Teses / dissertações sobre o tema "Tishre"
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Halse, Tore Egil, e Thomas Tøkje. "Tissue". Thesis, Norges teknisk-naturvitenskapelige universitet, Institutt for teknisk kybernetikk, 2012. http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-18790.
Texto completo da fonteShazly, Tarek (Tarek Michael). "Tissue-material interactions : bioadhesion and tissue response". Thesis, Massachusetts Institute of Technology, 2009. http://hdl.handle.net/1721.1/54577.
Texto completo da fonteCataloged from PDF version of thesis.
Includes bibliographical references (p. 159-162).
Diverse interactions between soft tissues and implanted biomaterials directly influence the success or failure of therapeutic interventions. The nature and extent of these interactions strongly depend on both the tissue and material in question and can presumably be characterized for any given clinical application. Nevertheless, optimizing biomaterial performance remains a challenge in many implant scenarios due to complex relationships between intrinsic material properties and tissue response. Soft tissue sealants are clinically-relevant biomaterials which impart therapeutic benefit through adhesion to tissue, thus exhibiting a direct functional dependence on tissue-material reactivity. Because adhesion can be rigorously quantified and correlated to the local tissue response, sealants provide an informative platform for studying material properties, soft tissues, and their interplay. We developed a model hydrogel sealant composed of aminated polyethylene glycol and dextran aldehyde (PEG:dextran) that can possess a wide range of bulk and adhesive properties by virtue of constituent polymer modifications. Through comparison to traditional sealants, we established that highly viscoelastic adhesion promotes tissue-sealant interfacial failure resistance without compromising underlying tissue morphology.
(cont.) We analyzed multiple soft tissues to substantiate the notion that natural biochemical variability facilitates the design of tissue-specific sealants which have distinct advantages over more general alternatives. We confirmed that hydrogel-based materials are an attractive material class for ensuring sealant biocompatibility, but found that a marked reduction in adhesive strength following characteristic swell can potentially limit clinical efficacy. To mitigate the swell-induced loss of hydrogel-based sealant functionality, a biomimetic conjugation strategy derived from marine mussel adhesion was applied to PEG:dextran and shown to favorably modulate adhesion. In all phases of this research, we defined material design principles that extend beyond the immediate development of PEG:dextran with potential to enhance the clinical performance of a range of biomaterials.
by Tarek Shazly.
Ph.D.
Tam, Y. Y. A. "Connective tissue growth factor in tissue fibrosis". Thesis, University College London (University of London), 2014. http://discovery.ucl.ac.uk/1448702/.
Texto completo da fonteLe, Thua Trung Hau. "Multimodality Treatment of Soft Tissue and Bone Defect: from Tissue Transfer to Tissue Engineering". Doctoral thesis, Universite Libre de Bruxelles, 2015. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/220961.
Texto completo da fonteDoctorat en Sciences médicales (Médecine)
info:eu-repo/semantics/nonPublished
Dean, Drew W. Kane Robert R. "Meniscal tissue bonding and exploration of sonochemical tissue modification". Waco, Tex. : Baylor University, 2008. http://hdl.handle.net/2104/5291.
Texto completo da fonteGhezzi, Chiara Elia. "Dense collagen-based tubular tissue constructs for airway tissue engineering". Thesis, McGill University, 2013. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=114489.
