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1
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2
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3Academic Journal
Subject Terms: эмболизация, non-adhesive glue composition, эндоваскулярная окклюзия, неадгезивная клеевая композиция, endovascular occlusion, периферическая артериовенозная мальформация, peripheral arteriovenous malformation, embolization, жидкие эмболические агенты, liquid embolic agents, 3. Good health
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4Academic Journal
Authors: Perlovskaya V.V., Stal'makhovich V.N.
Source: Russian Journal of Pediatric Surgery, Anesthesia and Intensive Care; Vol 13 (2023): Supplement; 135 ; Российский вестник детской хирургии, анестезиологии и реаниматологии; Vol 13 (2023): Supplement; 135 ; 2587-6554 ; 2219-4061 ; 10.17816/psaic.2023
Subject Terms: артериовенозная мальформация, гемангиома, лечебная тактика
File Description: application/pdf
Availability: https://rps-journal.ru/jour/article/view/1696
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5Academic Journal
Authors: P. A. Shatokha, A. A. Novak, A. R. Shudueva, Yu. L. Mizernitskiy, O. S. Groznova, П. А. Шатоха, А. А. Новак, А. Р. Шудуева, Ю. Л. Мизерницкий, О. С. Грознова
Contributors: This study was not sponsored, Спонсорская и финансовая поддержка исследования отсутствовала
Source: PULMONOLOGIYA; Том 33, № 2 (2023); 251-258 ; Пульмонология; Том 33, № 2 (2023); 251-258 ; 2541-9617 ; 0869-0189
Subject Terms: ENG, primary ciliary dyskinesia, hereditary hemorrhagic telangiectasia (type 1), Randu - Osler - Weber disease, arteriovenous malformation, DRC1, первичная цилиарная дискинезия, наследственная геморрагическая телеангэктазия (тип 1), болезнь Рандю-Ослера-Вебера, артериовенозная мальформация
File Description: application/pdf
Relation: https://journal.pulmonology.ru/pulm/article/view/4231/3517; https://journal.pulmonology.ru/pulm/article/downloadSuppFile/4231/1827; https://journal.pulmonology.ru/pulm/article/downloadSuppFile/4231/1839; https://journal.pulmonology.ru/pulm/article/downloadSuppFile/4231/1840; https://journal.pulmonology.ru/pulm/article/downloadSuppFile/4231/1859; Новак А.А., Мизерницкий Ю.Л. Первичная цилиарная дискинезия: состояние проблемы и перспективы. Медицинский совет. 2021; (1): 276-285. DOI:10.21518/2079-701X-2021-1-276-285.; Bequignon E., Dupuy L., Zerah-Lancner F. et al. Critical evaluation of sinonasal disease in 64 adults with primary ciliary dyskinesia. J. Clin. Med. 2019; 8 (5): 619. DOI:10.3390/jcm8050619.; Bush A., Hogg C. Primary ciliary dyskinesia: recent advances in epidemiology, diagnosis, management and relationship with the expanding spectrum of ciliopathy. Expert Rev. Respir. Med. 2012; 6 (6): 663-682. DOI:10.1586/ers.12.60.; Fliegauf M., Olbrich H., Horvath J. et al. Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia. Am. J. Respir. Crit. Care Med. 2005; 171 (12): 1343-1349. DOI:10.1164/rccm.200411-1583OC.; Fretzayas A., Moustaki M. Etiology and clinical features of viral bronchiolitis in infancy. World J. Pediatr. 2017; 13 (4): 293-299. DOI:10.1007/s12519-017-0031-8.; Раджабова Г.М., Смирнова А.В., Князева А.А. и др. Клиническая значимость молекулярно-генетических подходов на основе технологий NGS в выборке пациентов с первичной цилиарной дискинезией. Медицинская генетика. 2022; 21 (10): 38-42. DOI:10.25557/2073-7998.2022.10.38-42.; Новак А.А., Мизерницкий Ю.Л. Клинико-генетические варианты первичной цилиарной дискинезии у детей. Российский вестник перинатологии и педиатрии. 2023; 68: (1): 39-46. DOI:10.21508/1027-4065-2023-68-1-39-38.; Wirschell M., Olbrich H., Werner C. et al. The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans. Nat. Genet. 2013; 45 (3): 262-268. DOI:10.1038/ng.2533.; Кузьмина Т.Н., Новак А.А, Мизерницкий Ю.Л. Особенности функций внешнего дыхания у пациентов с различными клинико-генетическими вариантами первичной цилиарной дискинезии. Пульмонология детского возраста: проблемы и решения. 2022; (22): 34-36.; Новак А.А., Мизерницкий Ю.Л. Клинико-генетические варианты первичной цилиарной дискинезии у детей. Российский вестник перинатологии и педиатрии. 2022; 67 (4): 307. DOI:10.21508/1027-4065-congress-2022.; Maori A., Wilson A.M., Shafaat O., Sharma S. Osler-Weber-Rendu disease. Updated: August 8, 2022. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022. Available at: https://www.ncbi.nlm.nih.gov/books/NBK482361/; Мизерницкий Ю.Л., Соколова Л.В. Поражения легких при болезни Рендю-Ослера-Вебера. В кн.: Розинова Н.Н., Мизерницкий Ю.Л. Орфанные заболевания легких у детей. М.: Мед-практика-М; 2015: 187-189.; Westermann C.J., Rosina A.F., De Vries V., De Coteau P.A. The prevalence and manifestations of hereditary hemorrhagic telangiectasia in the Afro-Caribbean population of the Netherlands Antilles: a family screening. Am. J. Med. Genet. A. 2003; 116A (4): 324-328. DOI:10.1002/ajmg.a.10002.; Jackson S.B., Villano N.P., Benhammou J.N. et al. Gastrointestinal manifestations of hereditary hemorrhagic telangiectasia (HHT): a systematic review of the literature. Dig. Dis. Sci. 2017; 62 (10): 2623-2630. DOI:10.1007/s10620-017-4719-3.; Morgan T., McDonald J., Anderson C. et al. Intracranial hemorrhage in infants and children with hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome). Pediatrics. 