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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.
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.
Kabuki syndrome
Kondratenko I.V., Suspitsin E.N., Vakhlyarskaya S.S., Bologov A.A., Imyanitov E.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.
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.
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.
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.
Haematopoietic development and leukaemia in Down syndrome
Roberts I..., Izraeli S...
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.
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.
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.
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.
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.
Genetic and clinical characteristics of a group of patients with hereditary angioedema type 1 and 2
Kuzmenko N.B., Viktorova E.A., Pavlova A.V., Kurnikova M.A., Laberko A.L., Raikina E.V., Shcherbina A.Y.
Shwachman–Diamond syndrome: a hematologist's view
Tesakov I.P., Deordieva E.A., Brontveyn T.G., Sveshnikova A.N.
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.
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.
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.
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.
Autoimmune lymphoproliferative syndrome (Review of literature)
Shvets O.A., Shcherbina A.Y.
1 - 20 of 20 Items

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