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5Academic Journal
Authors: A. M. Antonova, A. N. Lodyagin, Ch. B. Batotsyrenov, S. V. Kuznetsov, V. I. Rusakova, I. D. Mishchenkov, А. М. Антонова, А. Н. Лодягин, Ч. Б. Батоцыренов, С. В. Кузнецов, В. И. Русакова, И. Д. Мищенков
Source: Diagnostic radiology and radiotherapy; Том 16, № 1 (2025); 74-84 ; Лучевая диагностика и терапия; Том 16, № 1 (2025); 74-84 ; 2079-5343
Subject Terms: КТ диагностика, clinical death, acute poisoning, toxic-hypoxic encephalopathy, post-resuscitation encephalopathy, brain, CT diagnostics, клиническая смерть, острое отравление, токсико-гипоксическая энцефалопатия, постреанимационная энцефалопатия, головной мозг
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Relation: https://radiag.bmoc-spb.ru/jour/article/view/1068/678; Брагина Н.В., Маркова Т.Г., Горбачев В.И. Постреанимационная болезнь // Анестезиология и реаниматология. 2021. № 4. С. 140–150 https://doi.org/10.17116/anaesthesiology2021041140.; Jozwiak M., Bougouin W., Geri G. et al. Post-resuscitation shock: recent advances in pathophysiology and treatment // Ann. Intensive Care. 2020. Vol. 10. Article number: 170 https://doi.org/10.1186/s13613-020-00788-z.; Neumar R.W., Nolan J.P., Christophe A. et. al. Post-Cardiac Arrest Syndrome: Epidemiology, Pathophysiology, Treatment, and Prognostication A Consensus Statement From the International Liaison Committee on Resuscitation (American Heart Association, Australian and New Zealand Council on Resuscitation, European Resuscitation Council, Heart and Stroke Foundation of Canada, InterAmerican Heart Foundation, Resuscitation Council of Asia, and the Resuscitation Council of Southern Africa); the American Heart Association Emergency Cardiovascular Care Committee; the Council on Cardiovascular Surgery and Anesthesia; the Council on Cardiopulmonary, Perioperative, and Critical Care; the Council on Clinical Cardiology; and the Stroke Council // Circulation. 2008. Vol. 118, No. 23. https://doi.org/10.1161/CIRCULATIONAHA.108.190652.; Srinivasan V., Hall J., Wahlster S. et. al. Associations between clinical characteristics of cardiac arrest and early CT head findings of hypoxic ischaemic brain injury following out-of-hospital cardiac arrest // Resuscitation. 2023. Vol. 190. 109858. doi:10.1016/j.resuscitation.2023.109858.; Аврущенко М.Ш., Мороз В.В., Острова И.В. Значение нейроморфологических исследований в изучении постреанимационной патологии организма: развитие взглядов академика ВА Неговского // Общая реаниматология. 2009. Т. 5, № 1. С. 14–20.; Shprecher D., Mehta L. The syndrome of delayed post-hypoxic leukoencephalopathy // NeuroRehabilitation. 2010. Vol. 26, No. 1. Р. 65–72.; Platt A., Collins J., Ramos E., Goldenberg F.D. Pseudosubarachnoid hemorrhage: A systematic review of causes, diagnostic modalities, and outcomes in patients who present with pseudosubarachnoid hemorrhage // Surg. Neurol. Int. 2021. Vol. 12. Р. 29. doi:10.25259/SNI_905_2020.; Avrahami E., Katz R., Rabin A., Friedman V. CT diagnosis of non-traumatic subarachnoid haemorrhage in patients with brain edema // European Journal of Radiology. 1998. Vol. 28, No. 3. P. 222–225.; Faeez M.S., Abdul Rashid A.M. Development of pseudo-subarachnoid hemorrhage secondary to hypoxic-ischemic injury due to bleeding pulmonary arterio-venous malformation // BMC Neurol. 2018. Vol. 18. Article number: 157. https://doi.org/10.1186/s12883-018-1161-x.; Ефимов А.А. и др. Диффузное аксональное повреждение мозга с судебно-медицинских позиций // Современные проблемы науки и образования. 2020. № 5. С. 142.; Шай А.Н., Федулова М.В., Квачева Ю.Е. и др. Аспекты изучения диффузного аксонального повреждения: возможность использования структурных компонентов нервной ткани в качестве биомаркеров при его диагностике // Лечебное дело. 2016. № 4. С. 96–100; Колударова Е.