Εμφανίζονται 1 - 20 Αποτελέσματα από 26 για την αναζήτηση '"СИНДРОМ ВОЛЬФА-ПАРКИНСОНА-УАЙТА"', χρόνος αναζήτησης: 0,63δλ Περιορισμός αποτελεσμάτων
  1. 1
    Academic Journal

    Πηγή: Pediatric pharmacology; Том 20, № 1 (2023); 59-62 ; Педиатрическая фармакология; Том 20, № 1 (2023); 59-62 ; 2500-3089 ; 1727-5776

    Περιγραφή αρχείου: application/pdf

    Relation: https://www.pedpharma.ru/jour/article/view/2268/1464; Бокарев И.Н., Попова Л.В. Современные проблемы тромбозов артерий и вен // Практическая медицина. — 2014. — № 6. — С. 13–17.; Свирин П.В., Румянцев С.А., Ларина Л.Е. и др. Лечение неонатальных тромбозов. Проект клинического протокола // Неонатология: Новости. Мнения. Обучение. — 2013. — № 1. — С. 76–85.; Shaik M, Patel D, Mihir B, et al. Epidemiology, Diagnosis and Management of Neonatal Thrombosis. Blood. 2019;134(Suppl 1):3656. doi: https://doi.org/10.1182/blood-2019-129914; Dieffenbach BV, Nath BD, Tracy ET, Kim HB. Management of symptomatic neonatal aortic thrombosis: When is surgery indicated? J Pediatr Surg Case Rep. 2019;47:101247. doi: https://doi.org/10.1016/j.epsc.2019.101247; Chhabra L, Goyal A, Benham MD. Wolff Parkinson White Syndrome. [Updated 2022 Aug 8]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022.; Джанашия П.Х., Шевченко Н.М., Рыжова Т.В. Роль амиодарона в лечении аритмий // Лечащий врач. — 2006. — № 3. Доступно по: https://www.lvrach.ru/2006/03/4533545. Ссылка активна на 08.02.2023.; Мкртумян А.М., Бирюкова Е.В., Егшатян Л.В. и др. Амиодарон-индуцированный тиреотоксикоз 1 типа: особенности ведения пациентов // Эффективная фармакотерапия. — 2019. — Т. 15. — № 25. — С. 8–11. — doi: https://doi.org/10.33978/2307-3586-2019-15-25-8-11; Стародубова А.В. Амиодарон. Что должен знать практикующий врач // АтмосферА. Новости кардиологии. — 2011. — № 1. — С. 19–25.; Narayana SK, Woods DR, Boos CJ. Management of amiodarone-related thyroid problems. Ther Adv Endocrinol Metab. 2011;2(3):115–126. doi: https://doi.org/10.1177/2042018811398516; Danzi S, Klein I. Amiodarone-induced thyroid dysfunction. J Intensive Care Med. 2015;30(4):179–185. doi: https://doi.org/10.1177/0885066613503278; Лебедева Е.А., Яблонская Ю.А., Булгакова С.В. Амиодарониндуцированный тиреотоксикоз. Современный взгляд на проблему // Клиническая и экспериментальная тиреоидология. — 2017. — Т. 13. — № 2. — С. 31–38. — doi: https://doi.org/10.14341/ket2017231-38; https://www.pedpharma.ru/jour/article/view/2268

  2. 2
    Academic Journal

    Πηγή: Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics); Том 67, № 4 (2022); 99-107 ; Российский вестник перинатологии и педиатрии; Том 67, № 4 (2022); 99-107 ; 2500-2228 ; 1027-4065