2002; 109 (1): e12. DOI:10.1542/peds.109.1.e12.; Byard R.W., Schliebs J., Koszyca B.A. Osler-Weber-Rendu syndrome-pathological manifestations and autopsy considerations. J. Forensic Sci. 2001; 46 (3): 698-701. DOI:10.1520/JFS15025J.; Shovlin C.L., Jackson J.E., Bamford K.B. et al. Primary determinants of ischaemic stroke/brain abscess risks are independent of severity of pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia. Thorax. 2008; 63 (3): 259-266. DOI:10.1136/thx.2007.087452.; Poisson A., Vasdev A., Brunelle F. et al. Acute paraplegia due to spinal arteriovenous fistula in two patients with hereditary hemorrhagic telangiectasia. Eur. J. Pediatr. 2009; 168 (2): 135-149. DOI:10.1007/s00431-008-0863-2.; Robert F., Desroches-Castan A., Bailly S. et al. Future treatments for hereditary hemorrhagic telangiectasia. Orphanet J. Rare Dis. 2020; 15 (1): 4. DOI:10.1186/s13023-019-1281-4.; https://journal.pulmonology.ru/pulm/article/view/4231
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6Academic Journal
Authors: A. V. Belopasova, P. S. Shlapakova, L. A. Dobrynina, A. S. Kadykov, А. В. Белопасова, П. С. Шлапакова, Л. А. Добрынина, А. С. Кадыков
Contributors: The investigation has not been sponsored, Исследование не имело спонсорской поддержки
Source: Neurology, Neuropsychiatry, Psychosomatics; Vol 15, No 6 (2023); 78-84 ; Неврология, нейропсихиатрия, психосоматика; Vol 15, No 6 (2023); 78-84 ; 2310-1342 ; 2074-2711 ; 10.14412/2074-2711-2023-6
Subject Terms: инсульт в молодом возрасте, hereditary hemorrhagic telangiectasia, Rendu–Osler–Weber disease, pulmonary arteriovenous malformation, paradoxical embolism, stroke at a young age, наследственная геморрагическая телеангиэктазия, болезнь Рандю–Ослера–Вебера, легочная артериовенозная мальформация, парадоксальная эмболия
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Relation: https://nnp.ima-press.net/nnp/article/view/2142/1609; Добрынина ЛА, Калашникова ЛА, Павлова ЛН. Ишемический инсульт в молодом возрасте. Журнал неврологии и психиатрии им. С.С. Корсакова. 2011;111(3):4-8.; Schöberl F, Ringleb PA, Wakili R, et al. Juvenile Stroke. Dtsch Arztebl Int. 2017 Aug 7;114(31-32):527-34. doi:10.3238/arztebl.2017.0527; Hart RG, Catanese L, Perera KS, et al. Embolic Stroke of Undetermined Source: A Systematic Review and Clinical Update. Stroke. 2017 Apr;48(4):867-72. doi:10.1161/STROKEAHA.116.016414. Epub 2017 Mar 6.; Кулеш АА, Демин ДА, Виноградов ОИ. Криптогенный инсульт. Часть 1: аорто-артериальная эмболия. Медицинский совет. 2021;(4):78-87. doi:10.21518/2079-701X-2021-4-78-87; Li L, Yiin GS, Geraghty OC, et al; Oxford Vascular Study. Incidence, outcome, risk factors, and long-term prognosis of cryptogenic transient ischaemic attack and ischaemic stroke: a population-based study. Lancet Neurol. 2015 Sep;14(9):903-13. doi:10.1016/S14744422(15)00132-5. Epub 2015 Jul 27.; Putaala J, Nieminen T, Haapaniemi E, et al. Undetermined stroke with an embolic pattern – a common phenotype with high early recurrence risk. Ann Med. 2015;47(5):406-13. doi:10.3109/07853890.2015.1057612. Epub 2015 Aug 4.; Faughnan ME, Mager JJ, Hetts SW, et al. Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia. Ann Intern Med. 2020 Dec 15;173(12):989-1001. doi:10.7326/M20-1443. Epub 2020 Sep 8.; Rendu M. Epistaxis repetes chez unsujet porteur de petits angiomies cutaneset muqueux. Bulletins et Memoires de la Societe Medicale des Hopitaux de Paris. 1886;13:731-3 (In French).; Osler W. On a family form of recurring epistaxis, associated with multiple telangiectases of the skin and mucous membranes. Johns Hopkins Med J. 1901;12:333.; Weber FP. Multiple hereditary developmental angiomata (telangiectases) of the skin and mucous membranes associated with recurring haemorrhages. Lancet. 1907;170:160-2.; Hanes FM. Multiple hereditary telangiectases causing hemorrhages. Bull John Hopkins Hospital. 1909;20:63-73.; Macri A, Wilson AM, Shafaat O, Sharma S. Osler-Weber-Rendu disease (hereditary hemorrhagic telangiectasia, HHT). In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing LLC. 2019. Available from: https://www.ncbi.nlm.nih.gov/books/NBK482361/; Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-OslerWeber syndrome). Am J Med Genet. 2000 Mar 6;91(1):66-7. doi:10.1002/(sici)10968628(20000306)91:13.0.co;2-p; Faughnan ME, Palda VA, Garcia-Tsao G, et al; HHT Foundation International – Guidelines Working Group. International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia. J Med Genet. 2011 Feb;48(2):73-87. doi:10.1136/jmg.2009.069013. Epub 2009 Jun 23.; Pahl KS, Choudhury A, Wusik K, et al. Applicability of the CuraНao Criteria for the Diagnosis of Hereditary Hemorrhagic Telangiectasia in the Pediatric Population. J Pediatr. 2018 Jun;197:207-13. doi:10.1016/j.jpeds.2018.01.079. Epub 2018 Apr 11.; Morgan T, McDonald J, Anderson C, et al. Intracranial hemorrhage in infants and children with hereditary hemorrhagic telangiectasia (Osler–Weber–Rendu syndrome). Pediatrics. 2002 Jan;109(1):E12. doi:10.1542/peds.109.1.e12; Schoonderwoerd MJA, Goumans MTH, Hawinkels LJAC. Endoglin: Beyond the Endothelium. Biomolecules. 2020 Feb 12;10(2):289. doi:10.3390/biom10020289; Berg J, Porteous M, Reinhardt D, et al. Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations. J Med Genet. 