Лазерная терапия в онкологии
2011. Lacour J. Low-power laser and recurrent labial herpes // Ann. Dermatol. Venereol. – 2000, 127 (6–7): 652–656. [Article in French].
2012. Ladas E.J., Post-White J., Hawks R., Taromina K. Evidence for symptom management in the child with cancer // J. Pediatr. Hematol. Oncol. – 2006, 28 (9): 601–615.
2013. Lalla R.V., Bowen J., Barasch A. et al. MASCC/ISOO clinical practice guidelines for the management of mucositis secondary to cancer therapy // Cancer. – 2014, 120: 1453–1461. doi: 10.1002/cncr.28592.
2014. Lampl Y., Zivin J.A., Fisher M. et al. Infrared laser therapy for ischemic stroke: a new treatment strategy: results of the NeuroThera Effectiveness and Safety Trial-1 (NEST-1) // Stroke. – 2007, 38 (6): 1843–1849. 2015. Lanzafame R., Myakishev M., Stadler I. et al. Photoradiation at 670 nm does not influence UVB-induced squamous cell carcinoma in hairless mice treated after tumor induction // American Society for Laser Medicine and Surgery Тwenтy-NinтhAnnual ConferenceApril 1–5,Abstracts. – 2009, 41 (S21): 61–62.
2016. Lanzafame R.J. Photobiomodulation and cancer and other musings // Photomedicine and Laser Surgery. – 2011, 29 (1): 3–4. doi: 10.1089/pho.2011.9922.
2017. Lapchak P.A., De Taboada L. Transcranial near infrared laser treatment (NILT) increases cortical adenosi- ne-5’-triphosphate (ATP) content following embolic strokes in rabbits // Brain Res. – 2010, 1306 (8): 100–105. 2018. Lapchak P.A., Han M.K., Salgado K.F. et al. Safety profile of transcranial near-infrared laser therapy administered in combination with thrombolytic therapy to embolized rabbits // Stroke. – 2008, 39 (11): 3073–3078. 2019. Lapchak P.A., Salgado K.F., Chao C.H., Zivin J.A. Transcranial near-infrared light therapy improves motor function following embolic strokes in rabbits:An extended therapeutic window study using continuous and pulse frequency delivery modes // Neuroscience. – 2007, 148 (4): 907–914.
2020. Lapchak P.A., Wei J., Zivin J.A. Transcranial infrared laser therapy improves clinical rating scores after embolic strokes in rabbits // Stroke. – 2004, 35 (8): 1985–1988.
2021. Lapeyre M., Charra-Brunaud C., Kaminsky M.C. et al. Management of mucositis following radiotherapy forheadandneckcancers//CancerRadiother.–2001,5Suppl1:121s–130s.doi:10.1016/s1278-3218(01)80018- 4. [Article in French].
2022. Lara R.N., da Guerra E.N., de Melo N.S. Macroscopic and microscopic effects of GaAIAs diode laser and dexamethasone therapies on oral mucositis induced by fluorouracil in rats // Oral Health Prev. Dent. – 2007, 5 (1): 63–71.
2023. Lasinski B.B., Thrift K.M., Squire D. et al. A systematic review of the evidence for complete decongestive therapy in the treatment of lymphedema from 2004 to 2011 // PM&R. – 2012, 4 (8): 580–601. doi: 10.1016/j. pmrj.2012.05.003.
2024. Lau R.W.L., Cheing G.L.Y. Managing postmastectomy lymphedema with low-level laser therapy // Photomedicine and Laser Surgery. – 2009, 27 (5): 763–769. doi: 10.1089/pho.2008.2330.
2025. Leal N.F., Carrara H.H., Vieira K.F., Ferreira C.H. Physiotherapy treatments for breast cancer-related lymphedema: a literature review // Rev. Lat. Am. Enfermagem. – 2009, 17 (5): 730–736. doi: 10.1590/s010411692009000500021.
2026. Lee B.B., Bergan J., Rockson S.G. Lymphoedema: A Concise Compendium of Theory and Practice. – Springer-Verlag, London, 2011. – 599 p.
2027. Lee J.-Y., Kim I.-R., Park B.-S. et al. Effect of low-level laser therapy on oral keratinocytes exposed to bisphosphonate // Lasers in Medical Science. – 2015, 30 (2): 635–643. doi: 10.1007/s10103-013-1382-6. 2028. Lee N., Wigg J., Carroll J.D. The use of low level light therapy in the treatment of head and neck oedema // Journal of Lymphoedema. – 2013, 8 (1): 35–42.
2029. Legouté F., Bensadoun R.J., Seegers V. et al. Low-level laser therapy in treatment of chemoradiotherapyinduced mucositis in head and neck cancer: results of a randomised, triple blind, multicentre phase III trial // Radiat. Oncol. – 2019, 14 (1): 83. doi: 10.1186/s13014-019-1292-2.
2030. Lemanne D., Maizes V. Advising women undergoing treatment for breast cancer: A narrative review // J. Altern. Complement. Med. – 2018, 24 (9–10): 902–909. doi: 10.1089/acm.2018.0150.
2031. Li K., Zhang Z., Liu N.F. et al. Efficacy and safety of far infrared radiation in lymphedema treatment: clinical evaluation and laboratory analysis // Lasers in Medical Science. – 2017, 32 (3): 485–494. doi: 10.1007/ s10103-016-2135-0.
2032. Li L., Yuan L., Chen X. et al. Current treatments for breast cancer-related lymphoedema: a systematic review //Asian Pac. J. Cancer Prev. – 2016, 17 (11): 4875–4883. doi: 10.22034/APJCP.2016.17.11.4875.
2033. Li Q., Guo K., Kang J., Jiang B. Clinic analysis of endonasal low energy He-Ne laser treatment of 39 cases of intractable headache //ActaAcademiae medicinae Qingdao Universitatis. – 1998, 1: 53. [Article in Chinese]. 2034. Li X., Ferrel G.L., Guerra M.C. et al. Preliminary safety and efficacy results of laser immunotherapy for the treatment of metastatic breast cancer patients // Photochemical & Photobiological Sciences. – 2011, 10 (5): 817–821. doi: 10.1039/c0pp00306a.
940
Список литературы
2035. Lievens P. The influence of laser-irradiation on the motoricity of the lymphatic system and on the wound healing process // Proceedings from the International Congress on Laser in Medicine and Surgery, Bologna, 1985. – P. 171–174.
2036. Lievens P.C. The effect of a combined HeNe and I.R. laser treatment on the regeneration of the lymphatic system during the process of wound healing // Lasers in Medical Science. – 1991, 6 (2): 193–199. doi: 10.1007/ BF02032548.
2037. Lievens P.C. The effect of I.R. laser irradiation on the vasomotoricity of the lymphatic system // Lasers in Medical Science. – 1991(1), 6 (2): 189–191. doi: 10.1007/BF02032547.
2038. LimaA.A.M., Spínola L.G., Baccan G. et al. Evaluation of corticosterone and IL-1в, IL-6, IL-10 andTNF-β expression after 670-nm laser photobiomodulation in rats // Lasers in Medical Science. – 2014, 29 (2): 709–715. doi: 10.1007/s10103-013-1356-8.
2039. Lima A.G., Antequera R., Peres M.P. et al. Efficacy of low-level laser therapy and aluminum hydroxide in patients with chemotherapy and radiotherapy-induced oral mucositis // Braz. Dent. J. – 2010, 21 (3): 186–192. doi: 10.1590/s0103-64402010000300002.
2040. Lino M.D., Carvalho F.B., Oliveira L.R. et al. Laser phototherapy as a treatment for radiotherapy-induced oral mucositis // Braz. Dent. J. – 2011, 22 (2): 162–165. doi: 10.1590/s0103-64402011000200013.
