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Books on the topic 'Fibring'

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Published: 4 June 2021
Last updated: 20 February 2023

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1

Gabbay, Dov M. Fibring logics. Oxford: Clarendon Press, 1999.

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2

Lane, D. A., ed. Fibrin formation and Fibrinolysis. Berlin, Boston: De Gruyter, 1986. http://dx.doi.org/10.1515/9783110871951.

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3

Waclawiczek, Hans-Werner, ed. Progress in Fibrin Sealing. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-48362-2.

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4

Günther, Schlag, and Redl Heinz, eds. Fibrin sealant in operative medicine. Berlin: Springer-Verlag, 1986.

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5

Schlag, Günther, and Heinz Redl, eds. Fibrin Sealant in Operative Medicine. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71359-0.

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6

Schlag, Günther, and Heinz Redl, eds. Fibrin Sealant in Operative Medicine. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71391-0.

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7

Schlag, Günther, and Heinz Redl, eds. Fibrin Sealant in Operative Medicine. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71453-5.

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8

Schlag, Günther, and Heinz Redl, eds. Fibrin Sealant in Operative Medicine. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-82880-5.

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9

Schlag, Günther, and Heinz Redl, eds. Fibrin Sealant in Operative Medicine. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-95513-6.

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10

Schlag, Günther, and Heinz Redl, eds. Fibrin Sealant in Operative Medicine. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-95515-0.

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11

Schlag, Günther, and Heinz Redl, eds. Fibrin Sealant in Operative Medicine. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71633-1.

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12

1949-, Lane D. A., Henschen A. 1935-, and Jasani M. K, eds. Fibrinogen, fibrin formation and fibrinolysis: Proceedings Workshop in Fibrinogen, April 2-3, 1985, London, England. Berlin: W. de Gruyter, 1986.

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13

Schlag, Günther, Ernst Wolner, and Franz Eckersberger, eds. Fibrin Sealing in Surgical and Nonsurgical Fields. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-79227-4.

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14

Schlag, Günther, and Heinz Redl, eds. Fibrin Sealing in Surgical and Nonsurgical Fields. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-95720-8.

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15

Schlag, Günther, H. W. Waclawiczek, and R. Daum, eds. Fibrin Sealing in Surgical and Nonsurgical Fields. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-85101-8.

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16

Schlag, Günther, and Jürgen Holle, eds. Fibrin Sealing in Surgical and Nonsurgical Fields. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-79346-2.

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17

Schlag, Günther, Peter Bösch, and Helene Matras, eds. Fibrin Sealing in Surgical and Nonsurgical Fields. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-79010-2.

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18

Bense, Christine Adelle. The in vitro stability of cross-linked fibrin and fibrin/hyaluronan-coated polyurethanes in the presence of plasmin. Ottawa: National Library of Canada, 1998.

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19

Otzen, Daniel Erik, ed. Amyloid Fibrils and Prefibrillar Aggregates. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527654185.

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20

1935-, Henschen A., ed. Fibrinogen: Proceedings. Berlin: W. de Gruyter, 1985.

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21

McRitchie, Donna Isabelle. The role of fibrin in the pathogenesis of intraabdominal sepsis. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1993.

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22

Kadler, Karl. Extracellular matrix 1: fibril-forming collagens. London: Academic Press, 1995.

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23

Kadler, Karl. Extracellular matrix 1: fibril-forming collagens. London: Academic Press, 1994.

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24

F, Ebert Ray, ed. Index of variant human fibrinogens. Boca Raton: CRC Press, 1994.

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25

U, Kyŏng-mi. Chʻisu mit chʻiju chojik chʻangsang chʻiyu esŏ pʻibŭrin nano sŏmyu kijil ŭi yŏkhal kyumyŏng =: Role of fibrin nanofibrous matrix in pulpal and periodontal wound healing. [Seoul]: Pogŏn Pokchibu, 2007.

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26

Fromstein, Joanna Dawn. Development and characterization of fibrin and hyaluronan coated biodegradable polyurethane films. Ottawa: National Library of Canada, 2001.

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27

Miron, Richard J., and Joseph Choukroun, eds. Platelet Rich Fibrin in Regenerative Dentistry: Biological Background and Clinical Indications. Oxford, UK: John Wiley & Sons, Ltd, 2017. http://dx.doi.org/10.1002/9781119406792.

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28

IARC Working Group on the Evaluation of Carcinogenic Risks to Humans. Silica, some silicates, coal dust and para-Aramid fibrils. Lyon, France: IARC, 1997.

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29

Endoscopic Fibrin Glueing. Blackwell Science Ltd, 1998.

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30

Leiris, Michel. Fibrils. Yale University Press, 2019. http://dx.doi.org/10.12987/9780300227857.

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31

Waclawiczek, Hans-Werner. Progress in Fibrin Sealing. Springer, 1989.

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32

Miron, Richard J. Understanding Platelet-Rich Fibrin. Quintessence Publishing Company, Incorporated, 2021.