2003 Aug;40(8):585-90. doi:10.1136/jmg.40.8.585; Bayrak-Toydemir P, McDonald J, Markewitz B, et al. Genotype-phenotype correlation in hereditary hemorrhagic telangiectasia: mutations and manifestations. Am J Med Genet A. 2006 Mar 1;140(5):463-70. doi:10.1002/ajmg.a.31101; McDonald J, Wooderchak-Donahue W, VanSant Webb C, et al. Hereditary hemorrhagic telangiectasia: genetics and molecular diagnostics in a new era. Front Genet. 2015 Jan 26;6:1. doi:10.3389/fgene.2015.00001; Halpern M, Turner AF, Citron BP. Hereditary hemorrhagic telangiectasia. An angiographic study of abdominal visceral angiodysplasias associated with gastrointestinal hemorrhage. Radiology. 1968 Jun;90(6):1143-9. doi:10.1148/90.6.1143; Dupuis-Girod S, Cottin V, Shovlin CL. The Lung in Hereditary Hemorrhagic Telangiectasia. Respiration. 2017;94(4):315-30. doi:10.1159/000479632. Epub 2017 Aug 30.; White RI Jr, Lynch-Nyhan A, Terry P, et al. Pulmonary arteriovenous malformations: techniques and long-term outcome of embolotherapy. Radiology. 1988 Dec;169(3):663-9. doi:10.1148/radiology.169.3.3186989; Белопасова АВ, Добрынина ЛА, Калашникова ЛА и др. Легочный артериовенозный шунт – редкая причина рецидивирующих нарушений мозгового кровообращения по механизму парадоксальной эмболии. Журнал неврологии и психиатрии им. С.С. Корсакова. 2020;120(9):107-13. doi:10.17116/jnevro2020120091107; Байдарова МД, Тупикин КА, Андрейцева ОИ. Наследственная геморагическая телеангиэктазия: современные проблемы диагностики и тактики хирургического лечения. Доказательная гастроэнтерология. 2016;(4):36-43. doi:10.17116/dokgastro20165436-43; Кулеш АА, Демин ДА, Белопасова АВ и др. Криптогенный инсульт. Часть 2: парадоксальная эмболия. Медицинский совет. 2021;(19):16-33. doi:10.21518/2079701X-2021-19-16-33; Shovlin CL, Jackson JE, Bamford KB, et al. Primary determinants of ischaemic stroke/brain abscess risks are independent of severity of pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia. Thorax. 2008 Mar;63(3):259-66. doi:10.1136/thx.2007.087452. Epub 2007 Nov 2.; Jauss M, Zanette E. Detection of right-toleft shunt with ultrasound contrast agent and transcranial Doppler sonography. Cerebrovasc Dis. 2000 Nov-Dec;10(6):490-6. doi:10.1159/000016119; Silvestry FE, Cohen MS, Armsby LB, et al; American Society of Echocardiography; Society for Cardiac Angiography and Interventions. Guidelines for the Echocardiographic Assessment of Atrial Septal Defect and Patent Foramen Ovale: From the American Society of Echocardiography and Society for Cardiac Angiography and Interventions. J Am Soc Echocardiogr. 2015 Aug;28(8):910-58. doi:10.1016/j.echo.2015.05.015; Чечеткин АО, Каршиева АР, Кравченко МА и др. Легочный артерио-венозный шунт как причина парадоксальной церебральной эмболии: возможности ультразвуковой диагностики. Известия Российской Военно-медицинской академии. 2019;38(3):162-4. doi:10.17816/rmmar26170
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7Academic Journal
Authors: Kulabukhova P.V., Kondrashina O.S., Akinfiev D.M., Bychenko V.G.
Contributors: 1
Source: Almanac of Clinical Medicine; Vol 51, No 8 (2023); 478-484 ; Альманах клинической медицины; Vol 51, No 8 (2023); 478-484 ; 2587-9294 ; 2072-0505
Subject Terms: chorion, placenta increta, post-cesarean scar incompetency, arteriovenous malformation, хорион, несостоятельность рубца от кесарева сечения, артериовенозная мальформация
File Description: application/pdf
Relation: https://almclinmed.ru/jour/article/view/15290/1630; https://almclinmed.ru/jour/article/view/15290/1636; https://almclinmed.ru/jour/article/downloadSuppFile/15290/138835; https://almclinmed.ru/jour/article/downloadSuppFile/15290/138836; https://almclinmed.ru/jour/article/downloadSuppFile/15290/159764; https://almclinmed.ru/jour/article/downloadSuppFile/15290/159765; https://almclinmed.ru/jour/article/downloadSuppFile/15290/159766; https://almclinmed.ru/jour/article/downloadSuppFile/15290/159767; https://almclinmed.ru/jour/article/downloadSuppFile/15290/159768; https://almclinmed.ru/jour/article/downloadSuppFile/15290/159769; https://almclinmed.ru/jour/article/downloadSuppFile/15290/159770; https://almclinmed.ru/jour/article/downloadSuppFile/15290/159771; https://almclinmed.ru/jour/article/downloadSuppFile/15290/159772; https://almclinmed.ru/jour/article/downloadSuppFile/15290/159773; https://almclinmed.ru/jour/article/view/15290
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8Academic Journal
Authors: A. S. Brusyanskaya, A. L. Krivoshapkin, K. Yu. Orlov, A. A. Alshevskaya, A. V. Moskalev, G. S. Sergeev, A. S. Gaytan, A. E. Simonovich
Source: Патология кровообращения и кардиохирургия, Vol 23, Iss 1, Pp 54-60 (2019)
Subject Terms: артериовенозная мальформация головного мозга, RD1-811, 0203 mechanical engineering, эпилептический тип течения артериовенозной мальформации, Surgery, эндоваскулярная эмболизация, 02 engineering and technology, 0101 mathematics, геморрагический тип течения артериовенозной мальформации, 01 natural sciences, 3. Good health
Access URL: https://doaj.org/article/4707708620fb48ed844883466df46862
https://cyberleninka.ru/article/n/sravnenie-rezultatov-i-vyyavlenie-prediktorov-neblagopriyatnogo-ishoda-posle-endovaskulyarnoy-embolizatsii-u-bolnyh-s-raznymi-tipami/pdf
http://journalmeshalkin.ru/index.php/heartjournal/article/download/683/566
https://journalmeshalkin.ru/index.php/heartjournal/article/view/683/566
https://cyberleninka.ru/article/n/sravnenie-rezultatov-i-vyyavlenie-prediktorov-neblagopriyatnogo-ishoda-posle-endovaskulyarnoy-embolizatsii-u-bolnyh-s-raznymi-tipami -
9Academic Journal
Authors: Inkina, A.V., Arevina, V.E.
