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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Neuromuscular Diseases</journal-id><journal-title-group><journal-title xml:lang="en">Neuromuscular Diseases</journal-title><trans-title-group xml:lang="ru"><trans-title>Нервно-мышечные болезни</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2222-8721</issn><issn publication-format="electronic">2413-0443</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">105</article-id><article-id pub-id-type="doi">10.17650/2222-8721-2015-1-10-18</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>LECTURES AND REVIEWS</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ЛЕКЦИИ И ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Acute rhabdomyolysis</article-title><trans-title-group xml:lang="ru"><trans-title>Острый рабдомиолиз</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name><surname>de Lonlay</surname><given-names>Pascale</given-names></name><address><country country="FR">France</country></address><bio xml:lang="en"><p>Paris</p></bio><bio xml:lang="ru"><p>Hôpital Necker, AP-HP, Paris</p></bio><email>pascale.delonlay@nck.aphp.fr</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Mamoune</surname><given-names>Asmaa</given-names></name><address><country country="FR">France</country></address><bio xml:lang="en"><p>Paris</p></bio><bio xml:lang="ru"><p>Hôpital Necker, AP-HP, Paris</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Hamel</surname><given-names>Yamina</given-names></name><address><country country="FR">France</country></address><bio xml:lang="en"><p>Paris</p></bio><bio xml:lang="ru"><p>Hôpital Necker, AP-HP, Paris</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Bahuau</surname><given-names>Michel</given-names></name><address><country country="FR">France</country></address><bio xml:lang="en"><p>Créteil</p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Vergnaud</surname><given-names>Sabrina</given-names></name><address><country country="FR">France</country></address><bio><p>Grenoble</p></bio><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Piraud</surname><given-names>Moniqu</given-names></name><name xml:lang="ru"><surname>Piraud</surname><given-names>Monique</given-names></name></name-alternatives><address><country country="FR">France</country></address><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name><surname>Lallemand</surname><given-names>Lætitia</given-names></name><address><country country="FR">France</country></address><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Nguyen More</surname><given-names>Marie-Ange</given-names></name><name xml:lang="ru"><surname>Ngu Nguyen Morel</surname><given-names>Marie-Ange</given-names></name></name-alternatives><address><country country="FR">France</country></address><xref ref-type="aff" rid="aff5"/><xref ref-type="aff" rid="aff8"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Vio</surname><given-names>Mai Thao</given-names></name><name xml:lang="ru"><surname>Viou</surname><given-names>Mai Thao</given-names></name></name-alternatives><address><country country="FR">France</country></address><xref ref-type="aff" rid="aff8"/></contrib><contrib contrib-type="author"><name><surname>Romero</surname><given-names>Norma Beatriz</given-names></name><address><country country="FR">France</country></address><bio><p>Paris</p></bio><xref ref-type="aff" rid="aff9"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Inserm U781, Institut Imagine des Maladies Génétiques, Université Paris Descartes, Centre de Référence des Maladies Héréditaires&#13;
