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1 or viral coinfections and immunosuppression (corticosteroids).
2 ents were treated with local infiltration of corticosteroid.
3 act development among eyes receiving topical corticosteroids.
4 IL-10) generally impaired by frequently used corticosteroids.
5 usion of food triggers and swallowed topical corticosteroids.
6  that are treated with high doses of inhaled corticosteroids.
7 n of offending drug and short course of oral corticosteroids.
8 ywords for oral corticosteroids and systemic corticosteroids.
9 use of lopinavir-ritonavir, interferons, and corticosteroids.
10 sk while limiting calcineurin inhibitors and corticosteroids.
11 andard-dose CNIs, mycophenolate mofetil, and corticosteroids.
12 ndard-exposure TAC (MMF + sTAC; n = 54) with corticosteroids.
13 ttenuated with concomitant use of statins or corticosteroids.
14 ed with attention paid to the use of topical corticosteroids.
15 body weight include progesterone analogs and corticosteroids.
16 sed optic canal decompression and the use of corticosteroids.
17 d were successfully treated with intravenous corticosteroids.
18 arding remission, and (4) no use of systemic corticosteroids.
19 p inhibitors, elimination diets, and topical corticosteroids.
20 cause the stunting of growth seen with these corticosteroids.
21 nation of intranasal H(1)-antihistamines and corticosteroids.
22  progesterone analogs and short-term (weeks) corticosteroids.
23 rential trabeculotomy or using postoperative corticosteroids.
24 JIA)-associated uveitis treated with topical corticosteroids.
25  common, used in 31%, followed by iNO (13%), corticosteroids (10%), prone positioning (10%), HFOV (9%
26 ampreys produces two predominant circulating corticosteroids, 11-deoxycortisol (S) and 11-deoxycortic
27  orbital disease with inadequate response to corticosteroids (44.4%) or a high suspicion of malignanc
28 ed intravenous immune globulin (IVIG) (71%), corticosteroids (61%), and anakinra (18%).
29 ts were more commonly treated with long-term corticosteroids (73%), whereas German patients were more
30 0% IE vs. 13% WNE, P < .001) and use inhaled corticosteroids (77% FE vs. 15% IE vs. 18% WNE, P < .001
31                Thirty-four were treated with corticosteroids (83%), 11 with an immunosuppressant trea
32 sporine, both with mycophenolate mofetil and corticosteroids; 95/115 randomized patients were followe
33 oved from the study and treated with topical corticosteroids according to best medical judgment.
34 s used in eight studies as a measure of oral corticosteroid adherence, and fractional exhaled nitric
35 itric oxide (FeNO) in 17 studies for inhaled corticosteroid adherence.
36  patients continue to be prescribed systemic corticosteroids after CSC diagnosis.
37                            Patients who used corticosteroids after surgery were more likely to experi
38          In this mouse model, treatment with corticosteroid allows for initial proliferation and sust
39 scale) after a 1-hour treatment with an oral corticosteroid and 3 inhaled albuterol and ipratropium t
40  caused by type 2 cytokines is responsive to corticosteroid and biologic therapies, many severe asthm
41                                              Corticosteroid and high-dose intravenous immunoglobulin
42 uding 208 (44%) prescribed high-dose inhaled corticosteroids and 122 (31%) with severe asthma.
43 active NIPPU after failure of treatment with corticosteroids and a second-line immunosuppression drug
44 logic agents after failure of treatment with corticosteroids and a second-line immunosuppression drug
45                     The patient refused oral corticosteroids and any intravitreal injection therapies
46 eviously unsuspected roles for oncostatin M, corticosteroids and ephrins in mediating cellular respon
47 g function, require more courses of systemic corticosteroids and have greater limitation of activitie
48  by conventional therapy only, consisting of corticosteroids and immunosuppressants.
