コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 esponse in LAP can be partially modulated by periodontal therapy.
2 ity of periodontal disease and the effect of periodontal therapy.
3 and six oral antibiotics of potential use in periodontal therapy.
4 critical to optimize the results of surgical periodontal therapy.
5 otics are emerging as a promising adjunctive periodontal therapy.
6 t and control sites as an adjunct to Phase 1 periodontal therapy.
7 (n = 20) included patients who did not have periodontal therapy.
8 eatment of intrabony defects during surgical periodontal therapy.
9 essure and subclinical atherosclerosis after periodontal therapy.
10 Serum analytes were not influenced by periodontal therapy.
11 raphic indicators of bone regeneration after periodontal therapy.
12 matrix derivative (EMD) is commonly used in periodontal therapy.
13 before and after completion of non-surgical periodontal therapy.
14 of D-ROM (P < 0.01) were observed following periodontal therapy.
15 nd did not undergo resective or regenerative periodontal therapy.
16 enzyme inhibitors or receptor antagonists in periodontal therapy.
17 loss, are the actual and desired outcomes of periodontal therapy.
18 icient calculus removal is a primary goal in periodontal therapy.
19 s in practice, and referral for non-surgical periodontal therapy.
20 f depression on their patients' responses to periodontal therapy.
21 s remaining after completion of non-surgical periodontal therapy.
22 ma denticola before and following mechanical periodontal therapy.
23 n patients usually not receiving concomitant periodontal therapy.
24 CAL, or BOP 2 years after completion of the periodontal therapy.
25 cerns about medications as a risk factor for periodontal therapy.
26 ion of migrated teeth sometimes occurs after periodontal therapy.
27 is often the motivation for patients to seek periodontal therapy.
28 delivery of a standard non-surgical phase of periodontal therapy.
29 attachment compared to non-smokers following periodontal therapy.
30 ts represents a unique treatment approach in periodontal therapy.
31 ts to be initially treated with non-surgical periodontal therapy.
32 mos after delivery of standard non-surgical periodontal therapy.
33 trends in referral patterns of patients for periodontal therapy.
34 tigated further for possible development for periodontal therapy.
35 monitored before and up to 5 years following periodontal therapy.
36 le-dose drug delivery systems appropriate to periodontal therapy.
37 to and at 3, 6, 12, 24, and 36 months after periodontal therapy.
38 in assessing disease status and response to periodontal therapy.
39 teroid therapy as an adjunct to non-surgical periodontal therapy.
40 regard it as osteoinductive when utilized in periodontal therapy.
41 odontal healing in barrier membrane-assisted periodontal therapy.
42 th EB present a unique challenge in terms of periodontal therapy.
43 urgical treatment and a period of supportive periodontal therapy.
44 inical outcomes of non-surgical and surgical periodontal therapy.
45 uate the effect of smoking on the outcome of periodontal therapy.
46 ant role in achieving a desirable outcome in periodontal therapy.
47 ing used clinically than any other agents in periodontal therapy.
48 ccess needs after completion of non-surgical periodontal therapy.
49 of 134 patients were screened 10 years after periodontal therapy.
50 al disease in smokers remains a challenge of periodontal therapy.
51 of statins or bisphosphonates as adjuncts to periodontal therapy.
52 acebo capsules as an adjunct to conservative periodontal therapy.
53 ows the efficacy of platelet concentrates in periodontal therapy.
54 ividuals that respond poorly to conventional periodontal therapy.
55 emains poorly investigated in the context of periodontal therapy.
56 ) would enhance the outcomes of non-surgical periodontal therapy.
57 lent alternative for dentists in nonsurgical periodontal therapy.
58 mise as a diagnostic and therapeutic tool in periodontal therapy.
59 ment of gingival condition and changes after periodontal therapy.
60 periodontitis before and after non-surgical periodontal therapy.
61 ATV or placebo gels as adjunct to mechanical periodontal therapy.
62 e of Gram-negative bacteria before and after periodontal therapy.
63 periodontitis were treated with non-surgical periodontal therapy.
64 Periodontitis patients received non-surgical periodontal therapy.
65 patients are more compliant with supportive periodontal therapy.