du Métabolisme, Hôpital Necker, AP-HP</institution></aff><aff><institution xml:lang="ru">Inserm U781, Institut Imagine des Maladies Génétiques, Université Paris Descartes, Centre de Référence des Maladies Héréditaires du Métabolisme</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Département de Génétique, CHU Henri-Mondor, AP-HP</institution></aff><aff><institution xml:lang="ru">Département de Génétique, CHU Henri-Mondor, AP-HP, Créteil</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Département de Biochimie, Toxicologie et Pharmacologie, CHU de Grenoble, Centre de Référence Rhône-Alpes des Maladies&#13;
Neuromusculaires</institution></aff><aff><institution xml:lang="ru">Département de Biochimie, Toxicologie et Pharmacologie, CHU de Grenoble, Centre de Référence Rhône-Alpes des Maladies Neuromusculaires</institution></aff></aff-alternatives><aff id="aff4"><institution>Laboratoire Maladies Héréditaires du Métabolisme, Centre de Biologie et Pathologie Est, Hospices Civils de Lyon</institution></aff><aff id="aff5"><institution>Clinique Universitaire de Pédiatrie, Hôpital couple enfant, CHU de Grenoble</institution></aff><aff-alternatives id="aff6"><aff><institution xml:lang="ru"></institution></aff><aff><institution xml:lang="en">Clinique Universitaire de Pédiatrie, Hôpital couple enfant, CHU de Grenoble</institution></aff></aff-alternatives><aff-alternatives id="aff7"><aff><institution xml:lang="ru">Clinique Universitaire de Pédiatrie, Hôpital couple enfant, CHU de Grenoble</institution></aff><aff><institution xml:lang="en">Université Pierre et Marie Curie, UM 76, Inserm U974, CNRS UMR 7215, Institut de Myologie, GHU Pitié-Salpêtrière, AP-HP,&#13;
Centre de Référence des Maladies Neuromusculaires</institution></aff></aff-alternatives><aff id="aff8"><institution></institution></aff><aff id="aff9"><institution>Université Pierre et Marie Curie, UM 76, Inserm U974, CNRS UMR 7215, Institut de Myologie, GHU Pitié-Salpêtrière, AP-HP, Centre de Référence des Maladies Neuromusculaires</institution></aff><pub-date date-type="pub" iso-8601-date="2015-05-22" publication-format="electronic"><day>22</day><month>05</month><year>2015</year></pub-date><volume>5</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>10</fpage><lpage>18</lpage><history><date date-type="received" iso-8601-date="2015-05-21"><day>21</day><month>05</month><year>2015</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2015, de Lonlay P., Mamoune A., Hamel Y., Bahuau M., Vergnaud S., Piraud M., Lallemand L., Nguyen More M., Vio M., Romero N.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2015, de Lonlay P., Mamoune A., Hamel Y., Bahuau M., Vergnaud S., Piraud M., Lallemand L., Ngu Nguyen Morel M., Viou M.T., Romero N.</copyright-statement><copyright-year>2015</copyright-year><copyright-holder xml:lang="en">de Lonlay P., Mamoune A., Hamel Y., Bahuau M., Vergnaud S., Piraud M., Lallemand L., Nguyen More M., Vio M., Romero N.</copyright-holder><copyright-holder xml:lang="ru">de Lonlay P., Mamoune A., Hamel Y., Bahuau M., Vergnaud S., Piraud M., Lallemand L., Ngu Nguyen Morel M., Viou M.T., Romero N.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://nmb.abvpress.ru/jour/article/view/105">https://nmb.abvpress.ru/jour/article/view/105</self-uri><abstract xml:lang="en"><p/></abstract><trans-abstract xml:lang="ru"><p/></trans-abstract><kwd-group xml:lang="en"><kwd>rhabdomyolysis</kwd><kwd>fever</kwd><kwd>temperature-dependent rhabdomyolysis</kwd><kwd>inherited rhabdomyolysis</kwd><kwd>environment</kwd><kwd>thermolability</kwd><kwd>aldolase A</kwd><kwd>myopathy</kwd><kwd>myoglobinuria</kwd><kwd>pro-inflammatory mediators</kwd><kwd>hemolytic anemia</kwd><kwd>myositis</kwd><kwd>ATP</kwd><kwd>statins</kwd><kwd>lipid droplets</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>рабдомиолиз</kwd><kwd>лихорадка</kwd><kwd>термочувствительный рабдомиолиз</kwd><kwd>наследственный рабдомиолиз</kwd><kwd>окружающая среда</kwd><kwd>термолабильность</kwd><kwd>альдолаза А</kwd><kwd>миопатия</kwd><kwd>миоглобинурия</kwd><kwd>провоспалительные медиаторы</kwd><kwd>гемолитическая анемия</kwd><kwd>миозит</kwd><kwd>аденозинтрифосфат</kwd><kwd>статины</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. Sauret J.M., Marinides G., Wang G.K. Rhabdomyolysis. Am Fam Physician 2002;65(5):907– 12.