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Alfonso Gil is receiving a 5-year post-graduate education in Fixed and Removable Prosthodontics and Dental Material Sciences from the University of Zurich. He obtained his DDS Degree from the University of the Basque Country (2013). His Master of Science and Advanced Periodontology Implantology Certificate from the University of Southern California (USC) (2013-2016) were followed by a Certificate in Advanced Surgical Implant Dentistry from the University of California Los Angeles (UCLA) (2016-2017). He is a Diplomate of the American Board of Periodontology. He obtained his PhD with highest honors from the University International of Catalunya in November 2019. His research focuses on the treatment of peri-implant disease, soft tissue augmentation of teeth and implants and fixed prosthodontics.
Issue cycle: quarterly Language: German Category: Esthetic Dentistry Editor-in-chief: Dr. Martina Stefanini PhD, ZTM Vincent Fehmer BDT, MDT, Dr. Alfonso Gil DDS, PhD QP Deutschland
Issue cycle: quarterly Language: English Category: Esthetic Dentistry Editor-in-chief: Dr. Martina Stefanini PhD, ZTM Vincent Fehmer BDT, MDT, Dr. Alfonso Gil DDS, PhD QP Deutschland
Events
1st EAED Academy Meeting
Red Carpet for Digital & Biological Esthetic Dentistry1. Jun 2023 — 3. Jun 2023Hôtel Martinez, Cannes, France
Speakers: Sam Alawie, Hadi Antoun, Wael Att, Nitzan Bichacho, Álvaro Blasi, Gonzalo Blasi, Ignacio Blasi, Franck Bonnet, Marie Bonnet, Renato Cocconi, Vincent Fehmer, Jean-Pierre Gardella, Alfonso Gil, Howard Gluckman, Stefano Gracis, Ueli Grunder, Effrat Habsha, Arndt Happe, Joseph Kan, Amélie Mainjot, Tidu Mankoo, Siegfried Marquardt, Francesco Mintrone, Nikolaos Perakis, Andrea Ricci, Miguel Roig, Rafi Romano, Irena Sailer, David Winkler, Giovanni Zucchelli
European Academy of Esthetic Dentistry
29th EAO annual scientific meeting
Uniting Nations through Innovations29. Sep 2022 — 1. Oct 2022Palexpo, Le Grand-Saconnex, Switzerland
Speakers: Thabo Beeler, Nitzan Bichacho, Rino Burkhardt, Luigi Canullo, Matteo Chiapasco, Luca De Stavola, Mirela Feraru, Alfonso Gil, Klaus Gotfredsen, Markus Gross, Ueli Grunder, Christoph Hämmerle, Björn Klinge, Ivo Krejci, Sebastian Kühl, Niklaus P. Lang, Sonia Leziy, Daniele Manfredini, Konrad H. Meyenberg, Francesco Mintrone, Ricardo Mitrani, Sven Mühlemann, José M. Navarro, Florian Probst, Pablo Ramírez, Christoph Andreas Ramseier, mario roccuzzo, Fidel Ruggia, Mariano Sanz, Rubens Spin-Neto, Dennis P. Tarnow, Daniel Thoma, Istvan Urban, Hans-Peter Weber
European Association for Osseintegration (EAO)
This author's journal articles
International Journal of Computerized Dentistry, 3/2023
ScienceDOI: 10.3290/j.ijcd.b3781703, PubMed ID (PMID): 36632986Pages 237-245, Language: English, GermanGil, Alfonso / Eliades, George / Özcan, Mutlu / Jung, Ronald E. / Hämmerle, Christoph H. F. / Ioannidis, Alexis
Aim: To evaluate the fracture load and type of failure of two different monolithic restorative materials bonded to standardized titanium bases and fabricated by two different procedures regarding the bonding interface.
Materials and methods: All screw-retained implant crown specimens (n = 40), subjected to fatigue by thermomechanical loading, differed in the restorative material (lithium disilicate [LDS] or polymer-infiltrated ceramic network [PICN], referred to as ‘hybrid ceramic’ [HYC]) and the interface type between the restorative material and the titanium base abutment (prefabricated ex-factory or produced during a CAM-milling procedure). This resulted in the following groups (n = 10/group): 1) LDS-M: lithium disilicate crown with a CAM-milled interface; 2) LDS-P: lithium disilicate crown with a prefabricated interface; 3) HYC-M: PICN crown with a CAM-milled interface; and 4) HYC-P: PICN crown with a prefabricated interface. Aged specimens underwent static fracture load testing. The load (N) at which the initial crack occurred was denoted as Finitial, and the maximal load (N) at which the restorations fractured as Fmax. All specimens were examined under a stereomicroscope to determine the failure mode.
Results: The median Finitial values were 180 N for LDS-M, 343 N for LDS-P, 340 N for HYC-M, and 190 N for HYC-P. The median Fmax values were 1822 N for LDS-M, 2039 N for LDS-P, 1454 N for HYC-M, and 1581 N for HYC-P. The intergroup differences were significant for Finitial (KW: P = 0.0042) and for Fmax (KW: P = 0.0010). The failure types also showed differences between the restorative groups.
Conclusions: The choice of restorative material had a stronger influence on the fracture load than the abutment interface workflow. Lithium disilicate showed the highest load for initial crack appearance (Finitial) and for complete fracture of the restoration (Fmax).
Keywords: lithium disilicate, dental materials, polymer-infiltrated ceramic network, thermomechanical aging, fracture load, failure mode, prosthetic dentistry, restorative material, abutment interface
Phenotype modification therapy has emerged as one of the main treatment objectives of periodontal plastic surgery. However, long-term data on the stability of gingival thickness gains are not available. This study examined the kinetics of mucosal thickness gain as a measure of phenotype modification therapy following treatment of multiple gingival recession defects with vestibular incision subperiosteal tunnel access (VISTA). Six patients with 14 recession type (RT) II teeth were treated using VISTA and subepithelial connective tissue grafts (SCTG). Scanned images of study casts at pre- and postoperative periods (6 to 66 months) were digitally superimposed for quantitative evaluation of soft tissue dimensional changes. Mucosal thickness gains ranged from 1.0 ± 0.7 mm (1 mm apical to cement-enamel junction [CEJ]) to 1.4 ± 0.4 mm (5 mm apical to CEJ). The gingival thickness gains remained relatively stable, with thickness gains at 66 months of 0.5 ± 0.8, 0.9 ± 0.6, 1.1 ± 0.6, 1.0 ± 0.4, and 1.2 ± 0.6 mm at 1, 2, 3, 4 and 5 mm apical to the CEJ, respectively. Treatment of multiple gingival recession defects with VISTA and SCTG led to stable gingival thickness gains and shows promise as a strategy for phenotype modification therapy.