<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<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">120</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="ru">Опыт ведения пациентов с болезнью Фабри после изменения дозы или смены препарата в процессе проведения ферментозаместительной терапии</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Weidemann</surname><given-names>F.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Krämer</surname><given-names>J.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Duning</surname><given-names>T.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Lenders</surname><given-names>M.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name><surname>Canaan-Kühl</surname><given-names>S.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name><surname>Krebs</surname><given-names>A.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name><surname>González</surname><given-names>H. G.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff5"/></contrib><contrib contrib-type="author"><name><surname>Sommer</surname><given-names>C.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff5"/></contrib><contrib contrib-type="author"><name><surname>Üçeyler</surname><given-names>N.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff6"/></contrib><contrib contrib-type="author"><name><surname>Niemann</surname><given-names>M.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff6"/></contrib><contrib contrib-type="author"><name><surname>Störk</surname><given-names>S.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Schelleckes</surname><given-names>M.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name><surname>Reiermann</surname><given-names>S.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name><surname>Stypmann</surname><given-names>J.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff7"/></contrib><contrib contrib-type="author"><name><surname>Brand</surname><given-names>S.-M.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff8"/></contrib><contrib contrib-type="author"><name><surname>Wanner</surname><given-names>C.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Brand</surname><given-names>E.</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff3"/></contrib></contrib-group><aff id="aff1"><institution>Department of Medicine, Divisions of Cardiology and Nephrology, Comprehensive Heart Failure Center, Fabry Center for Interdisciplinary Therapy</institution></aff><aff id="aff2"><institution>Department of Neurology Divisions of Cardiology and Nephrology, Comprehensive Heart Failure Center, Fabry Center for Interdisciplinary Therapy</institution></aff><aff id="aff3"><institution>Internal Medicine D, Department of Nephrology, Hypertension and Rheumatology, Interdisciplinary Fabry Center Muenster</institution></aff><aff id="aff4"><institution>Department of Medicine, Charité, Campus Virchow-Klinikum, Berlin, Germany</institution></aff><aff id="aff5"><institution>Department of Neurology, University of Wuerzburg, Wuerzburg, Germany</institution></aff><aff id="aff6"><institution></institution></aff><aff id="aff7"><institution>Department of Cardiovascular Medicine, Division of Cardiology</institution></aff><aff id="aff8"><institution>Institute of Sports Medicine, Molecular Genetics of Cardiovascular Disease, &#13;
University Hospital Muenster, Muenster, Germany</institution></aff><pub-date date-type="pub" iso-8601-date="2015-09-21" publication-format="electronic"><day>21</day><month>09</month><year>2015</year></pub-date><volume>5</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>15</fpage><lpage>30</lpage><history><date date-type="received" iso-8601-date="2015-09-21"><day>21</day><month>09</month><year>2015</year></date><date date-type="accepted" iso-8601-date="2015-09-21"><day>21</day><month>09</month><year>2015</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2015, ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., .