66 line and at the first and third months after periodontal therapy.
67 of furcation defects is a core component of periodontal therapy.
68 djunct to resective or regenerative surgical periodontal therapy.
69 defects is an important therapeutic goal of periodontal therapy.
70 ver (FMF) and their response to non-surgical periodontal therapy.
71 quires effective endodontic and regenerative periodontal therapy.
72 onization of flora may affect the outcome of periodontal therapy.
73 tool for calculus detection in non-surgical periodontal therapy.
74 -1 genotypes on the outcomes of non-surgical periodontal therapy.
75 periodontitis before and after non-surgical periodontal therapy.
76 erapy (PDT) as monotherapy during supportive periodontal therapy.
77 tors of poor response following non-surgical periodontal therapy.
78 at baseline and 3 months after non-surgical periodontal therapy.
79 received an intensive course of non-surgical periodontal therapy.
80 on periodontitis progression and response to periodontal therapy.
81 nts responding poorly to mechanical forms of periodontal therapy.
82 t was treated with non-surgical and surgical periodontal therapies.
83 iscuss strategies for future applications in periodontal therapies.
84 is, randomly assigned into test group (basic periodontal therapy + 0.12% chlorhexidine) with 61 impla
86 d to either (a) one-time, shortened outreach periodontal therapy adapted to German statutory health g
87 ects with above average clinical response to periodontal therapy after correction for possible confou
89 ficantly reduced 3 months after non-surgical periodontal therapy, although they never reached the sam
90 ation lesions are a challenging scenario for periodontal therapy and a serious threat for tooth progn
92 rous and insightful look into the origins of periodontal therapy and anesthesia in "Happy Memories of
93 ria reduction process, it was suggested that periodontal therapy and chlorhexidine (CHX) rinse could
94 dontal disease before and after non-surgical periodontal therapy and correlate these values with clin
95 mproves the clinical outcome of non-surgical periodontal therapy and may be an appropriate adjunctive
96 dy is to evaluate the effect of non-surgical periodontal therapy and medical treatment on the level o
101 uence cytokine expression after non-surgical periodontal therapy and supportive periodontal care.
102 iologic effects of a two-phase antimicrobial periodontal therapy and tested microbiologic, clinical,
106 vercome limitations associated with existing periodontal therapies, and may provide a new direction i
107 nce of periodontal disease, poor response to periodontal therapy, and a high risk for developing head
108 ical and radiographic response to mechanical periodontal therapy, and assess the factors associated w
109 etween host-parasite interaction, outcome of periodontal therapy, and systemic factors is best repres
110 erties of tetracycline (TCN) are valuable in periodontal therapy, and TCN treatment can remove the sm
111 Care include tobacco cessation as a part of periodontal therapy, and the 2000 Surgeon General's Repo
112 pathologically migrated teeth after routine periodontal therapy, and to study the relation between t
114 Periodontal treatment consists of active periodontal therapy (APT) and supportive periodontal the
115 postoperative care and subsequent supportive periodontal therapy are essential to achieve sustainable
116 ied bone allograft (DFDBA) is widely used in periodontal therapy as a scaffold for new bone formation
118 Ts) consistently demonstrate that mechanical periodontal therapy associates with approximately a 0.4%
120 enhance the effectiveness of these agents in periodontal therapy by enhancing or sustaining their the
121 chronic periodontitis receiving non-surgical periodontal therapy by SRP with (test) and without (cont
122 itis (good responders [GR]) before and after periodontal therapy by using the Human Oral Microbe Iden
125 ng the level of PGRN in GCF before and after periodontal therapy could in the future be useful for pe
126 vious studies have suggested that success of periodontal therapy depends on the specific attachment,
129 tion with the use of lasers for non-surgical periodontal therapy due to ablation, vaporization, hemos
130 ontal Therapy [OPT] Study) demonstrated that periodontal therapy during pregnancy improved periodonta
131 ffect of intensive oral hygiene regimens and periodontal therapy during pregnancy on periodontal heal
133 minimum 12 months) with CP with non-surgical periodontal therapy either alone or associated with loca
137 indings from interventional studies in which periodontal therapy failed to alleviate systemic health
138 atients were treated with four modalities of periodontal therapy followed by supportive periodontal t
139 eatment and after completion of non-surgical periodontal therapy for 213 sextants in 38 patients by t
143 cal role for smoking cessation counseling in periodontal therapy for smokers in order to effectively
144 uld improve clinical results of non-surgical periodontal therapy for smokers with chronic periodontit
145 of Glanzmann's thrombasthenia presented for periodontal therapy for spontaneous gingival hemorrhage.
