2011
DOI: 10.1002/ca.21271
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Study of the vascular architecture of bones using the plastination technique

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Cited by 6 publications
(5 citation statements)
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“…The study of the three-dimensional (3D) spatial distribution of the vasoductal elements can be carried out by: ( i ) classical dissection [ 32 , 40 ], ( ii ) by making and examining corrosion casts [ 41 ], ( iii ) by making two-dimensional plastination preparations followed by 3D reconstruction of anatomical structures and [ 42 , 43 ]; ( iv ) by modern imaging methods, of which MDCT angiography is the easiest method [ 19 , 20 , 24 , 25 , 26 , 38 , 44 ].…”
Section: ⧉ Discussionmentioning
confidence: 99%
“…The study of the three-dimensional (3D) spatial distribution of the vasoductal elements can be carried out by: ( i ) classical dissection [ 32 , 40 ], ( ii ) by making and examining corrosion casts [ 41 ], ( iii ) by making two-dimensional plastination preparations followed by 3D reconstruction of anatomical structures and [ 42 , 43 ]; ( iv ) by modern imaging methods, of which MDCT angiography is the easiest method [ 19 , 20 , 24 , 25 , 26 , 38 , 44 ].…”
Section: ⧉ Discussionmentioning
confidence: 99%
“…-Type II (17 casts, 10.25% of cases) in which from the ombilical part of the left branch arise three LBrs with two subtypes: -Type IIA (4 pieces, 2.500% of cases) in which from the ombilical part of the left branch arise three LBrs: two superior LBrs -for segments II and IIa, and one inferior LBr -for segment III ( fig.1 C); -Type IIB (13 pieces, 8.125% of cases) in which from the ombilical part of the left branch arise three LBrs: one superior LBr -for segments II, and two inferior LBrs -for segments IIIa and III ( fig.1 D). [18][19][20] and the corrosion casts [2,8,9,14,21]. In the case of parenchymal organs, the corrosion casts most closely outline the three-dimensional distribution of vascularductal elements.…”
Section: Resultsmentioning
confidence: 99%
“…The standard method for producing 1–3 mm thick E12‐plastinated sections (Sora et al, ; Sora and Matusz, ), pioneered by von Hagens, is carried out by freezing a fresh tissue sample and cutting sections with a band‐saw; the tissue loss is in the order 0.9 mm per slice (von Hagens, ) (Figs. and A, B).…”
Section: Introductionmentioning
confidence: 99%
“…A different technique is used for plastinating ultra‐thin sections, between 0.3 and 1.0 mm (Sora and Matusz, ). In general, 3–5 mm sections are used for descriptive and morphometric analysis, and ultra‐thin sections (<1 mm) for three‐dimensional reconstruction or histological examination (Cook, ; Gruber et al, ; Sora et al, , ).…”
Section: Introductionmentioning
confidence: 99%