М., Тучик Е.С. Методология судебно-медицинской диагностики диффузного аксонального повреждения головного мозга // Судебно-медицинская экспертиза. 2022. Т. 65, № 1. С. 14–19. https://doi.org/10.17116/sudmed20226501114.; Palmieri M., Frati A., Santoro A. et al. Diffuse Axonal Injury: Clinical рrognostic factors, molecular experimental models and the impact of the trauma related oxidative stress. An extensive review concerning milestones and advances // International Journal of Molecular Sciences. 2021. Vol. 22, No. 19. Р. 10865. https://doi.org/10.3390/ijms221910865.; Арефьева Е.Г., Гатин Д.В., Мошнегуц С.В. и др. Диффузное аксональное повреждение: КТ-картина и клинические наблюдения // Медицинская визуализация. 2012. № 1. С. 45–50.
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6Academic Journal
Authors: M. S. Maslov, A. M. Sviridova, M. A. Zalevskaya, М. С. Маслов, А. М. Свиридова, М. А. Залевская
Source: Russian Journal of Child Neurology; Том 20, № 1 (2025); 32-38 ; Русский журнал детской неврологии; Том 20, № 1 (2025); 32-38 ; 2412-9178 ; 2073-8803
Subject Terms: фармакорезистентная эпилепсия, infantile epilepsy, microcephaly-capillary malformation syndrome, STAMBP gene, early infantile epileptic encephalopathy, early infantile myoclonic epileptic encephalopathy, antiepileptic therapy, pharmacoresistant epilepsy, младенческая эпилепсия, синдром микроцефалии с капиллярными мальформациями, ген STAMBP, ранняя младенческая эпилептическая энцефалопатия, ранняя младенческая миоклоническая эпилептическая энцефалопатия, антиэпилептическая терапия
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Relation: https://rjdn.abvpress.ru/jour/article/view/510/348; Демикова Н.С., Какаулина В.С., Печатникова Н.Л. и др. Синдром микроцефалии с капиллярными мальформациями. Педиатрия 2016;95(5);110–4.; Щугарева Л.М., Потешкина О.В., Шумеева А.Г., Галактионова С.М. Резистентная эпилепсия у ребенка с микроцефальнокапиллярным мальформационным синдромом. Журнал неврологии и психиатрии им. С.С. Корсакова 2020;120(8):110–6.; Carter M., Geraghty M., de la Cruz L. et al. A new syndrome with multiple capillary malformations, intractable seizures, and brain and limb anomalies. Am J Med Genet A 2011;155(2):301–6.; Carter M.T., Mirzaa G., McDonell L.M., Boycott K.M. Microcephaly-Capillary Malformation Syndrome. In: GeneReviews®. Seattle: University of Washington, 1993–2024.; Isidor B., Barbarot S., Bénéteau C. et al. Multiple capillary skin malformations, epilepsy, microcephaly, mental retardation, hypoplasia of the distal phalanges: Report of a new case and further delineation of a new syndrome. Am J Med Genet A 2011;155(6):1458–60.; McDonell L.M., Mirzaa G.M., Alcantara D. et al. Mutations in STAMBP, encoding a deubiquitinating enzyme, cause microcephaly-capillary malformation syndrome. Nat Genet 2013;45(5):556–62. DOI:10.1038/ng.2602; Pavlović M., Neubauer D., Al Tawari A., Heberle L. The microcephaly-capillary malformation syndrome in two brothers with novel clinical features. Pediatr Neurol 2014;51(4):560–5.; Postma J.K., Zambonin J.L., Khouj E. et al. Further clinical delineation of microcephaly-capillary malformation syndrome. Am J Med Genet A 2022;188A:3350–7. DOI:10.1002/ajmg.a.62936; STAMPB Gene – STAM Building Protein. The GeneCards Suite: From Gene Data Mining to Disease Genome Sequence Analyses. Available at: hhtp://www.genecards.org/cgi-bin/carddisp.pl?gene=STAMPB.; Wang H., Wang Z., Ji T. et al. Novel STAMBP mutations in a Chinese girl with rare symptoms of microcephaly-capillary malformation syndrome and Mowat–Wilson syndrome. Heliyon 2023;9(12):e22989. DOI:10.1016/j.heliyon.2023.e22989; https://rjdn.abvpress.ru/jour/article/view/510
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7Academic Journal
Source: Высшая школа: научные исследования.