2041. Litscher G., Litscher D. Alaser watch for simultaneous laser blood irradiation and laser acupuncture at the wrist // Integr. Med. Int. – 2016, 3: 75–81. doi: 10.1159/000448099.
2042. Liu T.C.Y. Indirect photobiomodulation on tumors // Lasers in Surgery and Medicine. – 2012, 44 (4): 358. 2043. Liu T.C.Y., Wu D.F., Gu Z.Q., Wu M. Applications of intranasal low intensity laser therapy in sports medicine // Journal of Innovation in Optical Health Science. – 2010, 3(1): 1–16. doi: 10.1142/s1793545810000836. 2044. Liu T.C.Y., Zhang J., Li X-E. The balance between normal and tumor tissues in phototherapy of tissues harboring cancer // Photomedicine and Laser Surgery. – 2013, 31 (3): 93–94. doi: 10.1089/pho.2012.3355.
2045. Liu Y-H., Ho C-C., Cheng C-C. et al. Photoradiation could influence the cytoskeleton organization and inhibit the survival of human hepatoma cells in vitro // Lasers in Medical Science. – 2006, 21 (1): 42–48. doi: 10.1007/s10103-005-0369-3.
2046. Lončar B., Stipetić M.M., Baričević M., Risović D. The effect of low-level laser therapy on salivary glands in patients with xerostomia // Photomedicine and Laser Surgery. – 2011, 29 (3): 171–175. doi: 10.1089/ pho.2010.2792.
2047. Lopes C.O., Mas J.R.I., Zângaro R.A. Low level laser therapy in the prevention of radiotherapy-induced xerostomia and oral mucositis // Radiol. Bras. – 2006, 39 (2): 131–136. [Article in Portuguese].
2048. Lopes N.N., Plapler H., Chavantes M.C. et al. Cyclooxygenase-2 and vascular endothelial growth factor expression in 5-fluorouracil-induced oral mucositis in hamsters: evaluation of two low-intensity laser protocols // Support Care Cancer. – 2009, 17 (11): 1409–1415. doi: 10.1007/s00520-009-0603-9.
2049. Lopes N.N.F., Plapler H., Lalla R.V. et al. Effectsoflow-levellasertherapyoncollagenexpressionandneu- trophil infiltrate in 5-fluorouracil-induced oral mucositis in hamsters // Lasers in Surgery and Medicine. – 2010, 42 (6): 546–552. doi: 10.1002/lsm.20920.
2050. Lopez T.C., Martins M.D., Pavesi V.C. et al. Effect of laser phototherapy in the prevention and treatment of chemo-induced mucositis in hamsters // Braz. Oral Res. – 2013, 27 (4): 342–348. doi: 10.1590/S180683242013005000019.
2051. Løvschall H., Arenholt-Bindslev D. Effect of low level diode laser irradiation of human oral mucosa fi broblasts in vitro // Lasers in Surgery and Medicine. – 1994, 14 (4): 347–354.
2052. Løvschall H., Scharff O., Foder B., Arenholdt-Bindslev D. Effect of low level laser irradiation on cytosolic Cа2+ in human neutrophils in vitro // Laser Therapy. – 1994, 6 (1): 31.
2053. Low-level laser therapy for preventing or treating oral mucositis caused by radiotherapy or chemotherapy: Interventional procedures guidance. – The National Institute for Health and Care Excellence (NICE), 2018. ISBN: 978-1-4731-2954-2.
2054. Lubart R., Friedman H., Sinyakov M. et al. Change in calcium transport in mammalian sperm mitochondria and plasma membranes caused by 780-nm irradiation // Lasers in Surgery and Medicine. – 1997, 21 (5): 493–499. 2055. Lubart R., Friedmann H., Sinyakov M. et al. The effect of HeNe laser (633 nm) radiation on intracellular Сa2+ concentration in fibroblasts // Laser Therapy. – 2005, 14 (0_Pilot_Issue_2): 35–40.
2056. Lubart R., Friedmann H., Sinyakov M. et al. The effect of HeNe laser (633 nm) radiation on intracellular Cа2+ concentration in fibroblasts // Laser Therapy. – 1997(1), 9 (3): 115–120.
2057. Luo L., Sun Z., Zhang L. et al. Effects of low-level laser therapy on ROS homeostasis and expression of IGF-1 and TGF-β1 in skeletal muscle during the repair process // Lasers in Medical Science. – 2012, 28 (3): 725–734.
2058. Mafra de Lima F., Costa M.S., Albertini R. et al. Low level laser therapy (LLLT):Attenuation of cholinergic hyperreactivity, β2-adrenergic hyporesponsiveness and TNF-α mRNA expression in rat bronchi segments in
941
Рекомендовано к покупке и изучению сайтом МедУнивер - https://meduniver.com/
Лазерная терапия в онкологии
E. coli lipopolysaccharide-induced airway inflammation by a NF-κB dependent mechanism // Lasers in Surgery and Medicine. – 2009, 41 (1): 68–74. doi: 10.1002/lsm.20735.
2059. Magné N., Pivot X., Marcy P.Y. et al. Concomitant bifractionated radiotherapy and chemotherapy with cisplatin and 5-fluorouracil in locally progressive, non-resectable epidermoid carcinomas of the pharynx: ten years experience at theAntoine Lacassagne center // Cancer Radiother. – 2001, 5 (4): 413–424. [Article in French].
2060. Magrini T.D., dos Santos N.V., Milazzotto M.P. et al. Low-level laser therapy on MCF-7 cells: a mic- ro-Fourier transform infrared spectroscopy study // J. Biomed. Opt. – 2012, 17 (10): 101516. doi: 10.1117/1. jbo.17.10.101516.
2061. Mahram M., Rajabi M.Treatment of lymphedema praecox through low level laser therapy (LLLT) // J. Res. Med. Sci. – 2011, 16 (6): 848–851.
2062. Maiya A., Olivia E., Dibya A. Effect of low energy laser therapy in the management of post-mastectomy lymphoedema // Physiotherapy Singapore. – 2008, 11 (1): 2–5.
2063. Mallick S., Benson R., Rath G.K. Radiation induced oral mucositis: a review of current literature on prevention and management // Eur.Arch. Otorhinolaryngol. – 2016, 273 (9): 2285–2293. doi: 10.1007/s00405-015- 3694-6.
2064. Manteifel V., Karu T. Activation of chromatin in T-lymphocytes under the He-Ne laser radiation // Proc. SPIE 3569, Effects of Low-Power Light on Biological Systems IV. – 1999: 12–16. doi: 10.1117/12.334394. 2065. Manteifel V., Karu T., Bakeeva L. Ultrastructural changes in chondriome of human lymphocytes after irradiation with He-Ne laser:Appearance of giant mitochondria // J. Photochem. Photobiol. B. – 1997, 38 (1): 25–30. doi: 10.1016/S1011-1344 (96)07426-X.
2066. Manteifel V.M., Andreichuk T.N., Karu T.I. Influence of He-Ne laser radiation and phytohemagglutinin on the ultrastructure of chromatin of human lymphocytes // Lasers in the Life Sciences. – 1994, 6 (1): 1–8.
2067. Manteifel V.M., Bakeeva L., Karu T.I. Ultrastructural changes in mitohondria of human lymphocytes after irradiation with HeNe laser: formation of giant mitochondria // Laser Therapy. – 1994(1), 6 (1): 20–21.
2068. Manteifel V.M., Karu T.I. Activation of chromatin inT-lymphocyte nuclei under the He-Ne laser radiation // Lasers in the Life Sciences. – 1998, 8 (3): 117–125.