Texto completo da fonteÀ ce jour, seuls les tissus synthétisés de forme plane, comme les substituts dermiques et épidermiques, ont réussi à percer le marché, surtout en raison de leur complexité relativement faible et de leur géométrie simple. À l'opposé, les exigences mécaniques et fonctionnelles des tissus tubulaires imposent un plus grand nombre de contraintes que les tissus planaires. Principales composantes de plusieurs systèmes biologiques (circulatoire, urinaire ou respiratoire), les tissus tubulaires sont non seulement plus complexes sur le plan de la géométrie et de l'architecture tissulaire, mais ils sont aussi composés de cellules de différents types. De plus, ils sont continuellement exposés à des stimuli mécaniques cycliques. Voilà pourquoi il est essentiel de comprendre les milieux physiologiquement équivalents et de pouvoir les reproduire si on veut obtenir des néotissus ou des modèles tissulaires fonctionnels sur le plan mécanique et biologique.La présente recherche de doctorat visait donc à produire et à caractériser des constructions tubulaires 3D à base de CD, les tissus des voies respiratoires dans des conditions de culture physiologiquement pertinentes. Le premier objectif était de concevoir des constructions à base de CD et d'évaluer la réaction des fibroblastes ensemencés à la CP et à la culture dans un milieu à base de CD; de fabriquer et de caractériser des hybrides multicouches CD-fibroïne-CD ensemencés de cellules souches mésenchymateuses (CSM); et d'évaluer la différenciation.Le deuxième objectif de la présente recherche était de concevoir et de caractériser des constructions tubulaires faites de collagène dense (CTCD). Le troisième objectif était d'implanter des constructions tubulaires à base de CD comme modèle tissulaire des voies respiratoires par l'évaluation de la réponse des cellules musculaires lisses (CML) des voies respiratoires dans les CTCD en présence de stimuli mécaniques physiologiques.En leur fournissant une niche physiologiquement équivalente, et grâce à la stimulation de l'écoulement pulsatoire, in vitro, les CML des voies respiratoires ont pris leur orientation naturelle, maintenu leur phénotype contractile et amélioré les propriétés mécaniques de la CTCD grâce au remodelage matriciel. La capacité de la CTCD à transférer la stimulation physiologique pulsatile aux CSM résidentes a donné une orientation des cellules s'apparentant à leur orientation naturelle et induit l'expression phénotypique.En conclusion, les constructions tubulaires à base de collagène dense qui ont été développées et implantées sont parvenues à fournir in vitro un modèle tissulaire des voies respiratoires pour d'éventuelles études précliniques visant à reproduire les conditions physiologiques et pathologiques.
Chik, Tsz-kit, e 戚子傑. "Fabrication of multi-component tissue for intervertebral disc tissue engineering". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hub.hku.hk/bib/B47849447.
Texto completo da fontepublished_or_final_version
Mechanical Engineering
Doctoral
Doctor of Philosophy
Banani, M. A., M. Rahmatullah, N. Farhan, Zoe Hancox, Safiyya Yousaf, Z. Arabpour, Moghaddam Z. Salehi, M. Mozafari e Farshid Sefat. "Adipose tissue-derived mesenchymal stem cells for breast tissue regeneration". Future Medicine, 2021. http://hdl.handle.net/10454/18391.
Texto completo da fonteWith an escalating incidence of breast cancer cases all over the world and the deleterious psychological impact that mastectomy has on patients along with several limitations of the currently applied modalities, it's plausible to seek unconventional approaches to encounter such a burgeoning issue. Breast tissue engineering may allow that chance via providing more personalized solutions which are able to regenerate, mimicking natural tissues also facing the witnessed limitations. This review is dedicated to explore the utilization of adipose tissue-derived mesenchymal stem cells for breast tissue regeneration among postmastectomy cases focusing on biomaterials and cellular aspects in terms of harvesting, isolation, differentiation and new tissue formation as well as scaffolds types, properties, material–host interaction and an in vitro breast tissue modeling.
Killich, Markus. "Tissue Doppler Imaging". Diss., lmu, 2007. http://nbn-resolving.de/urn:nbn:de:bvb:19-67089.
Texto completo da fonteHeidegger, Simon. "Tissue-specific migration". Diss., lmu, 2010. http://nbn-resolving.de/urn:nbn:de:bvb:19-131476.
Texto completo da fonteDawson, Jennifer Elizabeth. "Cardiac Tissue Engineering". Thèse, Université d'Ottawa / University of Ottawa, 2011. http://hdl.handle.net/10393/20071.
