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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.
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.
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.
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.
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.
Granulomatous skin lesion as a manifestation of primary immunodeficiency in children
Selezneva O.S., Shcherbina A.Y.
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.
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.
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.
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.
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.
Genetic diversity in pediatric patients with inborn errors of immunity in Russia
Kuzmenko N.B., Alexenko M.A., Mukhina A.A., Rodina Y.A., Fadeeva M.S., Pershin D.E., Kieva A.M., Varlamova T.V., Yukhacheva D.V., Burlakov V.I., Kan N.Y., Deripapa E.V., Kozlova A.L., Nesterenko Z.A., Avedova A.Y., Moiseeva A.A., Deordieva E.A., Shvets O.A., Viktorova E.A., Bludova A.O., Ogneva A.L., Bogdanova D.V., Mersiyanova I.V., Raykina E.V., Maschan M.A., Novichkova G.A., Grachev N.S., Shcherbina A.Y.
Clinical and laboratory characteristics of a group of patients with ataxia-telangiectasia syndrome
Asekretova T.V., Anderzhanova L.H., Leontyeva M.E., Rodina Y.A., Panferova A.V., Alexenko M.Y., Pеrshin D.E., Khadzhieva M.B., Larin S.S., Raykina E.V., Lebedev V.V., Myakova N.V., Shcherbina A.Y., Deripapa E.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.
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.
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.
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.
Verification of X-linked lymphoproliferative syndrome type 1 and 2 using a flow cytometry method
Pershin D.Е., Vedmedskaya V.А., Fadeeva M.S., Vladimirov I.S., Kulakovskaya E.A., Roppelt A.A., Kieva A.M., Raykina E.V., Rodina Y.A., Maschan M.A., 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.
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.
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.
Гранулематозное поражение кожи как проявление первичного иммунодефицитного состояния у детей.
Kabuki syndrome
Kondratenko I.V., Suspitsin E.N., Vakhlyarskaya S.S., Bologov A.A., Imyanitov E.N.
Treatment of lymphoid malignancies in patients with primary immunodeficiencies associated with DNA repair defects
Anderzhanova L.K., Rodina Y.A., Mukhina A.A., Abugova Y.G., Abramov D.S., Aleksenko M.Y., Vavilova L.A., Dyakonova Y.Y., Evstratov D.A., Raykina E.V., Fominykh V.V., Shcherbina A.Y., Deripapa E.V., Myakova N.V.
A familial case of Louis–Bar syndrome
Asekretova T.V., Sineokova A.V., Lebedev V.V., Rodina Y.A., Deripapa E.V.
A rare case of combined immunodeficiency due to a deletion of 11(q) – Jacobsen syndrome
Kuzmenko N.B., Shvets O.A., Mukhina A.A.
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.
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.
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.
1 - 29 of 29 Items

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