Osteogenesis imperfektalı yetişkin hastada zoledronik asit tedavisi: Bir olgu ve literatür derlemesi
Abstract
Keywords
References
- Martin E, Shapiro JR. Osteogenesis Imperfecta: epidemiol- ogy and pathophysiology. Curr Osteoporos Rep 2007;5:91- 97.
- Marini JC, Cabral WA, Barnes AM. Null mutations in LEP- RE and CRTAP cause severe recessive osteogenesis imper- fecta. Cell Tissue Res 2010;339:59-70.
- Sillence D, Senn A, Danks D. Genetic heterogeneity In os- teogenesis imperfecta. J Med Genet 1979;16:101-106.
- Glorieux FH, Rauch F, Plotkin H et al: Type V osteogenesis imperfecta: A new form of brittle bone disease. J Bone Min Res 2000;15:1650-1658
- Cabral W, Chang W, Barnes A. et al. Protyl 3-hydroxylase 1 deficiency causes a recessive metabolic disorder re- sembling lethal/severe osteogenesis imperfecta. Nat Gen 2007;39:359-365.
- Cheung MS, Glorieux FH. Osteogenesis Imperfecta: update on presentation and management. Rev Endocr Metab Dis- ord 2008;9:153-160.
- Rebelo M, Lima J, Vieira JD, Costa JN. An unusual presenta- tion of osteogenesis imperfecta type I. Int Med Case Rep J 2011;4:25-29.
- Balkefors V, Mattsson E, Pernow Y, Sääf M. Functioning and quality of life in adults with mild-to-moderate osteogenesis imperfecta. Physiother Res Int 2013;18:203-211.
Details
Primary Language
Turkish
Subjects
-
Journal Section
-
Authors
Levent Yazmalar
This is me
İbrahim Batmaz
This is me
Abdullah Zübeyr Dağlı
This is me
Erkam Hattapoğlu
This is me
Mustafa Akif Sarıyıldız
This is me
Publication Date
June 1, 2014
Submission Date
March 2, 2015
Acceptance Date
-
Published in Issue
Year 2014 Volume: 41 Number: 2