Subject Terms: полихимиотерапиия, лимфомы, гепатотоксичность, гипераммониемия, энцефалопатия
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8Academic Journal
Source: Высшая школа: научные исследования.
Subject Terms: рецепторыврожденного иммунитета, гипоксически-ишемическая энцефалопатия, генный полиморфизм
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9Academic Journal
Authors: Л. В. Никонова, С. В. Тишковский, О. Н. Мартинкевич
Source: Žurnal Grodnenskogo Gosudarstvennogo Medicinskogo Universiteta, Vol 22, Iss 4, Pp 299-303 (2024)
Subject Terms: сахарный диабет, инсулинорезистентность, когнитивные нарушения, деменция, диабетическая энцефалопатия, Medicine
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10Academic Journal
Authors: Batyrov M.A., Per Н., Mamytova E.M., Nurbekova U.A.
Contributors: The work was performed without external funding., Работа выполнена без спонсорской поддержки.
Source: Russian Journal of Child Neurology; Vol 20, No 2 (2025); 71-77 ; Русский журнал детской неврологии; Vol 20, No 2 (2025); 71-77 ; 2412-9178 ; 2073-8803
Subject Terms: HECW2 mutations, epileptic encephalopathy, genetic epilepsy, phenobarbital, drug-resistant seizures, neurogenesis, мутации гена HECW2, эпилептическая энцефалопатия, генетическая эпилепсия, фенобарбитал, резистентные приступы, нейрогенез
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Relation: https://rjdn.abvpress.ru/jour/article/view/523/359; https://rjdn.abvpress.ru/jour/article/view/523
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11Academic Journal
Authors: Kolesnikova E.V., Vyshlova I.A., Karpov S.M., Soboleva O.A.
Source: Russian Journal of Child Neurology; Vol 19, No 4 (2024); 20-28 ; Русский журнал детской неврологии; Vol 19, No 4 (2024); 20-28 ; 2412-9178 ; 2073-8803
Subject Terms: cerebral palsy, perinatal encephalopathy, clinical picture, etiology, diagnosis, treatment, prevention, детский церебральный паралич, перинатальная энцефалопатия, клиническая картина, этиология, диагностика, лечение, профилактика
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Relation: https://rjdn.abvpress.ru/jour/article/view/492/337; https://rjdn.abvpress.ru/jour/article/view/492
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12Academic Journal
Authors: Rakhmanina О.A., Volkov I.V., Tomenko Т.R., Shestakova O.I., Volkova О.К.
Contributors: The authors express their gratitude to neurologists PhD O.V. Belyaev, PhD N.N. Omelchenko and I.V. Panyukova for their participation in the initial collection of data used in the dynamic comparative analysis., Авторы выражают благодарность врачам-неврологам к.м.н. О.В. Беляеву, к.м.н. Н.Н. Омельченко и И.В. Панюковой за участие в первичном сборе данных, использованных в динамическом сравнительном анализе.
