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1 stasis at various time points post-PDT (post photodynamic therapy).
2 sensitizers for photocontrolled-delivery and photodynamic therapy.
3 erved between added reovirus before or after photodynamic therapy.
4 a history of choroidal neovascularization or photodynamic therapy.
5 orescence probes, as well as sensitizers for photodynamic therapy.
6 al wastewater treatment, photochemistry, and photodynamic therapy.
7 oninvasive optical imaging, optogenetics and photodynamic therapy.
8 ch as imaging combined with drug delivery or photodynamic therapy.
9 r photocoagulation, CyberKnife radiation, or photodynamic therapy.
10 therapy, hyper- or hypothermic therapy, and photodynamic therapy.
11 s, which makes them potentially suitable for photodynamic therapy.
12 s in photothermal therapy, chemotherapy, and photodynamic therapy.
13 lation of photosensitizer drugs in tumors in photodynamic therapy.
14 for light-triggered biological reactions and photodynamic therapy.
15 n of disease and any previous treatment with photodynamic therapy.
16 ential as photosensitizers for metal-organic photodynamic therapy.
17 topical or injection interferon alfa-2b, and photodynamic therapy.
18 oxaliplatin chemotherapy, radiotherapy, and photodynamic therapy.
19 adverse effects, and cost, limit the use of photodynamic therapy.
20 itization, a limitation often encountered in photodynamic therapy.
21 rget proteins or to kill cell populations in photodynamic therapy.
22 itor, sensitizes xenotransplanted tumours to photodynamic therapy.
23 gulation, multipolar electrocoagulation, and photodynamic therapy.
24 plications in photobiology or O2-independent photodynamic therapy.
25 otactic radio surgery, and vascular-targeted photodynamic therapy.
26 modified silica nanoparticles for two-photon photodynamic therapy.
27 nding probes and photosensitizers for use in photodynamic therapy.
28 role of singlet oxygen and (1)O2 carriers in photodynamic therapy.
29 as effective and well-tolerated as daylight photodynamic therapy.
30 VEGF) interventions, dietary supplements, or photodynamic therapy.
31 econtouring, and antitumor and antimicrobial photodynamic therapy.
32 echanism for PIT as compared to conventional photodynamic therapies.
33 alfa-2b (0% vs 1%), cryotherapy (0% vs 3%), photodynamic therapy (0% vs 1%), excisional biopsy and c
34 therapy and the other half treated with AWL photodynamic therapy 1 week apart and randomly allocated
35 randomly assigned (1:1) to vascular-targeted photodynamic therapy (4 mg/kg padeliporfin intravenously
38 ing oxidant production by transition metals, photodynamic therapy, activated macrophages, and platele
40 hospholipid monolayer or with the lipophilic photodynamic therapy agent, tetra-t-butyl-silicon phthal
41 bial and antiviral agents, anticancer drugs, photodynamic therapy agents, radiotherapy agents and bio
42 occurs following topical aminolevulinic acid-photodynamic therapy (ALA-PDT), but its nature and media
43 or 0.5 mg), sham injections plus verteporfin photodynamic therapy (ANCHOR), or sham injections alone
44 y assigned 206 patients to vascular-targeted photodynamic therapy and 207 patients to active surveill
45 e findings may help to alleviate pain during photodynamic therapy and also allow for disease modifica
46 mes were after vs before the introduction of photodynamic therapy and anti-vascular endothelial growt
48 ffectiveness and adverse effects of daylight photodynamic therapy and artificial white light (AWL) LE
53 ies based on oxygen free radicals, including photodynamic therapy and radiotherapy, have emerged as p
54 ad half of their scalp treated with daylight photodynamic therapy and the other half treated with AWL
55 Of the new non-invasive treatments, only photodynamic therapy and topical imiquimod have become e
56 e studies that evaluated submacular surgery, photodynamic therapies, and anti-angiogenic therapies, a
57 diagnostics and analytics, photothermal and photodynamic therapies, and delivery of target molecules
58 emonstrates a highly promising new agent for photodynamic therapy, and attracts attention to photosta
59 peutics and biologics, chemotherapeutics and photodynamic therapy, and chemotherapeutics and radiothe
64 Ablative treatments, including Nd:YAG laser, photodynamic therapy, and thermal contact treatments hav
65 ts of repeated applications of antimicrobial photodynamic therapy (aPDT) adjunctive to scaling and ro
66 im of this study is to compare antimicrobial photodynamic therapy (aPDT) as an adjunctive therapy to
70 low-intensity laser (LIL); 2) antimicrobial photodynamic therapy (aPDT); or 3) toluidine blue O (TBO
71 mus) and the most promising absorptivity for photodynamic therapy application, was tested as efficien
73 Near-IR absorption, desired for potential photodynamic therapy applications, was not pursuable for
75 ession in cancer cells and susceptibility to photodynamic therapy based on their increased ability to
76 e most promising candidate in this study for photodynamic therapy because it has the longest waveleng
77 atoses (AKs) is as effective as conventional photodynamic therapy but has the advantage of being almo
79 cations, including therapeutic (photothermal/photodynamic therapy, chemotherapy and synergistic thera
80 prolonging long-term survival, and although photodynamic therapy combined with stenting has been rep
83 -VEGF therapy increased from 60.3% to 72.7%, photodynamic therapy decreased from 12.8% to 5.3%, and t
86 imaging and synergetic photothermal therapy/photodynamic therapy derived from the porphyrin-like moi
87 osensitizers into nanostructures can improve photodynamic therapy efficacy and the safety profile of
88 niques include endoscopic mucosal resection, photodynamic therapy, electrocoagulation, and laser ther
89 as photosynthesis, vision, photolithography, photodynamic therapy, etc., is yet to become a common to
90 re to sunlight and other patients undergoing photodynamic therapy experience similar pain, which can
91 e variety of potential applications, such as photodynamic therapy for accelerated drug screening, mag
92 diotherapy, brachytherapy, radiosurgery, and photodynamic therapy for recurrent high-grade glioma.