</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2015, Weidemann F., Krämer J., Duning T., Lenders M., Canaan-Kühl S., Krebs A., González H.G., Sommer C., Üçeyler N., Niemann M., Störk S., Schelleckes M., Reiermann S., Stypmann J., Brand S., Wanner C., Brand E.</copyright-statement><copyright-year>2015</copyright-year><copyright-holder xml:lang="en">., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., .</copyright-holder><copyright-holder xml:lang="ru">Weidemann F., Krämer J., Duning T., Lenders M., Canaan-Kühl S., Krebs A., González H.G., Sommer C., Üçeyler N., Niemann M., Störk S., Schelleckes M., Reiermann S., Stypmann J., Brand S., Wanner C., Brand E.</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/120">https://nmb.abvpress.ru/jour/article/view/120</self-uri><abstract xml:lang="ru"><p/></abstract><kwd-group xml:lang="ru"><kwd>болезнь Фабри</kwd><kwd>болезни накопления</kwd><kwd>лизомальные болезни</kwd><kwd>Х-сцепленная лизосомальная болезнь</kwd><kwd>глоботри- аозилцерамид</kwd><kwd>GL-3</kwd><kwd>Gb3</kwd><kwd>гликосфинголипиды</kwd><kwd>кардиомиопатия</kwd><kwd>почечная недостаточность</kwd><kwd>микроальбуминурия</kwd><kwd>ферменто- заместительная терапия</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. Desnick R., Ionnou Y., Eng C. Fabry disease: alpha galactosidase A deficiency. In: The metabolic and molecular bases of inherited disease. Ed. by Scriver C., Beaudet A., Sly W., Valle D., New York, McGraw-Hill, 1995, pp. 2741– 2784.</mixed-citation><mixed-citation xml:lang="ru">Desnick R., Ionnou Y., Eng C. Fabry disease: alpha galactosidase A deficiency. In: The metabolic and molecular bases of inherited disease. Ed. by Scriver C., Beaudet A., Sly W., Valle D., New York, McGraw-Hill, 1995, pp. 2741– 2784.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Zarate Y.A., Hopkin R.J. Fabry’s disease. Lancet 2008;372:1427–35.</mixed-citation><mixed-citation xml:lang="ru">Zarate Y.A., Hopkin R.J. Fabry’s disease. Lancet 2008;372:1427–35.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. Desnick R.J., Brady R., Barranger J. et al. Fabry disease, an under-recognized multisystemic disorder: Expert recommendations for diagnosis, management, and enzyme replacement therapy. Ann Intern Med 2003;138:338–46.</mixed-citation><mixed-citation xml:lang="ru">Desnick R.J., Brady R., Barranger J. et al. Fabry disease, an under-recognized multisystemic disorder: Expert recommendations for diagnosis, management, and enzyme replacement therapy. Ann Intern Med 2003;138:338–46.</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. Banikazemi M., Bultas J., Waldek S. et al. Fabry Disease Clinical Trial Study Group: Agalsidase-beta therapy for advanced Fabry disease: A randomized trial. Ann Intern Med 2007;146:77–86.</mixed-citation><mixed-citation xml:lang="ru">Banikazemi M., Bultas J., Waldek S. et al. Fabry Disease Clinical Trial Study Group: Agalsidase-beta therapy for advanced Fabry disease: A randomized trial. Ann Intern Med 2007;146:77–86.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Eng C.M., Guffon N., Wilcox W.R. et al. International Collaborative FabryDisease Study Group: Safety and efficacy of recombinant human alpha-galactosidase A – replacement therapy in Fabry’s disease. N Engl J Med 2001;345:9–16.</mixed-citation><mixed-citation xml:lang="ru">Eng C.M., Guffon N., Wilcox W.R. et al. International Collaborative FabryDisease Study Group: Safety and efficacy of recombinant human alpha-galactosidase A – replacement therapy in Fabry’s disease. N Engl J Med 2001;345:9–16.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Hughes D.A., Elliott P.M., Shah J. et al. Effects of enzyme replacement therapy on the cardiomyopathy of Anderson-Fabry disease: A randomised, double-blind, placebocontrolled clinical trial of agalsidase alfa. Heart 2008;94:153–8.</mixed-citation><mixed-citation xml:lang="ru">Hughes D.A., Elliott P.M., Shah J. et al. Effects of enzyme replacement therapy on the cardiomyopathy of Anderson-Fabry disease: A randomised, double-blind, placebocontrolled clinical trial of agalsidase alfa. Heart 2008;94:153–8.