Zobrazeno 1 - 10
of 35
pro vyhledávání: '"E.V. Raikina"'
Autor:
Yu.A. Dmitrieva, A.L. Zaplatnikov, O.A. Kuznetsova, E. R. Radchenko, A. L. Gorelik, A. Yu. Kharitonova, M.E. Lokhmatova, Immunology named after Dmitry Rogachev, Moscow, Russia, E.V. Raikina, O. V. Karaseva, Traumatology, Moscow, Russia
Publikováno v:
Pediatria. Journal named after G.N. Speransky. 100:279-283
Diseases of the gastrointestinal tract (GIT) are one of the reasons for the development of iron deficiency anemia (IDA). The presence of gastroenterological pathology often leads to the refracterity of anemia to standard therapy, which necessitates t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::675c0fe6d257a77be7d9a17f76a74c01
https://doi.org/10.24110/0031-403x-2021-100-3-279-283
https://doi.org/10.24110/0031-403x-2021-100-3-279-283
Autor:
A.Yu. Shcherbina, D.S. Abramov, Immunology named after Dmitry Rogachev, Moscow, Russia, Yu.E. Belkina, S.V. Ivanovsky, Z.A. Nesterenko, O.V. Zhogova, Yu.A. Rodina, A. A. Moiseeva, V.I. Burlakov, Viktoria Zakharova, A.V. Pavlova, D.V. Konovalov, K.K. Egorova, E.V. Raikina, N. Yu. Kan, M.E. Dubrovina, A.L. Khoreva, A.L. Kozlova
Publikováno v:
Pediatria. Journal named after G.N. Speransky. 100:246-253
This article is dedicated to one of the auto-respiratory syndromes – adenosine deaminase deficiency 2 (deficiency of adenosine deaminase 2 – DADA2) in the 12-year-old. This rare disease is caused by mutations in the ADA2 gene (CECR1), that encode
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2872837ecb1895e8a09f11be9e968f9b
https://doi.org/10.24110/0031-403x-2021-100-2-246-253
https://doi.org/10.24110/0031-403x-2021-100-2-246-253
Autor:
I.V. Mersiyanova, V. A. Vedmedskaya, M.A. Maschan, E.A. Kulakovskaya, M.S. Fadeeva, A.L. Khoreva, A.Yu. Shcherbina, E.A. Malakhova, I.S. Vladimirov, Dmitry Pershin, E.V. Raikina, Yu.A. Rodina, A. M. Kieva, O.B. Lodoeva, Immunology named after Dmitry Rogachev, Moscow, Russia
Publikováno v:
Pediatria. Journal named after G.N. Speransky. 100:31-40
Compensatory or revertant somatic mutations (RSM) is a well-known phenomenon in patients with PIs. RSM can lead to the restoration of functional protein expression in some cell populations and thus influence the severity of clinical manifestations in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53d027a4fffca189cf382dab44f7fda2
https://doi.org/10.24110/0031-403x-2021-100-2-31-40
https://doi.org/10.24110/0031-403x-2021-100-2-31-40
Autor:
Dmitry Balashov, A.A. Roppelt, Alexandr G. Rumiantsev, E.V. Raikina, Dmitry Pershin, V.I. Burlakov, Alexandra Laberko, Ekaterina V. Kalinina, D.V. Yukhacheva, E.V. Deripapa, Yulia Rodina, Anna Shcherbina
Publikováno v:
Russian Journal of Allergy. 17:97-114
Severe combined immunodeficiency (SCID) is the most life-threatening form of primary immunodeficiency, fatal within the first years of life if hematopoietic stem cell transplantation (HSCT) is not performed. Early diagnosis is crucial for prevention
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f250ce8fe73ea444cac464797e4e4c8
https://doi.org/10.36691/rja1381
https://doi.org/10.36691/rja1381
Autor:
Goronkova Ov, E.V. Raikina, I.A. Demina, A.M. Popov, I. I. Kalinina, Alexey Maschan, G. S. Ovsyannikova, N.S. Smetanina, E.V. Suntsova
Publikováno v:
Pediatria. Journal named after G.N. Speransky. 96:97-103
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4658a8b154902ecccd6f37ff6ae6738c
https://doi.org/10.24110/0031-403x-2017-96-5-97-103
https://doi.org/10.24110/0031-403x-2017-96-5-97-103
Autor:
Alexei Maschan, Anna Shcherbina, E.V. Deripapa, Dmitry Balashov, Olga Soldatkina, Galina Novichkova, Alexandra Laberko, E.V. Raikina
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-5 (2019)
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-5 (2019)
Background Mosaic variegated aneuploidy (MVA) syndrome is a chromosomal instability disorder that leads to aneuploidies of different chromosomes in various tissues. Type 1 MVA (MVA1) is caused by mutations in the budding uninhibited by benzimidazoles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::478e84bcff5505f4cd76adfca324340e
https://pubmed.ncbi.nlm.nih.gov/31053147
https://pubmed.ncbi.nlm.nih.gov/31053147
Autor:
V. Bobrynina, E.V. Raikina, T.V. Varlamova, A.Yu. Shcherbina, I.V. Mersiyanova, N.B. Kuzmenko
Publikováno v:
Voprosy gematologii/onkologii i immunopatologii v pediatrii. 15:10-16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b7b151bf86d601ae03937a26d041cff
https://doi.org/10.20953/1726-1708-2016-1-10-16
https://doi.org/10.20953/1726-1708-2016-1-10-16
Autor:
N.V. Smirnova, Yu.V. Skvortsova, T.V. Gabrusskaya, A.A. Roppelt, A.Yu. Shcherbina, E.V. Raikina, N.B. Ulanova, T.V. Varlamova, D.S. Abramov, N.V. Myakova, D.V. Yukhacheva
Publikováno v:
Voprosy gematologii/onkologii i immunopatologii v pediatrii. 15:17-26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1623b26b5ef278e1976259769c9f6444
https://doi.org/10.20953/1726-1708-2016-1-17-26
https://doi.org/10.20953/1726-1708-2016-1-17-26
Publikováno v:
Voprosy gematologii/onkologii i immunopatologii v pediatrii. 15:41-45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30535a0ee2558fc8f2c0f651615aff21
https://doi.org/10.20953/1726-1708-2016-1-41-45
https://doi.org/10.20953/1726-1708-2016-1-41-45
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