Source: Russian Journal of Child Neurology; Vol 19, No 4 (2024); 10-19 ; Русский журнал детской неврологии; Vol 19, No 4 (2024); 10-19 ; 2412-9178 ; 2073-8803
Subject Terms: epilepsy, developmental and epileptic encephalopathy, gene mutations, sequencing, эпилепсия, энцефалопатия развития и эпилептическая, генные мутации, секвенирование
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Relation: https://rjdn.abvpress.ru/jour/article/view/491/336; https://rjdn.abvpress.ru/jour/article/view/491
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13Academic Journal
Authors: Irina F. Fedoseeva, Alexey V. Goncharenko, Tatyana V. Poponnikova, Vladimir A. Goncharenko, И. Ф. Федосеева, А. В. Гончаренко, Т. В. Попонникова, В. А. Гончаренко
Contributors: Not specified., Отсутствует.
Source: Current Pediatrics; Том 24, № 1 (2025); 6–12 ; Вопросы современной педиатрии; Том 24, № 1 (2025); 6–12 ; 1682-5535 ; 1682-5527
Subject Terms: мозжечковая атаксия, Kinsbourne encephalopathy, children, cerebellar ataxia, энцефалопатия Кинсбурна, дети
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Five Years Follow-up of Opsoclonus-Myoclonus-Ataxia Syndrome-Associated Neurogenic Tumors in Children. Neuropediatrics. 2024;55(1):57–62. doi: https://doi.org/10.1055/s-0043-1768143; Румянцева К.А., Полушин А.Ю., Абдулоева Н.Х. и др. Развитие синдрома опсоклонус-миоклонус-атаксии у взрослого пациента на фоне терапии пембролизумабом (описание клинического случая и анализ литературных данных) // Эпилепсия и пароксизмальные состояния. — 2023. — Т. 15. — № 1. — С. 26–35. — doi: https://doi.org/10.17749/2077-8333/epi.par.con.2023.131; Tate ED, Allison TJ, Pranzatelli MR, Verhulst SJ. Neuroepidemiologic trends in 105 US cases of pediatric opsoclonusmyoclonus syndrome. J Pediatr Oncol Nurs. 2005;22(1):8–19. doi: https://doi.org/10.1177/1043454204272560; Pang KK, de Sousa C, Lang B, Pike MG. A prospective study of the presentation and management of dancing eye syndrome/ opsoclonus-myoclonus syndrome in the United Kingdom. Eur J Paediatr Neurol. 2010;14(2):156–161. doi: https://doi.org/10.1016/j.ejpn.2009.03.002; Hasegawa S, Matsushige T, Kajimoto M, et al. A nationwide survey of opsoclonus-myoclonus syndrome in Japanese children. Brain Dev. 2015;37(7):656–660. doi: https://doi.org/10.1016/j.braindev.2014.10.010; Rossor T, Yeh EA, Khakoo Y, et al. Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International Perspective. Neurol Neuroimmunol Neuroinflamm. 2022;9(3):e1153. doi: https://doi.org/10.1212/NXI.0000000000001153; Малевич О.Б., Ильина Е.С., Хомякова С.П. и др. Синдром опсоклонус–миоклонус у детей с нейрогенными опухолями: взгляд невролога // Педиатрия. Журнал им. Г.Н. Сперанского. — 2019. — Т. 98. — № 2. — С. 221–226. — doi: https://doi.org/10.24110/0031-403X-2019-98-2-221-226; Качанов Д.Ю., Шаманская Т.В., Ильина Е.С. и др. Особенности нейрогенных опухолей у пациентов с синдромом опсоклонусмиоклонус // Онкопедиатрия. — 2016. — Т. 3. — № 3. — С. 228–239. — doi: https://doi.org/10.15690/onco.v3i3.1602; Pranzatelli MR, Tate ED, McGee NR. Multifactorial analysis of opsoclonus-myoclonus syndrome etiology (“Tumor” vs. “No tumor”) in a cohort of 356 US children. Pediatr Blood Cancer. 