Source: Head and neck. Russian Journal. 10
Subject Terms: vascular anomalies, гемангиома, нос, paranasal sinuses, arteriovenous malformation, артериовенозная мальформация, nose, сосудистые аномалии, Hemangioma, 3. Good health, околоносовые пазухи
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10Academic Journal
Authors: V. V. Krylov, V. A. Rak, A. S. Tokarev, M. V. Sinkin, I. S. Trifonov, O. L. Yevdokimova, V. N. Stepanov, E. N. Rozhnova, G. V. Koinash, В. В. Крылов, В. А. Рак, А. С. Токарев, М. В. Синкин, И. С. Трифонов, О. Л. Евдокимова, В. Н. Степанов, Е. Н. Рожнова, Г. В. Койнаш
Source: Russian Sklifosovsky Journal "Emergency Medical Care"; Том 10, № 1 (2021); 73-82 ; Журнал им. Н.В. Склифосовского «Неотложная медицинская помощь»; Том 10, № 1 (2021); 73-82 ; 2541-8017 ; 2223-9022 ; 10.23934/2223-9022-2021-10-1
Subject Terms: артериовенозная мальформация, epilepsy, hippocampal sclerosis, meningioma, diffuse astrocytoma, cavernous angioma, arteriovenous malformation, эпилепсия, склероз гиппокампа, менингиома, диффузная астроцитома, кавернозная ангиома
File Description: application/pdf
Relation: https://www.jnmp.ru/jour/article/view/1075/923; https://www.jnmp.ru/jour/article/view/1075/1018; Thijs RD, Surges R, O’Brien TJ, Sander JW. Epilepsy in adults. Lancet. 2019;393(10172):689–701. PMID: 30686584 https://doi.org/10.1016/S0140-6736(18)32596-0; Голанов А.В., Костюченко В.В. (ред.) Нейрорадиохирургия на гамма-ноже. Москва: Т. А. Алексеева; 2018. ISBN: 978-5-905221-19-4; Sutcliffe JC, Forster DM, Walton L, Dias PS, Kemeny AA. Untoward clinical effects after stereotactic radiosurgery for intracranial arteriovenous malformations. Br J Neurosurg. 1992;6(3):177–185. PMID: 1632916 https://doi.org/10.3109/02688699209002925; Kondziolka D, Shin SM, Brunswick A, Kim I, Silverman JS. The biology of radiosurgery and its clinical applications for brain tumors. Neuro Oncol. 2015;17(1):29–44. PMID: 25267803 https://doi.org/10.1093/neuonc/nou284; Gewirtz RJ, Steinberg GK, Crowley R, Levy RP. Pathological changes in surgically resected angiographically occult vascular malformations after radiation. Neurosurgery. 1998;42(4):738–742; discussion 742–743. PMID: 9574637 https://doi.org/10.1097/00006123-199804000-00031; Awad IA, Polster SP. Cavernous angiomas: deconstructing a neurosurgical disease. J Neurosurg. 2019;131(1):1–13. PMID: 31261134 https://doi.org/10.3171/2019.3.JNS181724; Szeifert GT, Kemeny AA, Timperley WR, Forster DM. The potential role of myofibroblasts in the obliteration of arteriovenous malformations after radiosurgery. Neurosurgery. 1997;40(1):61–65; discussion 65–66. PMID: 8971825 https://doi.org/10.1097/00006123-199701000-00013; Lunsford LD, Niranjan A, Kano H, Monaco Iii EA, Flickinger JC. Leksell Stereotactic Radiosurgery for Cavernous Malformations. Prog Neurol Surg. 2019;34:260–266. PMID: 31096254 https://doi.org/10.1159/000493072; McGonigal A, Sahgal A, de Salles A, Hayashi M, Levivier M, Ma L, et al. Radiosurgery for epilepsy: Systematic review and International Stereotactic Radiosurgery Society (ISRS) practice guideline. Epilepsy Res. 2017;137:123–131. PMID: 28939289 https://doi.org/10.1016/j.eplepsyres.2017.08.016; Pallud J, McKhann GM. Diffuse Low-Grade Glioma-Related Epilepsy. Neurosurg Clin North Am. 2019;30(1):43–54. PMID: 30470404 https://doi.org/10.1016/j.nec.2018.09.001; Manford M. Recent advances in epilepsy. J Neurol. 2017;264(8):1811–1824. PMID: 28120042 https://doi.org/10.1007/s00415-017-8394-2; Soldozy S, Norat P, Yağmurlu K, Sokolowski JD, Sharifi KA, Tvrdik P, et al. Arteriovenous malformation presenting with epilepsy: a multimodal approach to diagnosis and treatment. Neurosurg Focus. 2020;48(4):E17. PMID: 32234990 https://doi.org/10.3171/2020.1.FOCUS19899; Tanti MJ, Marson AG, Chavredakis E, Jenkinson MD. The impact of epilepsy on the quality of life of patients with meningioma: A systematic review. Br J Neurosurg. 2016;30(1):23–28. 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11Academic Journal
Authors: A. A. Kulesh, D. A. Demin, A. V. Belopasova, S. A. Mekhryakov, O. I. Vinogradov, L. I. Syromyatnikova, A. A. Ziankou, А. А. Кулеш, Д. А. Демин, А. В. Белопасова, С. А. Мехряков, О. И. Виноградов, Л. И. Сыромятникова, А. А. Зеньков
Source: Meditsinskiy sovet = Medical Council; № 19 (2021); 16-33 ; Медицинский Совет; № 19 (2021); 16-33 ; 2658-5790 ; 2079-701X
Subject Terms: легочная артериовенозная мальформация, ESUS, paradoxical embolism, open foramen ovale, atrial septal defect, pulmonary arteriovenous malformation, парадоксальная эмболия, открытое овальное окно, дефект межпредсердной перегородки
