viktorova E.A., Salnikova E.A., Papusha L.I., Shchukin V.V., Nechesnyuk A.V., Gornostaev V.V., Kuzmenko N.B. | |||
| Vol 20, No 3 (2021) | Clinical case of type I interferonopathy: homozygous STAT2 gain-of-function mutation |
(Rus) |
|
| Kozlova А.L., Leonteva М.Е., Burlakov V.I., Nesterenko Z.А., Laba О.М., Pisareva М.V., Kan N.Y., Khoreva А.L., Roppelt А.А., Yukhacheva D.V., Rodina Y.A., Shvets O.A., Deordieva E.A., Kuzmenko N.B., Mukhina A.A., Scherbakov A.P., Abramov D.S., Tereshchenko G.V., Konovalov D.M., Novichkova G.A. | |||
| Vol 20, No 2 (2021) | Long-term persistent mixed chimerism in a patient with Wiskott–Aldrich syndrome after allogeneic hematopoietic stem cell transplantation |
(Rus) |
|
| Bludova V.О., Laberko A.L., Rodina Y.A., Brilliantova V.V., Raykina E.V., Khoreva A.L., Pershin D.E., Tereshchenko G.V., Shcherbina A.Y. | |||
| Vol 20, No 2 (2021) | Long-term persistent mixed chimerism in a patient with Wiskott–Aldrich syndrome after allogeneic hematopoietic stem cell transplantation |
(Rus) |
|
| Bludova V.О., Laberko A.L., Rodina Y.A., Brilliantova V.V., Raykina E.V., Khoreva A.L., Pershin D.E., Tereshchenko G.V., Shcherbina A.Y. | |||
| Vol 18, No 4 (2019) | Granulomatous inflammation in the manifestation of chronic granulomatous disease: a clinical case report |
(Rus) |
|
| Yukhacheva D.V., Pershin D.E., Uskova N.G., Tereshchenko G.V., Kuzmenko N.B. | |||
| Vol 18, No 3 (2019) | The phenomenon of reverse mutation in a patient with Wiskott–Aldrich syndrome |
(Rus) |
|
| Nesterenko Z.A., Kuzmenko N.B., Burlakov V.I., Victorova E.A., Vedmedskaya V.A., Pershin D.E., Kieva A.M., Mersiyanova I.V., Varlamova T.V., Raykina E.V., Deripapa E.V. | |||
| Vol 18, No 1 (2019) | Lymphoma as a rare complication of severe combined immunodeficiency |
(Rus) |
|
| Venyov D.A., Deripapa E.V., Roppelt A.A., Laberko A.L., Abramov D.S., Varalamova T.V., Mukhina A.A., Balashov D.N., Shcherbina A.Y. | |||
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