2018;65(8):e27097. doi: https://doi.org/10.1002/pbc.27097; Anand S, Agarwala S, Jain V, et al. Neuroblastoma with Opsoclonus-Myoclonus-Ataxia Syndrome: Role of Chemotherapy in the Management: Experience From a Tertiary Care Center in a Resource-limited Setting. J Pediatr Hematol Oncol. 2021;43(7): e924–e929. doi: https://doi.org/10.1097/MPH.0000000000002131; Kumar R, Vankadari K, Mittal BR, et al. Diagnostic values of 68Ga-labelled DOTANOC PET/CT imaging in pediatric patients presenting with paraneoplastic opsoclonus myoclonus ataxia syndrome. 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Cerebellum. 2024;23(3):1245–1248. doi: https://doi.org/10.1007/s12311-023-01610-36; Cannilla H, Messe M, Girardin F, et al. Drug- and Toxin-Induced Opsoclonus — a Systematized Review, including a Case Report on Amantadine-Induced Opsoclonus in Multiple System Atrophy. Tremor Other Hyperkinet Mov (N Y). 2024;14:23. doi: https://doi.org/10.5334/tohm.832; Hsu M, Tejani I, Shah N, et al. Review of Opsoclonus-Myoclonus Ataxia Syndrome in Pediatric Patients. Children (Basel). 2024;11(3):367. doi: https://doi.org/10.3390/children11030367; Ghia T, Kanhangad M, Alessandri AJ, et al. Opsoclonus-Myoclonus Syndrome, Neuroblastoma, and Insulin-Dependent Diabetes Mellitus in a Child: A Unique Patient. Pediatr Neurol. 2016;55:68–70. doi: https://doi.org/10.1016/j.pediatrneurol.2015.09.021; Alburaiky S, Dale RC, Crow YJ, et al. Opsoclonus-myoclonus in Aicardi-Goutières syndrome. Dev Med Child Neurol. 2021;63(12):1483–1486. doi: https://doi.org/10.1111/dmcn.14969; Almudhry M, Wagner MW, Longoni G, et al. Brain Volumes in Opsoclonus-Myoclonus Ataxia Syndrome: A Longitudinal Study. J Child Neurol. 2024;39(3-4):129–134. doi: https://doi.org/10.1177/08830738241240181; Chekroud AM, Anand G, Yong J, et al. Altered functional brain connectivity in children and young people with opsoclonusmyoclonus syndrome. Dev Med Child Neurol. 2017;59(1):98–104. doi: https://doi.org/10.1111/dmcn.13262; Santoro JD, Kerr LM, Codden R, et al. Increased Prevalence of Familial Autoimmune Disease in Children with Opsoclonus-Myoclonus Syndrome. Neurol Neuroimmunol Neuroinflamm. 2021;8(6):e1079. doi: https://doi.org/10.1212/NXI.0000000000001079; Mitoma H, Manto M. Recent advances in diagnosis of immune-mediated cerebellar ataxias: novel concepts and fundamental questions on autoimmune mechanisms. 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J Pediatr Hematol Oncol. 2021;43(2):e176–e179. doi: https://doi.org/10.1097/MPH.0000000000001953; Noguchi K, Ikawa Y, Takenaka M, et al. Presence of identical B-cell clone in both cerebrospinal fluid and tumor tissue in a patient with opsoclonus-myoclonus syndrome associated with neuroblastoma. Pediatr Hematol Oncol. 2023;40(4):363–370. doi: https://doi.org/10.1080/08880018.2022.2109784; Ding X, Yang W, Ren Q, et al. Serum IgG-induced microglial activation enhances neuronal cytolysis via the NO/sGC/PKG pathway in children with opsoclonus-myoclonus syndrome and neuroblastoma. J Neuroinflammation. 2020;17(1):190. doi: https://doi.org/10.1186/s12974-020-01839-9; Sun Q, Wang Y, Xie Y, et al. Long-term neurological outcomes of children with neuroblastoma with opsoclonus-myoclonus syndrome. Transl Pediatr. 2022;11(3):368–374. doi: https://doi.org/10.21037/tp-21-519; Rosenberg MI, Greenstein E, Buchkovich M, et al. 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14Academic Journal
Authors: Nabieva, Shoxista