93 therapy and artificial white light (AWL) LED photodynamic therapy for the treatment of AKs on the for
94 cholangiopancreatography, and refinements in photodynamic therapy for the treatment of cholangiocarci
95 eporfin (VP), a light-activated drug used in photodynamic therapy for the treatment of choroidal neov
96 The use of endoscopic mucosal resection and photodynamic therapy for treatment of dysplastic Barrett
97 was 58 (28%) of 206 in the vascular-targeted photodynamic therapy group compared with 120 (58%) of 20
99 tatitis (three [2%] in the vascular-targeted photodynamic therapy group vs one [<1%] in the active su
100 rious adverse event in the vascular-targeted photodynamic therapy group was retention of urine (15 pa
105 for phototherapeutic interventions, such as photodynamic therapy, has transformed medicine and biolo
109 strated the enhanced role of cholangioscopy, photodynamic therapy in cholangiocarcinoma, and biliary
111 lar endothelial growth factor or verteporfin photodynamic therapy in combination with systemic chemot
113 inical trials suggest excellent efficacy for photodynamic therapy in the treatment of subretinal neov
116 interventions (argon laser photocoagulation, photodynamic therapy, intravitreal corticosteroids, and
117 TERPRETATION: Padeliporfin vascular-targeted photodynamic therapy is a safe, effective treatment for
120 iolet and visible light, and also to develop photodynamic therapy, it is important to resolve the mec
124 ndoscopic therapies including mucosectomy or photodynamic therapy may be emerging options in patients
126 ng for subsequent surgical excision (n = 3), photodynamic therapy (n = 1), or cryotherapy (n = 1) for
129 guided sensitizer delivery for the potential photodynamic therapy of hypoxic structures requiring cyt
131 vironments and (ii) "trackable" NO donors in photodynamic therapy of malignancies (such as skin cance
136 bined with protoporphyrin IX (PpIX)-mediated photodynamic therapy on a variety of human pancreatic ca
137 gnosed as having exudative ARMD who received photodynamic therapy or anti-VEGF therapy compared with
139 onthermal ablation with alcohol injection or photodynamic therapy, or displacement of tumor with endo
141 ffect compared with reovirus monotherapy and photodynamic therapy (p=0.042) with 100% cell death obse
143 ing pigment (methylene blue - MB) to mediate photodynamic therapy (PDT) against Streptococcus mutans
145 es are needed to identify and optimize novel photodynamic therapy (PDT) agents with greater efficacy
148 e recently contributed to the progression of photodynamic therapy (PDT) and microbial photodynamic in
150 , presumably through the combined effects of photodynamic therapy (PDT) and released chemotherapy dru
151 Cationic antimicrobial peptides (CAMPs) and photodynamic therapy (PDT) are attractive tools to comba
152 inical experiments addressing the effects of photodynamic therapy (PDT) as an adjunct to conventional
153 and imaging functions in one agent, choosing photodynamic therapy (PDT) as an appropriate cancer trea
155 opportunities of NP imaging and therapy on a photodynamic therapy (PDT) based NP system that has been
157 we have found that addition of erlotinib to photodynamic therapy (PDT) can improve treatment respons
161 neration and exhibits significantly enhanced photodynamic therapy (PDT) efficacy on two colon cancer
164 n angiograms taken before and 3 months after photodynamic therapy (PDT) for CNV (6 patients, group 1)
171 n photoreceptor degeneration associated with photodynamic therapy (PDT) in a laser-induced model of c
172 mate visual system after a single session of photodynamic therapy (PDT) in an intact nonhuman primate
173 for their potential as photosensitizers for photodynamic therapy (PDT) in P-glycoprotein (P-gp) expr
174 herapy in ancient texts and the discovery of photodynamic therapy (PDT) in the early 1900s, the landm
198 ial of this conjugate as photosensitizer for photodynamic therapy (PDT) of cancers overexpressing the
199 cteriochlorins are attractive candidates for photodynamic therapy (PDT) of diverse medical indication
200 onthly ranibizumab (0.3 or 0.5 mg) with sham photodynamic therapy (PDT) or sham ocular injections wit