148 terns of SAEs indicated that subjects in the periodontal therapy group tended to be less likely to ex
152 sive techniques in non-surgical and surgical periodontal therapy has not progressed to the same exten
153 namel matrix protein derivative (EMD) during periodontal therapy have been shown to be safe for the p
154 growing interest in the use of probiotics in periodontal therapy; however, until now, most research h
157 nhance the clinical benefits of non-surgical periodontal therapy in adults who are otherwise healthy.
158 In this context, the support of nonsurgical periodontal therapy in diabetics with host modulation ag
160 e to conduct a secondary prevention trial of periodontal therapy in patients who have had coronary he
161 biotic supplementation adjunctive to initial periodontal therapy in patients with chronic periodontit
164 on clinical response following non-surgical periodontal therapy in patients with severe periodontiti
165 polymorphisms are associated with success of periodontal therapy in pregnant women with periodontal d
166 e evidence suggesting a negligible effect of periodontal therapy in reducing interleukin-6 and lipids
167 microbials improved efficacy of non-surgical periodontal therapy in reducing PD and improving CAL at
168 th SRP improves the efficacy of non-surgical periodontal therapy in reducing probing depth and improv
169 t reduction in HbA1c observed as a result of periodontal therapy in subjects with type 2 diabetes is
170 statistically significant improvement after periodontal therapy in the BS compared with the obese gr
173 ary or even justified to evaluate effects of periodontal therapy in these defects, and can be substit
174 rant secretion of chemerin, and non-surgical periodontal therapy influenced the decrease of GCF cheme
175 it mouth study evaluated a new model to test periodontal therapy involving a novel bioerodible copoly
176 d the impact of standard (SPT) and intensive periodontal therapy (IPT) on serum inflammatory markers
179 tion of whether the additional use of EMD in periodontal therapy is more effective compared with a co
183 modulation of host inflammatory response in periodontal therapy, it is important to control the bact
185 of patients with periodontitis submitted to periodontal therapy/maintenance and implant placement.
186 These findings suggest that non-surgical periodontal therapy may be associated with a substantial
188 ies suggest that initial patient response to periodontal therapy may be related to emotional intellig
194 ed randomly to either a control group (C; no periodontal therapy) (n = 35) or an experimental group (
195 ilure or success 5 years after completion of periodontal therapy, none of the four strategies produce
197 tudy investigated the impact of non-surgical periodontal therapy (NSPT) on clinical and immunological
198 ssess the short-term effects of non-surgical periodontal therapy (NSPT) on the gingival crevicular fl
204 effective adjuvant treatments to nonsurgical periodontal therapy offering strong antiresorptive prope
205 in-1, (b) limited evidence on the effects of periodontal therapy on arterial blood pressure, leucocyt
206 zithromycin in combination with non-surgical periodontal therapy on clinical and microbiologic parame
208 authors aim to assess the effect of initial periodontal therapy on exacerbation frequency in COPD pa
210 dy was to examine the effect of non-surgical periodontal therapy on GCF levels of ICTP and IL-1.
211 vidence is available regarding the effect of periodontal therapy on major disease endpoints such as t
212 ect of two modes of delivery of non-surgical periodontal therapy on patient experience of pain and or
213 eriod of 6 months the effect of non-surgical periodontal therapy on serum levels of high-sensitivity
214 sulted in: (a) no evidence on the effects of periodontal therapy on subclinical atherosclerosis, seru
215 zed controlled trials testing the effects of periodontal therapy on systemic health outcomes were con
218 All published trials included non-surgical periodontal therapy; only two included systemic antimicr
221 A recent clinical trial (Obstetrics and Periodontal Therapy [OPT] Study) demonstrated that perio
222 levels of HbA1c, FPG, and CML, and improves periodontal therapy outcome in people with DMt2 and CP.