2069. Marchese C., Chedid M., Dirsch O.R. et al. Modulation of keratinocyte growth factor and its receptor in reepithelializing human skin // J. Exp. Med. – 1995, 182 (5): 1369–1376.
2070. Marchesini R., Dasdia T., Melloni E., Rocca E. Effect of low-energy laser irradiation on colony formation capability in different human tumor cells in vitro // Lasers in Surgery and Medicine. – 1989, 9 (1): 59–62. 2071. Marín-Conde F., Castellanos-Cosano L., Pachón-Ibañez J. et al. Photobiomodulation with low-level laser therapy reduces oral mucositis caused by head and neck radio-chemotherapy: prospective randomized controlled trial // Int. J. Oral Maxillofac. Surg. – 2019, 48 (7): 917–923. doi: 10.1016/j.ijom.2018.12.006.
2072. Markovic A, Todorovic L. Effectiveness of dexamethasone and low-power laser in minimizing oedema after third molar surgery: a clinical trial // Int. J. Oral Maxillofac. Surg. – 2007, 36 (3): 226–229. doi: 10.1016/j. ijom.2006.10.006.
2073. Marotti J. Herpes // Lasers in dentistry: guide for clinical practice / P.M. de Freitas, A. Simões (Eds.). – Ames (USA), West Sussex, Oxford (UK): Blackwell Publishing, 2015. – P. 272–284.
2074. Martins M.A., Martins M.D., Lascala C.A. et al. Association of laser phototherapy with PRP improves healing of bisphosphonate-related osteonecrosis of the jaws in cancer patients: a preliminary study // Oral Oncol. – 2012, 48 (1): 79–84. doi: 10.1016/j.oraloncology.2011.08.010.
2075. Matsumoto Y., Akita Y. Safety guidelines for PDT of cutaneous lesions // Laser Therapy. – 2012, 21 (2): 124–128. doi: 10.5978/islsm.12-SG-03.
2076. Matsumura C., Ishikawa F., Imai M., Kemmotsu O. Useful effect of application of helium-neon LLLT on an early stage case of Herpes Zoster:Acase report // Laser Therapy. – 1993, 5 (1): 43–46. doi: 10.5978/islsm.93- CR-01.
2077. Matsumura Y., Moodycliffe A.M., Nghiem D.X. et al. Resistance of CD1d-/- mice to ultraviolet-induced skin cancer is associated with increased apoptosis //Am. J. Pathol. – 2004, 165 (3): 879–887. doi: 10.1016/s0002- 9440(10)63350-0.
2078. Mayrovitz H.N. The standard of care for lymphedema: current concepts and physiological considerations // Lymphat. Res. Biol. – 2009, 7: 101–108. doi: 10.1089/lrb.2009.0006.
2079. Mayrovitz H.N., Davey S. Changes in tissue water and indentation resistance of lymphedematous limbs accompanying low level laser therapy (LLLT) of fibrotic skin // Lymphology. – 2011, 44 (4): 168–177.
2080. Mazhari F., Shirazi A.S., Shabzendehdar M. Management of oral mucositis in pediatric patients receiving cancer therapy: A systematic review and meta-analysis // Pediatr. Blood Cancer. – 2019, 66 (3): e27403. doi: 10.1002/pbc.27403.
942
Список литературы
2081. McCallin M., Johnston J., Bassett S. How effective are physiotherapy techniques to treat established secondary lymphoedema following surgery for cancer?Acritical analysis of the literature // N. Z. J. Physiother. – 2005, 33 (3): 101–112.
2082. McGarvey A.C., Osmotherly P.G., Hoffman G.R. et al. Lymphoedema following treatment for head and neck cancer: impact on patients, and beliefs of health professionals // Eur. J. Cancer Care (Engl). – 2014, 23 (3): 317–327. doi: 10.1111/ecc.12134.
2083. McGuff P.E., Deterling R.A. Jr, Bushnell D. et al. Laser radiation of malignancies // Ann. NYAcad. Sci. – 1965, 122 (2): 747–757. doi: 10.1111/j.1749-6632.1965.tb20256.x.
2084. McGuff P.E., Deterling R.A. Jr, Gottlieb L.S. et al. Effects of laser radiation on tumor transplants // Federation Proceedings. – 1965(1), 24 (14): 150–154.
2085. McGuff P.E., Deterling R.A. Jr, Gottlieb L.S. et al. The laser treatment of experimental malignant tumours // Canad. Med.Ass. J. – 1964, 91 (21): 1089–1995.
2086. McNeely M.L., Peddle C.J., Yurick J.L. et al. Conservative and dietary interventions for cancer-related lymphedema: a systematic review and meta-analysis // Cancer. – 2011, 117 (6): 1136–1148. doi: 10.1002/cncr.25513. 2087. Medeiros N.J., Medeiros N.F., Santos C.C. et al. Low-power laser therapy in chemical-induced oral mucositis: a case study // Braz. J. Otorhinolaryngol. – 2013, 79 (6): 792. doi: 10.5935/1808-8694.20130143.
2088. Medeiros-Filho J.B., Maia Filho E.M., Ferreira M.C. Laser and photochemotherapy for the treatment of oral mucositis in young patients: randomized clinical trial // Photodiagnosis Photodyn. Ther. – 2017, 18: 39–45. doi: 10.1016/j.pdpdt.2017.01.004.
2089. Meneguzzo D.T., Lopes L.A., Pallota R. et al. Prevention and treatment of mice paw edema by near-infrared low-level laser therapy on lymph nodes // Lasers in Medical Science. – 2013, 28 (3): 973–980. doi: 10.1007/ s10103-012-1163-7.
2090. Merchant S.J., Chen S.L. Prevention and management of lymphedema after breast cancer treatment // Breast J. – 2015, 21 (3): 276–284. doi: 10.1111/tbj.12391.
2091. Metelitsa A.I., Dover J.S. Should we use light-emitting diode photomodulation to minimize radiation-indu- ced dermatitis? // Dermatol. Surg. – 2010, 36 (12): 1928–1929. doi: 10.1111/j.1524-4725.2010.01802.x.
2092. Michalikova S., Ennaceur A., van Rensburg R., Chazot P.L. Emotional responses and memory performance of middle-aged CD1 mice in a 3D maze: effects of low infrared light // Neurobiol. Learn. Mem. – 2008, 89 (4): 480–488.
2093. Migliorati C., Hewson I., Lalla R.V. et al. Systematic review of laser and other light therapy for the management of oral mucositis in cancer patients // Support Care Cancer. – 2013, 21 (1): 333–341. doi: 10.1007/ s00520-012-1605-6.
2094. Migliorati C., Massumoto C., De Paula Eduardo F. et al. Low-energy laser therapy in oral mucositis // J. Oral LaserAppl. – 2001, 1 (2): 97–101.
2095. Migliorati C.A., Oberle-Edwards L., Schubert M. The role of alternative and natural agents, cryotherapy, and/or laser for management of alimentary mucositis // Support Care Cancer. – 2006, 14 (6): 533–540.
2096. Mikhailov V.A., Denisov I.N., Frank G.A., Voltchenko N.N. Results of treatment of patients with IInd–IIIrd stage breast cancer by combination of low level laser therapy (LLLT) and surgery (10 – year experience). – Proc. SPIE 4166, Laser Florence’99: A Window on the Laser Medicine World, Vol. 40 (June 28, 2000). doi: org/10.1117/12.389507.
2097. Mikhailov V.A., Skobelkin O.K, Andreeva C.P., Petuchov M.I. Study of the accumulative function of tumour cells after the injection of haematoporphyrin derivatives under low-intensity laser energy irradiation // Laser Therapy. – 1994, 6 (4): 209–212.