</mixed-citation><mixed-citation xml:lang="ru">Sauret J.M., Marinides G., Wang G.K. Rhabdomyolysis. Am Fam Physician 2002;65(5):907– 12.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Brown C.V., Rhee P., Chan L. et al. Preventing renal failure in patients with rhabdomyolysis: do bicarbonate and mannitol make a difference? J Trauma 2004;56(6):1191–6.</mixed-citation><mixed-citation xml:lang="ru">Brown C.V., Rhee P., Chan L. et al. Preventing renal failure in patients with rhabdomyolysis: do bicarbonate and mannitol make a difference? J Trauma 2004;56(6):1191–6.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. Alpers J.P., Jones L.K. Jr. Natural history of exertional rhabdomyolysis: a populationbased analysis. Muscle Nerve 2010;42(4): 487–91.</mixed-citation><mixed-citation xml:lang="ru">Alpers J.P., Jones L.K. Jr. Natural history of exertional rhabdomyolysis: a populationbased analysis. Muscle Nerve 2010;42(4): 487–91.</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. Perreault S., Birca A., Piper D., et al. Transient creatine phosphokinase elevations in children: a single-center experience. J Pediatr. 2011 Oct;159(4):682–5.</mixed-citation><mixed-citation xml:lang="ru">Perreault S., Birca A., Piper D., et al. Transient creatine phosphokinase elevations in children: a single-center experience. J Pediatr. 2011 Oct;159(4):682–5.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Mackay M.T., Kornberg A.J., Shield L.K. et al. Benign acute childhood myositis: laboratory and clinical features. Neurology 1999;53(9):2127–31.</mixed-citation><mixed-citation xml:lang="ru">Mackay M.T., Kornberg A.J., Shield L.K. et al. Benign acute childhood myositis: laboratory and clinical features. Neurology 1999;53(9):2127–31.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Zutt R., van der Kooi A.J., Linthorst G.E. et al. Rhabdomyolysis: review of the literature. Neuromuscul Disord 2014;24(8):651–9.</mixed-citation><mixed-citation xml:lang="ru">Zutt R., van der Kooi A.J., Linthorst G.E. et al. Rhabdomyolysis: review of the literature. Neuromuscul Disord 2014;24(8):651–9.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. Tein I., DiMauro S., DeVivo D.C. Recurrent childhood myoglobinuria. Adv Pediatr 1990;37:77–117.</mixed-citation><mixed-citation xml:lang="ru">Tein I., DiMauro S., DeVivo D.C. Recurrent childhood myoglobinuria. Adv Pediatr 1990;37:77–117.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. Tonin P., Lewis P., Servidei S. et al. Metabolic causes of myoglobinuria. Ann Neurol 1990;27(2):181–5.</mixed-citation><mixed-citation xml:lang="ru">Tonin P., Lewis P., Servidei S. et al. Metabolic causes of myoglobinuria. Ann Neurol 1990;27(2):181–5.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Berardo A., DiMauro S., Hirano M. A diagnostic algorithm for metabolic myopathies. Curr Neurol Neurosci Rep 2010;10(2):118–26.</mixed-citation><mixed-citation xml:lang="ru">Berardo A., DiMauro S., Hirano M. A diagnostic algorithm for metabolic myopathies. Curr Neurol Neurosci Rep 2010;10(2):118–26.</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. DiMauro S., Garone C., Naini A. Metabolic myopathies. Curr Rheumatol Rep 2010;12(5):386–93.</mixed-citation><mixed-citation xml:lang="ru">DiMauro S., Garone C., Naini A. Metabolic myopathies. Curr Rheumatol Rep 2010;12(5):386–93.