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Journal articles on the topic 'Guided tissue regeneration. eng'

Author: Grafiati
Published: 4 June 2021
Last updated: 2 February 2022

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1

Cahaya, Cindy, and Sri Lelyati C. Masulili. "Perkembangan Terkini Membran Guided Tissue Regeneration/Guided Bone Regeneration sebagai Terapi Regenerasi Jaringan Periodontal." Majalah Kedokteran Gigi Indonesia 1, no. 1 (June 1, 2015): 1. http://dx.doi.org/10.22146/majkedgiind.8810.

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Periodontitis adalah salah satu penyakit patologis yang mempengaruhi integritas sistem periodontal yang menyebabkan kerusakan jaringan periodontal yang berlanjut pada kehilangan gigi. Beberapa tahun belakangan ini banyak ketertarikan untuk melakukan usaha regenerasi jaringan periodontal, tidak saja untuk menghentikan proses perjalanan penyakit namun juga mengembalikan jaringan periodontal yang telah hilang. Sasaran dari terapi regeneratif periodontal adalah menggantikan tulang, sementum dan ligamentum periodontal pada permukaan gigi yang terkena penyakit. Prosedur regenerasi antara lain berupa soft tissue graft, bone graft, biomodifikasi akar gigi, guided tissue regeneration sertakombinasi prosedur-prosedur di atas, termasuk prosedur bedah restoratif yang berhubungan dengan rehabilitasi oral dengan penempatan dental implan. Pada tingkat selular, regenerasi periodontal adalah proses kompleks yang membutuhkan proliferasi yang terorganisasi, differensiasi dan pengembangan berbagai tipe sel untuk membentuk perlekatan periodontal. Rasionalisasi penggunaan guided tissue regeneration sebagai membran pembatas adalah menahan epitel dan gingiva jaringan pendukung, sebagai barrier membrane mempertahankan ruang dan gigi serta menstabilkan bekuan darah. Pada makalah ini akan dibahas sekilas mengenai 1. Proses penyembuhan terapi periodontal meliputi regenerasi, repair ataupun pembentukan perlekatan baru. 2. Periodontal spesific tissue engineering. 3. Berbagai jenis membran/guided tissue regeneration yang beredar di pasaran dengan keuntungan dan kerugian sekaligus karakteristik masing-masing membran. 4. Perkembangan membran terbaru sebagai terapi regenerasi penyakit periodontal. Tujuan penulisan untuk memberi gambaran masa depan mengenai terapi regenerasi yang menjanjikan sebagai perkembangan terapi penyakit periodontal. Latest Development of Guided Tissue Regeneration and Guided Bone Regeneration Membrane as Regenerative Therapy on Periodontal Tissue. Periodontitis is a patological state which influences the integrity of periodontal system that could lead to the destruction of the periodontal tissue and end up with tooth loss. Currently, there are so many researches and efforts to regenerate periodontal tissue, not only to stop the process of the disease but also to reconstruct the periodontal tissue. Periodontal regenerative therapy aims at directing the growth of new bone, cementum and periodontal ligament on the affected teeth. Regenerative procedures consist of soft tissue graft, bone graft, roots biomodification, guided tissue regeneration and combination of the procedures, including restorative surgical procedure that is connected with oral rehabilitation with implant placement. At cellular phase, periodontal regeneration is a complex process with well-organized proliferation, distinction, and development of various type of cell to form attachment of periodontal tissue. Rationalization of the use of guided tissue regeneration as barrier membrane is to prohibit the penetration of epithelial and connective tissue migration into the defect, to maintain space, and to stabilize the clot. This research discusses: 1. Healing process on periodontal therapy including regeneration, repair or formation of new attachment. 2. Periodontal specific tissue engineering. 3. Various commercially available membrane/guided tissue regeneration in the market with its advantages and disadvantages and their characteristics. 4. Recent advancement of membrane as regenerative therapy on periodontal disease. In addition, this review is presented to give an outlook for promising regenerative therapy as a part of developing knowledge and skills to treat periodontal disease.
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2

Iviglia, Giorgio, Saeid Kargozar, and Francesco Baino. "Biomaterials, Current Strategies, and Novel Nano-Technological Approaches for Periodontal Regeneration." Journal of Functional Biomaterials 10, no. 1 (January 2, 2019): 3. http://dx.doi.org/10.3390/jfb10010003.

