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A cutaneous manifestation of Stenotrophomonas maltophilia infection in a patient previously treated with allogeneic haematopoietic stem cell transplantation
Lyudovskikh E.I., Kozlovskaya S.N., Suvorova N.V., Pinegina O.N., Skvortsova Y.V., Solopova G.G., Balashov D.N.
Chediak-Higashi syndrome (Review of literature and clinical case reports)
Rodina Y.A., Matveev V.E., Balashov D.N., Dubrovina M.E., Shcherbina A.Y.
X-linked agammaglobulinemia: a review of literature and a case report
Mgdsyan E.K., Yukhacheva D.V., Malakhova E.A., Pershin D.E., Kieva A.M., Raikina E.V., Kondratieva N.M., Alekseeva E.I., Rodina Y.A., Shcherbina A.Y.
Non-infectious complications in the group of pediatric patients with chronic granulomatous disease
Yukhacheva D.V., Rodina Y.A., Laberko A.L., Roppelt A.A., Burlakov V.I., Deripapa E.V., Kan N.Y., Khoreva A.L., Abramov D.S., Konovalov D.M., Podlipaeva S.G., Zakharov I.V., Kulakovskaya E.A., Pershin D.E., Varlamova T.V., Raykina E.V., Tereshchenko G.V., Shcherbina A.Y.
X-Linked lymphoproliferative syndrome types 1 and 2 (Review of literature and clinical case reports)
Roppelt A.A., Yukhacheva D.V., Myakova N.V., Smirnova N.V., Skvortsova Y.V., Varlamova T.V., Raikina E.V., Abramov D.S., Ulanova N.B., Gabrusskya T.V., Shcherbina A.Y.
The use of next generation sequencing technologies for the diagnosis of inborn errors of immunity
Polyakova E.A., Guryanova I.E., Vertelko V.R., Liubushkin A.V., Skapavets K.Y., Aleshkevich S.N., Zharankova Y.S., Sharapova S.O., Belevtsev M.V.
Immune dysregulation symptoms as a rare manifestation of X-linked lymphoproliferative syndrome type 1
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.
Immune thrombocytopenia as the first symptom of primary immunodeficiency with immune dysregulation: a clinical case report and literature review
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.
Clinical characteristics of patients with the SAMD9/SAMD9L gene defects
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.
Гранулематозное поражение кожи как проявление первичного иммунодефицитного состояния у детей.
The use of adoptive cell therapy for the treatment of SARS-CoV-2 in a patient after allogeneic hematopoietic stem cell transplantation
Leontyeva M.E., Sultanova E.R., Radygina S.A., Skvortsova Y.V., Muzalevskiy Y.O., Kurnikova E.E., Pershin D.E., Maschan M.A., Balashov D.N.
Haematological complications of X-linked lymphoproliferative syndrome type 1 and 2
Roppelt A.A., Laberko A.L., Burlakov V.I., Kan N.Y., Rodina Y.A., Yukhacheva D.V., Viktorova E.A., Selezneva O.S., Pershin D.E., Vedmedskaya V.A., Raykina E.V., Varlamova T.V., Кieva A.M., Mann S.G., Polyakov A.V., Sermyagina I.G., Petrova U.N., Kalinina I.I., Shelikhova L.N., Balashov D.N., Kondratenko I.V., Maschan A.A., Shcherbina A.Y.
A case of allogeneic hematopoietic stem cell transplantation in a patient with hyper-IgE syndrome
Bazaev A.A., Kozlovskaya S.N., Vasilyeva A.P., Skvortsova Y.V., Balashov D.N.
A familial case of Louis–Bar syndrome
Asekretova T.V., Sineokova A.V., Lebedev V.V., Rodina Y.A., Deripapa E.V.
Hematopoietic stem cell transplantation with TCRαβ+/CD19+ - graft depletion for hemophagocytic lymphohistiocytosis
Kantulaeva A.K., Gutovskaya E.I., Laberko A.L., Radygina S.A., Kozlovskaya S.N., Livshits A.M., Shelikhova L.N., Balashov D.N., Maschan M.A.
Experience with the use of Hizentra, an immunoglobulin preparation for subcutaneous administration, in patients with primary immunodeficiency diseases
Avedova A.Y., Rodina Y.А., Yukhacheva D.V., Burlakov V.I., Deripapa E.V., Shcherbina A.Y.
A case of medulloblastoma in a patient with hereditary angioedema with C1 inhibitor deficiency
Viktorova E.A., Salnikova E.A., Papusha L.I., Shchukin V.V., Nechesnyuk A.V., Gornostaev V.V., Kuzmenko N.B.
Therapy features of interstitial lymphocytic lung disease (ILLD) in patients with immune dysregulation syndromes: case report
Rodina Y.A., Horeva A.L., Abramova I.N., Shvets O.A., Burlakov V.I., Tereshenko G.V., Abramov D.S., Deripapa E.V.
The assessment of the efficacy and safety of the personalized rehabilitation of the second stage using modern methods and technologies in children with primary immunodeficiencies
Mgdsyan E.K., Rodina Y.A., Abrosimov A.B., Zhukovskaya E.V., Karelin A.F., Shcherbina A.Y., Novichkova G.A.
Evans syndrome in children: the results of a retrospective study of 54 patients
Kuzminova Z.A., Pshonkin A.V., Raikina E.V., Pavlova A.V., Kurnikova M.A., Mersiyanova I.V., Suntsova E.V., Shvets O.A., Mukhina A.A., Kuzmenko N.B., Shcherbina A.Y., Maschan A.A., Smetanina N.S.
Clinical experience using selective immunomodulating targeted therapy of Interstitial lymphocytic lung disease in a group of pediatric patients with primary immunodeficiencies
Rodina Y.A., Deripapa E.V., Shvets O.A., Muhina A.A., Roppelt A.A., Yuhacheva D.V., Laberko A.L., Burlakov V.I., Abramov D.S., Golbitc A.B., Tereshenko G.V., Rumiantsev A.G., Shcherbina A.Y.
Secondary Fisher–Evans syndrome in a child with activated PI(3)kd syndrome and lymphoma
Kuzminova Z.A., Fominykh V.V., Kotskaya N.N., Mitrakov K.V., Moiseeva A.A., Shvets O.A., Livshits A.M., Kurnikova M.A.
Granulomatous skin lesion as a manifestation of primary immunodeficiency in children
Selezneva O.S., Shcherbina A.Y.
1 - 23 of 23 Items

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