49                                              Corticosteroids and immunosuppressive drugs were largely
50  (6) optimal dosing regimens for intravenous corticosteroids and infliximab in these patients, and (7
51                            Dispensed inhaled corticosteroids and inhaled beta-agonists were associate
52  airway obstruction despite massive doses of corticosteroids and maximal pharmacologically induced br
53 -term use of anti-inflammatory drugs such as corticosteroids and nonsteroidal anti-inflammatory drugs
54 he age of fourteen, and the addition of oral corticosteroids and omalizumab to regular inhaled cortic
55             Management is primarily based on corticosteroids and other immunomodulatory agents, which
56 ry to traditional antirejection therapy with corticosteroids and polyclonal antilymphocyte globulin.
57 verity, exacerbations, and responsiveness to corticosteroids and potential for response to anti-Type
58 ment options were confined to application of corticosteroids and symptomatic management, without prov
59 arch terms for asthma with keywords for oral corticosteroids and systemic corticosteroids.
60 a aged 6 to 16 years taking low-dose inhaled corticosteroids and with serum 25-hydroxyvitamin D level
61 te GVHD respond to first-line treatment with corticosteroids and, for several decades, there was no o
62 ts with fast-acting immunosuppressive drugs (corticosteroids and/or cyclosporine) to reduce inflammat
63 RSwNP with inadequate response to intranasal corticosteroids, and it was well tolerated.
64 clude discontinuation of the specific agent, corticosteroids, and other immune suppressing agents for
65            The combination of ascorbic acid, corticosteroids, and thiamine has been identified as a p
66 multicenter clinical trial of ascorbic acid, corticosteroids, and thiamine vs placebo for adult patie
67 tic shock, the combination of ascorbic acid, corticosteroids, and thiamine, compared with placebo, di
68               Of these, 10 were treated with corticosteroids, and three of these patients also receiv
69                            Race, gender, and corticosteroids apparently did not influence RNA positiv
70                                              Corticosteroids are a possible therapeutic option.
71 vir has not been shown to have efficacy, and corticosteroids are currently not recommended.
72                     Swallowed topical-acting corticosteroids are effective in bringing active EoE int
73                 However, inhaled or systemic corticosteroids are ineffective treatments in many patie
74                             Depot parenteral corticosteroids are not recommended for treatment of AR
75 effects of allergic immune dysregulation and corticosteroids are poorly understood.
76 rine and antihistamines followed by systemic corticosteroids are the mainstays of therapy for acute e
77 o help ameliorate the inflammatory response, corticosteroids are used as an adjuvant to standard anti
78                                         When corticosteroids are used for a long time in patients wit
79 d effects of asthma-controlling medications (corticosteroids) as factors that predispose patients wit
80                                              Corticosteroid-associated AEs of elevated intraocular pr
81  effects of vamorolone on motor outcomes and corticosteroid-associated safety concerns.
82 egy to avoid both calcineurin inhibitors and corticosteroids at this time.
83 pt-based strategies employing tacrolimus and corticosteroid avoidance.
84 are not fully understood, and treatment with corticosteroids, biologics, and surgical intervention ar
85 and transplant-related covariates and use of corticosteroids, bisphosphonates, vitamin D and calcium
86 uch as chronic lymphopenia and/or history of corticosteroid boluses could be useful to avoid life-thr
87 osuppressive drugs and the administration of corticosteroid boluses used in acute rejection.
88                                         Oral corticosteroid bursts are frequently prescribed in the g
89 here appropriate, we estimated the effect of corticosteroids by random-effects meta-analyses using th
90 sivir, lopinavir-ritonavir, interferon beta, corticosteroids, chloroquine and hydroxychloroquine, and
91  inflammatory markers 1 week after receiving corticosteroids (CS) (p<0.003).
92                                     Although corticosteroids dampen the dysregulated immune system an
93  2009 compared to 51.4% in 2018) and topical corticosteroids decreased (57.3%-52.0%).
94 at high risk for colectomy, hospitalization, corticosteroid dependence, and serious infections.
95 lucocorticoid receptor (GR) by the synthetic corticosteroid dexamethasone (DEX) stimulates bovine her
96 e natural polyphenol curcumin (CURC) and the corticosteroid dexamethasone (DEX).
97                                The synthetic corticosteroid dexamethasone consistently induces BoHV-1
98 ncy is consistently induced by the synthetic corticosteroid dexamethasone.
