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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.
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.
Haptoglobin polymorphisms and their relationship to the activities of liver function enzymes in sickle cell anemia and hepatitis C patients
Jumaa S.S., Maktoof A.A., Nuhiar R.S.
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.
Kabuki syndrome
Kondratenko I.V., Suspitsin E.N., Vakhlyarskaya S.S., Bologov A.A., Imyanitov E.N.
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.
The prognostic significance of partner genes and breakpoint locations in children with KMT2A-rearranged acute myeloid leukemia
Lebedeva S.A., Kalinina I.I., Olshanskaya Y.V., Kazakova A.N., Bankole V.A., Vasileva M.S., Venyov D.A., Baydildina D.D., Aleinikova O.V., Popa A.V., Maschan A.A., Novichkova G.A., Zerkalenkova E.A.
Transient abnormal myelopoiesis, myelodysplastic syndrome and acute myeloid leukemia in children with Down syndrome
Abashidze Z.A., Kalinina I.I., Khachatryan L.A., Vasilieva M.S., Gaskova M.V., Zerkalenkova E.A., Kazakova A.N., Olshanskaya Y.V., Mikhailova E.V., Popov A.M., Voronin K.A., Maschan A.A., Novichkova G.A.
Sarcoma with BCOR gene alterations (BCOR-ITD) of the L3 vertebra in an 8-year-old boy
Sidorov I.V., Fedorova A.S., Makarova N.P., Konopleva E.I., Sharlai A.S., Panferova A.V., Druy A.E., Konovalov D.M.
Clinical significance of methylenetetrahydrofolate reductase gene polymorphism in children with acute lymphoblastic leukemia receiving protocol therapy
Petina O.V., Zborovskaya A.A., Matevosyan M.L., Savitskaya T.V., Aleinikova O.V.
The phenomenon of reverse mutation in a patient with Wiskott–Aldrich syndrome
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.
MYH9-related inherited thrombocytopenia
Suntsova E.V., Kalinina M.P., Aksenova M.E., Arseneva A.E., Playsunova S.A., Raikina E.V., Mersianova I.V., Demina I.A., Goronkova O.V., Maschan A.A., Novichkova G.A.
Clinical features and treatment of hemophilia B
Zozulya N.I., Andreeva T.A., Zharkov P.A., Vdovin V.V.
The first results of genetic screening and exploration of genotype-phenotype correlations in retinoblastoma patients from Belarus
Guryanova I.E., Liubushkin A.V., Makarevich O.O., Litvinova D.Y., Vertеlko V.R., Valochnik A.V., Polyakova E.A., Migas A.A., Konoplya N.E.
Case report of the inflammatory myofibroblastic tumor of the liver in infant
Suleymanova A.M., Filin A.V., Kachanov D.Y., Shamanskaya T.V., Metelin A.V., Feoktistova E.V., Roschin V.Y., Shcherbakov A.P., Tereschenko G.V., Zemcova L.V., Preobrazhenskaya E.V., Suspitsin E.N., Varfolomeeva S.R.
Relapses of congenital mesoblastic nephroma: description of three clinical cases and literature review
Kasich I.N., Smirnova L.A., Teleshova M.V., Merkulov N.N., Mitrofanova A.M., Erega E.P., Osipova I.V., Zatsarinnaya O.S., Shamanskaya T.V., Konovalov D.M., Grachev N.S., Kachanov D.Y.
Immunophenotypic characterization of pediatric acute myeloid leukemia with inv(16)(p13.1q22)/t(16;16)(p13.1;q22)/CBFb-MYH11
Mikhailova E.V., Kashpor S.A., Zerkalenkova E.A., Semchenkova A.A., Dubrovina M.E., Plyasunova S.A., Olshanskaya Y.V., Kalinina I.I., Maschan M.A., Maschan A.A., Novichkova G.A., Popov A.M.
Prognostic value of molecular, genetic and clinical characteristics of SHH group medulloblastoma
Papusha L.I., Druy A.E., Yasko L.A., Supik Z.S., Zemtsova L.Z., Ektova A.P., Konovalov D.M., Voronin K.A., Merishavyan A.A., Borodina I.D., Shapochnik A.P., Belogurova M.B., Makhonin v.B., Zaychikov A.N., Sharapova G.R., Nesterova Y.A., Tarasova E.M., Novichkova G.A., Karachunsky A.I.
Shwachman–Diamond syndrome: a hematologist's view
Tesakov I.P., Deordieva E.A., Brontveyn T.G., Sveshnikova A.N.
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.
Genetic predictors of an unfavorable course of severe congenital neutropenia in patients with ELANE gene mutation
Deordieva E.A., Varlamova T.V., Raikina E.V., Shcherbina A.Y.
Acute myeloid leukemia with translocations involving the KMT2A gene in twins as a model for the study of leukemogenesis: clinical case reports and genetic characteristics
Askerova Z.Z., Zerkalenkova E.A., Lebedeva S.A., Iskakova K.S., Venyov D.A., Petrova U.N., Baydildina D.D., Balashov D.N., Bronin G.O., Tomilin I.Y., Natrusova M.V., Gaskova M.V., Soldatkina O.I., Olshanskaya Y.V., Kazakova A.N., Popov A.M., Kashpor S.A., Dubrovina M.E., Konyukhova T.V., Maschan A.A.
The efficacy of the TRK inhibitor entrectinib in patients with extracranial NTRK fusion-positive tumors
Stradomskaya T.V., Suleymanova A.M., Konovalov D.M., Druy A.E., Panfyorova A.V., Preobrazhenskaya E.V., Andreeva N.A., Sagoyan G.B., Teleshova M.V., Smirnova L.A., Zacarinnaya O.S., Shamanskaya T.V., Grachev N.S., Rubanskaya M.V., Kirgizov K.I., Imyanitov E.N., Varfolomeeva S.R., Kachanov D.Y.
Autoimmune lymphoproliferative syndrome (Review of literature)
Shvets O.A., Shcherbina A.Y.
Molecular genetic diagnosis in the group of hemophilia A patients in Belarus: 12 new allelic variants in the F8 gene
Liubushkin A.V., Guryanova I.E., Dmitriev E.V., Vertelko V.R., Polyakova E.A., Volkova L.I., Aleinikova O.V.
Low-grade gliomas with the V600E mutation in the BRAF gene in children: clinical features and treatment options
Papusha L.I., Valiakhmetova E.F., Druy A.E., Yasko L.A., Voronin K.A., Zaitseva M.A., Salnikova E.A., Raikina E.V., Novichkova G.A., Karachunsky A.I.
Iron-refractory iron deficiency anemia in children: first genetically confirmed cases in Russia
Lunyakova M.A., Demikhov V.G., Inyakova N.V., Raykina E.V.
MYCN-amplified stage 1 neuroblastoma: results of a retrospective multicenter study
Belogurova M.B., Kotlyarova T.V., Kachanov D.Y., Fechina L.G., Zaychikov A.N., Mitrofanova E.S., Slinin A.S., Shamanskaya T.V.
Modern approaches in hemophilia therapy
Florinskiy D.B., Zharkov P.A.
Monitoring of minimal residual disease in the perspective of treatment of acute lymphoblastic leukemias in children
Zakharova E.S., Gnuchev N.V., Georgiev G.P., Larin S.S.
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