Zobrazeno 1 - 7
of 7
pro vyhledávání: '"I. O. Schederkina"'
Autor:
N. V. Bronina, I. O. Schederkina, B. M. Kurmanov, E. A. Burtsev, M. V. Natrusova, G. O. Bronin
Publikováno v:
Русский журнал детской неврологии, Vol 18, Iss 2-3, Pp 52-58 (2023)
Glutamic acid decarboxylase (GAD) is an intracellular enzyme expressed in brain neurons and insulin-secreting β-cells of the pancreas. Anti-GAD-anitibodies are associated with type 1 diabetes mellitus, limbic encephalitis, cerebellar ataxia, tempora
Externí odkaz:
https://doaj.org/article/dc0de348d52b4d06bae46230bbd9c608
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 10, Iss 2, Pp 82-94 (2018)
There are considerable variations in the reported incidence of early and late epilepsy in children with lymphoproliferative diseases. The etiology of seizures in pediatric patients with hemoblastosis during polychemotherapy can be diverse: dysmetabol
Externí odkaz:
https://doaj.org/article/22ebe590cf754ce68b9c850f52ff85b2
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 9, Iss 1, Pp 69-78 (2017)
Childhood absence epilepsy (CAE) is an idiopathic generalized epilepsy, which could be attributed to genetic forms according to the latest proposals of the Commission on Classification and Terminology of the International League Against Epilepsy (201
Externí odkaz:
https://doaj.org/article/10ee7e2bdc464da2b8b3b9cee35dd2da
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 5, Iss 4, Pp 49-53 (2016)
Abstract: the article presents the clinical observation of outpatients with a diagnosis of epilepsy in the children’s neurological department Morozovsky Children Hospital translation from the original on generic drug valproic acid. Such changes in
Externí odkaz:
https://doaj.org/article/e3ee7bdcc2d24b2f90c4450de4abac65
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 5, Iss 1, Pp 56-58 (2016)
Externí odkaz:
https://doaj.org/article/fc2ff9b9e2d441479564fe970bd1304a
Autor:
M. Yu. Bobylova, T. M. Krasilshikova, M. B. Mironov, S. G. Burd, I. O. Schederkina, T. T. Batysheva, D. N. Smirnov
Publikováno v:
Siberian Medical Review. :77-81
Publikováno v:
Scopus-Elsevier
Diabetes mellitus type 1 (DM1) is an etiologically heterogeneous group of metabolic diseases characterized by chronic hyperglycemia. This autoimmune disease develops in people genetically predisposed to it. DM1 can combine with other autoimmune disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ac7fdc3dcba7c9f369325b27501dcdb
http://www.scopus.com/inward/record.url?eid=2-s2.0-85017561521&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-85017561521&partnerID=MN8TOARS