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. Mehta A., Beck M., Elliott P. et al. Fabry Outcome Survey investigators: Enzyme replacement therapy with agalsidase alfa in patients with Fabry’s disease: An analysis of registry data. Lancet 2009;374:1986–96.</mixed-citation><mixed-citation xml:lang="ru">Mehta A., Beck M., Elliott P. et al. Fabry Outcome Survey investigators: Enzyme replacement therapy with agalsidase alfa in patients with Fabry’s disease: An analysis of registry data. Lancet 2009;374:1986–96.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. Schiffmann R., Kopp J.B., Austin H.A. 3rd et al. Enzyme replacement therapy in Fabry disease: A randomized controlled trial. JAMA 2001;285:2743–9.</mixed-citation><mixed-citation xml:lang="ru">Schiffmann R., Kopp J.B., Austin H.A. 3rd et al. Enzyme replacement therapy in Fabry disease: A randomized controlled trial. JAMA 2001;285:2743–9.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Wraith J.E., Tylki-Szymanska A., Guffon N. et al. Safety and efficacy of enzyme replacement therapy with agalsidase beta: An international, open-label study in pediatric patients with Fabry disease. J Pediatr 2008;152:563–70.</mixed-citation><mixed-citation xml:lang="ru">Wraith J.E., Tylki-Szymanska A., Guffon N. et al. Safety and efficacy of enzyme replacement therapy with agalsidase beta: An international, open-label study in pediatric patients with Fabry disease. J Pediatr 2008;152:563–70.</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. Tsuboi K., Yamamoto H. Clinical observation of patients with Fabry disease after switching from agalsidase beta (Fabrazyme) to agalsidase alfa (Replagal). Genet Med 2012;14:779–86.</mixed-citation><mixed-citation xml:lang="ru">Tsuboi K., Yamamoto H. Clinical observation of patients with Fabry disease after switching from agalsidase beta (Fabrazyme) to agalsidase alfa (Replagal). Genet Med 2012;14:779–86.</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. Linthorst G.E., Germain D.P., Hollak C.E. et al. European Medicines Agency: Expert opinion on temporary treatment recommendations for Fabry disease during the shortage of enzyme replacement therapy (ERT). Mol Genet Metab 2011;102:99–102.</mixed-citation><mixed-citation xml:lang="ru">Linthorst G.E., Germain D.P., Hollak C.E. et al. European Medicines Agency: Expert opinion on temporary treatment recommendations for Fabry disease during the shortage of enzyme replacement therapy (ERT). Mol Genet Metab 2011;102:99–102.</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. Pisani A., Spinelli L., Visciano B. et al. Effects of switching from agalsidase Betato agalsidase alfa in 10 patients with andersonfabry disease. JIMD Rep 2013;9:41–8.</mixed-citation><mixed-citation xml:lang="ru">Pisani A., Spinelli L., Visciano B. et al. Effects of switching from agalsidase Betato agalsidase alfa in 10 patients with andersonfabry disease. JIMD Rep 2013;9:41–8.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13. Smid B.E., Rombach S.M., Aerts J.M. et al. Consequences of a global enzyme shortage of agalsidase beta in adult Dutch Fabry patients. Orphanet J Rare Dis 2011;6:69.</mixed-citation><mixed-citation xml:lang="ru">Smid B.E., Rombach S.M., Aerts J.M. et al. Consequences of a global enzyme shortage of agalsidase beta in adult Dutch Fabry patients. Orphanet J Rare Dis 2011;6:69.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14. Weidemann F., Breunig F., Beer M. et al. Improvement of cardiac function during enzyme replacement therapy in patients with Fabry disease: A prospective strain rate imaging study. Circulation 2003;108:1299–301.</mixed-citation><mixed-citation xml:lang="ru">Weidemann F., Breunig F., Beer M. et al. Improvement of cardiac function during enzyme replacement therapy in patients with Fabry disease: A prospective strain rate imaging study. Circulation 2003;108:1299–301.</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15. Weidemann F., Niemann M., Breunig F. et al. Long-termeffects of enzyme replacement therapy on fabry cardiomyopathy: Evidence for a better outcome with early treatment. Circulation 2009;119:524–9.