In memoriam. Rebecca Katz, M.B., Ch.B.
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Biomedical subjects
Publications and source records attributed to H Cooper.
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This study evaluated the antimicrobial activity of Universal Bond II adhesive and two experimental versions of Universal Bond II adhesives against the bacteria, Streptococcus mutans. The zones of bacterial inhibition produced by three samples of the adhesive (identified as Batches 1, 2, and 3) were measured and compared. Batch 1 contained 0.7% glutaraldehyde, Batch 2 contained 1.0% glutaraldehyde, and Batch 3 contained 0.45% glutaraldehyde (current Universal Bond II adhesive). The bacteria was swabbed over the surface of agar plates in two directions. The plates were divided into the following two groups: Group I-Batches 1, 2, 3 were placed into wells for 1 minute before being cured. Group II-Batches 1, 2, 3 were placed into wells for 20 seconds before being cured. Zones of microbial inhibition were measured in millimeters at the end of 24, 48, and 72 hours. All batches of the adhesive produced zones of inhibition against S. mutans. All batches of the adhesive maintained zones of inhibition throughout the 72 hours of the study.
All porcelain restorations, especially intra- and extracoronal restorations, have become an accepted treatment modality for the esthetic restoration of posterior teeth. One problem with these restorations is the limited ability to modify the porcelain when a proximal contact is not present or there is an open margin. Using a low-fusing porcelain in a glazing oven, practitioners can easily accomplish such modifications during the try-in and cementation appointment for porcelain inlays. This technique eliminates the need for returning the porcelain inlay to the laboratory for modification and a second patient visit to complete the restoration. This paper describes an in-office procedure for modifying porcelain restorations and a scanning electron micrographic evaluation of the etched porcelain surface after using this modification technique.
An analysis by scanning electron microscopy was undertaken to investigate the effects of bleaching on enamel-cementum surface morphology. Teeth were investigated in five groups: control; vital bleached for 5, 15, and 30 days; and 37 percent phosphoric acid gel etched for 20 seconds. Only the gel-etched group exhibited etching patterns. Shade change in vital bleached teeth was noted in the group vital bleached for 30 days.
This study evaluated the effects of an at-home vital bleaching system on gingival responses over a 6-week period. Objective measures were utilized to measure and monitor gingival inflammation over this period of time. Vital bleaching was performed as follows: (1) bleaching gel in a prefabricated mouthguard and (2) an ad-mix technique--bleaching gel and toothpaste in a 1:1 ratio. In addition a control group used a placebo in a prefabricated mouthguard. The at-home vital bleaching system produced no adverse gingival tissue responses. Furthermore, the at-home vital bleaching system helped produce a therapeutic effect on inflamed gingival tissues over the course of the study.
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This study in vivo evaluated the sensitivity of class 1 and 2 amalgam restorations which had bases of either zinc phosphate or an admix, silver-reinforced glass ionomer. The evaluation of sensitivity was done by providing the patient with five postcard questionnaires to be mailed to the clinic over a period of time from one to 28 days. Teeth restored with amalgam and silver-reinforced glass ionomer were significantly less sensitive to cold than those restored with amalgam and zinc phosphate.
The congenital absence of teeth, total anodontia, may involve both the primary and permanent dentitions. This paper updates the dental history of a twenty-eight-year-old Greek-American woman first reported in 1977 by Herman and Moss, when she was fourteen. Five complete sets of dentures had been made for her in thirteen years. Treatment was more complex due to an underdeveloped maxilla and a prognathic mandible.
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