</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. Laforêt P., Vianey-Saban C. Disorders of muscle lipid metabolism: diagnostic and therapeutic challenges. Neuromuscul Disord 2010;20(11):693–700.</mixed-citation><mixed-citation xml:lang="ru">Laforêt P., Vianey-Saban C. Disorders of muscle lipid metabolism: diagnostic and therapeutic challenges. Neuromuscul Disord 2010;20(11):693–700.</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. Zeharia A., Shaag A., Houtkooper R.H. et al. Mutations in LPIN1 cause recurrent acute myoglobinuria in childhood. Am J Hum Genet 2008;83(4):489–94.</mixed-citation><mixed-citation xml:lang="ru">Zeharia A., Shaag A., Houtkooper R.H. et al. Mutations in LPIN1 cause recurrent acute myoglobinuria in childhood. Am J Hum Genet 2008;83(4):489–94.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13. Michot C., Hubert L., Brivet M. et al. LPIN1 gene mutations: a major cause of severe rhabdomyolysis in early childhood. Hum Mutat 2010;31(7):E1564–73.</mixed-citation><mixed-citation xml:lang="ru">Michot C., Hubert L., Brivet M. et al. LPIN1 gene mutations: a major cause of severe rhabdomyolysis in early childhood. Hum Mutat 2010;31(7):E1564–73.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14. Michot C., Hubert L., Romero N.B. et al. Study of LPIN1, LPIN2 and LPIN3 in rhabdomyolysis and exercise-induced myalgia. J Inherit Metab Dis 2012;35(6):1119–28.</mixed-citation><mixed-citation xml:lang="ru">Michot C., Hubert L., Romero N.B. et al. Study of LPIN1, LPIN2 and LPIN3 in rhabdomyolysis and exercise-induced myalgia. J Inherit Metab Dis 2012;35(6):1119–28.</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15. Kapina V., Sedel F., Truffert A. et al. Relapsing rhabdomyolysis due to peroxisomal alpha-methylacyl-coa racemase deficiency. Neurology 2010;75(14):1300–2.</mixed-citation><mixed-citation xml:lang="ru">Kapina V., Sedel F., Truffert A. et al. Relapsing rhabdomyolysis due to peroxisomal alpha-methylacyl-coa racemase deficiency. Neurology 2010;75(14):1300–2.</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16. Darras B.T., Friedman N.R. Metabolic myopathies: a clinical approach; part I. Pediatr Neurol 2000;22(2):87–97.</mixed-citation><mixed-citation xml:lang="ru">Darras B.T., Friedman N.R. Metabolic myopathies: a clinical approach; part I. Pediatr Neurol 2000;22(2):87–97.</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17. Quinlivan R., Jungbluth H. Myopathic causes of exercise intolerance with rhabdomyolysis. Dev Med Child Neurol 2012; 54(10):886–91.</mixed-citation><mixed-citation xml:lang="ru">Quinlivan R., Jungbluth H. Myopathic causes of exercise intolerance with rhabdomyolysis. Dev Med Child Neurol 2012; 54(10):886–91.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18. Rosenberg H., Davis M., James D. et al. Malignant hyperthermia. Orphanet J Rare Dis 2007;2:21.</mixed-citation><mixed-citation xml:lang="ru">Rosenberg H., Davis M., James D. et al. Malignant hyperthermia. Orphanet J Rare Dis 2007;2:21.</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19. Shapiro M.L., Baldea A., Luchette F.A. Rhabdomyolysis in the intensive care unit. J Intensive Care Med 2012;27(6):335–42.</mixed-citation><mixed-citation xml:lang="ru">Shapiro M.L., Baldea A., Luchette F.A. Rhabdomyolysis in the intensive care unit. J Intensive Care Med 2012;27(6):335–42.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20. Cervellin G., Comelli I., Lippi G. Rhabdomyolysis: historical background, clinical, diagnostic and therapeutic features. Clin Chem Lab Med 2010;48(6):749–56.</mixed-citation><mixed-citation xml:lang="ru">Cervellin G., Comelli I., Lippi G. Rhabdomyolysis: historical background, clinical, diagnostic and therapeutic features. Clin Chem Lab Med 2010;48(6):749–56.