223 th factor (PDGF) have significantly enhanced periodontal therapy outcomes with a high degree of varia
232 ible participants were randomized to receive periodontal therapy provided by the study or community d
233 ied, intensive instructions and non-surgical periodontal therapy provided during 8 weeks at early pre
234 d discuss all published RCTs testing whether periodontal therapy reduces rates of preterm birth and l
235 systemic antibiotic usage, with non-surgical periodontal therapy resulted in improvement in clinical
236 lementation in conjunction with conventional periodontal therapy (scaling and root planing [SRP]) on
239 fects of two different forms of non-surgical periodontal therapy, scaling and root planing (SRP) per
243 icillin plus metronidazole in the context of periodontal therapy should be limited to patients with s
245 gnant women with periodontitis, non-surgical periodontal therapy significantly reduced levels of peri
246 lth" should be considered a true endpoint of periodontal therapy, since this outcome provides a condi
250 tudy aims to assess compliance to supportive periodontal therapy (SPT) among patients treated with de
251 t the time of routinely scheduled supportive periodontal therapy (SPT) appointments by 2 evaluators.
253 Patients did not receive regular supportive periodontal therapy (SPT) from 2 to 5 years post-treatme
258 and if results are substantiated, adjunctive periodontal therapies subsequently need to be evaluated.
259 d at 3 months following completion of active periodontal therapy supplemented by amoxicillin plus met
260 study assesses the differential outcomes of periodontal therapy supplemented with amoxicillin-metron
261 and 1.5, 3, and 6 months after non-surgical periodontal therapy: supra- and subgingival plaque from
262 ays) during the first, non-surgical phase of periodontal therapy (T1) and placebo during the second,
263 rivative (EMD) as an adjunct to non-surgical periodontal therapy (test) versus non-surgical therapy a
265 onsidered the gold standard for non-surgical periodontal therapy, then the evidence supporting laser-
267 to the 3-month visit, and from completion of periodontal therapy to each annual visit up to the 5-yea
268 eplacement graft (BRG) materials are used in periodontal therapy to encourage new bone formation.
269 ceutical agents has been proposed for use in periodontal therapy to inhibit loss of alveolar bone and
270 SETTING, AND PARTICIPANTS: The Diabetes and Periodontal Therapy Trial (DPTT), a 6-month, single-mask
271 ontitis who participated in the Diabetes and Periodontal Therapy Trial (DPTT); and associations among
273 ects on both hard and soft tissues following periodontal therapy using a single statistical test.
274 compare disease progression and response to periodontal therapy using both individual site activity
277 to assess whether the degree of response to periodontal therapy was associated with changes in serol
278 h locally and systemically, and non-surgical periodontal therapy was effective in reducing LRG levels
281 itis and Vascular Events (PAVE) pilot study, periodontal therapy was provided as an intervention in a
284 GCF and a significant decrease after initial periodontal therapy were determined in the CP group (P <
285 to receive immediate or delayed non-surgical periodontal therapy were evaluated at baseline and 6 mon
286 6.33 +/- 3.79 months after steps 1 and 2 of periodontal therapy were included and retrospectively an
288 A smoking cessation program and non-surgical periodontal therapy were offered to 80 smokers with peri
292 tenance program and provided with supportive periodontal therapy with 3 to 4 appointments annually.
294 is to evaluate the influence of non-surgical periodontal therapy with adjunctive systemic antibiotics
295 bout the protocol of choice for non-surgical periodontal therapy with adjuvant use are still reported
296 review if they reported outcomes of surgical periodontal therapy with and without the use of lasers.
298 mly assigned to receive initial non-surgical periodontal therapy with scaling/root planing and oral h
299 l conditions in pregnant women, case-related periodontal therapy, with or without systemic antibiotic
300 s and periodontal burden, shortened outreach periodontal therapy yielded improvements in periodontal