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    Relation: https://www.ped-perinatology.ru/jour/article/view/1681/1269; Blair E., Redwood C., Ashrafian H., Oliveira M., Broxholme J., Kerr В. et al. Mutations in the gamma (2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis. Hum Mol Genet 2001; 10: 1215- 1220. DOI:10.1093/hmg/10.11.1215 (2001); Lopez-Sainz A., Dominguez F., Lopes L.R., Ochoa J.P., Barriales-Villa R., Climent V., et. al. Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis J Am Coll Cardiol 2020; 76(2): 186-197. DOI:10.1016/j.jacc.2020.05.029; Porto A.G., Brun F., Severini G.M., Losurdo P., Fabris E., Taylor M.R.G. et al. Clinical Spectrum of PRKAG2 Syndrome. Circ Arrhythm Electrophysiol 2016; 9(1): e003121. DOI:10.1161/CIRCEP.115.003121; Banankhah P., Fishbein G.A., Dota A., Ardehali R. Cardiac manifestations of PRKAG2 mutation. BMC Med Genet 2018; 19(1): 1. DOI:10.1186/s12881-017-0512-6; Gollob M.H., Green M.S., Tang A.S., Roberts R. PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy. Curr Opin Cardiol 2002;17: 229-234. DOI:10.1097/00001573-200205000-00004; Thevenon J., Laurent G., Ader F., Laforêt P., Klug D., Duva Pentiah A. et al. High prevalence of arrhythmic and myocardial complications in patients with cardiac glycogenosis due to PRKAG2 mutations. Europace 2017; 19: 651-659. DOI:10.1093/europace/euw067; Arad M., Maron B.J., Gorham J.M., Johnson W.H. Jr., Saul J.P., Perez-Atayde A.R. et al. Glycogen storage diseases presenting as hypertrophic cardiomyopathy. N Engl J Med 2005; 352: 362-372. DOI:10.1056/NEJMoa033349; Fabris E., Brun F., Porto A.G., Losurdo P., Vitali Serdoz L., Zecchin M. et al. Cardiac hypertrophy, accessory pathway, and conduction system disease in an adolescent: the PRKAG2 cardiac syndrome. J Am Coll Cardiol 2013; 62(9): e17. DOI:10.1016/j.jacc.2013.02.099; Aggarwal V., Dobrolet N., Fishberger S., Zablah J., Jayakar P., Ammous Z. PRKAG2 mutation: An easily missed cardiac specific non-lysosomal glycogenosis. Ann Pediatr Cardiol 2015; 8(2): 153-156. DOI:10.4103/0974-2069.154149; van der Steld L.P., Campuzano O., Pérez-Serra A., Moura de Barros Zamorano M., Sousa Matos S., Brugada R. Wolff-Parkinson-White Syndrome with Ventricular Hypertrophy in a Brazilian Family. Am J Case Rep 2017; 18: 766-776. DOI:10.12659/AJCR.904613; Hu J., Tang B., Wang J., Huang K., Wang Y., Lu S. et al. Familial Atrial Enlargement, Conduction Disorder and Symmetric Cardiac Hypertrophy Are Early Signs of PRKAG2 R302Q. Curr Med Sci 2020; 40(3): 486-492. DOI:10.1007/s11596-020-2207-z

  3. 3
    Academic Journal

    Πηγή: Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics); Том 67, № 3 (2022); 111-116 ; Российский вестник перинатологии и педиатрии; Том 67, № 3 (2022); 111-116 ; 2500-2228 ; 1027-4065