File Description: application/pdf
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Ann Thorac Cardiovasc Surg. 2008;14(1):35–37. Available at: https://pubmed.ncbi.nlm.nih.gov/18292739/; Faughnan M., Palda V., Garcia-Tsao G., Geisthoff U., McDonald J., Proctor D. et al. International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia. J Med Genet. 2011;48:73–87. https://doi.org/10.1136/jmg.2009.069013.; Devlin H.L., Hosman A.E., Shovlin C.L. Antiplatelet and anticoagulant agents in hereditary hemorrhagic telangiectasia. N Engl J Med. 2013;368(9):876–878. https://doi.org/10.1056/NEJMc1213554.; Shovlin C.L., Millar C.M., Droege F., Kjeldsen A., Manfredi G., Suppressa P. et al. Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia. Orphanet J Rare Dis. 2019;14(1):210. https://doi.org/10.1186/s13023-019-1179-1.; Kleindorfer D.O., Towfighi A., Chaturvedi S., Cockroft K.M., Gutierrez J., Lombardi-Hill D. et al. 2021 Guideline for the Prevention of Stroke in Patients With Stroke and Transient Ischemic Attack: A Guideline From the American Heart Association / American Stroke Association. Stroke. 2021;52(7):e364-e467. https://doi.org/10.1161/STR.0000000000000375.; Baumgartner H., De Backer J., Babu-Narayan S.V., Budts W., Chessa M., Diller G.P. et al. 2020 ESC Guidelines for the management of adult congenital heart disease. Eur Heart J. 2021;42(6):563–645. https://doi.org/10.1093/eurheartj/ehaa554.; Shovlin C.L., Condliffe R., Donaldson J.W., Kiely D.G., Wort S.J. British Thoracic Society Clinical Statement on Pulmonary Arteriovenous Malformations. Thorax. 2017;72(12):1154–1163. https://doi.org/10.1136/thoraxjnl-2017-210764.
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12Academic Journal
Authors: L. V. Rozhchenko, N. V. Dryagina, Л. В. Рожченко, Н. В. Дрягина
Source: Translational Medicine; Том 7, № 5 (2020); 43-52 ; Трансляционная медицина; Том 7, № 5 (2020); 43-52 ; 2410-5155 ; 2311-4495 ; 10.18705/2311-4495-2020-7-5
Subject Terms: эмболизация, cerebral arteriovenous malformation, embolization, factors of angiogenesis, факторы ангиогенеза, церебральная артериовенозная мальформация
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Relation: https://transmed.almazovcentre.ru/jour/article/view/584/400; Парфенов В.Е., Свистов Д.В., Элиава Ш.Ш. и др. Клинические рекомендации по диагностике и лечению артериовенозных мальформаций центральной нервной системы. М.: Ассоциация нейрохирургов Российской Федерации, 2014. С. 34.; Amin-Hanjani S. ARUBA results are not applicable to all patients with arteriovenous malformation. Stroke. 2014; 45 (5): 1539–1540.; Рожченко Л.В., Дрягина Н.В., Панунцев В.С. и др. Исследование факторов ангиогенеза при церебральных артериовенозных мальформациях с различным клиническим течением. Российский нейрохирургический журнал имени профессора А. Л. Поленова. 2014; 6 (1): 35–41.; Rangel-Castilla L, Russin JJ, Martinez-DelCampo E, et al. Molecular and cellular biology of cerebral arteriovenous malformations: a review of current concepts and future trends in treatment. Neurosurg Focus. 2014; 37 (3): E1.; Chapot R, Stracke P, Velasco A, et al. The pressure cooker technique for the treatment of brain AVMs. J Neuroradiol. 2014; 41 (1): 87–91.; Starke RM, Komotar RJ, Hwang BY, et al. Systemic expression of matrix metalloproteinase-9 in patients with cerebral arteriovenous malformations. Neurosurgery. 2010; 66(2): 343–348.; Moftakhar P, Hauptman JS, Malkasian D, et al. Cerebral arteriovenous malformations. Part 1: cellular and molecular biology. Neurosurg Focus. 2009; 26 (5): E10.; Karamysheva A.F. The Mechanisms of angiogenesis. Biochemistry (Moscow). 2008; 73 (7): 751–762. I; Chen W, Choi E-J, McDougall CM, et al. Brain arteriovenous malformation modeling, pathogenesis, and novel therapeutic targets. Transl Stroke Res. 2014; 5 (3): 316–329.; Hashimoto T, Lam T, Boudreau NJ, et al. Abnormal balance in the angiopoietin-tie2 system in human brain arteriovenous malformations. Circ Res. 2011; 89 (2): 111–113.; https://transmed.almazovcentre.ru/jour/article/view/584
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13Academic Journal
Authors: M. L. Lagunavichene, S. N. Larionov, Yu. A. Alexandrov, A. V. Livadarov, P. G. Gruzin, G. S. Zhdanovich, М. Л. Лагунавичене, С. Н. Ларионов, Ю. А. Александров, А. В. Ливадаров, П. Г. Грузин, Г. С. Жданович
Source: Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics); Том 65, № 3 (2020); 126-130 ; Российский вестник перинатологии и педиатрии; Том 65, № 3 (2020); 126-130 ; 2500-2228 ; 1027-4065 ; 10.21508/1027-4065-2020-65-3
