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| 1 | Enamel microabrasion: An overview of clinical and scientific considerations显示文摘Superficial stains and irregularities of the enamelare generally what prompt patients to seek dental intervention to improve their smile. These stains or defects may be due to hypoplasia, amelogenesis imperfecta, mineralized white spots, or fluorosis, for which enamel microabrasion is primarily indicated. Enamel microabrasion involves the use of acidic and abrasive agents, such as with 37% phosphoric acid and pumice or 6% hydrochloric acid and silica, applied to the altered enamel surface with mechanical pressure from a rubber cup coupled to a rotatory mandrel of a lowrotation micromotor. If necessary, this treatment can be safely combined with bleaching for better esthetic results. Recent studies show that microabrasion is a conservative treatment when the enamel wear is minimal and clinically imperceptible. The most important factor contributing to the success of enamel microabrasion is the depth of the defect, as deeper, opaque stains, such as those resulting from hypoplasia, cannot be resolved with microabrasion, and require a restorative approach. Surface enamel alterations that result from microabrasion, such as roughness and microhardness, are easily restored by saliva. Clinical studies support the efficacy and longevity of this safe and minimally invasive treatment. The present article presents the clinical and scientific aspects concerning the microabrasion technique, and discusses the indications for and effects of the treatment, including recent works describing microscopic and clinical evaluations. | Núbia Inocencya Pavesi Pini Daniel Sundfeld-Neto Flavio Henrique Baggio Aguiar Renato Herman Sundfeld Luis Roberto Marcondes Martins José Roberto Lovadino Débora Alves Nunes Leite Lima | 2015 | World Journal of Clinical Cases2015，3，1： | 6 |
| 2 | Acidic heteroxylans from medicinal plants and their anti-ulcer activity显示文摘 | Thales R. Cipriani Caroline G. Mellinger Lauro M. de Souza Cristiane H. Baggio Cristina S. Freitas Maria C.A. Marques Philip A.J. Gorin Guilherme L. Sassaki Marcello Iacomini | 2008 | Carbohydrate Polymers2008，，2： | 2 |
| 3 | Biology of Incretins: GLP-1 and GIP显示文摘 | Laurie L. Baggio Daniel J. Drucker | 2007 | Gastroenterology2007，，6： | 2 |
| 4 | Therapeutic approaches to preserve islet mass in type 2 diabetes显示文摘 | BAGGIO L L DRUCKER D J | 2006 | Annu Rev Med2006，57，： | 1 |
| 5 | Biology of incretins: GLP-1 and GIP 显示文摘 | Baggio L L Drucker D J | 2007 | Gastroenterology2007，132，： | 1 |
| 6 | Growth factors and the kidney in diabetes mellitus显示文摘 | Gambaro G Baggio B | 1998 | Crit Rev Clin Lab Sci1998，35，1： | 1 |
| 7 | Biology of incretins:GLP-1 and GIP显示文摘 | Baggio LL Drucker DJ | 2007 | Gastroenterology2007，132，6： | 1 |
| 8 | Exendin-4 modulates diabetes onset in nonobese diabetic mice显示文摘 | Hadjiyanni I Baggio LL Poussier P | | 0，，： | 1 |
| 9 | Biology of ineretins: GLP- 1 and GIP显示文摘 | BAGGIO LL DRUCKER DJ | 2007 | Gastroenterology2007，132，6： | 1 |
| 10 | Improving tourism destination governance:a complexity science approach显示文摘 | Baggio R SCOTT N COOPER C | | 0，，04： | 1 |
| 11 | Monte Carlo localization formobile wireless sensor networks 显示文摘 | BAGGIO A LANGENDOEN K | 2008 | Ad Hoe Networks2008，6，5： | 1 |
| 12 | Biology of incretins: GLP-1 and GIP 显示文摘 | Baggio LL Drucker DJ | 2007 | Gastroenterology2007，132，6： | 1 |
| 13 | Destination networks: four Aus- tralian cases 显示文摘 | Scott N Cooper C Baggio R | 2008 | Annals of Tourism Research2008，35，1： | 1 |
| 14 | Network Science: A Review Fo- cused on Tourism 显示文摘 | Baggio R Scott N Cooper C | 2010 | Annals of Tourism Research2010，37，3： | 1 |
| 15 | Chronic exposure to GLP-1R agonists promotes homologous GLP-I receptor desensitization in vitro but does not attenuate GLP-1R- dependent glucose homeostasis in vivo 显示文摘 | Baggio LL Kim JG Drucker DJ | 2005 | Diabetes2005，53，： | 1 |
| 16 | Biology of ineretins: GLP-1 and GIP显示文摘 | Baggio LL Drueker DJ | 2007 | Gastroenterology2007，132，6： | 1 |
| 17 | GLP-1 receptor activation im- proves beta cell function and survival following induction of endoplas- mic reticulum stress显示文摘 | Yusta B Baggio L L Estall J L | 2006 | Cell Metab2006，4，5： | 1 |
| 18 | Inhibition of Mn^2+ 2-arginase by borate Ieads to the design of a transition state analogue inhibitor, 2 (S)-amino-6-boronohexanoic acid 显示文摘 | Baggio R Elbaum D Kanyo ZF | 1997 | JAm Chem Soc1997，119，34： | 1 |
| 19 | Lipoprotein-X and diagnosis of cholestasis: comparison with other biochemical parameters and liver biopsy显示文摘 | Fellin R Manzato E Zotti S Baggio G Briani G Rugge M | 1978 | Clin Chim Acta1978，85，： | 1 |
| 20 | Monte Carlo Localization for Mobile Wireless Sensor Networks显示文摘 | Baggio A Langendoen K | 2008 | Ad Hoc Networks2008，6，5： | 1 |
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