Source: Medical science of Uzbekistan; No. 3 (2025): May-June; 59-63 ; Медицинская наука Узбекистана; № 3 (2025): Май-Июнь; 59-63 ; O`zbekiston tibbiyot ilmi; No. 3 (2025): May-Iyun; 59-63 ; 2181-3612
Subject Terms: perinatal encephalopathy, chin tremor, intracranial hypertension syndrome, hypotension, hypertension, horizontal nystagmus, перинатальная энцефалопатия, тремор подбородка, синдром внутричерепной гипертензии, гипотонус, гипертонус, горизонтальный нистагм, perinatal ensefalopatiya, iyakning tremori, intrakranial gipertenziya sindromi, gipotonus, gipertoniklik, gorizontal nistagmus
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Relation: https://fdoctors.uz/index.php/journal/article/view/161/124; https://fdoctors.uz/index.php/journal/article/view/161
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15Academic Journal
Authors: Набиева, Шоиста
Source: International Journal of Scientific Pediatrics; Vol. 4 No. 3 (2025): May-June; 992-996 ; Международный журнал научной педиатрии; Том 4 № 3 (2025): Май-Июнь; 992-996 ; Xalqaro ilmiy pediatriya jurnali; Nashr soni. 4 No. 3 (2025): May-Iyun; 992-996 ; 2181-2926
Subject Terms: ССС, ЦНС, акроцианоз, тахикардия, брадикардия, перинатальная энцефалопатия, cardiovascular disorders, acrocyanosis, tachycardia, bradycardia, perinatal encephalopathy, yurak-qon tomir tizimi, markaziy asab tizimi, akrotsianoz, taxikardiya, bradikardiya, perinatal ensefalopatiya
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Relation: https://ijsp.uz/index.php/journal/article/view/342/272; https://ijsp.uz/index.php/journal/article/view/342
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16Academic Journal
Authors: Жамалова, Феруза, Хулаева, Алия
Source: International Journal of Scientific Pediatrics; Vol. 4 No. 3 (2025): May-June; 1009-1012 ; Международный журнал научной педиатрии; Том 4 № 3 (2025): Май-Июнь; 1009-1012 ; Xalqaro ilmiy pediatriya jurnali; Nashr soni. 4 No. 3 (2025): May-Iyun; 1009-1012 ; 2181-2926
Subject Terms: гипоксически-ишемическая энцефалопатия, новорождённые, гестационный возраст, клиническая картина, недоношенность, hypoxic-ischemic encephalopathy, newborns, gestational age, clinical picture, prematurity, gipoksik-ishemik entsefalopatiya, yangi tug‘ilganlar, gestatsiya yoshi, klinik tasvir, muddatidan oldin tug‘ilish
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Relation: https://ijsp.uz/index.php/journal/article/view/346/275; https://ijsp.uz/index.php/journal/article/view/346
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17Academic Journal
Authors: Ходжаева, Светлана
Source: International Journal of Scientific Pediatrics; Vol. 4 No. 2 (2025): March-April; 895-899 ; Международный журнал научной педиатрии; Том 4 № 2 (2025): Март-Апрель; 895-899 ; Xalqaro ilmiy pediatriya jurnali; Nashr soni. 4 No. 2 (2025): Mart-Aprel; 895-899 ; 2181-2926
Subject Terms: новорожденные, факторы риска, перинатальная энцефалопатия, относительный риск, достоверность, newborns, risk factors, perinatal encephalopathy, relative risk, reliability, chaqaloqlar, xavf omillari, perinatal ensefalopatiya, nisbiy xavf, ishonchlilik
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Relation: https://ijsp.uz/index.php/journal/article/view/322/256; https://ijsp.uz/index.php/journal/article/view/322
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18Academic Journal