201 e purpose of this study was to determine how photodynamic therapy (PDT) promotes stabilization and re
205 very (fluence rate) plays a critical role in photodynamic therapy (PDT) through its control of tumor
206 treatment, it allowed delivery of selective photodynamic therapy (PDT) to the cancerous tissues, wit
208 e entrapped agents that harnesses sub-lethal photodynamic therapy (PDT) using a photosensitiser that
209 3 months, additional treatment with laser or photodynamic therapy (PDT) was considered if any fluores
211 chanisms how the efficacy of photofrin based photodynamic therapy (PDT) was enhanced by miR-99a trans
212 racellular localization and cell response to photodynamic therapy (PDT) were analyzed in MCF10A norma
214 integration of fluorescence imaging (FL) and photodynamic therapy (PDT) with positron emission tomogr
216 2 and Bcl-xL, are recognized phototargets of photodynamic therapy (PDT) with the mitochondrion-target
217 nalysis evaluated patients who had undergone photodynamic therapy (PDT) within the preceding year (N
218 val of combining surgery with intraoperative photodynamic therapy (PDT), a light-based cancer treatme
219 nstrate that benzoporphyrin derivative-based photodynamic therapy (PDT), a photochemical cytotoxic mo
222 f cancer and dermatological diseases through photodynamic therapy (PDT), and advanced materials for e
223 nd emerging therapies, such as radiation and photodynamic therapy (PDT), can induce angiogenic molecu
225 additional limitations of porphyrin-mediated photodynamic therapy (PDT), including low depths of tiss
226 ent procedures, such as laser irradiation or photodynamic therapy (PDT), may provide some additional
227 anced technologies such as optical limiting, photodynamic therapy (PDT), organic field-effect transis
228 each clinical treatment tool (chemotherapy, photodynamic therapy (PDT), radiotherapy (RT)) by contro
230 ptake of photosensitizers by cancer cells in photodynamic therapy (PDT), we designed a smart plasma m
253 MRI contrasting agents, and sensitizers for photodynamic therapy (PDT); and more recently as models
254 (MARINA), or were randomized to verteporfin photodynamic therapy (PDT; n=143), 0.3-mg ranibizumab mo
256 atform for the high-throughput assessment of photodynamic therapy photosensitizer (PDT) efficacy on E
257 addition, light activation has potential in photodynamic therapy, photothermal therapy, radiotherapy
258 , which is used as an antimicrobial agent in photodynamic therapy, potentiates tellurite toxicity.
260 gated as cytotoxic agents and inhibitors, in photodynamic therapy, radiation therapy, drug/gene deliv
261 rapies were identified: electrochemotherapy, photodynamic therapy, radiotherapy, intralesional therap
270 re either ineligible for or nonresponsive to photodynamic therapy, the standard treatment at the time
271 c function, which directs the development of photodynamic therapy to be safer and more selective.
277 on with Photodynamic Therapy; Verteporfin in Photodynamic Therapy; VEGF Inhibition Study in Ocular Ne
278 ent of Age-Related Macular Degeneration with Photodynamic Therapy; Verteporfin in Photodynamic Therap
279 vitreal anti-VEGF injection; (3) verteporfin photodynamic therapy (vPDT); or (4) laser photocoagulati
280 xamine the hypothesis that vascular-targeted photodynamic therapy (VTP) with WST11 and clinically rel
287 ects of reovirus combined with PpIX-mediated photodynamic therapy were analysed in methylthiazoltetra
289 omy, cryotherapy, laser photocoagulation, or photodynamic therapy, were excluded from the analysis.
290 in rare diseases, such as porphyrias, and in photodynamic therapy where short-term toxicity is intend
291 itization represents a promising approach in photodynamic therapy where the design of the active phot
293 photothermal therapy and porphyrin-mediated photodynamic therapy which results in complete tumor eli
294 mour cells with low or no PTEN expression to photodynamic therapy, which is based on the ability of p
295 l of oral infections, including their use in photodynamic therapy, will be discussed in this review.
299 f vascular endothelial growth factor A--with photodynamic therapy with verteporfin in the treatment o
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