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33

Waclawiczek, Hans-Werner. Progress in Fibrin Sealing. Springer, 1989.

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34

Waclawiczek, Hans-Werner. Progress in Fibrin Sealing. Springer London, Limited, 2012.

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35

Kahn, S. Lowell. Fibrin Sheath Removal Techniques. Edited by S. Lowell Kahn, Bulent Arslan, and Abdulrahman Masrani. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199986071.003.0045.

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Abstract:
Although autogenous arteriovenous fistula creation is the gold-standard dialysis access, catheters represent between 40% and 60% of dialysis access in the United States. Catheters are placed for a variety of reasons, commonly as temporary access for acute renal failure or as a bridge to a more permanent access in patients with end-stage renal disease. Fibrin sheaths represent a heterogeneous matrix of cells and debris that form around catheters and are a known common cause of catheter failure and central venous stenosis. Their formation is ubiquitous in the dialysis population, occurring with 80–100% of catheters within 1 week of implantation. This chapter presents several techniques for the management of the fibrin sheath—the traditional catheter stripping technique, the internal catheter stripping technique, and the fibrin sheath angioplasty technique.
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36

Günther, Schlag, and Redl Heinz, eds. Fibrin sealant in operative medicine. Berlin: Springer-Verlag, 1986.

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37

Fibrin Sealant in Operative Medicine. Springer-Verlag Berlin and Heidelberg GmbH & Co. KG, 1986.

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38

Bleyl, Uwe. Arteriosklerose und Fibrininkorporation: Untersuchungen zur Pathogenese der Aortensklerose. Springer, 2012.

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39

Badimon, Lina, Felix C. Tanner, Giovanni G. Camici, and Gemma Vilahur. Pathophysiology of thrombosis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198755777.003.0018.

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Ischaemic heart disease and stroke are major causes of death and morbidity worldwide. Coronary and cerebrovascular events are mainly a consequence of a sudden thrombotic occlusion of the vessel lumen. Arterial thrombosis usually develops on top of a disrupted atherosclerotic plaque because of the exposure of thrombogenic material, such as collagen fibrils and tissue factor (TF), to the flowing blood. TF, either expressed by subendothelial cells, macrophage- and/or vascular smooth muscle-derived foam-cells in atherosclerotic plaques, is a key element in the initiation of thrombosis due to its ability to induce thrombin formation (a potent platelet agonist) and subsequent fibrin deposition at sites of vascular injury. Adhered platelets at the site of injury also play a crucial role in the pathophysiology of atherothrombosis. Platelet surface receptors (mainly glycoproteins) interact with vascular structures and/or Von Willebrand factor triggering platelet activation signalling events, including an increase in intracellular free Ca2+, exposure of a pro-coagulant surface, and secretion of platelet granule content. On top of this, interaction between soluble agonists and platelet G-coupled protein receptors further amplifies the platelet activation response favouring integrin alpha(IIb)beta(3) activation, an essential step for platelet aggregation. Blood-borne TF and microparticles have also been shown to contribute to thrombus formation and propagation. As thrombus evolves different circulating cells (red-blood cells and leukocytes, along with occasional undifferentiated cells) get recruited in a timely dependent manner to the growing thrombus and further entrapped by the formation of a fibrin mesh.
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40

ABRAMOWITZ, Laurent. Fistules Anales: Utilisation des Colles de Fibrine. Springer Paris, 2010.

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41

Günther, Schlag, and Redl Heinz, eds. Fibrin sealing in surgical and nonsurgical fields. Berlin: Springer-Verlag, 1994.

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42

Redl, H., and G. Schlag. Fibrin Sealant in Operative Medicine: Traumatology-Orthopaedics. Springer, 1987.

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43

Schlag, G. Fibrin Sealant in Operative Medicine: Ophthalmology-Neurosurgery. Springer Verlag, 1986.

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44

Sabeti, Mohammad. Platelet-Rich Fibrin Prf Applications in Endodontics. Quintessence Publishing Company, Incorporated, 2020.

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45

Galzitskaya, Oxana V., and Vijay Kumar. Structural Biology of Amyloid Fibrils. Elsevier Science & Technology Books, 2023.

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46

Amyloid Fibrils And Prefibrillar Aggregates. Wiley-VCH Verlag GmbH, 2013.

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47

Fibrin Sealant in Operative Medicine : Volume 1: Otorhinolaryngology. Springer, 2012.

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48

Redl, H., and G. Schlag. Fibrin Sealant in Operative Medicine : Volume 1: Otorhinolaryngology. Springer London, Limited, 2012.

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49

Henschen, A., and D. A. Lane. Fibrinogen: Fibrin Formation and Fibrinolysis : Proceedings, Workshop on Fibrinogen, April 2-3, 1985, London England. Walter De Gruyter Inc, 1986.

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50

Fibrinogen. Walter de Gruyter & Co, 1986.

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