    Περιγραφή αρχείου: application/pdf

    Relation: https://www.ped-perinatology.ru/jour/article/view/1661/1253; Elliott P.M., Anastasakis A., Borger M.A., Borggrefe M., Cecchi F., Charron P. et al. 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy The Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology. Eur Heart J 2014; 35: 2733–2779. DOI:10.1093/eurheartj/ehu284; Maron B., Rowin E., Casey S., Lesser J., Garberich R., McGriff D.M., Maron M.S. Hypertrophic Cardiomyopathy in Children, Adolescents, and Young Adults Associated With Low Cardiovascular Mortality With Contemporary Management Strategies. Circulation 2016; 133(1): 62–73. DOI:10.1161/circulationaha.115.01763; Lipshultz S.E., Orav E.J., Wilkinson J. D., Towbin J.A., Messere J.E., Lowe A.M. et al. Risk stratification at the time of diagnosis for children with hypertrophic cardiomyopathy: a report from the Pediatric Cardiomyopathy Registry Study Group. Lancet 2013; 382(9908): 1889–1897. DOI:10.1016/S0140–6736(13)61685–2; Леонтьева И.В. Дифференциальная диагностика гипертрофической кардиомиопатии Российский вестник перинатологии и педиатрии 2017; 62(3): 20–31.; Arad M., Maron B.J., Gorham J.M., Johnson W.H. Jr., Saul J.P., Perez-Atayde A.R. et al. Glycogen storage diseases presenting as hypertrophic cardiomyopathy. N Engl J Med 2005; 352: 362–372. DOI:10.1056/NEJMoa033349; Blair E., Redwood C., Ashrafian H., Oliveira M., Broxholme J., Kerr В., Salmon А. et al. Mutations in the gamma (2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis. Hum Mol Genet 2001; 10: 1215–1220. DOI:10.1093/hmg/10.11.1215; Lopez-Sainz A., Dominguez F., Lopes L.R., Ochoa J.P., Barriales-Villa R., Climent V. et al. Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis J Am Coll Cardiol 2020; 76(2): 186–197. DOI:10.1016/j.jacc.2020.05.029; Murphy R.T., Mogensen J., McGarry K., Bahl A., Evans A., Osman E. Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff–Parkinson–White syndrome: natural history. J Am Coll Cardiol 2005; 45: 922–930. DOI:10.1016/j.jacc.2004.11.053; Porto A.G., Brun F., Severini G.M., Losurdo P., Fabris E., Taylor M.R.G. et al. Clinical Spectrum of PRKAG2 Syndrome. Circ Arrhythm Electrophysiol 2016; 9: e003121. DOI:10.1161/CIRCEP.115.003121; MacRae С.A., Ghaisas N., Kass S., Donnell S., Basson C., Watkins H. et al. Familial Hypertrophic cardiomyopathy with Wolff–Parkinson–White syndrome maps to a locus on chromosome 7q3 l. Clin Invest 1995; 96(3): 1216–1220. DOI:10.1172/JCI118154; Yang K.Q., Lu C.X., Zhang Y., Yang Y.K., Li J.C., Lan T. et al. A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation. Sci Rep 2017; 7(1): 2407. DOI:10.1038/s41598-017-02455-z; Lang T., Yu L., Tu Q., Jiang J., Chen, Z., Xin Y. et al. Molecular cloning, genomic organization, and mapping of PRKAG2, a heart abundant Ȗ2 subunit of 5 -AMP-activated protein kinase, to human chromosome 7q36. Genomics 2000; 70: 258–263. DOI:10.1006/geno.2000.6376; Merante F., Tein I., Benson L., Robinson B.H. Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA (glycine) gene. Am J Hum Genet 1994; 55: 437–446.; Puccio H., Koenig M. Recent advances in the molecular pathogenesis of Friedreich ataxia. Hum Mol Genet 2000; 9: 887–892. DOI:10.1093/hmg/9.6.887; Bonnet D., Martin D., De Lonlay P., Villain E., Jouvet P., Rabier D. et al. Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children. Circulation 1999; 100: 2248–2253. DOI:10.1161/01.cir.100.22.2248; Arad M., Moskowitz I.P., Patel V.V., Ahmad F., PerezAtayde A.R., Sawyer D.B. et al. Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff–Parkinson–white syndrome in glycogen storage cardiomyopathy. Circulation 2003; 107: 2850–2856. DOI:10.1161/01.CIR.0000075270.13497.2B; Banankhah P., Fishbein G.A., Dota A., Ardehali R. Cardiac manifestations of PRKAG2 mutation. BMC Med Genet 2018; 19(1): 1. DOI:10.1186/s12881-017-0512-6; Gollob M.H., Green M.S., Tang A.S., Roberts R. PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy. Curr Opin Cardiol 2002; 17: 229–234. DOI:10.1097/00001573-200205000-00004; Sternick E.B., Oliva A., Gerken L.M., Hong K., Santana O., Brugada P. et al. Clinical, electrocardiographic, and electrophysiologic characteristics of patients with a fasciculoventricular pathway: the role of PRKAG2 mutation. Hear Rhythm 2011; 8: 58–64. DOI:10.1016/j.hrthm.2010.09.081; Wolf C.M., Arad M., Ahmad F., Sanbe A., Bernstein S.A., Toka O. et al. Reversibility of PRKAG2 glycogen-storage cardiomyopathy and electrophysiological manifestations. Circulation 2008; 117: 144–154. DOI:10.1161/CIRCULATIONAHA.107.726752; Gollob M. H., Seger J. J., Gollob T. N., Tapscott Т., Gonzales О., Bachinski L., Roberts R. Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy. Circulation 2001; 104: 3030–3033. DOI:10.1161/hc5001.102111; Thevenon J., Laurent G., Ader F., Laforêt P., Klug D., Duva Pentiah A. et al. High prevalence of arrhythmic and myocardial complications in patients with cardiac glycogenosis due to PRKAG2 mutations. Europace 2017; 19: 651–659. DOI:10.1093/europace/euw067; van der Steld L.P., Campuzano O., Pérez-Serra A., Moura de Barros Zamorano M., Sousa Matos S., Brugada R. Wolff–Parkinson–White Syndrome with Ventricular Hypertrophy in a Brazilian Family. Am J Case Rep 2017; 18: 766–776. DOI:10.12659/AJCR.904613; Sternick E.B., Oliva A., Magalhaes L.P., Gerken L.M., Hong K., Santana O. et al. Familial pseudo-Wolff–Parkinson–White syndrome. J Cardiovasc Electrophysiol 2006; 17: 724–732 DOI:10.1111/j.1540-8167.2006.00485; Burwinkel B., Scott J.W., Buhrer C., van Landeghem F.K., Cox G.F., Wilson C.J. et al. Fatal congenital heart glycogenosis caused by a recurrent activating R531Q mutation in the gamma 2-subunit of AMP-activated protein kinase (PRKAG2), not by phosphorylase kinase deficiency. Am J Hum Genet 2005; 76: 1034–1049. DOI:10.1086/430840; Zhang L.P., Hui B., Gao B.R. High risk of sudden death associated with a PRKAG2-related familial Wolff–Parkinson–White syndrome. J Electrocardiol 2011; 44: 483–486. DOI:10.1016/j.jelectrocard. 2010.02.009; Fabris E., Brun F., Porto A.G., Losurdo P., Vitali Serdoz L., Zecchin M. et al. Cardiac hypertrophy, accessory pathway, and conduction system disease in an adolescent: the PRKAG2 cardiac syndrome. J Am Coll Cardiol 2013; 62(9): e17. DOI:10.1016/j.jacc.2013.02.099; Lorenzini M., Anastasiou Z., O’Mahony C., Gimeno J.R., Monserrat L., Anastasakis А. et al. Mortality among referral patients with hypertrophic cardiomyopathy vs the general European population. JAMA Cardiol 2020; 5: 73–80. DOI:10.1001/jamacardio.2019.4534; Гандаева Л.А., Кондакова О.Б., Басаргина Е.Н., Пушков А.А., Колоскова Н.Н., Жарова О.П. и др. Гликогеновая болезнь сердца — синдром PRKAG2. Российский вестник перинатологии и педиатрии 2022; 67(2): 133–137.; Gene Therapy for Male Patients With Danon Disease (DD) Using RP-A501; AAV9.LAMP2B. Clinical Study Evaluating a Recombinant Adeno-Associated Virus Serotype 9 (rAAV9) Capsid Containing the Human Lysosome-Associated Membrane Protein 2 Isoform B (LAMP2B) Transgene (RP-A501; AAV9.LAMP2B) in Male Patients With DD (NCT03882437). https://ichgcp.net/ru/clinical-trials-registry/NCT03882437 / Ссылка активна на 16.04.2022