Texto completo da fonteSomasundaram, Murali. "Intestinal tissue engineering". Thesis, University of Oxford, 2016. https://ora.ox.ac.uk/objects/uuid:54e0f17f-fe04-4012-b0d3-04f436e9af9a.
Texto completo da fonteVanhook, Patricia M., Lynne M. Dunphy, M. Zycowizc e C. Luskin. "Soft Tissue Disorders". Digital Commons @ East Tennessee State University, 2019. https://dc.etsu.edu/etsu-works/7410.
Texto completo da fonteMiller, Jeri L. "Ultrasonic tissue characterization of the tongue : spectral features of tissue morphology". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape8/PQDD_0022/NQ50222.pdf.
Texto completo da fonteLiu, Xuerong. "Comparison of Methods For Estimating Tissue Components In Mixed Tissue Sample". University of Akron / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=akron1467971800.
Texto completo da fonteHajeer, Mohammad Younis. "3D soft-tissue, 2D hard-tissue and psychosocial changes following orthognathic surgery". Thesis, University of Glasgow, 2003. http://theses.gla.ac.uk/3126/.
Texto completo da fonteBrown, Andrew. "Development of an autonomous parallel action tissue grasper to minimise tissue trauma". Thesis, University of Dundee, 2014. https://discovery.dundee.ac.uk/en/studentTheses/8151b394-f604-4d5f-98c5-dc8516ac0c42.
Texto completo da fonteHatayama, Takahide. "Regeneration of gingival tissue using in situ tissue engineering with collagen scaffold". Kyoto University, 2019. http://hdl.handle.net/2433/243271.
Texto completo da fonteGrasbon-Frodl, Eva Maria. "Parameters affecting the survival of cultured and grafted embryonic neurons". Lund : Section of Neuronal Survival, Wallenberg Neuroscience Center, Dept. of Physiology and Neuroscience, University of Lund, 1996. http://books.google.com/books?id=XIVsAAAAMAAJ.
Texto completo da fonteMaksym, Geoffrey Nicholas. "Modelling lung tissue rheology". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp02/NQ30329.pdf.
Texto completo da fonteKilarski, Witold. "Mechanisms of Tissue Vascularization". Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4819.
Texto completo da fonteRouwkema, Jeroen. "Prevascularized bone tissue engineering". Enschede : University of Twente [Host], 2007. http://doc.utwente.nl/57929.
Texto completo da fonteMaksym, Geoffrey N. "Modelling lung tissue theology". Thesis, McGill University, 1997. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=42087.
Texto completo da fonteDickson, Jeanette. "Predicting normal tissue radiosensitivity". Thesis, University of Glasgow, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.366256.
Texto completo da fonteMirsadraee, Saeed. "Tissue engineering of pericardium". Thesis, University of Leeds, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.426783.
Texto completo da fonteGetgood, Alan Martin John. "Articular cartilage tissue engineering". Thesis, University of Cambridge, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.608764.
Texto completo da fonteTseng, Yuan-Tsan. "Heart valve tissue engineering". Thesis, University of Oxford, 2011. http://ora.ox.ac.uk/objects/uuid:e67c780d-d60f-42e7-9311-dd523f9141b3.
Texto completo da fonteRosengren, Agneta. "Tissue reactions to biomaterials". Lund : Dept. of Physiology and Neuroscience, Section for Neuroendocrine Cell Biology, and the Dept. of Experimental Research, University Hospital MAS, Lund University, 1997. http://catalog.hathitrust.org/api/volumes/oclc/38986628.html.
Texto completo da fonteBapat, S. "Tissue culture in cereals". Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 1992. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/3020.
Texto completo da fonteSandino, Velásquez Clara Inés. "Simulation of mechanoregulation and tissue differentiation in calcium phosphate scaffolds for tissue engineering". Doctoral thesis, Universitat Politècnica de Catalunya, 2010. http://hdl.handle.net/10803/6211.