</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21. Luck R.P., Verbin S. Rhabdomyolysis: a review of clinical presentation, etiology, diagnosis, and management. Pediatr Emerg Care 2008;24(4):262–8.</mixed-citation><mixed-citation xml:lang="ru">Luck R.P., Verbin S. Rhabdomyolysis: a review of clinical presentation, etiology, diagnosis, and management. Pediatr Emerg Care 2008;24(4):262–8.</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">22. Hotamisligil G.S., Shargill N.S., Spiegelman B.M. Adipose expression of tumor necrosis factor-alpha: direct role in obesitylinked insulin resistance. Science. 1993;259(5091):87–91.</mixed-citation><mixed-citation xml:lang="ru">Hotamisligil G.S., Shargill N.S., Spiegelman B.M. Adipose expression of tumor necrosis factor-alpha: direct role in obesitylinked insulin resistance. Science. 1993;259(5091):87–91.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">23. Xu H., Barnes G.T., Yang Q. et al. Chronic inflammation in fat plays a crucial role in the development of obesity-related insulin resistance. J Clin Invest 2003;112(12): 1821–30.</mixed-citation><mixed-citation xml:lang="ru">Xu H., Barnes G.T., Yang Q. et al. Chronic inflammation in fat plays a crucial role in the development of obesity-related insulin resistance. J Clin Invest 2003;112(12): 1821–30.</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">24. Weisberg S.P., McCann D., Desai M. et al. Obesity is associated with macrophage accumulation in adipose tissue. J Clin Invest 2003; 112(12):1796–808.</mixed-citation><mixed-citation xml:lang="ru">Weisberg S.P., McCann D., Desai M. et al. Obesity is associated with macrophage accumulation in adipose tissue. J Clin Invest 2003; 112(12):1796–808.</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">25. Molenaar J.P., Voermans N.C., van Hoeve B.J et al. Fever-induced recurrent rhabdomyolysis due to a novel mutation in the ryanodine receptor type 1 gene. Intern Med J 2014; 44(8):819–20.</mixed-citation><mixed-citation xml:lang="ru">Molenaar J.P., Voermans N.C., van Hoeve B.J et al. Fever-induced recurrent rhabdomyolysis due to a novel mutation in the ryanodine receptor type 1 gene. Intern Med J 2014; 44(8):819–20.</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">26. East C., Alivizatos P.A., Grundy S.M. et al. Rhabdomyolysis in patients receiving lovastatin after cardiac transplantation. N Engl J Med 1988;318(1):47–8.</mixed-citation><mixed-citation xml:lang="ru">East C., Alivizatos P.A., Grundy S.M. et al. Rhabdomyolysis in patients receiving lovastatin after cardiac transplantation. N Engl J Med 1988;318(1):47–8.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">27. Santos J. Jr. Exertional rhabdomyolysis. Potentially life-threatening consequence of intense exercise. JAAPA 1999;12(7):46–9, 53–5.</mixed-citation><mixed-citation xml:lang="ru">Santos J. Jr. Exertional rhabdomyolysis. Potentially life-threatening consequence of intense exercise. JAAPA 1999;12(7):46–9, 53–5.</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">28. Hopkins P.M. Malignant hyperthermia: advances in clinical management and diagnosis. Br J Anaesth 2000;85(1):118–28.</mixed-citation><mixed-citation xml:lang="ru">Hopkins P.M. Malignant hyperthermia: advances in clinical management and diagnosis. Br J Anaesth 2000;85(1):118–28.</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">29. Späte U., Schulze P.C. Proinflammatory cytokines and skeletal muscle. Curr Opin Clin Nutr Metab Care 2004;7(3):265–9.</mixed-citation><mixed-citation xml:lang="ru">Späte U., Schulze P.C. Proinflammatory cytokines and skeletal muscle. Curr Opin Clin Nutr Metab Care 2004;7(3):265–9.</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">30. Ostrowski K., Rohde T., Asp S. et al. Chemokines are elevated in plasma after strenuous exercise in humans. Eur J Appl Physiol 2001;84(3):244–5.