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Periodontal diseases involve injuries to the supporting structures of the tooth and, if left untreated, can lead to the loss of the tooth. Regenerative periodontal therapies aim, ideally, at healing all the damaged periodontal tissues and represent a significant clinical and societal challenge for the current ageing population. This review provides a picture of the currently-used biomaterials for periodontal regeneration, including natural and synthetic polymers, bioceramics (e.g., calcium phosphates and bioactive glasses), and composites. Bioactive materials aim at promoting the regeneration of new healthy tissue. Polymers are often used as barrier materials in guided tissue regeneration strategies and are suitable both to exclude epithelial down-growth and to allow periodontal ligament and alveolar bone cells to repopulate the defect. The problems related to the barrier postoperative collapse can be solved by using a combination of polymeric membranes and grafting materials. Advantages and drawbacks associated with the incorporation of growth factors and nanomaterials in periodontal scaffolds are also discussed, along with the development of multifunctional and multilayer implants. Tissue-engineering strategies based on functionally-graded scaffolds are expected to play an ever-increasing role in the management of periodontal defects.
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3

Dueñas-Villamil., Ricardo Ernesto, Leticia Belén Bernard-Gutiérrez, Diana Susely Hernández-Chavarría, Mercedes Olaya-Contreras, Nelly Stella Roa-Molina, and Adriana Rodriguez-Ciodaro. "Expression of CD44 in previously grafted alveolar bone." Journal of Oral Research 9, no. 6 (December 30, 2020): 449–56. http://dx.doi.org/10.17126/joralres.2020.089.

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Objetive: To determine the expressions of the bone surface marker CD44 in samples of alveolar bone previously regenerated with allograft, xenograft, and mixed, using the technique of guided bone regeneration. Material and Methods: This exploratory study was approved by the institutional research and ethics committee. By means of intentional sampling and after obtaining informed consent for tissue donation, 20 samples of alveolar bone previously regenerated with guided bone regeneration therapy with particulate bone graft and membrane were taken during implant placement. The samples were stained with hematoxylin-eosin for histological analysis, and by immunohistochemistry for the detection of CD44. Results: Sections with hematoxylin-eosin showed bone tissue with the presence of osteoid matrix and mature bone matrix of usual appearance. Of the CD44+ samples, 80% were allograft and 20% xenograft. The samples with allograft-xenograft were negative. There were no differences in the intensity of CD44 expression between the positive samples. The marker was expressed in osteocytes, stromal cells, mononuclear infiltrate, and some histiocytes. Eighty percent of the CD44+ samples and 100% of the samples in which 60 or more cells were labelled corresponded to allografts (p=0.000). A total of 67% of the samples from the anterior sector, and 40% from the posterior sector were CD44+ (p=0.689). Conclusion: This study shows for the first time that guided bone regeneration using allografts is more efficient for the generation of mature bone determined by the expression of CD44, compared to the use of xenografts and mixed allograft-xenograft, regardless of the regenerated anatomical area.
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4

Bernabe, Pedro Felicio Estrada, Mariane Maffei Azuma, Luciana Louzada Ferreira, Eloi Dezan-Junior, Joao Eduardo Gomes-Filho, and Luciano Tavares Angelo Cintra. "Root Reconstructed with Mineral Trioxide Aggregate and Guided Tissue Regeneration in Apical Surgery: A 5-year Follow-up." Brazilian Dental Journal 24, no. 4 (July 2013): 428–32. http://dx.doi.org/10.1590/0103-6440201302242.