2098. Mikhailov V.A., Skobelkin O.K., Denisov I.N. et al. Investigations on the influence of low level diode laser irradiation on the growth of experimental tumours // Laser Therapy. – 1993, 5 (1): 33–38.
2099. Mikhailov V.A., Sudakov I.B., Denisov I.N., Osin V.L. Use of low-level laser therapy (LLLT) for treatment of the patients with a cancer of esophagus T3N0Mx // VIII nternational Congress the European Medical Laser Association (EMLA), Dubrovnik-Cavtat, Croatia, June 22–25 May, 2000. – P. 69.
2100. Miller M.M., Donald D.V., Hagemann T.M. Prevention and treatment of oral mucositis in children with cancer // J. Pediatric Pharmacol. Ther. – 2012, 17: 340–350. doi: 10.5863/1551-6776-17.4.340.
2101. Milojević M., Kuruc V. Lowpowerlaserbiostimulationinthetreatmentofbronchialasthma//Med.Pregl.– 2003, 56 (9–10): 413–418. [Article in Serbian].
2102. Mognato M., Squizzato F., Facchin F. et al. Cell growth modulation of human cells irradiated in vitro with low-level laser therapy // Photomedicine and Laser Surgery. – 2004, 22 (6): 523–526. doi: 10.1089/ pho.2004.22.523.
2103. Monteiro J.S.D.C., de Oliveira S.C., Reis Júnior J.A. et al. Effects of imiquimod and low-intensity laser (λ660 nm) in chemically induced oral carcinomas in hamster buccal pouch mucosa // Lasers in Medical Science. – 2013, 28 (3): 1017–1024. doi: 10.1007/s10103-012-1192-2.
943
Рекомендовано к покупке и изучению сайтом МедУнивер - https://meduniver.com/
Лазерная терапия в онкологии
2104. Monteiro J.S.D.C., PinheiroA.L.B., de Oliveira S.C.P.S. et al. Influence of laser phototherapy (λ660 nm) on the outcome of oral chemical carcinogenesis on the hamster cheek pouch model: histological study // Photomedicine and Laser Surgery. – 2011, 29 (11): 741–745. doi: 10.1089/pho.2010.2896.
2105. Monteiro S.E., Resende L.V., Felicíssimo M.F. et al. Treatment of upper limb lymphedema with lowlevel laser: a systematic review // Fisioterapia em Movimento – 2014, 27 (4): 663–674. doi: 10.1590/01035150.027.004.ar01.
2106. Moore K.C. Laser therapy in post herpetic neuralgia // Laser Therapy. – 1996, 8 (1): 48.
2107. Moore K.C. Postherpetic neuralgia as a complication of malignant disease and its treatment using a GaAlAs diode laser // Laser Therapy. – 1996, 8 (1): 49.
2108. Moore K.C. PostherpeticneuralgiaasacomplicationofmalignantdiseaseanditstreatmentusingaGaAIAs diode laser // Lasers in Medical Science. – 1994, 9 (3): 217.
2109. Moore P., Ridgway T.D., Higbee R.G. et al. Effect of wavelength on low-intensity laser irradiation-stimula- ted cell proliferation in vitro // Lasers in Surgery and Medicine. – 2005, 36 (1): 8–12.
2110. Moraes J.J.C., Queiroga A.S., De Biase R.C.C.G. et al. The effect of low-level laser therapy in different wavelengths in the treatment of oral mucositis-proposal for extra-oral implementation // Laser Physics. – 2009, 19 (9): 1912–1919. doi: 10.1134/S1054660X09170150.
2111. Morton A.R., Fazio S.M., Miller D. Efficacy of laser-acupuncture in the prevention of exercise-induced asthma //Ann.Allergy. – 1993, 70 (4): 295–258.
2112. Moseley A.L., Carati C.J., Piller N.B. A systematic review of common conservative therapies for arm lymphoedema secondary to breast cancer treatment //Ann. Oncol. – 2007, 18 (4): 639–646. doi: 10.1093/annonc/ mdl182.
2113. Moskvin S., Pritiko D., Sergeenko E. et al. Abrief literature review and own clinical experience in prophylaxis of oral mucositis in children using low level laser therapy // Biomedicine. – 2019, 9 (1): 1–10. doi: 10.1051/ bmdcn/2019090101.
2114. Moskvin S.V. Low-intensity laser therapy apparatuses // Proceedings of SPIE, Vol. 4422. – USA, 2001. – P. 65–73.
2115. Moskvin S.V. Low-level laser therapy and light energy // Photobiomodulation, Photomedicine, and Laser Surgery. – 2019, 37 (5): 267–268. doi: 10.1089/photob.2019.4622.
2116. Moskvin S.V. Low-level laser therapy in Russia: history, science and practice // J. Lasers Med. Sci. – 2017, 8 (2): 56–65. doi: 10.15171/jlms.2017.11.
2117. Moskvin S.V. Low-Level Laser Therapy: Western Science vs. Eastern Science // The Annals of Laser Therapy Research. – 2017(1), 4. URL: http://www.laserannals.com/2018/01/14/low-level-laser-therapy-western-sci- ence-vs-eastern-science/.
2118. Moskvin S.V. Only lasers can be used for low level laser therapy // BioMedicine. – 2017(1), 7(4): 4–11. doi: 10.1051/bmdcn/2017070422.
2119. Moskvin S.V. Therapeutic action mechanisms of low intensity laser radiation (LILR) // Photodiagnosis and Photodynamic Therapy. – 2012, 9 (1): 5–6.
2120. Moskvin S.V., Apolikhin O.I. Effectiveness of low level laser therapy for treating male infertility // BioMedicine. – 2018, 8 (2): 1–15. doi: 10.1051/bmdcn/2018080207.
2121. Moskvin S.V., Geynitz A.V., Askhadulin E.V. Efficiency of a new combined laser therapy in patients with trophic ulcers of lower extremities and chronic venous insufficiency // J. Lasers Med. Sci. – 2017, 8 (3): 132–135. doi: 10.15171/jlms.2017.24.
2122. Moskvin S.V., Khadartsev A.A. Basic Techniques of Low Level Laser Therapy. – M.–Tver: Triada, 2017. – 144 p. ISBN 978-5-94789-772-2.
2123. Moskvin S.V., Khadartsev A.A. Laser Blood Illumination. The Main Therapeutic Techniques. – M.–Tver: Triada, 2018. – 64 p. ISBN 978-5-94789-818-7.
2124. Moskvin S.V., Kisselev S.B. Lasertherapyforjointandmusclepain.–M.–Tver:Triada,2017.–216p.ISBN 978-5-94789-787-6.
2125. Moskvin S.V., Kochetkov A.V. Effective Techniques of Low Level Laser Therapy. – M.–Tver: Triada, 2017. – 88 p. ISBN 978-5-94789-771-5.
2126. Moskvin S.V., Kochetkov A.V. Russian low level laser therapy techniques for brain disorders // Photobiomodulation in the Brain. Low-Level Laser (Light) Therapy in Neurology and Neuroscience / M.R. Hamblin, Y.-Y. Huang (Eds). – London:Academic Press is an imprint of Elsevier, 2019. – P. 545–572.
2127. Muñoz Sanchez P.J., Capote Femenías J.L., Díaz TejedaA., Tunér J. The effect of 670-nm low laser therapy onherpessimplextype1//PhotomedicineandLaserSurgery.–2012,30(1):37–40.doi:10.1089/pho.2011.3076. 2128. Muñoz-Corcuera M., González-Nieto A., López-Pintor Muñoz R.M. Use of laser for the prevention and treatment of oral mucositis induced by radiotherapy and chemotherapy for head and neck cancer // Med. Clin. (Barc). – 2014, 143 (4): 170–175. doi: 10.1016/j.medcli.2013.09.017. [Article in Spanish].