</mixed-citation><mixed-citation xml:lang="ru">Ostrowski K., Rohde T., Asp S. et al. Chemokines are elevated in plasma after strenuous exercise in humans. Eur J Appl Physiol 2001;84(3):244–5.</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">31. Chen X., Xun K., Chen L. et al. TNFalpha, a potent lipid metabolism regulator. Cell Biochem Funct 2009;27(7):407–16.</mixed-citation><mixed-citation xml:lang="ru">Chen X., Xun K., Chen L. et al. TNFalpha, a potent lipid metabolism regulator. Cell Biochem Funct 2009;27(7):407–16.</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">32. Feingold K.R., Grunfeld C. Tumor necrosis factor-alpha stimulates hepatic lipogenesis in the rat in vivo. J Clin Invest 1987;80(1):184–90.</mixed-citation><mixed-citation xml:lang="ru">Feingold K.R., Grunfeld C. Tumor necrosis factor-alpha stimulates hepatic lipogenesis in the rat in vivo. J Clin Invest 1987;80(1):184–90.</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">33. Grunfeld C., Adi S., Soued M. et al. Search for mediators of the lipogenic effects of tumor necrosis factor: potential role for interleukin 6. Cancer Res 1990;50(14): 4233–8.</mixed-citation><mixed-citation xml:lang="ru">Grunfeld C., Adi S., Soued M. et al. Search for mediators of the lipogenic effects of tumor necrosis factor: potential role for interleukin 6. Cancer Res 1990;50(14): 4233–8.</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">34. Vallerie S.N., Hotamisligil G.S. The role of JNK proteins in metabolism. Sci Transl Med 2010;2(60):60rv5.</mixed-citation><mixed-citation xml:lang="ru">Vallerie S.N., Hotamisligil G.S. The role of JNK proteins in metabolism. Sci Transl Med 2010;2(60):60rv5.</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">35. Chen C.W., Lin J., Chu Y.W. iStable: offtheshelf predictor integration for predicting protein stability changes. BMC Bioinformatics 2013;14 Suppl 2:S5.</mixed-citation><mixed-citation xml:lang="ru">Chen C.W., Lin J., Chu Y.W. iStable: offtheshelf predictor integration for predicting protein stability changes. BMC Bioinformatics 2013;14 Suppl 2:S5.</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">36. Yao D.C., Tolan D.R., Murray M.F. et al. Hemolytic anemia and severe rhabdomyolysis caused by compound heterozygous mutations of the gene for erythrocyte/muscle isozyme of aldolase, ALDO A(Arg303X/Cys338Tyr). Blood 2004;103(6):2401–3.</mixed-citation><mixed-citation xml:lang="ru">Yao D.C., Tolan D.R., Murray M.F. et al. Hemolytic anemia and severe rhabdomyolysis caused by compound heterozygous mutations of the gene for erythrocyte/muscle isozyme of aldolase, ALDO A(Arg303X/Cys338Tyr). Blood 2004;103(6):2401–3.</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">37. Michot C., Mamoune A., Vamecq J. et al. Combination of lipid metabolism alterations and their sensitivity to inflammatory cytokines in human lipin-1-deficient myoblasts. Biochim Biophys Acta 2013;1832(12):2103–14.</mixed-citation><mixed-citation xml:lang="ru">Michot C., Mamoune A., Vamecq J. et al. Combination of lipid metabolism alterations and their sensitivity to inflammatory cytokines in human lipin-1-deficient myoblasts. Biochim Biophys Acta 2013;1832(12):2103–14.</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">38. van Adel B.A., Tarnopolsky M.A. Metabolic myopathies: update 2009. J Clin Neuromuscul Dis 2009;10(3):97–121.</mixed-citation><mixed-citation xml:lang="ru">van Adel B.A., Tarnopolsky M.A. Metabolic myopathies: update 2009. J Clin Neuromuscul Dis 2009;10(3):97–121.</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">39. Kreuder J., Borkhardt A., Repp R. et al. Brief report: inherited metabolic myopathy and hemolysis due to a mutation in aldolase A. N Engl J Med 1996;334(17):1100–4.