Количество страниц: 6 с.
Анализ деятельности кабинета когнитивных расстройств центра нейродегеративных заболеваний клиники Якутского научного центра комплексных медицинских проблем / Ю. И. Хабарова, З. Н. Алексеева, Т. К. Давыдова, О. В. Татаринова // Якутский медицинский журнал. — 2020. — N 3 (71). — С. 119-124. – DOI: 10.25789/YMJ.2020.71.30.
DOI: 10.25789/YMJ.2020.71.30
Количество страниц: 4 с.
100 villous chorions at 9-12 weeks of pregnancy were studied in order to identify the relationship between the indicators of progesterone synthetic activity of the fetoplacental complex being formed and the nature of clinical and echographic manifestations of the threatened miscarriage in groups of women with different course of cytomegalovirus infection (CMV) infection. It was identified a significant dependence of the frequency of the threatened miscarriage and its clinical and echographic manifestations on the exacerbation of CMV infection in the first trimester of pregnancy, which was combined with low values of progesterone and 3β-hydroxy-5-pregnen-20-one-dehydrogenase in the villous chorion compared to the group with a latent course of infection
Никитина, М. А. Апатия как немоторный симптом болезни Паркинсона и болезни Гентингтона / М. А. Никитина, Н. Г. Бразовская, Н. Г. Жукова [и другие] // Якутский медицинский журнал. — 2020. — N 2 (70). — С. 24-27. – DOI: 10.25789/YMJ.2020.70.07.
DOI: 10.25789/YMJ.2020.70.07
Количество страниц: 8 с.
The article presents the results of a clinical and genetic study of a Yakut family with hereditary spastic paraplegia (HSP). Patients with clinically diagnosed HSP and healthy family members were studied. The disease is clinically characterized as a progressive spastic paraplegia of the lower extremities concomitant peripheral neuropathy in advanced case. The methods of exome sequencing of the entire genome, molecular modeling of dynamin-2 and experimental reproduction of key elements of the HSP pathogenesis have been applied. Genetic analysis revealed a novel missense c.2155C> T, p.R719W mutation in the highly conserved GTP-effector domain of the dynamin-2 gene (DNM2). In experiments on HeLa cells, it was shown that mutant dynamin-2 affected endocytosis process. In-silico modeling determined that the identified mutation is located in the DNM2 bundle-signaling element and potentially disrupts the assembly and functional properties of the protein. Testing of this mutation in other Yakut families with HSP showed a negative result, which once again confirms the genetic heterogeneity of this pathology
Аутосомно-доминантная спастическая параплегия в четырех поколениях якутской семьи, вызываемая мутацией в динамине-2 / Т. М. Сивцева, Л. Г. Гольдфарб, Т. К. Давыдова [и другие] // Якутский медицинский журнал. — 2020. — N 1 (69). — С. 6-12.
DOI: 10.25789/YMJ.2020.69.01
Количество страниц: 6 с.
- Математика. Естественные науки > Общая биология. Антропология. Вирусология. Микробиология,
- Прикладные науки. Медицина. Ветеринария. Техника. Сельское хозяйство > Медицина > Патология. Клиническая медицина > Неврология,
- НАУКА ЯКУТИИ > ПРИКЛАДНЫЕ НАУКИ. МЕДИЦИНА. ТЕХНИКА. СЕЛЬСКОЕ ХОЗЯЙСТВО > Медицина > Патология. Клиническая медицина > Неврология,
- НАУКА ЯКУТИИ > МАТЕМАТИКА. ЕСТЕСТВЕННЫЕ НАУКИ > Общая биология. Антропология. Вирусология. Микробиология.
This article considers the use of microRNAs as a possible biomarker of epilepsy. The presented studies have shown that microRNAs can be involved in the process of epileptogenesis by regulating the inflammatory response, apoptosis of neurons, and transcription factors involved in cell differentiation. Biological fluids (blood and CSF) of patients with epilepsy showed differences in the number of circulating microRNAs, which may allow further use of microRNAs as a diagnostic biomarker. Recent discoveries providethe sufficient source of new microRNA targets, but there are still significant problems of studying their role in pathogenesis and the possibility of their application in clinical practice
Биомаркеры эпилепсии: микроРНК / М. Р. Сапронова, К. Д. Яковлева, А. А. Усольцева [и другие] // Якутский медицинский журнал. — 2020. — N 4 (72). — С. 106-111
DOI: 10.25789/YMJ.2020.72.26
Количество страниц: 4 с.
Тихонов Д. Г., Вероятные причины вилюйского энцефаломиелита. Факты истории изучения и размышления // Якутский медицинский журнал. 2019. – N 1 (65). – С. 115-118.
DOI: 10.25789/YMJ.2019.65.35
Количество страниц: 6 с.