944
Список литературы
2129. Murayama H., Sadakane K., Yamanoha B., Kogure S. Low-power 808-nm laser irradiation inhibits cell proliferation of a human-derived glioblastoma cell line in vitro // Lasers in Medical Science. – 2012, 27 (1): 87–93. doi: 10.1007/s10103-011-0924-z.
2130. Murrey R.K., Granner D.K., Mayes P.A., Rodwell V.W. Harper’s biochemistry. –Appleton & Lange, 1996. – 700 p.
2131. Mussttaf R.A., Jenkins D.F.L., Jha A.N. Assessing the impact of low level laser therapy (LLLT) on biological systems: a review // International Journal of Radiation Biology. – 2019, 95 (2): 120–143. doi: 10.1080/09553002.2019.1524944.
2132. Myakishev-Rempel M., Stadler I., Brondon P. et al. A preliminary study of the safety of red light phototherapy of tissues harboring cancer // Photomedicine and Laser Surgery. – 2012, 30 (9): 551–558. doi: 10.1089/ pho.2011.3186.
2133. Nadur-Andrade N., Dale C.S., dos Santos A.S. et al. Photobiostimulation reduces edema formation induced in mice by Lys-49 phospholipasesA2 isolated from Bothrops moojeni venom // Photochemical & Photobiological Sciences. – 2014, 13 (11): 1561–1567. doi: 10.1039/c4pp00111g.
2134. Naeser M.A., Saltmarche A., Krengel M.H. et al. Improved cognitive function after transcranial, lightemitting diode treatments in chronic, traumatic brain injury: two case reports // Photomedicine and Laser Surgery. – 2010, 29 (5): 351–358.
2135. Nair R., Bensadoun R.J. Mitigation of cancer therapy side-effects with light. – San Rafael: Morgan & Claypool Publishers, 2016. – 34 p. doi: 10.1088/978-1-6817-4075-1.
2136. Navarro R., Marquezan M., Cerqueira D.F. et al. Low-level-laser therapy as an alternative treatment for primary herpes simplex infection: a case report // J. Clin. Pediatr. Dent. – 2007, 31 (4): 225–228. doi: 10.17796/ jcpd.31.4.yl4178275423171p.
2137. Navratil L., Dylevsky I. Mechanisms of the analgesic effect of therapeutic lasers in vivo // Laser Therapy. – 1997, 9 (1): 33–39.
2138. Nedeljković M., Ljustina-Pribić R., Savić K. Innovative approach to laser acupuncture therapy of acute obstruction in asthmatic children // Med. Pregl. – 2008, 61 (3–4): 123–130. doi: 10.2298/MPNS0804123N [Article in Serbian.
2139. Needham M.B., Martin M.C.H. Therapeutic laser treatment for post mastectomy lymphoedema: a perspective for nurses // Laser Therapy. – 2009, 18 (2): 103–110.
2140. Negri L.B., Martins T.J., da Silva R.S., Hamblin M.R. Photobiomodulation combined with photodynamic therapy using ruthenium phthalocyanine complexes in A375 melanoma cells: Effects of nitric oxide generation andATP production // J. Photochem. Photobiol. B. – 2019, 198: 111564. doi: 10.1016/j.jphotobiol.2019.111564. 2141. Nes A.G., Posso M.B. Patients with moderate chemotherapyinduced mucositis: pain therapy using low intensity lasers // Int. Nurs. Rev. – 2005, 52 (1): 68–72.
2142. Nussbaum E.L., Lilge L., Mazzulli T. Effects of 630-, 660-, 810-, and 905-nm laser irradiation delivering radiant exposure of 1–50 J/cm2 on three species of bacteria in vitro // Journal of Clinical Laser Medicine & Surgery. – 2002, 20 (6): 325–333.
2143. Oberoi S., Zamperlini-Netto G., Beyene J. et al. Effect of prophylactic low level laser therapy on oral mucositis: a systematic review and meta-analysis // PLoS One. – 2014, 9 (9): e107418. doi: 10.1371/journal. pone.0107418.
2144. Ocaña-Quero J.M., Perez de la Lastra J., Gomez-Villamandos R., Moreno-Millán M. Biological effect of helium-neon (He-Ne) laser irradiation on mouse myeloma (Sp2-Ag14) cell line in vitro // Lasers in Medical Science. – 1998, 13 (3): 214–218. doi: 10.1007/s101030050077.
2145. Oliveira P.C., Reis Junior J.A., Lacerda J.A. et al. Laser light may improve the symptoms of oral lesions of cicatricial pemphigoid: a case report // Photomedicine and Laser Surgery. – 2009, 27 (5): 825–828. doi: 10.1089=pho.2008.235.
2146. Olson R.A. In regard to de Lima et al. // Int. J. Radiat. Oncol. Biol. Phys. – 2013, 85 (4): 895. doi: 10.1016/j. ijrobp.2012.08.028.
2147. Omar M.T., Shaheen A.A., Zafar H. A systematic review of the effect of low-level laser therapy in the management of breast cancer-related lymphedema // Support Care Cancer. – 2012, 20 (11): 2977–2984. doi: 10.1007/s00520-012-1546-0.
2148. Oremus M., Dayes I., Walker K. et al. Systematic review: conservative treatments for secondary lymphedema // BMC Cancer. – 2012, 4 (12): 6. doi: 10.1186/1471-2407-12-6.
2149. Oron A., Oron U., Chen J. et al. Low-level laser therapy applied transcranially to rats after induction of stroke significantly reduces long-term neurological deficits // Stroke. – 2006, 37 (10): 2620–2624.
2150. OronA., Oron U., Streeter J. et al. Low-level laser therapy applied transcranially to mice following traumatic brain injury significantly reduces long-term neurological deficits // J. Neurotrauma. – 2007, 24 (4): 651–656.
945
Рекомендовано к покупке и изучению сайтом МедУнивер - https://meduniver.com/
Лазерная терапия в онкологии
2151. Oton-Leite A.F., Corrêa de Castro A.C., Morais M.O. et al. Effect of intraoral low-level laser therapy on quality of life of patients with head and neck cancer undergoing radiotherapy // Head & Neck. – 2012, 34 (3): 398–404. doi: 10.1002/hed.21737.
2152. Oton-LeiteA.F., Elias L.S., Morais M.O. et al. Effect of low level laser therapy in the reduction of oral complications in patients with cancer of the head and neck submitted to radiotherapy // Spec. Care Dentist. – 2013, 33 (6): 294–300. doi: 10.1111/j.1754-4505.2012.00303.x.
2153. Oton-Leite A.F., Silva G.B., Morais M.O. et al. Effect of low-level laser therapy on chemoradiotherapyinduced oral mucositis and salivary inflammatory mediators in head and neck cancer patients // Lasers in Surgery and Medicine. – 2015, 47 (4): 296–305. doi: 10.1002/lsm.22349.
2154. Otsuka H., Numazawa R., Okubo K. et al. Effects of helium-neon laser therapy on Herpes Zoster pain // Laser Therapy. – 1995, 7 (1): 27–32. doi: 10.5978/islsm.95-OR-05.
2155. Ottaviani G., Gobbo M., Sturnega M. et al. Effect of class IV laser therapy on chemotherapy-induced oral mucositis: a clinical and experimental study // Am. J. Pathol. – 2013, 183 (6): 1747–1757. doi. 10.1016/j. ajpath.2013.09.003.
2156. Ovsiannikov V.A. Analysis of the low-energy laser treatment of some cancers and infectious diseases // Journal of Clinical Laser Medicine & Surgery. – 1997, 15 (1): 39–44. doi: 10.1089/clm.1997.15.39.