</mixed-citation><mixed-citation xml:lang="ru">Weidemann F., Niemann M., Breunig F. et al. Long-termeffects of enzyme replacement therapy on fabry cardiomyopathy: Evidence for a better outcome with early treatment. Circulation 2009;119:524–9.</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16. Feriozzi S., Torras J., Cybulla M. et al. FOS Investigators: The effectiveness of longterm agalsidase alfa therapy in the treatment of Fabry nephropathy. Clin J Am Soc Nephrol 2012;7:60–9.</mixed-citation><mixed-citation xml:lang="ru">Feriozzi S., Torras J., Cybulla M. et al. FOS Investigators: The effectiveness of longterm agalsidase alfa therapy in the treatment of Fabry nephropathy. Clin J Am Soc Nephrol 2012;7:60–9.</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17. Germain D.P., Waldek S., Banikazemi M. et al. Sustained, long-term renal stabilization after 54 months of agalsidase beta therapy in patients with Fabry disease. J Am Soc Nephrol 2007;18:1547–57.</mixed-citation><mixed-citation xml:lang="ru">Germain D.P., Waldek S., Banikazemi M. et al. Sustained, long-term renal stabilization after 54 months of agalsidase beta therapy in patients with Fabry disease. J Am Soc Nephrol 2007;18:1547–57.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18. West M., Nicholls K., Mehta A. et al. Agalsidase alfa and kidney dysfunction in Fabry disease. J Am Soc Nephrol 2009;20:1132–9.</mixed-citation><mixed-citation xml:lang="ru">West M., Nicholls K., Mehta A. et al. Agalsidase alfa and kidney dysfunction in Fabry disease. J Am Soc Nephrol 2009;20:1132–9.</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19. Najafian B., Svarstad E., Bostad L. et al. Progressive podocyte injury and globotriao sylceramide (GL-3) accumulation in young patients with Fabry disease. Kidney Int 2011;79:663–70.</mixed-citation><mixed-citation xml:lang="ru">Najafian B., Svarstad E., Bostad L. et al. Progressive podocyte injury and globotriao sylceramide (GL-3) accumulation in young patients with Fabry disease. Kidney Int 2011;79:663–70.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20. Gansevoort R.T., de Jong P.E. The case for using albuminuria in staging chronic kidney disease. J Am Soc Nephrol 2009;20:465–8.</mixed-citation><mixed-citation xml:lang="ru">Gansevoort R.T., de Jong P.E. The case for using albuminuria in staging chronic kidney disease. J Am Soc Nephrol 2009;20:465–8.</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21. Miettinen H., Haffner S.M., Lehto S. et al. Proteinuria predicts stroke and other atherosclerotic vascular disease events in nondiabetic and non-insulin-dependent diabetic subjects. Stroke 1996;27:2033–9.</mixed-citation><mixed-citation xml:lang="ru">Miettinen H., Haffner S.M., Lehto S. et al. Proteinuria predicts stroke and other atherosclerotic vascular disease events in nondiabetic and non-insulin-dependent diabetic subjects. Stroke 1996;27:2033–9.</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">22. de Zeeuw D., Parving H.H., Henning R.H. Microalbuminuria as an early marker for cardiovascular disease. J Am Soc Nephrol 2006;17:2100–5.</mixed-citation><mixed-citation xml:lang="ru">de Zeeuw D., Parving H.H., Henning R.H. Microalbuminuria as an early marker for cardiovascular disease. J Am Soc Nephrol 2006;17:2100–5.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">23. Linthorst G.E., Hollak C.E., Donker-Koopman W.E. et al. Enzyme therapy for Fabry disease: Neutralizing antibodies toward agalsidase alpha and beta. Kidney Int 2004;66:1589–95.</mixed-citation><mixed-citation xml:lang="ru">Linthorst G.E., Hollak C.E., Donker-Koopman W.E. et al. Enzyme therapy for Fabry disease: Neutralizing antibodies toward agalsidase alpha and beta. Kidney Int 2004;66:1589–95.</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">24. Tanaka A., Takeda T., Hoshina T. et al. Enzyme replacement therapy in a patient with Fabry disease and the development of IgE antibodies against agalsidase beta but not agalsidase alpha. J Inherit Metab Dis 2010;33 (Suppl 3):249–52.