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Apical surgery should be considered as the last treatment option and employed when conventional endodontic treatment does not provide the expected result. In teeth undergoing apical surgery, the type of retrograde filling material is one of the factors interfering with the repair of periapical tissues. The material in intimate contact with the periapical tissues plays a fundamental role in the repair process. Several materials have been studied and indicated for use in apical surgery procedures, but the mineral trioxide aggregate (MTA) is still the most frequently used one. Guided tissue regeneration (GTR) techniques have been proposed as an adjunct to apical surgery to enhance bone healing. Here is reported a clinical case in which apical surgery was performed in conjunction with MTA-based root reconstruction of the maxillary right second incisor. After the apical surgery, a root-end cavity was prepared at the vestibular face of the involved tooth and filled with MTA. A bovine bone graft and a cortical collagen membrane were placed on the bone defect. After 5 years, clinical and radiographic assessments showed that the treatment was successful. It may be concluded that MTA presents favorable characteristics in adverse conditions and can be used in conjunction with GTR in cases involving root reconstruction.
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5

Anitua, Eduardo, Isabel Andia, Bruno Ardanza, Paquita Nurden, and Alan Nurden. "Autologous platelets as a source of proteins for healing and tissue regeneration." Thrombosis and Haemostasis 91, no. 01 (2004): 4–15. http://dx.doi.org/10.1160/th03-07-0440.

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SummaryPlatelets are known for their role in haemostasis where they help prevent blood loss at sites of vascular injury. To do this, they adhere, aggregate and form a procoagulant surface leading to thrombin generation and fibrin formation. Platelets also release substances that promote tissue repair and influence the reactivity of vascular and other blood cells in angiogenesis and inflammation. They contain storage pools of growth factors including PDGF, TGF-β and VEGF as well as cytokines including proteins such as PF4 and CD40L. Chemokines and newly synthesised active metabolites are also released. The fact that platelets secrete growth factors and active metabolites means that their applied use can have a positive influence in clinical situations requiring rapid healing and tissue regeneration. Their administration in fibrin clot or fibrin glue provides an adhesive support that can confine secretion to a chosen site. Additionally, the presentation of growth factors attached to platelets and/or fibrin may result in enhanced activity over recombinant proteins. Dental implant surgery with guided bone regeneration is one situation where an autologous platelet-rich clot clearly accelerates ossification after tooth extraction and/or around titanium implants. The end result is both marked reductions in the time required for implant stabilisation and an improved success rate. Orthopaedic surgery, muscle and/or tendon repair, reversal of skin ulcers, hole repair in eye surgery and cosmetic surgery are other situations where autologous platelets accelerate healing. Our aim is to review these advances and discuss the ways in which platelets may provide such unexpected beneficial therapeutic effects.
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6

Ventrelli, Letizia, Leonardo Ricotti, Arianna Menciassi, Barbara Mazzolai, and Virgilio Mattoli. "Nanoscaffolds for Guided Cardiac Repair: The New Therapeutic Challenge of Regenerative Medicine." Journal of Nanomaterials 2013 (2013): 1–16. http://dx.doi.org/10.1155/2013/108485.

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Cardiovascular diseases represent the leading cause of death and disability in the world. At the end-stage of heart failure, heart transplantation remains the ultimate option. Therefore, due to the numerous drawbacks associated with this procedure, new alternative strategies to repair the wounded heart are required. Cell therapy is a potential option to regenerate functional myocardial tissue. The characteristics of the ideal cardiac cell therapy include the use of the proper cell type and delivery methods as well as the choice of a suitable biomaterial acting as a cellular vehicle. Since traditional delivery methods are characterized by several counter backs, among which low cell survival, new engineered micro- and nanostructured materials are today extensively studied to provide a good cardiac therapy. In this review, we report the most recent achievements in the field of cell therapy for myocardial infarction treatment and heart regeneration, focusing on the most commonly used cell sources, the traditional approaches used to deliver cells at the damaged site, and a series of novel technologies based on recent advancements of bioengineering, highlighting the tremendous potential that nanoscaffolds have in this framework.
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7

Byun, Soo-Hwan, Sun-Hyun Kim, Sura Cho, Ho Lee, Ho-Kyung Lim, Ju-Won Kim, Ui-Lyong Lee, et al. "Tissue Expansion Improves the Outcome and Predictability for Alveolar Bone Augmentation: Prospective, Multicenter, Randomized Controlled Trial." Journal of Clinical Medicine 9, no. 4 (April 16, 2020): 1143. http://dx.doi.org/10.3390/jcm9041143.