2157. Palecek J., Lips M.B., Keller B.U. Calcium dynamics and buffering in motoneurones of the mouse spinal cord // J. Physiol. – 1999, 520 (2): 485–502.
2158. Palma L.F., Gonnelli F.A.S., Marcucci M. et al. Impact of low-level laser therapy on hyposalivation, salivary pH, and quality of life in head and neck cancer patients post-radiotherapy // Lasers in Medical Science. – 2017, 32 (4): 827–832. doi: 10.1007/s10103-017-2180-3.
2159. Papas A.S., Clark R.E., Martuscelli G. et al. A prospective, randomized trial for the prevention of mucositis in patients undergoing hematopoietic stem cell transplantation // Bone Marrow Transplant. – 2003, 31 (8): 705–712. doi: 10.1038/sj.bmt.1703870.
2160. Park J.E., Jang H.J., Seo K.S. Quality of life, upper extremity function and the effect of lymphedema treatment in breast cancer related lymphedema patients //Ann. Rehabil. Med. – 2012, 36 (2): 240–247. doi: 10.5535/ arm.2012.36.2.240.
2161. Paskett E.D., Dean J.A., Oliveri J.M., Harrop J.P. Cancer-related lymphedema risk factors, diagnosis, treatment, and impact: a review // J. Clin. Oncol. – 2012, 30 (30): 3726–3733. doi: 10.1200/JCO.2012.41.8574. 2162. Patent US 5231984. Laser therapeutic apparatus / Santana-Blank L.A. – Публикация 03.08.1993, приоритет 11.12.1989.
2163. Pavlić V. The effects of low-level laser therapy on xerostomia (mouth dryness) // Med. Pregl. – 2012, 65 (5–6): 247–250. [Article in Serbian].
2164. Payne S., Miles D. Mechanisms of anticancer drugs // M. Gleeson, G. Browning, J. Burton et al. (Eds.) Scott-Brown’s Otorhinolaryngology: Head and Neck Surgery 7Ed. CRC Press, London, 2008. – P. 34–46. 2165. Penha T.R., Botter B., Heuts E.M. et al. Quality of life in patients with breast cancer-related lymphedema andreconstructivebreastsurgery//J. Reconstr.Microsurg.–2016,32(6):484–90.doi:10.1055/s-0036-1572538. 2166. Peplow P.V., Chung T.-Y., Ryan B., Baxter G.D. Laser photobiomodulation of gene expression and release of growth factors and cytokines from cells in culture: a review of human and animal studies // Photomedicine and Laser Surgery. – 2011, 29 (5): 285–304. doi: 10.1089/pho.2010.2846.
2167. Perbeck L., Celebioglu F., Svensson L., Danielsson R. Lymph circulation in the breast after radiotherapy and breast conservation // Lymphology. – 2006, 39 (1): 33–40.
2168. Perrin D., Jolivald J.R., Triki H. et al. Effect of laser irradiation on latency of herpes simplex virus in a mouse model // Pathol. Biol. (Paris). – 1997, 45 (1): 24–27.
2169. Peševska S., Nakova M., Pejčić A. et al. Biostimulative laser therapy: base for favorized and accented results in dentistry //Acta Fac. Med. Naiss. – 2006, 23 (1): 75–78.
2170. Peterson D.E., Bensadoun R.-J., Roila F. Клинические рекомендации ESMO по лечению мукозитов слизистой ротовой полости и желудочно-кишечного тракта // Минимальные клинические рекомендации Европейского общества медицинской онкологии (ESMO). – М., 2010. – С. 397–403.
2171. Pezelj-Ribarić S., Kqiku L., Brumini G. et al. Proinflammatory cytokine levels in saliva in patients with burning mouth syndrome before and after treatment with low-level laser therapy // Lasers in Medical Science. – 2013, 28 (1): 297–301. doi: 10.1007/s10103-012-1149-5.
2172. Piller N., Carati C. The diagnosis and treatment of peripheral lymphedema (Letters to the editor) // Lymphology. – 2009, 42 (3): 146–147.
2173. Piller N.B., Thelander A. Treating chronic post-mastectomy lymphoedema with low level laser therapy: a cost effective strategy to reduce severity and improve the quality of survival // Laser Therapy. – 1995, 7 (4): 163–168.
946
Список литературы
2174. Piller N.B., Thelander A. Treatment of chronic postmastectomy lymphedema with low level laser therapy: a 2.5 year follow-up // Lymphology. – 1998, 31 (2): 74–86.
2175. Pinel B., Caillot E., Colson L., Bensadoun R.-J. Utilisation d’un laser de basse énergie transcutané dans la préventionetletraitementdesmuciteschimioradio-induites//Cancer/Radiothérapie.–2012,16(s5–6):516.doi: 10.1016/j.canrad.2012.07.006 [Article in French].
2176. Pinheiro A.L.B., Nascimento S.C., De Barros Vieira A.L. et al. Effects of Low-Level Laser Therapy on malignantcells:in vitro study//J.Clin.LaserMed.Surg.–2002,20(1):23–26.doi:10.1089/104454702753474977. 2177. Pinheiro A.L.B., Nascimento S.C., Vieira A.L.B. et al. Does LLLT stimulate laryngeal carcinoma cells?An in vitro study // Braz. Dent. J. – 2002(1), 13 (2): 109–112.
2178. Pinheiro A.L.B., Nascimento S.C., Vieira A.L.B. et al. Effects of LLLT on the proliferation of HEp2 cells: study in vitro // Lasers in dentistry VI. – 2000, Proceedings of SPIE, 3910: 75–81.
2179. Pinheiro S.L., Bonadiman A.C., Borges Lemos A.L.D.A. et al. Photobiomodulation therapy in cancer patients with mucositis: a clinical evaluation // Photobiomodul Photomed Laser Surg. – 2019, 37 (3): 142–150. doi: 10.1089/photob.2018.4526.
2180. Pires-Santos G.M., Ferreira M.F.L., Oliveira S.C.P.S. et al. Use of laser photobiomodulation in the evolution of oral mucositis associated with CMF chemotherapy protocol in patients with breast cancer-case report // Medicina Oral, Patologia Oral y Cirugia Bucal. – 2012, 17 (1): 252. doi: 10.4317/medoral.17643752.
2181. Plavnik L.M., De Crosa M.E., Malberti A.I. Effect of low-power radiation (Helium/Neon) upon submandibulary glands // Journal of Clinical Laser Medicine & Surgery. – 2003, 21 (4): 219–225. doi: 10.1089/104454703768247792.
2182. Plevová P. Prevention and treatment of chemotherapyand radiotherapyinduced oral mucositis.Areview // Oral Oncol. – 1999, 35 (5): 453–470.
2183. Podolskaya Е.Е. Radiation damage of lips and its treatment by low-intensity laser irradiation // Proceedings SPIE, Vol. – 1984: 245–246. doi: 10.1117/12.207033.
2184. Pourreau-Schneider N., Soudry M., Franquin J.C. et al. Soft-laser therapy for iatrogenic mucositis in cancer patients receiving high-dose fluorouracil: a preliminary report // J. Natl. Cancer Inst. – 1992, 84 (5): 358–359. doi: 10.1093/jnci/84.5.358.
2185. Powell K., Low P., McDonnell P.A. et al. The effect of laser irradiation on proliferation of human breast carcinoma, melanoma, and immortalized mammary epithelial cells // Photomedicine and Laser Surgery. – 2010, 28 (1): 115–123. doi: 10.1089/pho.2008.2445.
2186. Priezzhev A.V., Moskvin S.V., Titov M.N. et al. Laser therapeutical devices «Mustang» in clinical practice // Photonics West’95, Biomedical optics. Conference on clinical laser and optoelectronic systems. – San-Hose, 1995. – P. 96.