</mixed-citation><mixed-citation xml:lang="ru">Kreuder J., Borkhardt A., Repp R. et al. Brief report: inherited metabolic myopathy and hemolysis due to a mutation in aldolase A. N Engl J Med 1996;334(17):1100–4.</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">40. Miwa S., Fujii H., Tani K. et al. Two cases of red cell aldolase deficiency associated with hereditary hemolytic anemia in a Japanese family. Am J Hematol 1981;11(4):425–37.</mixed-citation><mixed-citation xml:lang="ru">Miwa S., Fujii H., Tani K. et al. Two cases of red cell aldolase deficiency associated with hereditary hemolytic anemia in a Japanese family. Am J Hematol 1981;11(4):425–37.</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">41. Beutler E., Scott S., Bishop A. et al. Red cell aldolase deficiency and hemolytic anemia: a new syndrome. Trans Assoc Am Physicians 1973;86:154–66.</mixed-citation><mixed-citation xml:lang="ru">Beutler E., Scott S., Bishop A. et al. Red cell aldolase deficiency and hemolytic anemia: a new syndrome. Trans Assoc Am Physicians 1973;86:154–66.</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">42. Kishi H., Mukai T., Hirono A. et al. Human aldolase A deficiency associated with a hemolytic anemia: thermolabile aldolase due to a single base mutation. Proc Natl Acad Sci USA 1987;84(23):8623–7.</mixed-citation><mixed-citation xml:lang="ru">Kishi H., Mukai T., Hirono A. et al. Human aldolase A deficiency associated with a hemolytic anemia: thermolabile aldolase due to a single base mutation. Proc Natl Acad Sci USA 1987;84(23):8623–7.</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">43. Pacheco P., Vieira-de-Abreu A., Gomes R.N. et al. Monocyte chemoattractant protein-1/CC chemokine ligand 2 controls microtubule-driven biogenesis and leukotriene B4-synthesizing function of macrophage lipid bodies elicited by innate immune response. J Immunol 2007;179(12):8500–8.</mixed-citation><mixed-citation xml:lang="ru">Pacheco P., Vieira-de-Abreu A., Gomes R.N. et al. Monocyte chemoattractant protein-1/CC chemokine ligand 2 controls microtubule-driven biogenesis and leukotriene B4-synthesizing function of macrophage lipid bodies elicited by innate immune response. J Immunol 2007;179(12):8500–8.</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">44. Gomes R.N., Figueiredo R.T., Bozza F.A. et al. Increased susceptibility to septic and endotoxic shock in monocyte chemoattractant protein 1/cc chemokine ligand 2-deficient mice correlates with reduced interleukin 10 and enhanced macrophage migration inhibitory factor production. Shock 2006;26(5):457–63.</mixed-citation><mixed-citation xml:lang="ru">Gomes R.N., Figueiredo R.T., Bozza F.A. et al. Increased susceptibility to septic and endotoxic shock in monocyte chemoattractant protein 1/cc chemokine ligand 2-deficient mice correlates with reduced interleukin 10 and enhanced macrophage migration inhibitory factor production. Shock 2006;26(5):457–63.</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><citation-alternatives><mixed-citation xml:lang="en">45. Beernink P.T., Tolan D.R. Subunit interface mutants of rabbit muscle aldolase form active dimers. Protein Sci 1994;3(9):1383–91.</mixed-citation><mixed-citation xml:lang="ru">Beernink P.T., Tolan D.R. Subunit interface mutants of rabbit muscle aldolase form active dimers. Protein Sci 1994;3(9):1383–91.</mixed-citation></citation-alternatives></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">46. Takahashi I., Takasaki Y., Hori K. Sitedirected mutagenesis of human aldolase isozymes: the role of Cys-72 and Cys-338 residues of aldolase A and of the carboxyterminal Tyr residues of aldolases A and B. J Biochem 1989;105(2):281–6.