Texto completo da fonteDos muestras de materiales porosos basados en fosfato de calcio fueron utilizadas. Se desarrollaron mallas de elementos finitos congruentes, discretizando la fase sólida y los macro poros interconectados, con el fin de tener en cuenta la morfología irregular de los andamios.
En primer lugar, se estudió la distribución de los estímulos mecánicos. La fase sólida y el fluido intersticial se simularon como material elástico lineal y como fluido Newtoniano, respectivamente. Se simuló una compresión del 0.5% en el sólido y un fluido con velocidades de entrada de 1, 10 y 100 µm/s en los poros. Se encontraron distribuciones de deformación similares en las paredes ambos materiales, con valores máximos de 1.6% en compresión y de 0.6% en tracción. En algunos poros, la velocidad del fluido aumentó a 100 y 1000 veces la velocidad de entrada. Este estudio mostró como estímulos mecánicos macroscópicos pueden causar distintos niveles de estímulos mecánicos microscópicos dentro los andamios, debido a la morfología.
A continuación se realizó un estudio en el tiempo de la diferenciación de tejido en un andamio sometido a condiciones in vitro. La compresión y la perfusión se modelaron como en el estudio anterior. Se simularon una compresión del 0.5% y una velocidad de entrada de fluido constante de 10 µm/s o una presión de entrada de fluido constante de 3 Pa. La deformación cortante octaédrica y el esfuerzo cortante del fluido se utilizaron como estímulos mecano-regulatorios basándose en la teoría de Prendergast et al. (1997). Al aplicar velocidad constante, se predijeron fluctuaciones entre los estímulos equivalentes a la formación de tejido y a la muerte celular, debido al aumento en el esfuerzo cortante del fluido cuando el tejido comienza a llenar los poros. Sin embargo, al aplicar presión constante, se predijo estímulo equivalente a la diferenciación de tejido óseo en la mitad del volumen de los poros. Estos resultados sugieren que para permitir la diferenciación de tejido, la velocidad del fluido debe disminuirse cuando el tejido empieza a mineralizarse.
Finalmente, se llevó acabo un estudio en el tiempo de la angiogénesis y de la diferenciación de tejido en un andamio bajo condiciones in vivo. La deformación cortante octaédrica y la velocidad relativa del fluido se utilizaron como estímulos mecano-regulatorios. Las fases sólida y porosa fueron tratadas como materiales poroelásticos. Se simuló la actividad individual de las células. Compresiones de 0.5 y 1% fueron simuladas. La mayoría de los vasos crecieron en los poros de la periferia del andamio y se bloquearon por las paredes. Se formaron redes capilares similares independientemente de la magnitud de deformación utilizada. Al aplicar 0.5% de compresión, estímulos correspondientes a la formación de hueso se predijeron en el 70% del volumen de los poros, sin embargo, sólo el 40% del volumen se llenó de osteoblastos debido a la falta de oxigeno. Este estudio mostró el efecto de la falta de vascularización en el centro del andamio en la diferenciación de tejido.
Ese tipo de estudios, combinados con estudios in vitro, deberían contribuir a la comprensión del proceso de diferenciación de los tejidos dentro de los andamios y por lo tanto a la mejora de los métodos de diseño de andamios.
Mechanical stimuli are one of the factors that affect cell differentiation in the process of bone tissue regeneration; therefore, in the development of scaffolds for tissue engineering, mechanical loads can be applied in order to induce cell activity. The specific mechanical stimuli transmitted to cells at a microscopic level when mechanical loads are applied can be studied using numerical techniques. The objective of this thesis was to study the mechanoregulation of tissue differentiation within calcium phosphate scaffolds using micro computed tomographed based finite element models.
Two samples of porous calcium phosphate based materials were used. Congruent finite element meshes, with the solid phase and the interconnected pores discretized, were developed in order to account for the scaffold irregular morphology.
