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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 | 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 |
| 3 | Biology of incretins: GLP-1 and GIP 显示文摘 | Baggio L L Drucker D J | 2007 | Gastroenterology2007，132，： | 1 |
| 4 | 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 |
| 5 | Single event upsets induced by 1-10 MeV neutrons in static-RAMs using monoenergetic neutron sources显示文摘 | BAGGIO J LAMBERT D FERLET-CAVROIS V | 2007 | IEEE Trans Nucl Sci2007，54，6： | 1 |
| 6 | Enhanced secretion and improved glucose tolerance in mice lacking CD26显示文摘 | Marguet D Baggio L Kobayasi T | 2000 | Proc Nat1 Acad Sci USA2000，97，12： | 1 |
| 7 | Neutron-induced SEU in SRAMs:Simulations with n-Si and n-O interactions显示文摘 | LAMBERT D BAGGIO J HUBERT G | 2005 | IEEE Trans Nucl Sci2005，52，6： | 1 |
| 8 | Neutron-induced SEU in hulk SRAMs in terrestrial environment:Simulations and experiments显示文摘 | LAMBERT D BAGGIO J FERLET-CAVROIS V | 2004 | IEEE Trans Nucl Sci2004，51，6： | 1 |
| 9 | Analysis of quasi-monoenergetic neutron and proton SEU cross sections for terrestrial applications显示文摘 | LAMBERT D BAGGIO J | 2006 | IEEE Trans Nucl Sci2006，53，4： | 1 |
| 10 | Single event upsets induced by 1-10 MeV neutrons in static-RAMs using mono-energetic neutrons sources显示文摘 | BAGGIO J LAMBERT D | 2007 | IEEE Trans Nucl Sci2007，54，6： | 1 |
| 11 | Development and characterization of a glucagon-like peptide 1-albumin conjugate: the ability to activate the glucagon-like peptide 1 receptor in vivo 显示文摘 | Kim J G Baggio L L Bridon D P | 2003 | Diabetes2003，52，： | 1 |
| 12 | Coupled heat, water and gas flow in deformable porous media显示文摘 | Gawin D Baggio P Schrefler B A | 1995 | Int J Numer Meth Fluids1995，20，89： | 1 |
| 13 | Development and characterization of a glucagon-like peptide 1-albumin conjugate显示文摘 | Kim J G Baggio L L Bridon D P | 2003 | Diabetes2003，52，： | 1 |
| 14 | Single event upsets induced by 1-10 MeV neutrons in staic-RAMs using mono-energtic neutron sources显示文摘 | Baggio J Lambert D Ferlet-Cavrois V | 2007 | IEEE Transactions on Nuclear Science2007，54，6： | 1 |
| 15 | Biology of Incretins: GLP-1 and GIP显示文摘 | BAGGIO L L DRUCKER D J | 2007 | Gastroenterology2007，32，： | 1 |
| 16 | Double incretin recep- tor knockout (DIRKO) mice reveal an essential role for the en- teroinsular axis in transducing the glucoregulatory actions of DPP- IV inhihitors 显示文摘 | Hansotia T Baggio LL Delmeire D | 2004 | Diabetes2004，53，5： | 1 |
| 17 | Biology of incretins: GLP-1 and GIP显示文摘 | Baggio L L Drucker D J | 2007 | Gastroenterology2007，132，6： | 1 |
| 18 | Neutron and proton-induced single event upsets in advanced commercial fully depleted SO1 SRAMS显示文摘 | Baggio J Ferlet-Cavrois V Lambert D | 2005 | IEEE Transactions on Nuclear Science2005，52，6： | 1 |
| 19 | Enhanced secretion and improved glucose tolerance in mice lacking CD26显示文摘 | MARGUET D BAGGIO L KOBAYASHI T | 2000 | Proc Natl Acad Sci USA2000，97，12： | 1 |
| 20 | Enhanced insulin secretion and improved glucose tolerance in mice lacking CD26 显示文摘 | Marguet D Baggio L Kobayashi T | 2000 | Proc Nail Acad Sci USA2000，97，： | 1 |
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