Subject Terms: тактика лечения, arteriovenous malformation, hemorrhage, obliteration, treatment tactics, артериовенозная мальформация, кровоизлияние, облитерация
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Relation: https://www.ped-perinatology.ru/jour/article/view/1160/943; Stapf C., Khaw A.V., Sciacco R.R., Hofmeister C., Schumacher H.C., Pile-Spellman J. et al. Effect of age on clinical and morphological characteristics in patients with brain arteriovenous malformations. Stroke 2003; 34: 2664–2670. DOI:10.1161/01.STR.0000094824.03372.9B; Холин А.В. Сосудистая патология головного мозга. Магнитно-резонансная томография при заболеваниях и травмах центральной нервной системы. М.: Медпресс, 2017; 144–145.; Börcek A.Ö. Clinical Outcomes of Stereotactic Radiosurgery for Cerebral Arteriovenous Malformations in Pediatric Patients: Systematic Review and Meta-Analysis. Neurosurgery 2019; 85: 629–640. DOI:10.1093/neuros/nyz146 4. Di Rocco C., Tamburrini G., Rollo M. Cerebral arteriovenous malformations in children. Acta Neurochirurgica 2000; 142(2): 145–158. DOI:10.1007/s007010050017; Орлов М.Ю. Артериовенозные мальформации головного мозга у детей. Український нейрохірургічний журнал 2007; 1: 15–20.; Buis D.R. Spontaneous regression of brain arteriovenous malformations A clinical study and a systematic review of the literature. J Neurol 2004; 251: 1375–1382. DOI:10.1007/s00415-004-0548-3; Malik G., Abdulrauf S., Yang X.Y., Gutierrez J.A., Rempel S.A. Expression of transforming growth factor-beta complex in arteriovenous malformations. Neurol Med Cbir 1998; 38: 161–164. DOI:10.2176/nmc.38.suppl_161; Jones B.V., Ball W.S., Tomsick T.A., Millard J., Crone K.R. Vein of Galen aneurismal malformation: diagnosis and treatment of 13 children with extended clinical follow-up. Am J Neuroradiol 2002; 23(10): 1717–1724.; Миронова А.К., Шарыкин А.С., Ватолин К.В., Пыков М.И., Османов И.М. Диагностика и тактика наблюдения новорожденных с артериовенозной мальформацией вены Галена в многопрофильном детском стационаре. Российский вестник перинатологии и педиатрии 2020; 65(3): 138–146.; Дан В.Н., Аракелян В.С., Богачев В.Ю., Бубнова Н.А., Кармазановский Г.Г., Карпенко А.А. и др. Ангиология и сосудистая хирургия. М.: Ангиология-ИНФО, 2015; 28.; Herbert С., Moiseenko V., McKenzie M., Redekop G., Hsu F., Gete E. et al. Factors Predictive of Obliteration After Arteriovenous Malformation Radiosurgery. Can J Neurol Sci 2011; 38: 845–850. DOI:10.1017/S0317167100012415; Patel M.C., Hodgson T.J., Kemeny A.A., Forster D.M. Spontaneous obliteration of pial arteriovenous malformations: a review of 27 cases. Am J Neuroradiol 2001; 22(3): 531–536.; Lim S.L., Foo A.S., Karlsson B., Yeo T.T. Spontaneous obliteration highlights the dynamic nature of cerebral arteriovenous malformations: A case report and review of the literature. Surg Neurol Int 2016; 7: 45. DOI:10.4103/2152-7806.180766; Mohr J.P. Medical management with or without interventional therapy for unruptured brain arteriovenous malformations (ARUBA): a multicentre, non-blinded, randomized trial. Lancet 2014; 9917(383): 614–621. DOI:10.1016/S0140-6736(13)62302-8; Leung K.M., Agid R., Brugge K. Spontaneous regression of cerebral arteriovenous malformation in hereditary hemorrhagic telangiectasia. J Neurosurg 2006; 105: 428–431. DOI:10.3171/ped.2006.105.5.428; Abdulrauf S.I., Malik G.M., Awad I.A. Spontaneous angiographic obliteration of cerebral arteriovenous malformations. Neurosurg 1999; 44: 280–287. DOI:10.1097/00006123-199902000-00021; Kano H., Flickinger J.C., Nakamura A., Jacobs R.C., Tonetti D.A., Lehocky C. et al. How to improve obliteration rates during volume-staged stereotactic radiosurgery for large arteriovenous malformations. J Neurosurg 2018; 130(3): 1–8. DOI:10.3171/2018.2.JNS172964
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14Academic Journal
Authors: A. K. Mironova, A. S. Sharykin, K. V. Vatolin, M. I. Pykov, I. M. Osmanov, А. К. Миронова, А. С. Шарыкин, К. В. Ватолин, М. И. Пыков, И. М. Османов
Source: Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics); Том 65, № 3 (2020); 138-146 ; Российский вестник перинатологии и педиатрии; Том 65, № 3 (2020); 138-146 ; 2500-2228 ; 1027-4065 ; 10.21508/1027-4065-2020-65-3
Subject Terms: лечение, preterm infants, very low birth weight, arteriovenous malformation, the Galena vein, neurosonography, heart failure, pulmonary hypertension, diagnostics, treatment, недоношенные, очень низкая масса при рождении, артериовенозная мальформация, вена Галена, нейросонография, сердечная недостаточность, легочная гипертензия, диагностика
