Zobrazeno 1 - 10
of 17
pro vyhledávání: '"G. S. Golosnaya"'
Autor:
G. S. Golosnaya, O. N. Krasnorutskaya, N. A. Ermolenko, V. L. Efimova, T. A. Larionova, D. M. Subbotin, D. A. Feklistov, M. D. Tysyachina
Publikováno v:
Русский журнал детской неврологии, Vol 19, Iss 2, Pp 72-79 (2024)
The etiology of cerebral palsy in children with intrauterine hypotrophy at birth and developmental delay is often explained by chronic intrauterine hypoxia. However, children with muscle hypotonia and developmental delay require genetic examination.
Externí odkaz:
https://doaj.org/article/9f37058c774a4129b6003238ffd44999
Publikováno v:
Русский журнал детской неврологии, Vol 18, Iss 2-3, Pp 38-44 (2023)
Background. Vasculoendothelial growth factor (VEGF) is responsible for vascular remodeling, influences the formation of post-hypoxic structural changes in the newborn brain and is synergistically closely related to neurotrophic factors, being an inhi
Externí odkaz:
https://doaj.org/article/56b8d2e0704a4d2bab145af3873349cf
Autor:
G. S. Golosnaya, N. A. Ermolenko, O. N. Krasnorutskaya, V. L. Efimova, T. A. Larionova, M. D. Tysyachina
Publikováno v:
Русский журнал детской неврологии, Vol 18, Iss 1, Pp 46-51 (2023)
In this article, we report a case of CTNNB1 syndrome (CTNNB1-NDD) in a child with cerebral palsy and also provide a literature review on the problem. CTNNB1 syndrome is an exceedingly rare and poorly studied disorder, which makes it particularly inte
Externí odkaz:
https://doaj.org/article/5acd7f06b81c4a38b4a32fd3b948992f
Autor:
G. S. Golosnaya, T. N. Belousova, M. Yu. Novikov, N. Yu. Knyazeva, D. Yu. Podkopaev, E. G. Trifonova, A. I. Makulova, Ya. Ya. Ginen, Z. A. Kozheurova, D. A. Kholichev, D. A. Politov, P. V. Baranova, N. A. Ermolenko, O. N. Krasnorutskaya, E. Ya. Kaledina, G. P. Tukabaev, A. V. Ogurtsov, K. A. Seleznev
Publikováno v:
Русский журнал детской неврологии, Vol 17, Iss 3, Pp 72-78 (2022)
Inherited metabolic disorders have a specific place among cases of sudden deterioration of the newborn’s condition. Therapies have been developed for some of these disorders. Accurate verification of the diagnosis is extremely important for choosin
Externí odkaz:
https://doaj.org/article/92c861fb959a4e0ab71105b12d2999cb
Autor:
G. S. Golosnaya, M. Yu. Novikov, N. Yu. Knyazeva, D. Yu. Volodina, A. A. Skobeltsyn, V. A. Perepelov, A. V. Ogurtsov, T. A. Larionova, L. V. Ledyaykina, K. A. Seleznev
Publikováno v:
Русский журнал детской неврологии, Vol 16, Iss 3, Pp 75-78 (2021)
In this article we report a case of pericallosal lipoma in a newborn with fetal alcohol syndrome, brain malformation (agenesis of the corpus callosum), and intrauterine infection (meningitis) diagnosed in a perinatal center.
Externí odkaz:
https://doaj.org/article/207103199498420981cd5281d3c80c5a
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 9, Iss 1, Pp 79-85 (2017)
Pharmacotherapy of epilepsy requires deep knowledge of anti-epileptic drugs (AEDs), including the following issues: spectrum of therapeutic efficacy and therapeutic strength, adverse effects (especially severe and life-threatening adverse reactions);
Externí odkaz:
https://doaj.org/article/dcc3bf7b424540fba2488f6d40c7de8a
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 7, Iss 1, Pp 46-55 (2016)
Alpers-Huttenlocher syndrome is a rare mitochondrial disease connected with mutations in the mitochondrial DNA replicase, polymerase gamma (POLG). The reduction of the activity within mitochondrial enzymes is connected with the reduction of replicati
Externí odkaz:
https://doaj.org/article/04ba02a98e9f4129bb312bca53dd50d1
Autor:
K. V. Voronkova, O. A. Pylayeva, A. A. Kholin, G. S. Golosnaya, T. V. Ananyeva, A. S. Petrukhin
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 5, Iss 1S, Pp 19-23 (2013)
A study was conducted to investigate electroclinical features in patients with epilepsy and autism and to determine the efficiency of antiepileptic therapy. A group of 113 patients aged 8 months to 10 years with autistic disorders was followed up. Al
Externí odkaz:
https://doaj.org/article/a3e738f8012c4a498862aadebccad272
Autor:
A. A. Skobeltsyn, D. Yu. Volodina, L. V. Ledyaykina, A. V. Ogurtsov, N. Yu. Knyazeva, V. A. Perepelov, M. Yu. Novikov, T. A. Larionova, K. A. Seleznev, G. S. Golosnaya
Publikováno v:
Russkij Žurnal Detskoj Nevrologii, Vol 16, Iss 3, Pp 75-78 (2021)
In this article we report a case of pericallosal lipoma in a newborn with fetal alcohol syndrome, brain malformation (agenesis of the corpus callosum), and intrauterine infection (meningitis) diagnosed in a perinatal center.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6027d26595ff6389ef7ec5f03b15f5b9
https://doi.org/10.17650/2073-8803-2021-16-3-75-78
https://doi.org/10.17650/2073-8803-2021-16-3-75-78
Autor:
D. Yu. Volodina, A. V. Ogurtsov, M. Yu. Novikov, T. A. Larionova, M.M. Vorokova, V. A. Perepelov, G. S. Golosnaya, N. Yu. Knyazeva, L. V. Ledyaykina, A. A. Skobeltsyn
Publikováno v:
Pediatria. Journal named after G.N. Speransky. 100:259-263
Diagnostics of hereditary diseases is one of the important tasks of the perinatal center (PC) team. Functioning conditions of PC pediatric departments allow to verify the diagnosis early, so doctors and parents of a child can receive complete informa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a8efbb5d711f60cbd4e3f105367c22e
https://doi.org/10.24110/0031-403x-2021-100-1-259-263
https://doi.org/10.24110/0031-403x-2021-100-1-259-263