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Objectives: The purpose of this study was to evaluate the effectiveness of the intraoral use of subperiosteally placed self-inflating tissue expanders for subsequent bone augmentation and implant integrity. Material and methods: A prospective, multicenter, randomized controlled trial was performed on patients requiring alveolar bone graft for dental implant insertion. Patients were assigned to three groups: tissue expansion and tunneling graft (TET group), tissue expansion and conventional bone graft (TEG), and control group without tissue expansion. Dimensional changes of soft tissue and radiographic vertical bone gain, retention, and peri-implant marginal bone changes were evaluated and secondary outcomes; clinical complications and thickness changes of expanded overlying tissue were assessed. Results: Among 75 patients screened, a total of 57 patients were included in the final analysis. Most patients showed uneventful soft tissue expansion without any inflammatory sign or symptoms. Ultrasonographic measurements of overlying gingiva revealed no thinning after tissue expansion (p > 0.05). Mean soft vertical and horizontal tissue measurements at the end of its expansion were 5.62 and 6.03 mm, respectively. Significantly higher vertical bone gain was shown in the TEG (5.71 ± 1.99 mm) compared with that in the control patients (4.32 ± 0.97 mm; p < 0.05). Hard tissue retention— measured by bone resorption after 6 months—showed that control group showed higher amount of vertical (2.06 ± 1.00 mm) and horizontal bone resorption (1.69 ± 0.81 mm) compared to that of the TEG group (p < 0.05). Conclusion: The self-inflating tissue expander effectively augmented soft tissue volume and both conventional bone graft and tunneling techniques confirmed their effectiveness in bone augmentation. With greater amount of bone gain and better 6 month hard tissue integrity, the TEG group compared to the control group—without tissue expansion—showed that the combined modality of tissue expander use and guided bone regeneration (GBR) technique may improve the outcome and predictability of hard tissue augmentation.
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8

Gilbert Triplett, R. "Guided Tissue Regeneration." Atlas of the Oral and Maxillofacial Surgery Clinics 2, no. 2 (September 1994): 93–108. http://dx.doi.org/10.1016/s1061-3315(18)30135-5.

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9

Dowell, P., J. Moran, and D. Quteish. "Guided tissue regeneration." British Dental Journal 171, no. 5 (September 1991): 125–27. http://dx.doi.org/10.1038/sj.bdj.4807634.

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10

Karring, Thorkild. "Guided Tissue Regeneration." Advances in Dental Research 9, no. 3_suppl (November 1995): 18. http://dx.doi.org/10.1177/0895937495009003s0901.

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11

Wagle, ShreeprasadVijay, AmitArvind Agrawal, Dinaz Bardoliwala, and Chhaya Patil. "Guided tissue regeneration." Journal of Oral Research and Review 13, no. 1 (2021): 46. http://dx.doi.org/10.4103/jorr.jorr_11_20.

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12

Laurell, Lars, and Jan Gottlow. "Guided tissue regeneration update." International Dental Journal 48, no. 4 (August 1998): 386–98. http://dx.doi.org/10.1111/j.1875-595x.1998.tb00701.x.

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13

Saravanakumar, R., M. Jananni, V. Arvind Raaj, and KR Vineela. "Guided Tissue Regeneration Membrane." Annals of SBV 3, no. 2 (2014): 7–13. http://dx.doi.org/10.5005/jp-journals-10085-3202.

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14

Villar, Cristina C., and David L. Cochran. "Regeneration of Periodontal Tissues: Guided Tissue Regeneration." Dental Clinics of North America 54, no. 1 (January 2010): 73–92. http://dx.doi.org/10.1016/j.cden.2009.08.011.

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15

van den Beucken, Jeroen J. J. P., Lise T. de Jonge, Adelina S. Plachokova, and John A. Jansen. "Enzymatically Enhanced Guided Tissue Regeneration." Bioceramics Development and Applications 1 (2011): 1–3. http://dx.doi.org/10.4303/bda/d110158.

