FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2017565340> ?p ?o ?g. }

• W2017565340 endingPage "95" @default.
• W2017565340 startingPage "89" @default.
• W2017565340 abstract "Abstract The object of this study was to analyze the cortical thickness (Ct.Th) of the ventral and dorsal shell of the vertebral bodies throughout the human spine in aging and in osteoporosis. Therefore, the complete front column of the spine of 26 autopsy cases (aged 17–90, mean 42 years) without diseases affecting the skeleton and of 11 cases (aged 58–92, mean 77 years) with proven osteoporosis were removed. A sagittal segment prepared through the center of all vertebral bodies was undecalcified, embedded in plastic, ground to a 1 mm thick block, and stained using a modification of the von Kossa method. The analysis included the measurement of the mean cortical thickness of both the ventral and dorsal shell, respectively (from the third cervical to the fifth lumbar vertebral body). The qualitative investigation of the structure of the cortical ring completed the analysis. The presented data revealed a biphasic curve for both the ventral and dorsal shell, skeletally intact with high values of the cortical thickness in the cervical spine (285 μm), and a decrease in the thoracic (244 μm) and an increase in the lumbar spine (290 μm). The mean thickness of the ventral shell is in general greater than the thickness of the dorsal shell in both skeletally normal and osteoporotic cases. The cortical thickness of the spine showed no gender‐specific differences ( p = NS). There was a slight decrease of the cortical thickness with aging; however, this decrease and the correlation of cortical thickness to age was only significant below vertebral body T8 ( r = 0.225–0.574; p r < 0.05–0.005). Most interestingly, however, osteoporosis presents itself with a highly significant loss of cortical thickness throughout the whole spine. This decrease of cortical thickness was more marked in the dorsal shell ( p < 0.05) than in the ventral shell (ventral from C3 to T6 [ p < 0.05] below T6 [ p = NS]). We therefore conclude that in osteoporosis the loss of spinal bone mass is not only a loss of trabecular structure but also a loss of cortical thickness. Furthermore, these results may explain the development of regions of least resistance within the spine in aging and the clustering of osteoporotic fractures in the lower thoracic and lumbar spine." @default.
• W2017565340 created "2016-06-24" @default.
• W2017565340 creator A5028116310 @default.
• W2017565340 creator A5029788399 @default.
• W2017565340 creator A5079425977 @default.
• W2017565340 creator A5086710024 @default.
• W2017565340 creator A5088451290 @default.
• W2017565340 date "1997-01-01" @default.
• W2017565340 modified "2023-10-17" @default.
• W2017565340 title "The Thickness of Human Vertebral Cortical Bone and its Changes in Aging and Osteoporosis: A Histomorphometric Analysis of the Complete Spinal Column from Thirty-Seven Autopsy Specimens" @default.
• W2017565340 cites W1596269324 @default.
• W2017565340 cites W1968079495 @default.
• W2017565340 cites W1971380056 @default.
• W2017565340 cites W1973586346 @default.
• W2017565340 cites W1982467614 @default.
• W2017565340 cites W1987395876 @default.
• W2017565340 cites W1987809980 @default.
• W2017565340 cites W1989240872 @default.
• W2017565340 cites W2001854130 @default.
• W2017565340 cites W2003285394 @default.
• W2017565340 cites W2009399798 @default.
• W2017565340 cites W2010035607 @default.
• W2017565340 cites W2034012970 @default.
• W2017565340 cites W2036564360 @default.
• W2017565340 cites W2037849952 @default.
• W2017565340 cites W2042721501 @default.
• W2017565340 cites W2049165136 @default.
• W2017565340 cites W2068224700 @default.
• W2017565340 cites W2070914367 @default.
• W2017565340 cites W2071366384 @default.
• W2017565340 cites W2090288107 @default.
• W2017565340 cites W2094084063 @default.
• W2017565340 cites W2101284439 @default.
