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implants_mukowiscydoza 10. Valenza G, Tappe D, Turnwald D, et al. Prevalence and antimicrobial susceptibility of microorganisms isolated from sputa of patients with cystic ibrosis. J Cyst Fibros 2008;7:123-127. 11. Button B, Toberts S, Kotsimbos T, Levvey B, Williams T, Bailey M, Snell G, Wilson J. Gastroesophageal relux (symptomatic and silent): a potentially signiicant problem in patients with cystic ibrosis before and after lung transplantation. J Heart Lung Transplant 2005;24:1522-1529. 12. Peker S, Mete S, Gokdemir Y, Karadag B, Kargul B. Related factors of dental caries and molar incisor hypomineralisa- tion in a group of children with cystic ibrosis. Eur Arch Pa- ediatr Dent 2014;15:275-280. 13. Dąbrowska E, Błahuszewska K, Minarowska A, Kaczmarski M, Niedźwiecka-Andrzejewicz I, Stokowska W. Assessment of dental status and oral hygiene in the study population of cystic ibrosis patients in the Podlasie province. Ad Med Sci 2006;51(Supl 1):100-3. 14. Ferrazzano GF, Orlando S, Sangianantoni G, Cantile T, In- genito A. Dental and periodontal health status in children affected by cystic ibrosis in a southern Italian region. Eur J Paediatr Dent 2009;10(2):65-68. 15. Arquitt CK, Boyd C, Wright JT. Cystic ibrosis transmem- brane regulator gene (CFTR) is associated with abnormal enamel formation. J Dent Res 2002; 81(7):492-496. 16. Sands KM, Wilson MJ, Lewis MAO, Wise MP, Palmer N, et al. Respiratory pathogen colonization of dental plaque, the _autorzy Sylwia Jarzynka, Gabriela Olędzka Zakład Biologii Medycznej, Warszawski Uniwersytet Medyczny Bartłomiej Iwańczyk, Tomasz Kamiński, Andrzej Wojtowicz Zakład Chirurgii Stomatologicznej, Warszawski Uniwersytet Medyczny Joanna Chudek, Paulina Gulatowska Studenckie Koło Naukowe, Warszawski Uniwersytet Medyczny Wojciech Skorupa I Klinika Chorób Płuc, Instytut Gruźlicy i Chorób Płuc, Warszawa Ewa Augustynowicz-Kopeć Zakład Mikrobiologii, Instytut Gruźlicy i Chorób Płuc, Warszawa Kontakt: lek. dent. Bartłomiej Iwańczyk E-mail: dent.iwanczyk@gmail.com lower airways, and endotracheal tube bioilms during ma- echanical ventilation. J Critical Care 2017;37:30-37. 17. Ferrazzano GF, Sangianantoni G, Cantile T, et al. Dental ena- mel defects in Italian children with cystic ibrosis: an obse- rvational study. Community Dent Health 2012;29:106-109. 18. Narang A, Maguire A, Nunn JH, Bush A. Oral health and re- lated factors in cystic ibrosis and other chronic respiratory disorders. Arch Dis Child 2003;88(8):702-707. 19. Aps JK, Van Maele GO, Claeys G, Martens LC. Mutans streptococci, lactobacilli and caries experience in cystic ibrosis homozygotes, heterozygotes and healthy controls. Caries Res 2001;35:407-411. 20. Mahboubi MA, Carmody LA, Foster BK, Kalikin LM, Van- Devanter DR, LiPuma JJ. Culture-based and culture-inde- pendent bacteriologic analysis of cystic ibrosis respiratory specimens. J ClinMicrobiol 2016;54(3):613-619. 21. Górska R, Konopka T. i wsp. Periodontologia współczesna. Med Tour Press International. 2013; 71-75. 22. Widmer RP. Oral health of children with respiratory dise- ases. PaediatrRespir Rev 2010;11:226-232. 23. Girón RM, Buendia B, Pinedo C, Casanova A, Hoyos N, Ancochea J. Methicillin-resistant Staphylococcus aureus in patients with cystic ibrosis. EnfermInfecc Microbiol Clin 2009;27(2):85-88. 24. Mazurek H. Mukowiscydoza. Med Dypl 2009; 05/09:35-39. 25. Patrick JRD, da Fonseca MA, Kaste LM, et al. Oral Health- -related quality of life in pediatric patients with cystic ibro- sis. Spec Care Dentist 2016;36(4):187-193. 26. Tunney MM, Field TR, Moriarty TF, Patrick S, Doering G, et al. Detection of anaerobic bacteria in high numbers in spu- tum from patients with cystic ibrosis. Am J RespirCrit Care Med 2008;177(9):995-1001. 27. Caldas RR, Le Gall F, Revert K, Rault G, Virmaux M, Gouriou S, Héry-Arnaud G, Barbier G, Boisramé S. Pseudomonas aeruginosa and periodontal pathogens in the oral cavity and lungs of cystic ibrosis patients: a case-control study. J ClinMicrobiol 2015;53(6):1898-1907. 28. Silva-Boghossian CM, Orrico SR, Gonçalves D, Correa FO, Colombo AP. Microbiological changes after periodontal the- rapy in diabetic patients with inadequate metabolic control. BrazOral Res 2014;28. 29. Chotirmall SH, McElvaney NG. Fungi in the cystic ibrosis lung: Bystanders or pathogens? Int J Biochem Cell Biol 2014;52: 161-173. 30. Mortensen KL, Jesen RH. Johansen HK et al. Aspergillus spp.and other moulds in respiratory samples from patients with cystic ibrosis: a laboratory-based study with focus on Aspergillus fumigates azole resistance. J Clin Microbiol 2011; 49:2243-2251. 32 1_2017 32 implants