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16

Richie-Gillespie, Ray. "Guided tissue regeneration in endodontics." Journal of Endodontics 22, no. 8 (August 1996): 443. http://dx.doi.org/10.1016/s0099-2399(96)80254-8.

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17

Baikm, B. E. "Guided Tissue and Bone Regeneration." Implant Dentistry 6, no. 1 (1997): 47. http://dx.doi.org/10.1097/00008505-199700610-00020.

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18

Dyer, Bret L., Raul G. Caffesse, Carlos E. Nasjleti, and Edith C. Morrison. "Guided Tissue Regeneration With Dentin Biomodification." Journal of Periodontology 64, no. 11 (November 1993): 1052–60. http://dx.doi.org/10.1902/jop.1993.64.11.1052.

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19

Tinti, Carlo, Giampaolo Vincenzi, and Roberto Cocchetto. "Guided Tissue Regeneration in Mucogingival Surgery." Journal of Periodontology 64, no. 11s (November 1993): 1184–91. http://dx.doi.org/10.1902/jop.1993.64.11s.1184.

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20

Lin, Louis, Melody Y. H. Chen, Domenico Ricucci, and Paul A. Rosenberg. "Guided Tissue Regeneration in Periapical Surgery." Journal of Endodontics 36, no. 4 (April 2010): 618–25. http://dx.doi.org/10.1016/j.joen.2009.12.012.

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21

GREENSTEIN, GARY, and JACK G. CATON. "Biodegradable barriers and guided tissue regeneration." Periodontology 2000 1, no. 1 (February 1993): 36–45. http://dx.doi.org/10.1111/j.1600-0757.1993.tb00205.x.

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22

Nyman, Sture R., and Niklaus P. Lang. "Guided tissue regeneration and dental implants." Periodontology 2000 4, no. 1 (February 1994): 109–18. http://dx.doi.org/10.1111/j.1600-0757.1994.tb00011.x.

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23

PRATO, GIOVANPAOLO PINI, CARLO CLAUSER, MAURIZIO S. TONETTI, and PIERPAOLO CORTELLINI. "Guided tissue regeneration in gingival recessions." Periodontology 2000 11, no. 1 (June 1996): 49–57. http://dx.doi.org/10.1111/j.1600-0757.1996.tb00182.x.

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24

Ferris, Robert T. "A review of guided tissue regeneration." International Dental Journal 48 (June 1998): 322–25. http://dx.doi.org/10.1111/j.1875-595x.1998.tb00723.x.

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25

Boyne, Philip J. "The Evolution of Guided Tissue Regeneration." Oral and Maxillofacial Surgery Clinics of North America 13, no. 3 (August 2001): 397–409. http://dx.doi.org/10.1016/s1042-3699(20)30126-6.

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26

Nyman, Sture. "Bone regeneration using the principle of guided tissue regeneration." Journal of Clinical Periodontology 18, no. 6 (July 1991): 494–98. http://dx.doi.org/10.1111/j.1600-051x.1991.tb02322.x.

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27

Agus Susanto, Susi Susanah, Bambang Pontjo, and Mieke Hemiawati Satari. "MEMBRAN GUIDED TISSUE REGENERATION UNTUK REGENERASI PERIODONTAL." Dentika Dental Journal 18, no. 3 (July 1, 2015): 300–304. http://dx.doi.org/10.32734/dentika.v18i3.1980.