First, a study of the distribution of mechanical stimuli was performed. The solid phase and the fluid flow within the pores were modeled as linear elastic solid material and Newtonian fluid respectively. Compressive strains of 0.5% of total deformation applied to the solid and interstitial fluid flows with inlet velocities of 1, 10 and 100 µm/s applied to the pores were simulated. Similar strain distributions for both materials were found, with compressive and tensile strain maximal values of 1.6% and 0.6% respectively. For the fluid flow models, the fluid velocity in some of the scaffold pores increased to 100 and 1000 times the inlet velocity. This study showed how mechanical loads and fluid flow applied to the scaffolds caused different levels of mechanical stimuli within the samples according to the morphology of the materials.
Next, a study of the mechanoregulation of tissue differentiation over time in a scaffold subjected to in vitro loads was performed. The solid phase and the fluid flow were modeled as in the study described above. Compressive strain of 0.5% and fluid flow with constant inlet velocity of 10 µm/s or constant inlet pressure of 3 Pa were applied. Octahedral shear strain and fluid shear stress were used as mechano-regulatory stimuli based on the theory of Prendergast et al. (1997). When a constant velocity was simulated, fluctuations between stimuli equivalent to tissue formation and cell death were predicted due to the increase in the fluid shear stress when tissue started to fill the pores. However, when constant pressure was applied, stimuli equivalent to bone formation were predicted in about half of the pore volume. These results suggest that in order to allow tissue differentiation within a scaffold, the fluid velocity should be decreased when tissue starts mineralizing.
Finally, a study of the angiogenesis and the mechanoregulation of tissue differentiation over time in a scaffold subjected to in vivo conditions was performed. Octahedral shear strain and relative fluid velocity were used as mechano-regulatory stimuli. The solid and pore phases were treated as poroelastic materials. Individual cell activity was simulated within the pore domain. Compressive strains of 0.5 and 1% of total deformation were simulated. Most vessels grew in the pores at the periphery of the scaffolds and were blocked by the scaffold walls. Similar capillary networks were formed independently of the magnitude of the mechanical strain applied. When 0.5% of strain was applied, 70% of the pore volume was affected by mechano-regulatory stimuli corresponding to bone formation; however, because of the lack of oxygen, only 40% of the volume was filled with osteoblasts. This study showed the effect of the lack of vascularization in the center of the scaffold on the tissue differentiation.
Such kind of studies, combined with in vitro studies, should contribute to the understanding of the process of tissue differentiation within the constructs and therefore to the improvement of scaffold design methods.
Starly, Binil Sun Wei. "Biomimetic design and fabrication of tissue engineered scaffolds using computer aided tissue engineering /". Philadelphia, Pa. : Drexel University, 2006. http://hdl.handle.net/1860/1114.
Texto completo da fonteWalsh, Joseph Tonry. "Pulsed laser ablation of tissue : analysis of the removal process and tissue healing". Thesis, Massachusetts Institute of Technology, 1988. http://hdl.handle.net/1721.1/14412.
Texto completo da fonteIncludes bibliographical references.
by Joseph T. Walsh, Jr.
Ph.D.
Rotenberg, Shaun. "Blood Flow, Tissue Thickness, and Molecular Changes during Connective Tissue Graft Early Healing". The Ohio State University, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=osu1273335634.
Texto completo da fonteAhn, Jinsoo. "Roles of Adipose Tissue-Derived Factors in Adipose Tissue Development and Lipid Metabolism". The Ohio State University, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=osu1430496153.
Texto completo da fonteChhaya, Mohit Prashant. "Additive tissue manufacturing for breast reconstruction: Combining CAD/CAM with adipose tissue engineering". Thesis, Queensland University of Technology, 2015. https://eprints.qut.edu.au/84762/9/Mohit_Prashant_Chhaya_Thesis.pdf.