2187. Ptaszyńska-Sarosiek I., Dunaj J., Zajkowska A. et al. Post-mortem detection of six human herpesviruses (HSV-1, HSV-2, VZV, EBV, CMV, HHV-6) in trigeminal and facial nerve ganglia by PCR // PeerJ. – 2019, 6: e6095. doi: 10.7717/peerj.6095.
2188. Puri M.M., Myneedu V.P., Jain R.C. Nitrogen and hellium-neon laser therapy in the treatment of drugresistant pulmonary tuberculosis // Laser Therapy. – 1995, 7(3): 123–127.
2189. Qu C., Cao W., Fan Y., Lin L. Near-infrared light protect the photoreceptor from light-induced damage in rats // Anderson R.E., editor. Retinal Degenerative Diseases. New York, NY: Springer Science; 2010. – P. 365– 374.
2190. Quadri T., Miranda L., Tunér J. et al. The short-term effects of lowlevel lasers as adjunct therapy in treatment of periodontal inflammation // J. Clin. Periodontol. – 2005, 32 (7): 714–719. doi: 10.1111/j.1600051x.2005.00749.x.
2191. Qutob A.F., Gue S., Revesz T. et al. Prevention of oral mucositis in children receiving cancer therapy: a systematic reviewand evidence-based analysis // Oral Oncol. – 2013, 49 (2): 102–107. doi: 10.1016/j.oraloncology.2012.08.008.
2192. Raber-Durlacher J.E., Elad S., Barasch A. Oral mucositis // Oral Oncol. – 2010, 46 (6): 452–456. doi: 10.1016/j.oraloncology.2010.03.012.
2193. Ramalho K.M., LuizA.C., de Paula Eduardo C. et al. Useoflaserphototherapyona delayedwoundhealing of oral mucosa previously submitted to radiotherapy: case report // Int. Wound J. – 2011, 8 (4): 413–418. doi: 10.1111/j.1742-481X.2011.00788.x.
2194. Rampini M.P., Ferreira E.M.S., Ferreira C.G.,Antunes H.S. Utilização da terapia com laser de baixa potência para prevenção de mucosite oral: revisão de literatura // Rev. Bras. Cancerol. – 2009, 55 (1): 59–68.
2195. Ravazzi T.P.Q., Ferreira H., Soares-Ferreira L. et al. A home care approach of low intensity laser therapy as adjuvant to prevent and treat oral complications in oncologic patients // ConferenceWALT.Abstacts. – Bergen, Norway, 2010. – P. 60.
947
Рекомендовано к покупке и изучению сайтом МедУнивер - https://meduniver.com/
Лазерная терапия в онкологии
2196. Ren C., McGrath C., Jin L. et al. Effect of diode low-level lasers on fibroblasts derived from human periodontal tissue: a systematic review of in vitro studies // Lasers in Medical Science. – 2016, 31 (7): 1493–1510. doi: 10.1007/s10103-016-2026-4.
2197. Renno A.C.M., McDonnell P.A., Parizotto N.A., Laakso, E.L. The effects of laser irradiation on osteoblast and osteosarcoma cell proliferation and differentiation in vitro // Photomedicine and Laser Surgery. – 2007, 25 (4): 275–280. doi: 10.1089/pho.2007.2055.
2198. Revazova E., Bryzgalov I., Sorokina Iu. et al. Stimulation of the growth of human tumor by low-power laser irradiation // Bull. Exp. Biol. Med. – 2001, 132 (2): 778–779.
2199. Rezk-Allah S.S., Abd Elshaf H.M., Farid R.J. et al. Effect of low-level laser therapy in treatment of chemotherapy induced oral mucositis // Journal of Lasers in Medical Sciences. – 2019, 10 (2): 125–130. doi: 10.15171/ jlms.2019.20.
2200. Rhee Y.-H., Moon J.-H., Choi S.-H. et al. Low-level laser therapy promoted aggressive proliferation and angiogenesis through decreasing of transforming growth factor-β1 and increasing of Akt/hypoxia inducible factor1α in anaplastic thyroid cancer // Photomedicine and Laser Surgery. – 2016, 34 (6): 229–235. doi: 10.1089/ pho.2015.3968.
2201. Ribeiro M.S., da Costa D.R., Prates R.A. et al. Study of the light parameters on cell cultures following low intensity red laser therapy // Conference WALT.Abstracts. – Bergen, Norway, 2010. – P. 38.
2202. Ridner S.H., Poage-Hooper E., Kanar C. et al. A pilot randomized trial evaluating low-level laser therapy as an alternative treatment to manual lymphatic drainage for breast cancer-related lymphedema // Oncol. Nurs. Forum. – 2013, 40 (4): 383–393. doi: 10.1188/13.ONF.383-393.
2203. Rigau J., Sun C.-H., Trelles M.A., Berns M.W. Effects of the 633-nm laser on the behavior and morphology of primary fibroblast culture // SPIE Proceedings. – 1996, 2630: 38–42.
2204. Rímulo A.L., Ferreira M.C., Abreu M.H. et al. Chemotherapy-induced oral mucositis in a patient with acute lymphoblastic leukaemia // EuropeanArchives of Paediatric Dentistry. – 2011, 12 (2): 124–127.
2205. Riquet M., Mordant P., Pricopi C. et al. A review of 250 ten-year survivors after pneumonectomy for nonsmall-cell lung cancer // Eur. J. Cardiothorac. Surg. – 2014, 45: 876–881. doi: 10.1093/ejcts/ezt494.
2206. Robb-Gaspers L.D., ThomasA.P. CoordinationofCa2+ signalingbyintercellularpropagationofCa2+ waves in the intact liver // J. Biol. Chem. – 1995, 270 (14): 8102–8107.
2207. Robijns J., Censabella S., Bulens P. et al. The use of low-level light therapy in supportive care for patients with breast cancer: review of the literature // Lasers in Medical Science. – 2017, 32 (1): 229–242. doi: 10.1007/ s10103-016-2056-y.
2208. Rocca J.-P., Zhao M., Fornaini C. et al. Effect of laser irradiation on aphthae pain management: A four different wavelengths comparison // J. Photochem. Photobiol. B. – 2018, 189: 1–4. doi: 10.1016/j.jphotobiol.2018.09.016.
2209. Rocha A.L., Souza A.F., Nunes L.F.M. et al. Treatment of oral manifestations of toxic epidermal necrolysis with low-level laser therapy in a pediatric patient // Pediatr. Dermatol. – 2019, 36 (1): e27–e30. doi: 10.1111/ pde.13719.
2210. Rodrigues G.H., Jaguar G.C., Alves F.A. et al. Variability of high-dose melphalan exposure on oral mucositis in patients undergoing prophylactic low-level laser therapy // Lasers in Medical Science. – 2017, 32 (5): 1089–1095. doi: 10.1007/s10103-017-2211-0.
2211. Rodríguez-Caballero A., Lagares D.T., García M.R. et al. Cancer treatment-induced oral mucositis: a critical review // Int. J. Oral Maxillofac. Surg. – 2012, 41 (2): 225–238. doi: 10.1016/j.ijom.2011.10.011.
2212. Rodriguez-Santana E., Reyes H., Santana-Rodriguez K.E., Santana-Blank L. Photo-infrared pulsed biomodulation in age-related macular degeneration associated to neurological disease: one interventional case report and mini-review // J. Chinese Clin. Med. – 2008, 3: 470–477.
2213. Rojas J.C., Gonzalez-Lima F. Low-level light therapy of the eye and brain // Eye and Brain. – 2011, 3: 49–67.
2214. Rojas J.C., Lee J., John J.M., Gonzalez-Lima F. Neuroprotective effects of near-infrared light in an in vivo model of mitochondrial optic neuropathy // J. Neurosci. – 2008, 28 (50): 13511–13521.
