Objectives: To assess clinical and radiographic outcomes as well as the profilometric contour alterations of peri-implant hard and soft tissues around single implants treated with simultaneous guided bone regeneration (GBR) at 5 years. Materials and methods: Twenty-seven patients presenting with a single tooth gap in the esthetic zone received a two-piece implant. GBR was randomly performed using a resorbable (RES) or a non-resorbable membrane (N-RES) combined with a bone substitute material. Follow-up examinations were performed at baseline (BL = crown insertion), 1 year (FU-1), 3 years (FU-3), and at 5 years (FU-5) including clinical and radiographic parameters as well as profilometric changes. Statistics were performed by means of param...
In aesthetic sites, the integrity of the facial bone wall dimension in the anterior maxilla is jeopa...
OBJECTIVES: To compare the clinical and histological outcomes of a resorbable modified polylactide/p...
Statement of problem: Whether increasing the space for peri-implant soft tissues by using implant sy...
OBJECTIVES To assess clinical and radiographic outcomes as well as the profilometric contour altera...
PURPOSE To test whether or not one of two membranes is superior for peri-implant-guided bone regene...
OBJECTIVES To assess two- and three-dimensional changes of the peri-implant tissues as well as clin...
AIM The aim was to evaluate the performance of implants placed with simultaneous guided bone regene...
Objectives: To assess contour changes of peri-implant tissues comparing a one- and a two-piece denta...
AimTo test whether implant placement with simultaneous guided bone regeneration (GBR) differs from i...
OBJECTIVES: To evaluate whether the adjunctive use of a bone substitute at immediate single implants...
Objectives: The aim of this study was to compare crown and soft tissue dimensions of single-tooth im...
PURPOSE To evaluate and compare crestal bone level changes and peri-implant status of implant-sup...
AIM To test whether soft-type block bone substitute used for guided bone regeneration (GBR) of peri...
OBJECTIVE: The aim of this randomized-controlled clinical trial was to evaluate the long-term outcom...
The aim of the present clinical study was to test whether peri-implant bone defects can successfully...
In aesthetic sites, the integrity of the facial bone wall dimension in the anterior maxilla is jeopa...
OBJECTIVES: To compare the clinical and histological outcomes of a resorbable modified polylactide/p...
Statement of problem: Whether increasing the space for peri-implant soft tissues by using implant sy...
OBJECTIVES To assess clinical and radiographic outcomes as well as the profilometric contour altera...
PURPOSE To test whether or not one of two membranes is superior for peri-implant-guided bone regene...
OBJECTIVES To assess two- and three-dimensional changes of the peri-implant tissues as well as clin...
AIM The aim was to evaluate the performance of implants placed with simultaneous guided bone regene...
Objectives: To assess contour changes of peri-implant tissues comparing a one- and a two-piece denta...
AimTo test whether implant placement with simultaneous guided bone regeneration (GBR) differs from i...
OBJECTIVES: To evaluate whether the adjunctive use of a bone substitute at immediate single implants...
Objectives: The aim of this study was to compare crown and soft tissue dimensions of single-tooth im...
PURPOSE To evaluate and compare crestal bone level changes and peri-implant status of implant-sup...
AIM To test whether soft-type block bone substitute used for guided bone regeneration (GBR) of peri...
OBJECTIVE: The aim of this randomized-controlled clinical trial was to evaluate the long-term outcom...
The aim of the present clinical study was to test whether peri-implant bone defects can successfully...
In aesthetic sites, the integrity of the facial bone wall dimension in the anterior maxilla is jeopa...
OBJECTIVES: To compare the clinical and histological outcomes of a resorbable modified polylactide/p...
Statement of problem: Whether increasing the space for peri-implant soft tissues by using implant sy...