Authors: G. A. Avakyan, Yu. V. Bykov, A. N. Obedin, Г. А. Авакян, Ю. В. Быков, А. Н. Обедин
Source: General Reanimatology; Том 21, № 2 (2025); 42-54 ; Общая реаниматология; Том 21, № 2 (2025); 42-54 ; 2411-7110 ; 1813-9779
Subject Terms: трансплантация печени, children and adolescents, hepatic encephalopathy, cerebral edema, extracorporeal methods, liver transplantation, дети и подростки, печеночная энцефалопатия, отек головного мозга, экстракорпоральные методы
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Letter to the Editor: Pediatric acute liver failure management-view from the other side of the pond. Liver Transpl. 2023; 29 (6): E9-E10. DOI:10.1097/LVT.0000000000000101. PMID: 36789651.; Mishra S., Pallavi P. Diagnosis and management of pediatric acute liver failure: ESPGHAN and NASPGHAN 2022. Indian Pediatr. 2022; 59 (4): 307–311. PMID: 35410966.; Coilly A., Samuel D. Paediatric acute liver failure: confirm the outbreak, find the cause and explore the mechanisms. United European Gastroenterol J. 2022; 10 (8): 789–790. DOI:10.1002/ueg2.12306. PMID: 36094884.; Hegarty R., Thompson R. J. Genetic aetiologies of acute liver failure. J Inherit Metab Dis. 2024; 47 (4): 582–597. DOI:10.1002/jimd.12733. PMID: 38499319.; Putra J., Ng V. L., Perez-Atayde A. R. Pediatric acute liver failure: a clinicopathological Pperspective. Pediatr Dev Pathol. 2022; 25 (4): 361–379. DOI:10.1177/10935266211067893. PMID: 35356839.; Deep A., Alexander E. C., Bulut Y., Fitzpatrick E., Grazioli S., Heaton N., Dhawan A. Advances in medical management of acute liver failure in children: promoting native liver survival. Lancet Child Adolesc Health. 2022; 6 (10): 725–737. DOI:10.1016/S2352-4642(22)00190-0. PMID: 35931098; Kim W. R., Lake J. R., Smith J. M. OPTN/SRTR 2017 annual data report: liver. Am J Transplant. 2019; 19 (Suppl 2): 184–283. DOI:10.1111/ajt.15276. PMID: 30811890.; Kwong A. J., Ebel N. H., Kim W. R., Lake J. R., Smith J. M., Schladt D. P., Skeans M., et al. OPTN/SRTR 2020 annual data report: liver. Am J Transplant. 2022; 22: 204–309. DOI:10.1111/ajt.16978. PMID: 35266621.; Kaya S., Ekşi Bozbulut N. Therapeutic plasma exchange in children with acute and acuteon-chronic liver failure: a single-center experience. Exp Clin Transplant. 2024; 22 (Suppl 1): 88–95. DOI:10.6002/ect.MESOT2023.O12. PMID: 38385381.; de Kleine R. H., Lexmond W. S., Buescher G., Sturm E., Kelly D., Lohse A. W., Lenz D., et al. 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19Academic Journal
Authors: Chyniak, O.S., Kolenko, O.I., Mudrenko, I.H., Lychko, V.S., Demikhov, A.A., Demikhova, N.V.
Source: Azerbaijan Medical Journal. :23-31
Subject Terms: Hentinqton xəstəliyi, damar mənşəli demensiya, Alsheymer xəstəliyi, постравматическая энцефалопатия, сосудистая деменция, vascular dementia, Huntington's disease, posttravmatik ensefalopatiya, Alzheimer's disease, 3. Good health, болезнь Гентингтона, болезнь Альцгеймера, post-traumatic dementia, neurophysiological diagnostics, electroencephalography
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20Academic Journal
Source: Наука и здравоохранение. :13-19
Subject Terms: острая некротизирующая энцефалопатия, цитокиновый шторм, SARS-CoV-2, жедел некроздаушы энцефалопатия, cytokine storm, цитокиндік дауыл, COVID 19, acute necrotizing encephalopathy, 3. Good health