</mixed-citation><mixed-citation xml:lang="ru">Takahashi I., Takasaki Y., Hori K. Sitedirected mutagenesis of human aldolase isozymes: the role of Cys-72 and Cys-338 residues of aldolase A and of the carboxyterminal Tyr residues of aldolases A and B. J Biochem 1989;105(2):281–6.</mixed-citation></citation-alternatives></ref><ref id="B47"><label>47.</label><citation-alternatives><mixed-citation xml:lang="en">47. Tsantes A.E., Bonovas S., Travlou A. et al. Redox imbalance, macrocytosis, and RBC homeostasis. Antioxid Redox Signal 2006;8 (7–8):1205–16.</mixed-citation><mixed-citation xml:lang="ru">Tsantes A.E., Bonovas S., Travlou A. et al. Redox imbalance, macrocytosis, and RBC homeostasis. Antioxid Redox Signal 2006;8 (7–8):1205–16.</mixed-citation></citation-alternatives></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">48. Marinkovic D., Zhang X., Yalcin S. et al. Foxo3 is required for the regulation of oxidative stress in erythropoiesis. J Clin Invest 2007;117(8):2133–44.</mixed-citation><mixed-citation xml:lang="ru">Marinkovic D., Zhang X., Yalcin S. et al. Foxo3 is required for the regulation of oxidative stress in erythropoiesis. J Clin Invest 2007;117(8):2133–44.</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">49. Matés J.M, Pérez-Gómez C., Olalla L. et al. Allergy to drugs: antioxidant enzymic activities, lipid peroxidation and protein oxidative damage in human blood. Cell Biochem Funct 2000;18(2):77–84.</mixed-citation><mixed-citation xml:lang="ru">Matés J.M, Pérez-Gómez C., Olalla L. et al. Allergy to drugs: antioxidant enzymic activities, lipid peroxidation and protein oxidative damage in human blood. Cell Biochem Funct 2000;18(2):77–84.</mixed-citation></citation-alternatives></ref><ref id="B50"><label>50.</label><citation-alternatives><mixed-citation xml:lang="en">50. Crawford J.H., Isbell T.S., Huang Z. et al. Hypoxia, red blood cells, and nitrite regulate NO-dependent hypoxic vasodilation. Blood 2006;107(2):566–74.</mixed-citation><mixed-citation xml:lang="ru">Crawford J.H., Isbell T.S., Huang Z. et al. Hypoxia, red blood cells, and nitrite regulate NO-dependent hypoxic vasodilation. Blood 2006;107(2):566–74.</mixed-citation></citation-alternatives></ref><ref id="B51"><label>51.</label><citation-alternatives><mixed-citation xml:lang="en">51. Berendse K., Ebberink M.S., Ijlst L. et al. Arginine improves peroxisome functioning in cells from patients with a mild peroxisome biogenesis disorder. Orphanet J Rare Dis 2013;8:138.</mixed-citation><mixed-citation xml:lang="ru">Berendse K., Ebberink M.S., Ijlst L. et al. Arginine improves peroxisome functioning in cells from patients with a mild peroxisome biogenesis disorder. Orphanet J Rare Dis 2013;8:138.</mixed-citation></citation-alternatives></ref><ref id="B52"><label>52.</label><citation-alternatives><mixed-citation xml:lang="en">52. Roth S.D., Schüttrumpf J., Milanov P. et al. Chemical chaperones improve protein secretion and rescue mutant factor VIII in mice with hemophilia A. PLoS One 2012;7(9):e44505.</mixed-citation><mixed-citation xml:lang="ru">Roth S.D., Schüttrumpf J., Milanov P. et al. Chemical chaperones improve protein secretion and rescue mutant factor VIII in mice with hemophilia A. PLoS One 2012;7(9):e44505.</mixed-citation></citation-alternatives></ref><ref id="B53"><label>53.</label><citation-alternatives><mixed-citation xml:lang="en">53. Senesi P., Luzi L., Montesano A. et al. Betaine supplement enhances skeletal muscle differentiation in murine myoblasts via IGF-1 signaling activation. J Transl Med 2013; 11:174.</mixed-citation><mixed-citation xml:lang="ru">Senesi P., Luzi L., Montesano A. et al. Betaine supplement enhances skeletal muscle differentiation in murine myoblasts via IGF-1 signaling activation. J Transl Med 2013; 11:174.</mixed-citation></citation-alternatives></ref></ref-list></back></article>
