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dc.contributor.authorAlper, S
dc.contributor.authorAki, S
dc.contributor.authorEskiyurt, N
dc.contributor.authorAkarirmak, U
dc.contributor.authorTuzun, F
dc.contributor.authorEryavuz, M
dc.contributor.authorArpacioglu, O
dc.contributor.authorAtalay, F
dc.contributor.authorKavuncu, V
dc.contributor.authorKokino, S
dc.contributor.authorKuru, O
dc.contributor.authorNas, K
dc.contributor.authorOzerbil, O
dc.contributor.authorSavas, G
dc.contributor.authorSendur, OF
dc.contributor.authorSoy, D
dc.contributor.authorAkyuz, G
dc.date.accessioned2021-03-06T10:31:08Z
dc.date.available2021-03-06T10:31:08Z
dc.date.issued2003
dc.identifier.citationAki S., Eskiyurt N., Akarirmak U., Tuzun F., Eryavuz M., Alper S., Arpacioglu O., Atalay F., Kavuncu V., Kokino S., et al., "Gastrointestinal side effect profile due to the use of alendronate in the treatment of osteoporosis", YONSEI MEDICAL JOURNAL, cilt.44, ss.961-967, 2003
dc.identifier.issn0513-5796
dc.identifier.othervv_1032021
dc.identifier.otherav_eabd58ff-f622-45b8-b8e1-cfd12a551965
dc.identifier.urihttp://hdl.handle.net/20.500.12627/154191
dc.identifier.urihttps://doi.org/10.3349/ymj.2003.44.6.961
dc.description.abstractThe aim of our study was to evaluate the upper gastrointestinal (GI) tract side effect profile in 759 female patients that had taken alendronate (10 mg/day), for at least 6 months, for the treatment of osteoporosis, in relation to the safety of alendronate and the compliance of patients to its absorption rules.
dc.language.isoeng
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectTIP, GENEL & İÇECEK
dc.titleGastrointestinal side effect profile due to the use of alendronate in the treatment of osteoporosis
dc.typeMakale
dc.relation.journalYONSEI MEDICAL JOURNAL
dc.contributor.department, ,
dc.identifier.volume44
dc.identifier.issue6
dc.identifier.startpage961
dc.identifier.endpage967
dc.contributor.firstauthorID170141


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