</mixed-citation><mixed-citation xml:lang="ru">Tanaka A., Takeda T., Hoshina T. et al. Enzyme replacement therapy in a patient with Fabry disease and the development of IgE antibodies against agalsidase beta but not agalsidase alpha. J Inherit Metab Dis 2010;33 (Suppl 3):249–52.</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">25. Helal I., Fick-Brosnahan G.M., Reed-Gitomer B., Schrier R.W. Glomerular hyperfiltration: Definitions, mechanisms and clinical implications. Nat Rev Nephrol 2012;8:293–300.</mixed-citation><mixed-citation xml:lang="ru">Helal I., Fick-Brosnahan G.M., Reed-Gitomer B., Schrier R.W. Glomerular hyperfiltration: Definitions, mechanisms and clinical implications. Nat Rev Nephrol 2012;8:293–300.</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">26. Levey A.S., Stevens L.A., Schmid C.H. et al. CKD-EPI (Chronic Kidney Disease Epidemiology Collaboration): A new equation to estimate glomerular filtration rate. Ann Intern Med 2009;150:604–12.</mixed-citation><mixed-citation xml:lang="ru">Levey A.S., Stevens L.A., Schmid C.H. et al. CKD-EPI (Chronic Kidney Disease Epidemiology Collaboration): A new equation to estimate glomerular filtration rate. Ann Intern Med 2009;150:604–12.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">27. Von Korff M., Ormel J., Keefe F.J., Dworkin S.F. Grading the severity of chronic pain. Pain 1992;50:133–49.</mixed-citation><mixed-citation xml:lang="ru">Von Korff M., Ormel J., Keefe F.J., Dworkin S.F. Grading the severity of chronic pain. Pain 1992;50:133–49.</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">28. Sommer C., Richter H., Rogausch J.P. et al. A modified score to identify and discriminate neuropathic pain: A study on the German version of the Neuropathic Pain Symptom Inventory (NPSI). BMC Neurol 2011;11:104.</mixed-citation><mixed-citation xml:lang="ru">Sommer C., Richter H., Rogausch J.P. et al. A modified score to identify and discriminate neuropathic pain: A study on the German version of the Neuropathic Pain Symptom Inventory (NPSI). BMC Neurol 2011;11:104.</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">29. Rolke R., Baron R., Maier C. et al. Quantitative sensory testing in the German Research Network on Neuropathic Pain (DFNS): Standardized protocol and reference values. Pain 2006;123:231–43.</mixed-citation><mixed-citation xml:lang="ru">Rolke R., Baron R., Maier C. et al. Quantitative sensory testing in the German Research Network on Neuropathic Pain (DFNS): Standardized protocol and reference values. Pain 2006;123:231–43.</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">30. Fukuda K., Straus S.E., Hickie I. et al. International Chronic Fatigue Syndrome Study Group: The chronic fatigue syndrome: A comprehensive approach to its definition and study. Ann Intern Med 1994;121:953–9.</mixed-citation><mixed-citation xml:lang="ru">Fukuda K., Straus S.E., Hickie I. et al. International Chronic Fatigue Syndrome Study Group: The chronic fatigue syndrome: A comprehensive approach to its definition and study. Ann Intern Med 1994;121:953–9.</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">31. Giannini E.H., Mehta A.B , Hilz M.J. et al. A validated disease severity scoring system for Fabry disease. Mol Genet Metab 2010;99:283–90.</mixed-citation><mixed-citation xml:lang="ru">Giannini E.H., Mehta A.B , Hilz M.J. et al. A validated disease severity scoring system for Fabry disease. Mol Genet Metab 2010;99:283–90.</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">32. Whybra C., Kampmann C., Krummenauer F. et al. Severity Score Index: A new instrument for quantifying the Anderson- Fabry disease phenotype, and the response of patients to enzyme replacement therapy. Clin Genet 2004;65:299–307.</mixed-citation><mixed-citation xml:lang="ru">Whybra C., Kampmann C., Krummenauer F. et al. Severity Score Index: A new instrument for quantifying the Anderson- Fabry disease phenotype, and the response of patients to enzyme replacement therapy. Clin Genet 2004;65:299–307.</mixed-citation></citation-alternatives></ref></ref-list></back></article>