2215. Romeo U., Del Vecchio A., Capocci M. et al. The low level laser therapy in the management of neurological burning mouth syndrome //Apilot study.Ann Stomatol (Roma). – 2010, 1 (1): 14–18.
2216. Romeo U., GalanakisA., Marias C. et al. Observation of pain control in patients with bisphosphonate-indu- ced osteonecrosis using low level laser therapy: preliminary results // Photomedicine and Laser Surgery. – 2011, 29 (7): 447–452. doi: 10.1089/pho.2010.2835.
2217. Roscoe J., Morrow G., Hickok J. et al. The efficacy of acupressure and acustimulation wrist bands for the relief of chemotherapy-induced nausea and vomiting.AUniversity of Rochester Cancer Center Community Clinical Oncology Program multicenter study // J. Pain Symptom Manage. – 2003, 26 (2): 731–742.
948
Список литературы
2218. RosenspireA.J., KindzelskiiA.L., Petty H.R. Interferon-γ and sinusoidal electric fields signal by modulating NAD(P)H oscillations in polarized neutrophils // Biophys. J. – 2000, 79 (6): 3001–3008.
2219. Rosenthal C., Karthaus M. Current approaches in prevention and therapy of chemoand radiotherapyinduced oral mucositis // Wien. Med. Wochenschr. – 2001, 151 (3–4): 53–65. [Article in German].
2220. Rosenthal D.S., Dean-Clower E. Integrative medicine in hematology/oncology: benefits, ethical considerations, and controversies // HematologyAm. Soc. Hematol. Educ. Program. – 2005: 491–497.
2221. Rozsa G. Laser therapy and its combinid treatments in the first provincial laser center of Hungary // Laser Therapy. – 1994, 6 (1): 69.
2222. Rozza-de-Menezes R., Souza P.H.C., Westphalen F.H. et al. Behaviour and prevention of 5’fluorouracil and doxorubicin-induced oral mucositis in immunocompetent patients with solid tumors: a randomised trial // Oral Health Prev. Dent. – 2018, 16 (6): 549–555. doi: 10.3290/j.ohpd.a41659.
2223. Rubenstein E., Peterson D., Schubert M. et al. Clinical practice guidelines for the prevention and treatment of cancer therapy-induced oral and gastrointestinal mucositis // Cancer. – 2004, 100 (9 Suppl): 2026–2046. doi: 10.1002/cncr.20163.
2224. Ruiz-Esquide G., Nervi B., Vargas A., Maíz A. Treatment and prevention of cancer treatment related oral mucositis // Rev. Med. Chil. – 2011, 139 (3): 373–381. doi: /S0034-98872011000300015.
2225. Rupel K., Zupin L., Colliva A. et al. Photobiomodulation at multiple wavelengths differentially modulates oxidative stress in vitro and in vivo // Oxid. Med. Cell. Longev. – 2018: 6510159. doi: 10.1155/2018/6510159. 2226. Rutkowski J.M., Moya M., Johannes J. et al. Secondary lymphedema in the mouse tail: Lymphatic hyperplasia, VEGF-C upregulation, and the protective role of MMP-9 // Microvasc Res. – 2006, 72 (3): 161–171. doi: 10.1016/j.mvr.2006.05.009.
2227. Saadeh C.E. Chemotherapyand radiotherapy-induced oral mucositis: review of preventive strategies and treatment // Pharmacotherapy. – 2005, 25 (4): 540–554.
2228. Sacono N.T. Uso de LED vermelho em mucosite induzida por quimioterápia. –Araraquara, 2007. – 162 p. [Book in Portuguese].
2229. Sacono N.T., Costa C.A.S., Bagnato V.S., Abreu-e-Lima F.C.B. Light-emitting diode therapy in chemothe- rapy-induced mucositis // Lasers in Surgery and Medicine. – 2008, 40 (9): 625–633. doi: 10.1002/lsm.20677. 2230. Sacono N.T., Ferrari J.C.L., Abreu-e-Lima F.C.B. Uso do LED vermelho e infravermelho para o tratamento da mucosite induzida por quimioterapia em hamsters // Anais da 22ª Reunião da Sociedade Brasileira de Pesquisa Odontológica–SBPqO; set. 3–7; Águas de Lindóia (SP). São Paulo: SBPqO, 2005. – P. 219. [Article in Portuguese].
2231. Safavi S.M., Kazemi B., Esmaeili M. et al. Effects of low-level He–Ne laser irradiation on the gene expression of IL-1β, TNF-α, IFN-γ, TGF-β, bFGF, and PDGF in rat’s gingiva // Lasers in Medical Science. – 2008, 23 (3): 331–335. doi: 10.1007/s10103-007-0491-5.
2232. Saikaly S.K., Saikaly T.S., Saikaly L.E. Recurrent aphthous ulceration: a review of potential causes and novel treatments // J. Dermatolog. Treat. – 2018, 29 (6): 542–552. doi: 10.1080/09546634.2017.1422079. 2233. Saleh H.M., Shaker A.S., Saafan A.M., Ibrahim A.K. Herpes virus reactivation by low-intensity diode and CO2 lasers // Photomedicine and Laser Surgery. – 2011, 29 (2): 83–90. doi: 10.1089/pho.2009.2744.
2234. Saleh J., Figueiredo M.A.Z., Cherubini K. et al. Effect of low-level laser therapy on radiotherapy-induced hyposalivation and xerostomia: a pilot study // Photomedicine and Laser Surgery. – 2014, 32 (10): 546–552. doi: 10.1089/pho.2014.3741.
2235. Salvador D.R.N., Soave D.F., Sacono N.T. et al. Effect of photobiomodulation therapy on reducing the che- mo-induced oral mucositis severity and on salivary levels of CXCL8/interleukin 8, nitrite, and myeloperoxidase in patients undergoing hematopoietic stem cell transplantation: a randomized clinical trial // Lasers in Medical Science. – 2017, 32 (8): 1801–1810. doi: 10.1007/s10103-017-2263-1.
2236. Sandoval R.L., Koga D.H., Buloto L.S. et al. Management of chemoand radiotherapy induced oral mucositis with low-energy laser: initial results ofA.C. Camargo Hospital // J.Appl. Oral Sci. – 2003, 11 (4): 337–341. doi: 10.1590/s1678-77572003000400012.
2237. Santana-Blank L., Rodríguez-Santana E., Santana-Rodríguez J.A. et al. Laser photobiomodulation as a potential multi-target anticancer therapy-review // Journal of Solid Tumors. – 2013, 3 (2): 50–62.
2238. Santana-Blank L., Rodríguez-Santana E., Santana-Rodríguez K.E. et al. Water’s many roles in laser photobiomodulation // Journal of Cancer Research and Treatment. – 2015, 3 (1): 1–5. doi: 10.12691/jcrt-3-1-1. 2239. Santana-Blank L.A., Reyes H., Rodríguez-Santana E., Santana-Rodríguez K.E. Microdensitometry of T2weighted magnetic resonance (MR) images from patients with advanced neoplasias in a phase I clinical trial of an infrared pulsed laser device (IPLD) // Lasers in Surgery and Medicine. – 2004, 34 (5): 398–406. doi: 10.1002/ lsm.20068.
2240. Santana-Blank L.A., Rodríguez-Santana E., Vargas F. et al. Phase I trial of an infrared pulsed laser device in patients with advanced neoplasias // Clinical Cancer Research. – 2002, 8 (10): 3082–3091.
949
Рекомендовано к покупке и изучению сайтом МедУнивер - https://meduniver.com/