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Berbagai teknik bedah dan bahan terus dikembangkan untuk meningkatkan regenerasi periodontal. Salah satu metode bedahyang sering digunakan pada defek periodontal adalah menggunakan barriermembranguided tissue regeneration (GTR) atauguided bone regeneration (GBR). Prinsip GTR/GBR adalah menggunakan barriermembran untuk menutupi tulang danligamen periodontal, kemudian memisahkannya sementara dari epitel gusi. Fungsi membran ini meningkatkan dan menjagabekuan darah dan bertindak sebagai scaffold untuk perlekatan dan proliferasi sel. Terdapat dua jenis membran yaitumembran non resorbable dan resorbable. Membran non resorbable pada umumnya terbuat dari polytetrafluoroethylene,membran ini sifatnya stabil, nondegradable dan biokompatibel, tetapi penggunaannya memerlukan bedah kedua untukmengambil membran. Membran resorbable berasal dari bahan sintetis seperti polyglycolic, polylactic acid dan bahan alamiseperti kolagen dan laminar bone. Pembuatan membran yang ideal masih terus dikembangkan, membran kolagen saat inilebih sering digunakan karena mempunyai biocompatibility yang optimal walaupun tingkat resorpsi membran sulit untukdiprediksi.
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Inuzuka, Akihiro, Toshiaki Shibutani, and Yukio Iwayama. "Effect of Bisphosphonate on Guided Tissue Regeneration." Nihon Shishubyo Gakkai Kaishi (Journal of the Japanese Society of Periodontology) 40, no. 1 (1998): 9–17. http://dx.doi.org/10.2329/perio.40.9.

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Sahu, Jigyasa, Deepti Rakesh Gattani, Rajvir Malik, Saurabh Lingala, and Nupur Kar. "MEMBRANES FOR GUIDED TISSUE REGENERATION - AN UPDATE." International Journal of Advanced Research 8, no. 7 (July 31, 2020): 1066–74. http://dx.doi.org/10.21474/ijar01/11369.

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Quin¯ones, Carlos R., and Raul G. Caffesse. "Current status of guided periodontal tissue regeneration." Periodontology 2000 9, no. 1 (October 1995): 55–68. http://dx.doi.org/10.1111/j.1600-0757.1995.tb00056.x.

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Giardino, Roberto, Milena Fini, Nicolo Nicoli Aldini, Gianluca Giavaresi, and Michele Rocca. "Polylactide Bioabsorbable Polymers for Guided Tissue Regeneration." Journal of Trauma: Injury, Infection, and Critical Care 47, no. 2 (August 1999): 303–8. http://dx.doi.org/10.1097/00005373-199908000-00014.

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32

Diedrich, Peter R. "Guided tissue regeneration associated with orthodontic therapy." Seminars in Orthodontics 2, no. 1 (March 1996): 39–45. http://dx.doi.org/10.1016/s1073-8746(96)80038-7.

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Tayebi, Lobat, Morteza Rasoulianboroujeni, Keyvan Moharamzadeh, Thafar K. D. Almela, Zhanfeng Cui, and Hua Ye. "3D-printed membrane for guided tissue regeneration." Materials Science and Engineering: C 84 (March 2018): 148–58. http://dx.doi.org/10.1016/j.msec.2017.11.027.

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Zhang, Ben, and Jie Song. "3D-Printed Biomaterials for Guided Tissue Regeneration." Small Methods 2, no. 9 (January 22, 2018): 1700306. http://dx.doi.org/10.1002/smtd.201700306.

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Nyman, Sture, Jan Gottlow, Jan Lindhe, Thorkild Karring, and Jan Wennstrom. "New attachment formation by guided tissue regeneration." Journal of Periodontal Research 22, no. 3 (May 1987): 252–54. http://dx.doi.org/10.1111/j.1600-0765.1987.tb01581.x.

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JT, Mellonig, and Triplett RG. "Guided tissue regeneration and endosseous dental implants." Implant Dentistry 3, no. 1 (1994): 56. http://dx.doi.org/10.1097/00008505-199404000-00015.

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CORTELLINI, PIERPAOLO, and MAURIZIO S. TONETTI. "Focus on intrabony defects: guided tissue regeneration." Periodontology 2000 22, no. 1 (February 2000): 104–32. http://dx.doi.org/10.1034/j.1600-0757.2000.2220108.x.

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SANZ, MARIANO, and JEAN LOUIS GIOVANNOLI. "Focus on furcation defects: guided tissue regeneration." Periodontology 2000 22, no. 1 (February 2000): 169–89. http://dx.doi.org/10.1034/j.1600-0757.2000.2220111.x.