• W2017565340 cites W2117135793 @default.
• W2017565340 cites W2123757980 @default.
• W2017565340 cites W2149793650 @default.
• W2017565340 cites W2156600737 @default.
• W2017565340 cites W2159246062 @default.
• W2017565340 cites W2231298957 @default.
• W2017565340 cites W4252543199 @default.
• W2017565340 doi "https://doi.org/10.1359/jbmr.1997.12.1.89" @default.
• W2017565340 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9240730" @default.
• W2017565340 hasPublicationYear "1997" @default.
• W2017565340 type Work @default.
• W2017565340 sameAs 2017565340 @default.
• W2017565340 citedByCount "186" @default.
• W2017565340 countsByYear W20175653402013 @default.
• W2017565340 countsByYear W20175653402014 @default.
• W2017565340 countsByYear W20175653402015 @default.
• W2017565340 countsByYear W20175653402016 @default.
• W2017565340 countsByYear W20175653402017 @default.
• W2017565340 countsByYear W20175653402018 @default.
• W2017565340 countsByYear W20175653402019 @default.
• W2017565340 countsByYear W20175653402020 @default.
• W2017565340 countsByYear W20175653402021 @default.
• W2017565340 countsByYear W20175653402022 @default.
• W2017565340 countsByYear W20175653402023 @default.
• W2017565340 crossrefType "journal-article" @default.
• W2017565340 hasAuthorship W2017565340A5028116310 @default.
• W2017565340 hasAuthorship W2017565340A5029788399 @default.
• W2017565340 hasAuthorship W2017565340A5079425977 @default.
• W2017565340 hasAuthorship W2017565340A5086710024 @default.
• W2017565340 hasAuthorship W2017565340A5088451290 @default.
• W2017565340 hasConcept C105702510 @default.
• W2017565340 hasConcept C140530291 @default.
• W2017565340 hasConcept C141071460 @default.
• W2017565340 hasConcept C142724271 @default.
• W2017565340 hasConcept C178910020 @default.
• W2017565340 hasConcept C2776541429 @default.
• W2017565340 hasConcept C2779504383 @default.
• W2017565340 hasConcept C2781012678 @default.
• W2017565340 hasConcept C2781451080 @default.
• W2017565340 hasConcept C2993931576 @default.
• W2017565340 hasConcept C44575665 @default.
• W2017565340 hasConcept C71924100 @default.
• W2017565340 hasConceptScore W2017565340C105702510 @default.
• W2017565340 hasConceptScore W2017565340C140530291 @default.
• W2017565340 hasConceptScore W2017565340C141071460 @default.
• W2017565340 hasConceptScore W2017565340C142724271 @default.
• W2017565340 hasConceptScore W2017565340C178910020 @default.
• W2017565340 hasConceptScore W2017565340C2776541429 @default.
• W2017565340 hasConceptScore W2017565340C2779504383 @default.
• W2017565340 hasConceptScore W2017565340C2781012678 @default.
• W2017565340 hasConceptScore W2017565340C2781451080 @default.
• W2017565340 hasConceptScore W2017565340C2993931576 @default.
• W2017565340 hasConceptScore W2017565340C44575665 @default.
• W2017565340 hasConceptScore W2017565340C71924100 @default.
• W2017565340 hasIssue "1" @default.
• W2017565340 hasLocation W20175653401 @default.
• W2017565340 hasLocation W20175653402 @default.
• W2017565340 hasOpenAccess W2017565340 @default.
• W2017565340 hasPrimaryLocation W20175653401 @default.
• W2017565340 hasRelatedWork W2417925853 @default.
• W2017565340 hasRelatedWork W2430296758 @default.
• W2017565340 hasRelatedWork W2483912283 @default.
• W2017565340 hasRelatedWork W2739425936 @default.
• W2017565340 hasRelatedWork W304603462 @default.
• W2017565340 hasRelatedWork W3124480230 @default.

• next