Parkinson’s disease and essential tremor are the most common neurodegenerative diseases, which are accompanied by the development of tremor - involuntary rhythmic hyperkinesis. In the essential tremor,tremor has a kinetically postural character with a frequency of 6 to 10 Hz, affectingarms, head, face, vocal cords, tongue, legs and trunk. Parkinson tremor has a frequency of 4-6 Hz, occurring at rest in the form of “counting coins” or “rolling pills”, decreasing with active movements until complete disappearance, and is characterized by resumption after 2 or more seconds after giving the pose (“renewed” tremor). The generation of tremors is associated with dysfunction of two main ways: basal nuclei - cerebellum - thalamus and cogwheel - olive complex. Consequently, damage to any of these levels leads to the development of tremors. Recently, the concept of a single continuum of essential tremor - Parkinson’s disease - is widely discussed.It has been established that these neurological disorders can coexist or transit into each other. So, essential tremor increases the risk of developing Parkinson’s disease by 3.5 times, and in patients with Parkinson’s disease the likelihood of attaching an essential tremor is as high. This is due to the cross pathophysiological mechanism, which is probably due to genetic mutations. This article discusses the pathophysiological mechanisms of the development of tremor in patients with Parkinson’s disease and essential tremor. We describe a patient with the essential tremor whose disease has been transformed into tremor predominant Parkinson’s disease
Таппахов, А. А. Взаимосвязь болезни Паркинсона и эссенциального тремора: обзор литературы и клинический случай /А. А. Таппахов, Т. Г. Говорова, Т. Е. Попова // Вестник Северо-Восточного федерального университета им. М. К. Аммосова. Серия: Медицинские науки.— 2018. — N 2 (11). — С. 44-49.
Количество страниц: 8 с.
Гольдфарб, Л. Г. Вилюйский энцефаломиелит. Организация клинико-эпидемиологических исследований в Якутии / Л. Г. Гольдфарб // Вестник Северо-Восточного федерального университета им. М. К. Аммосова. Серия "Медицинские науки". – 2021. – N 3 (24). – C. 19-25. – DOI: 10.25587/SVFU.2021.24.3.003
DOI: 10.25587/SVFU.2021.24.3.003
Количество страниц: 5 с.
Врожденные пороки центральной нервной системы и эффективность их профилактики за 2000-2009 гг. в Республике Саха (Якутия) / А. Н. Ноговицына, Н. Р. Максимова, А. Л. Сухомясова, А. Н. Григорьева // Якутский медицинский журнал. – 2010. – N 4 (32). – С. 9-13.
Ответственность: Костенко Ольга Ивановна (Составитель), Николаева Татьяна Яковлевна (Прочие), Попова Татьяна Егоровна (Прочие)
Издательство: ИП Боголепов А. А.
Год выпуска: 2008
Количество страниц: 28 с.
Вторичная профилактика инсульта : методическое письмо / Министерство здравоохранения Республики Саха (Якутия) [и др.] ; составитель О. И. Костенко. - Якутск: ИП Боголепов А. А., 2008. - 24 с.
Количество страниц: 3 с.
- Математика. Естественные науки > Общая биология. Антропология. Вирусология. Микробиология,
- Прикладные науки. Медицина. Ветеринария. Техника. Сельское хозяйство > Медицина > Патология. Клиническая медицина > Неврология,
- НАУКА ЯКУТИИ > ПРИКЛАДНЫЕ НАУКИ. МЕДИЦИНА. ТЕХНИКА. СЕЛЬСКОЕ ХОЗЯЙСТВО > Медицина > Патология. Клиническая медицина > Неврология,
- НАУКА ЯКУТИИ > МАТЕМАТИКА. ЕСТЕСТВЕННЫЕ НАУКИ > Общая биология. Антропология. Вирусология. Микробиология.
The purpose of the research work was the analysis of the ∆ 32 association of the gene CCR5 polymorphism with the risk of the multiple sclerosis development in the Russian and the Yakut population living on the territory of the Yakutia. Materials and methods: 63 patients with the reliable diagnosis of multiple sclerosis were examined according to the McDonald's criteria and 253 unallied healthy people selected on the basis of similarity to patients by age, sex and nationality characteristics were also surveyed. The polymorphic version ∆ 32 of CCR5 gene genotyping was carried out by polymerized chain reaction. Results: The Yakut population has no carriers of gene CCR5 deletion. The Russian population living on the territory of the republic has the frequency of CCR5 ∆ 32 allelic gene of 9,1%. There is a progressing speed increase in CCR5 ∆ 32- positive patients in comparison with CCR5 ∆ 32- negative ones (0.61±.013 versus 0.48±0.04).
Делеционный полиморфизм гена рецептора хемокина 5 и риск развития рассеянного склероза в Якутии / И. А. Николаева, Н. Р. Максимова, Т. Я. Николаева, В. П. Пузырев // Якутский медицинский журнал. – 2007. – N 2 (18). – C. 10-12.