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de Olyveira, Gabriel Molina, Márcio Luiz dos Santos, Ligia Maria Manzine Costa, Paula Braga Daltro, Pierre Basmaji, Gildásio de Cerqueira Daltro, and Antônio Carlos Guastaldi. "Bacterial Cellulose Biocomposites for Guided Tissue Regeneration." Science of Advanced Materials 6, no. 12 (December 1, 2014): 2673–78. http://dx.doi.org/10.1166/sam.2014.1985.

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40

Buser, D., U. Brägger, N. P. Lang, and S. Nyman. "Regeneration and enlargement of jaw bone using guided tissue regeneration." Clinical Oral Implants Research 1, no. 1 (December 1990): 22–32. http://dx.doi.org/10.1034/j.1600-0501.1990.010104.x.

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41

Funakoshi, Eiji. "The application of guided tissue regeneration, guided bone regeneration and implants to periodontal treatment." Nihon Shishubyo Gakkai Kaishi (Journal of the Japanese Society of Periodontology) 40, Supplement1 (1998): 55. http://dx.doi.org/10.2329/perio.40.supplement1_55.

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42

Polimeni, Giuseppe, Ki-Tae Koo, Mohammed Qahash, Andreas V. Xiropaidis, Jasim M. Albandar, and Ulf M. E. Wikesjo. "Prognostic factors for alveolar regeneration: effect of tissue occlusion on alveolar bone regeneration with guided tissue regeneration." Journal of Clinical Periodontology 31, no. 9 (September 2004): 730–35. http://dx.doi.org/10.1111/j.1600-051x.2004.00543.x.

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43

Mombelli, Andrea, Niklaus P. Lang, and Sture Nyman. "Isolation of Periodontal Species After Guided Tissue Regeneration." Journal of Periodontology 64, no. 11s (November 1993): 1171–75. http://dx.doi.org/10.1902/jop.1993.64.11s.1171.

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44

Al-Hamdan, Khalid, Robert Eber, David Sarment, Charles Kowalski, and Hom-Lay Wang. "Guided Tissue Regeneration-Based Root Coverage: Meta-Analysis." Journal of Periodontology 74, no. 10 (October 2003): 1520–33. http://dx.doi.org/10.1902/jop.2003.74.10.1520.

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45

Jang, Hyun-Seon. "Importancy of Guided Tissue Regeneration at Dental Clinic." Korean Journal of Oral and Maxillofacial Pathology 42, no. 4 (August 30, 2018): 91–94. http://dx.doi.org/10.17779/kaomp.2018.42.4.001.

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46

Gottlow, Jan. "Guided Tissue Regeneration using bioresorbable and nonresorbable devices." Nihon Shishubyo Gakkai Kaishi (Journal of the Japanese Society of Periodontology) 35, Supplement1 (1993): 37. http://dx.doi.org/10.2329/perio.35.supplement1_37.

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47

Hurzeler, Markus B., and Carlos R. Quinones. "Autotransplantation of a tooth using guided tissue regeneration." Journal of Clinical Periodontology 20, no. 7 (August 1993): 545–48. http://dx.doi.org/10.1111/j.1600-051x.1993.tb00404.x.

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48

BECKER, WILLIAM, and BURTON E. BECKER. "Clinical applications of guided tissue regeneration: surgical considerations." Periodontology 2000 1, no. 1 (February 1993): 46–53. http://dx.doi.org/10.1111/j.1600-0757.1993.tb00206.x.

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49

Taschieri, S., M. Del Fabbro, M. Saita, and T. Testori. "P.186 Guided tissue regeneration in endodontic microsurgery." Journal of Cranio-Maxillofacial Surgery 36 (September 2008): S214. http://dx.doi.org/10.1016/s1010-5182(08)71974-7.

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50

Kellert, Mitchell, Henry Chalfin, and Charles Solomon. "Guided Tissue Regeneration: An Adjunct to Endodontic Surgery." Journal of the American Dental Association 125, no. 9 (September 1994): 1229–33. http://dx.doi.org/10.14219/jada.archive.1994.0150.

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