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  5. 5
    Academic Journal

    Πηγή: Rational Pharmacotherapy in Cardiology; Vol 13, No 6 (2017); 856-862 ; Рациональная Фармакотерапия в Кардиологии; Vol 13, No 6 (2017); 856-862 ; 2225-3653 ; 1819-6446 ; 10.20996/1819-6446-2017-13-6

    Περιγραφή αρχείου: application/pdf

    Relation: https://www.rpcardio.com/jour/article/view/1579/1580; ESC guidelines for the diagnosis and treatment of acute and chronic heart failure 2008. Eur Heart J. 2008;29:2388-2442. doi:10.1093/eurheartj/ehn309.; Maisel W.H., Stevenson L.W. Atrial fibrillation in heart failure: epidemiology, pathophysiology and rationale for therapy. Am J Cardiol. 2003;93:2D-8D. doi:10.1016/S0002-9149(02)03373-8.; Schneider M.P., Hua T.A., Bohm M. et al. Prevention of atrial fibrillation by renin-angiotensin system inhibition: a meta-analysis. J Am Coll Cardiol. 2010;55:2299-307. doi:10.1016/j.jacc.2010.01.043.; Healey J.S., Baranchuk A., Crystal E. et al. Prevention of atrial fibrillation with angiotensin-converting enzyme inhibitors and angiotensin receptor blockers: a meta-analysis. J Am Coll Cardiol. 2005;45:1832-9. doi:10.1016/j.jacc.2004.11.070.; 2016 ESC guidelines for the management of atrial fibrillation developed in collaboration wit EACTS. Eur Heart J. 2016;37:2893-962. doi:10.1093/eurheartj/ehw210; Swedberg K., Zannad F., McMurray J.J. et al. Eplerinone and atrial fibrillation in mild systolic heart failure: results from the EMPHASIS-HF study. J Am Coll Cardiol. 2012;59:1598-603. doi:10.1016/j.jacc.2011.11.063.; Martin R.R., Pogoryelova O., Koref M.S. et al. Atrial fibrillation associated with ivabradine treatment: meta-analysis of randomized controlled trials. Heart. 2014;100:1506-10. doi:10.1136/heartjnl2014-305482.; Mc Murray J.J., Packer M., Desai A.S. et al. Paradigm-HF investigators and committees. Angiotensinneprilysin inhibition versus enalapril in heart failure. N Engl J Med. 2014;371:993-1004. doi:10.1056/NEJMoa1409077.; 2014 AHA/ACC/HRS guideline for the management of patients with atrial fibrillation. Circulation. 2014;130:e199–e267. https://doi.org/10.1161/CIR.0000000000000041; Hess P.L., Jackson K.P., Hasselblad V. Al-Khatib S.M. Is cardiac resynchronization therapy an antiarrhythmic therapy for atrial fibrillation? A Systematic Review and Meta-Analysis. Curr Cardiol Rep. 2013;15(2):330. doi:10.1007/s11886-012-0330-6; 2016 ESC guidelines for the diagnosis and treatment of acute and chronic heart failure. Eur Heart J. 2016;37:2129-200. doi:10.1093/eurheartj/ehw128.; Roskell N.S., Samuel M., Noack H. et al. Major bleeding in patients with atrial fibrillation receiving vitamin K antagonists: a systematic review of randomized and observational studies. Europace. 2013;15:787-97. doi:10.1093/europace/eut001.; Update European heart rhythm association practical guide on the use of non-vitamin K antagonist anticoagulants in patients with non-valvular atrial fibrillation. Europace. 2013;15:625-51. doi:10.1093/europace/euv309.; Connolly S.J., Ezekowitz M.D., Yusuf S. et al. RE-LY steering committee and investigators. Dabigatran vs warfarin in patients with atrial fibrillation. N Engl J Med. 2009;361:1139-51. doi:10.1056/NEJMoa0905561.; Patel M.R., Mahaffey K.W., Gard J. et al. ROCKET-AF investigators. Rivaroxaban vs warfarin in nonvalvular atrial fibrillation. N Engl J Med. 2011;365:883-91. doi:10.1056/NEJMoa1009638.; Granger C.B., Alexander J.H., Mc Murray J.J. et al. ARISTOTLE committees and investigators. Apixaban vs warfarin in patients with atrial fibrillation. N Engl J Med. 2011;365:981-92. doi:10.1056/NEJMoa1107039.; Holmes D.R., Doshi S.K., Kar S. et al. Left atrial appendage closure as an alternative to warfarin for stroke prevention in atrial fibrillation: a patient-level meta-analysis. J Am Coll Cardiol. 2015;65:261423. doi:10.4330/wjc.v9.i2.139.; Bunin Yu.A., Miklishanskaya S.V. Clinical significance of new oral anticoagulants in the prevention of thromboembolic complications in patients with atrial fibrillation: not all dreams come true. Ration Pharmacother Cardiol. 2016;12(4):465-70. (In Russ.) [Бунин Ю.А., Миклишанская С.В. Клиническое значение новых оральных антикоагулянтов в профилактике тромбоэмболических осложнений у больных с фибрилляцией предсердий: не все мечты сбываются. Рациональная Фармакотерапия в Кардиологии. 2016;12(4):465-470]. doi:10.20996/1819-6446-201612-4-465-470.; Roy D., Talajic M., Nattel S. et al. Rhythm control versus rate control for atrial fibrillation and heart failure. N Engl J Med. 2008;385:2667-77. doi:10.1056/NEJMoa0708789.; Van Gelder I.C., Groenveld H.F., Crijns H.J. et al. Lenient versus strict rate control in patients with atrial fibrillation. N Engl J Med. 2010;362:1363-73. doi:10.1056/NEJMoa1001337.; Kotecha D., Holmes J., Krum H. et al. Beta-blockers in heart failure collaborative group. Efficacy of beta-blockers in patients with heart failure plus atrial fibrillation: an individual-patient data metaanalysis. Lancet. 2014;384:2235-43. doi:10.1016/S0140-6736(14)61373-8.; Sager P.T. New advances in class III antiarrhythmic drug therapy. Curr Opion Cardiol. 2000;15:4153.; Bardy G.H., Lee K.L., Mark D.B. et al. Amiadarone or an implantable cardioverter-defibrillator for congestive heart failure. N Engl J Med. 2005;352:225-37. doi:10.1056/NEJMoa043399; https://www.rpcardio.com/jour/article/view/1579