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Relation: https://www.ped-perinatology.ru/jour/article/view/1162/945; Anatomy, imaging and surgery of the intracranial dural venosus sinuses. Editor-in-Chief R. Shane Tubbs. 2020; 250. Elsevier, Inc. DOI: org/10.1016/C2018-0-00971-8; Jamil F., Khan H.F., Ahmad I. Anwer F. Aneurysmal dilation of the vein of Galen and straight sinus with resultant obstructive hydrocephalus. BMJ Case Rep. 2018; 27(9): pii: bcr- 2018-226742. DOI:10.1136/bcr-2018-226742; Recinos P.F., Rahmathulla G., Pearl M., Recinos V.R., Jallo G.I., Gailloud P., Ahn E.S. Vein of Galen Malformations: Epidemiology, Clinical Presentations, Management. Neu rosurg Clin N Am 2012; 23(1): 165-177. DOI:10.1016/j.nec.2011.09.006; Синельников Р.Д., Синельников Я.Р., Синельников А.Я. Атлас анатомии человека. В 4-х томах. Том 4. Учение о нервной системе и органах чувств. М: Новая волна, 2019.; Hosmann A., El-Garci A., Gatterbauer B., Bavinzski G., Knosp E., Gruber A. Multimodality management of vein of Galen malformations – An institutional experience. World Neurosurg 2018; 112: e837–847. DOI:10.1016/j.wneu.2018.01.172; Vein of Galen Malformation (VOGM). Diagnosis and Treatment. https://www.childrenshospital.org/conditions-and-treatments/conditions/v/vein-of-galen/diagnosis-and-treatment.Ссылка активна на 25.01.2020.; Li A.H., Armstrong D., terBrugge K.G. Endovascular treatment of vein of Galen aneurysmal malformation: management strategy and 21-year experience in Toronto. J Neurosurg Pediatr 2011; 7(1): 3–10. DOI:10.3171/2010.9.PEDS0956; Lasjaunias P.L., Chng S.M., Sachet M., Alvarez H., Rodesch G., Garcia-Monaco R. The management of vein of Galen aneurysmal malformations. Neurosurgery 2006; 59(5 Suppl 3): S184–194.; Трунина И.И., Шарыкин А.С., Лившиц М.И., Лаврова Т.Р., Османов И.М. Первый опыт использования бозентана в комплексном лечении сердечной недостаточности у ребенка с аневризмой вены Галена. Российский кардиологический журнал 2017; 141(1): 114–120.; Tiwary S., Geethanath R.M., Abu-Harb M. Vein of Galen malformation presenting as persistent pulmonary hypertension of newborn (PPHN). BMJ Case Rep 2013; 26(9). pii: bcr2013200425. DOI:10.1136/bcr-2013-200425; Firdouse M., Agarwal A., Mondal T. Vein of Galen arteriovenous malformation mimicking coarctation of the aorta. J Ultrasound 2014; 17(4): 297–301. DOI:10.1007/s40477-014-0080-y; Brinjikji W., Krings T., Murad M.H., Rouchaud A., Meila D. Endovascular Treatment of Vein of Galen Malformations: A Systematic Review and Meta-Analysis. AJNR Am J Neuroradiol 2017; 38(12): 2308–2314. DOI:10.3174/ajnr.A5403; Адаев А.Р., Яковлев С.Б., Хухлаева Е.А. Результаты лечения артериовенозных мальформаций вены Галена. Вопросы нейрохирургии 2012; 3: 54–60.; Karadeniz L., Coban A., Sencer S., Has R., Ince Z., Can G. Vein of Galen aneurysmal malformation: Prenatal diagnosis and early endovascular management. J Chin Med Assoc 2011; 74(3): 134–137. DOI:10.1016/j.jcma.2011.01.029; Авраменко Т.В., Шевченко А.А. Аневризма вены Галена: аспекты диагностики и терапии. Клиническое наблюдение. Репродуктивное здоровье. Восточная Европа 2014;33 (3): 83–90.; Лагунавичене М.Л., Ларионов С.Н., Александров Ю.А., Ливадаров А.В., Грузин П.Г., Жданович. Г.С. Спонтанная облитерация врожденной артериовенозной мальформации головного мозга в детском возрасте. Российский вестник перинатологии и педиатрии 2020; 65(3): 126–130.
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15Academic Journal
Authors: Linnik, O. V., Sidorovich, E. K., Likhachev, S. A., Chernukha, T. N., Linnik, Yu. I., Shevchenko, N. S., Линник, О. В., Сидорович, Э. К., Лихачев, С. А., Чернуха, Т. Н., Линник, Ю. И., Шевченко, Н. С.
Subject Terms: RENDU-OSLER-WEBER DISEASE, PULMONARY ARTERIOVENOUS MALFORMATION, STROKE, CLINICAL CASE, EMBOLOTHERAPY, БОЛЕЗНЬ РАНДЮ-ОСЛЕРА-ВЕБЕРА, ЛЕГОЧНАЯ АРТЕРИОВЕНОЗНАЯ МАЛЬФОРМАЦИЯ, ИНФАРКТ МОЗГА, КЛИНИЧЕСКИЙ СЛУЧАЙ, ЭМБОЛОТЕРАПИЯ
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Relation: Уральский медицинский журнал. 2018. Т. 166, № 11.; http://elib.usma.ru/handle/usma/12906
Availability: http://elib.usma.ru/handle/usma/12906
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16Academic Journal
Authors: K. Yu. Orlov, A. L. Krivoshapkin, A. P. Chupakhin, A. A. Cherevko, A. K. Khe, V. I. Baranov, V. A. Panarin, N. Yu. Telegina
Source: Патология кровообращения и кардиохирургия, Vol 16, Iss 3, Pp 39-43 (2015)
Subject Terms: ЭМБОЛИЗАЦИЯ, АРТЕРИОВЕНОЗНАЯ МАЛЬФОРМАЦИЯ, ФИСТУЛА, ONYX, HEMORRHAGE, Surgery, RD1-811
File Description: electronic resource
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17Academic Journal
Authors: Stepanov, Yu.M., Krylovа, O.O.