Texto completo da fonteLiaudanksaya, Volha. "Bottom-up Tissue Engineering:The Effect of 3D Tissue Fabrication Strategies on Cellular Behavior". Doctoral thesis, University of Trento, 2015. http://eprints-phd.biblio.unitn.it/2018/1/Final_Doctoral_thesis_Volha_Liaudanskaya.pdf.
Texto completo da fonteGrover, Chloe Natasha. "Physical properties and cell interactions of collagen-based scaffolds and films for use in myocardial tissue engineering". Thesis, University of Cambridge, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.610672.
Texto completo da fonteMullen, Leanne. "The incorporation of chondrogenic factors into a biomimetic scaffold to facilitate tissue regeneration". Thesis, University of Cambridge, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.609303.
Texto completo da fonteComeau, Benita M. "Fabrication of tissue engineering scaffolds using stereolithography". Diss., Atlanta, Ga. : Georgia Institute of Technology, 2007. http://hdl.handle.net/1853/26564.
Texto completo da fonteCommittee Chair: Henderson, Clilfford; Committee Member: Ludovice, Peter; Committee Member: Meredith, Carson; Committee Member: Prausnitz, Mark; Committee Member: Rosen, David; Committee Member: Wang, Yadong. Part of the SMARTech Electronic Thesis and Dissertation Collection.
Wilson, Christopher G. "Modeling the dynamic composition of engineered cartilage". Link to electronic thesis, 2002. http://www.wpi.edu/Pubs/ETD/Available/etd-0326102-204208/.
Texto completo da fonteWarncke, Urszula Osinska. "Profiling Fatty Acid Composition of Brown Adipose Tissue, White Adipose Tissue and Bone Marrow Adipose Tissue of Healthy and Diet-Induced Obese Mice". Wright State University / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=wright1440097081.
Texto completo da fonteVijayasekaran, Aparna. "Human Adipose Derived Stem Cells (hASC's) and Soft Tissue Reconstruction: Evaluation of Methods for Increasing the Vascularity of Tissue Engineered Soft Tissue Construct". Thesis, The University of Arizona, 2012. http://hdl.handle.net/10150/265352.
Texto completo da fonteAndersson, Jonas. "Adipose tissue as an active organ : blood flow regulation and tissue-specific glucocorticoid metabolism". Doctoral thesis, Umeå universitet, Medicin, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-48415.
Texto completo da fonteWatt, Gillian Fairfull. "Analysis of the cross-tissue expression of antagonist and agonist activity on isolated tissue". Thesis, King's College London (University of London), 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266521.
Texto completo da fonteSmith, Michael James. "Utilising mesenchymal stem cells from adipose tissue and dental pulp for epithelial tissue engineering". Thesis, University of Birmingham, 2017. http://etheses.bham.ac.uk//id/eprint/7394/.
Texto completo da fonteDroesch, Kristen L. "The Development of Gelatin Based Tissue Adhesives for Use in Soft Tissue Biomedical Applications". Thesis, Virginia Tech, 1999. http://hdl.handle.net/10919/46204.
Texto completo da fonteMaster of Science
Napolitano, Anthony P. "Directing cellular self-assembly for micro-scale tissue engineering and in vitro tissue models". View abstract/electronic edition; access limited to Brown University users, 2008. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3319111.
Texto completo da fonteLiaudanskaya, Volha. "Bottom-up Tissue Engineering: The Effect of 3D Tissue Fabrication Strategies on Cellular Behavior". Doctoral thesis, Università degli studi di Trento, 2015. https://hdl.handle.net/11572/367766.
Texto completo da fonteLiaudanskaya, Volha. "Bottom-up Tissue Engineering: The Effect of 3D Tissue Fabrication Strategies on Cellular Behavior". Doctoral thesis, University of Trento, 2015. http://eprints-phd.biblio.unitn.it/1471/1/10.03.15_Doctoral_thesis_modified.pdf.
Texto completo da fonteSodian, Ralf. "Tissue-Engineering von kardiovaskulären Geweben". [S.l.] : [s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=974660175.
Texto completo da fonte