  6. 6
    Academic Journal

    Πηγή: Complex Issues of Cardiovascular Diseases; № 1 (2017); 153-157 ; Комплексные проблемы сердечно-сосудистых заболеваний; № 1 (2017); 153-157 ; 2587-9537 ; 2306-1278 ; 10.17802/2306-1278-2017-1

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    Relation: https://www.nii-kpssz.com/jour/article/view/275/242; Ревишвили А.Ш., Давтян К.В., Лабарткава Е.З. Современное представление о трактах Махайма, электрофизиологические свойства и результаты интервенционного метода лечения. Вестник аритмологии. 2007; 47: 15-22. Revishvili A.Sh., Davtjan K.V.; Labartkava E.Z.Sovremennoe predstavle-nie o traktah Mahajma, jelektrofiziologicheskie svojstva i rezul’taty intervencion-nogo metoda lechenija. Vestnik aritmologii. 2007; 47: 15- 22. [In Russ.]; Ablation of right free wall and atriofascicular accessory pathways G. To-massoni [et al.] Interventional electrophysiology. 2nd ed. ed. I. Singer. Phila-delphia: Lippincott Williams & Wilkins. 2001; 193-219.; ACC/AHA/ESC guidelines for the management of patients with supraventric-ular arrhythmias – executive summary: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the European Society of Cardiology Committee for Practice Guidelines (Writing Committee to Develop Guidelines for the Management of Patients With Supraventricular Arrhythmias) C. Blomstrom- Lundqvist [et al.]. Circu-lation. 2003; 108: 1871–1909.; Kalbfleisch S., Bowman K., Augostini R. A single Mahaim fiber causing both antidromic and orthodromic reciprocating tachycardia J. Cardiovasc. Electro-physiol. 2008; 19(7): 740- 742.; Mahaim I., Bennett A. Nouvelle recherches sur les connexions superieures de la branche gauche du faiscesu de His-Tawara avec cloison interventriculaire Cardiologia. 1938; 1: 61-76.; Klein G. J., Guiraudon G.M., Kerr C.R., Sharma A.D., Yee R., Szabo T. et al. «Nodoventricular» accessory pathway: evidence for a distinct accessory atrio-ventricular pathway with AV node-like properties. J.A.C.C. 1988; 11: 1035- 1040.; Leitch J., Klein G.J., Yee R., Murdock C. New concepts of nodoventricular accessory pathways. J. Clin. Electrophysiol. 1990; 1: 220-230.; Hoffmayer K.S., Lee B.K., Vedantham V., Bhimani A.A., Cakulev I.T., Mackall J.A. et al. Variable clinical features and ablation of manifest nodofascicular/ventricular pathways. Circ. Arrhythm. Electrophysiol. 2015; 8(1): 117-127. doi:10.1161/CIRCEP.114.001924.

  7. 7
    Academic Journal

    Πηγή: Complex Issues of Cardiovascular Diseases; № 1 (2016) ; Комплексные проблемы сердечно-сосудистых заболеваний; № 1 (2016) ; 2587-9537 ; 2306-1278 ; 10.17802/2306-1278-2016-1

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    Πηγή: Complex Issues of Cardiovascular Diseases; № 4 (2014); 33-37 ; Комплексные проблемы сердечно-сосудистых заболеваний; № 4 (2014); 33-37 ; 2587-9537 ; 2306-1278 ; 10.17802/2306-1278-2014-4

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