Source: Gastroenterologìa, Vol 47, Iss 2.48, Pp 91-96 (2013)
GASTROENTEROLOGY; № 2.48 (2013); 91-96
Гастроэнтерология-Gastroenterologìa; № 2.48 (2013); 91-96
Гастроентерологія-Gastroenterologìa; № 2.48 (2013); 91-96Subject Terms: 03 medical and health sciences, тонка кишка, відеокапсульна ендоскопія, ангіодисплазія, артеріовенозна мальформація, шлунково-кишкова кровотеча, 0302 clinical medicine, video capsule endoscopy, angiodysplasia, arteriovenous malformation, gastrointestinal bleeding, RC799-869, Diseases of the digestive system. Gastroenterology, small intestine, тонкая кишка, видеокапсульная эндоскопия, ангиодисплазия, артериовенозная мальформация, желудочно-кишечное кровотечение, 3. Good health
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18Academic Journal
Authors: E. A. Salnikova, S. S. Ozerov, A. E. Samarin, N. P. Ananieva, D. A. Kobyzeva, A. V. Nechesnyuk, V. V. Emtsova, M. A. Alekseev, S. P. Khomyakova, O. A. Boginskaya, D. V. Litvinov, E. V. Kumirova, Е. А. Сальникова, С. С. Озеров, А. Е. Самарин, Н. П. Ананьева, Д. А. Кобызева, А. В. Нечеснюк, В. В. Емцова, М. А. Алексеев, С. П. Хомякова, О. А. Богинская, Д. В. Литвинов, Э. В. Кумирова
Source: Russian Journal of Pediatric Hematology and Oncology; Том 4, № 1 (2017); 71-76 ; Российский журнал детской гематологии и онкологии (РЖДГиО); Том 4, № 1 (2017); 71-76 ; 2413-5496 ; 2311-1267 ; 10.17650/2311-1267-2017-4-1
Subject Terms: несахарный диабет, arteriovenous malformations of the brain, children, radiation therapy, diabetes insipidus, артериовенозная мальформация головного мозга, дети, лучевая терапия
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Relation: https://journal.nodgo.org/jour/article/view/284/284; Arora R.S., Alston R.D., Eden T.O. et al. Age-incidence patterns of primary CNS tumors in children, adolescents, and adults in England. Neuro Oncol 2009;11(4):403–13.; Ostrom Q.T., Gittleman H., Farah P. et al. CBTRUS statistical report: primary brain and central nervous system tumors diagnosed in the United States in 2006–2010. Neuro Oncol 2013;15(Suppl. 2):ii1–ii56.; Wöhrer A., Waldhör T., Heinzl H. et al. The Austrian Brain Tumour Registry: a cooperative way to establish a population-based brain tumour registry. J Neurooncol 2009;95(3):401–11.; The Committee of Brain Tumor Registry of Japan. Special Report of Brain Tumor Registry of Japan (1969–1996). Neurol Med Chir (Tokyo), 2003. 11th edition. P. 1–111.; Lee C.H., Jung K.W., Yoo H. et al. Epidemiology of primary brain and central nervous system tumors in Korea. J Korean Neurosurg Soc 2010;48(2):145–52.; Report of Brain Tumor Registry of Japan (1984–2000). Neurol Med Chir (Tokyo), 2009. 12th edition. P. 1–96.; Wong T.T., Ho D.M., Chang K.P. et al. Primary pediatric brain tumors: statistics of Taipei VGH, Taiwan (1975–2004). Cancer 2005;104(10):2156–67.; Kamoshima Y., Sawamura Y. Update on current standard treatments in central nervous system germ cell tumors. Curr Opin Neurol 2010;23(6):571–5.; Dolecek T.A., Propp J.M., Stroup N.E. et al. CBTRUS statistical report: primary brain and central nervous system tumors diagnosed in the United States in 2005–2009. Neuro Oncol 2012;14(Suppl 5):1–49.; Packer R.J., Cohen B.H., Cooney K. Intracranial germ cell tumors. Oncologist 2000;5(4):312–20.; Schneider D.T., Calaminus G., Koch S. et al. Epidemiologic analysis of 1,442 children and adolescents registered in the German germ cell tumor protocols. Pediatr Blood Cancer 2004;42(2):169–75.; Kim J.Y., Park J. Understanding the Treatment Strategies of Intracranial Germ Cell Tumors: Focusing on Radiotherapy. J Korean Neurosurg Soc 2015;57(5):315–22.; Halperin E.C., Constine L.S., Tarbell N.J. et al. Pediatric Radiation Oncology. In: Supratentorial Brain Tumors. Kun L.E., MacDonald S., Tarbell N.J., eds. Philadelphia: Lippincott Williams & Wilkins, 2010. P. 26–52.; Jennings M.T., Gelman R., Hochberg F. Intracranial germ-cell tumors: natural history and pathogenesis. J Neurosurg 1985;63(2):155–67.; Phi J.H., Kim S.K., Lee J. et al. The enigma of bifocal germ cell tumors in the suprasellar and pineal regions: synchronous lesions or metastasis? J Neurosurg Pediatr 2013;11(2):107–14.; Weksberg D.C., Shibamoto Y., Paulino A.C. Bifocal intracranial germinoma: a retrospective analysis of treatment outcomes in 20 patients and review of the literature. Int J Radiat Oncol Biol Phys 2012;82(4):1341–51.; Cho J., Choi J.U., Kim D.S. et al. Lowdose craniospinal irradiation as a definitive treatment for intracranial germinoma. Radiother Oncol 2009;91(1):75–9.; Jinguji S., Yoshimura J., Nishiyama K. et al. Factors affecting functional outcomes in long-term survivors of intracranial germinomas: a 20-year experience in a single institution. J Neurosurg Pediatr 2013; 11(4):454–63.; Maity A., Shu H.K., Janss A. et al. Craniospinal radiation in the treatment of biopsy-proven intracranial germinomas: twenty-five years’ experience in a single center. Int J Radiat Oncol Biol Phys 2004;58(4):1165–70.; Merchant T.E., Sherwood S.H., Mulhern R.K. et al. CNS germinoma: disease control and long-term functional outcome for 12 children treated with craniospinal irradiation. Int J Radiat Oncol Biol Phys 2000;46(5):1171–6.; Shim K.W., Park E.K., Lee Y.H. et al. Treatment strategy for intracranial primary pure germinoma. Childs Nerv Syst 2013;29(2):239–48.; Kim J.W., Kim W.C., Cho J.H. et al. 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20Academic Journal
Authors: Arustamyan, R. R., Adamyan, L. V., Shifman, Е. М., Saribekyan, A. S., Kulikov, A. V., Lyashko, E. S., Арустамян, P. P., Адамян, Л. B., Шифман, Е. М., Сарибекян, А. С., Куликов, А. В., Ляшко, Е. С.
Subject Terms: ARTERIOVENOUS MALFORMATION, INTRACRANIAL HEMORRHAGE, PREGNANCY, PREECLAMPSIA, АРТЕРИОВЕНОЗНАЯ МАЛЬФОРМАЦИЯ, ВНУТРИЧЕРЕПНОЕ КРОВОИЗЛИЯНИЕ, БЕРЕМЕННОСТЬ, ПРЕЭКЛАМПСИЯ
File Description: application/pdf
Relation: Уральский медицинский журнал. 2016. T. 140, № 7.; http://elib.usma.ru/handle/usma/13700
Availability: http://elib.usma.ru/handle/usma/13700