99                   The ongoing use of inhaled corticosteroids did not increase the risk of hospitaliza
100  3 Ds: drugs (particularly swallowed topical corticosteroids), dietary restriction, and endoscopic di
101                                          The corticosteroid domain randomized participants to a fixed
102 mized to open-label interventions within the corticosteroid domain.
103 plications increase with the cumulative oral corticosteroid dosage.
104 alysis was used to assess the association of corticosteroid dose and mortality.
105 nib and corticosteroids had a 50% or greater corticosteroid dose reduction from baseline.
106 (2) agonist therapy to a maintenance inhaled corticosteroid dose that causes the same magnitude of sy
107       We analyzed relapse and temporal daily corticosteroid dose with and without co-administration o
108 ion, but the evidence relates mainly to high corticosteroid doses and is of low quality with potentia
109  a fall in FeNO following supervised inhaled corticosteroid dosing could indicate previous poor adher
110 ine (AZA), baricitinib, ciclosporin A (CSA), corticosteroids, dupilumab, interferon-gamma, intravenou
111 lation or >=2 courses of blinded rescue oral corticosteroids) during the study; in addition, patients
112 k 24 because of an increased placebo/topical corticosteroid effect (36.8% vs 21.1%, P = .06).
113               Systemic exposure to high-dose corticosteroids effectively combats acute rejection afte
114                        Greater oral/systemic corticosteroid exposure was also associated with increas
115 t comparison of its use with observation and corticosteroids failed to confirm the usefulness of this
116 x stromal keratitis who had not received any corticosteroids for at least 10 days before study enroll
117  right eye and the recent use of intravenous corticosteroids for bronchitis.
118 ith Septic Shock and Activated Protein C and Corticosteroids for Human Septic Shock trials.
119 ith Septic Shock and Activated Protein C and Corticosteroids for Human Septic Shock trials.
120  Shock) and $30,911 (Activated Protein C and Corticosteroids for Human Septic Shock) per patient.
121                  Per Activated Protein C and Corticosteroids for Human Septic Shock, adjunctive hydro
122 sex, CMV mismatch, interleukin-2 inhibitors, corticosteroids for rejection, and plasmapheresis were n
123 pic mucosal healing, clinical remission, and corticosteroid-free remission at week 44 (all P < .05) i
124 y higher percentage of patients establishing corticosteroid-free state for the first time throughout
125 ith placebo in out- and inpatients, systemic corticosteroids given for 9 to 56 days were associated w
126 d at a significantly lower rate in the early corticosteroid group (34.9% vs 54.3%, P = .005).
127 ength of stay was also observed in the early corticosteroid group (5 vs 8 days, P < .001).
128 Outcomes of standard of care (SOC) and early corticosteroid groups were evaluated, with a primary com
129 cts, 81 (38%) and 132 (62%) in SOC and early corticosteroid groups, respectively.
130 8%) of 43 patients receiving ruxolitinib and corticosteroids had a 50% or greater corticosteroid dose
131                  Immunosuppression devoid of corticosteroids has been investigated to avoid long-term
132                        Long-term use of oral corticosteroids has known adverse effects, but the risk
133                                      Inhaled corticosteroids have been the foundation for asthma trea
134 stimulatory blockade strategies that include corticosteroids have recently shown promise, despite the
135 gnaling System (RAAS) involve binding of the corticosteroid hormone, aldosterone to its mineralocorti
136                                              Corticosteroids, however, can have a wide range of effec
137              ICANS is currently managed with corticosteroids; however, the optimal dose and duration
138                              Intra-articular corticosteroid (IACS) injections are often used for pain
139 ns.Objectives: To understand whether inhaled corticosteroid (ICS) withdrawal affected IMPACT results,
140 lines were updated to recommend that inhaled corticosteroid (ICS)/long-acting beta (2)-adrenoceptor a
141              The combination drug of inhaled corticosteroid (ICS)/long-acting beta2 agonist is being
142 ms underlying hyperinflation and how inhaled corticosteroids (ICS) affect this important aspect of CO
143                                      Inhaled corticosteroids (ICS) are a mainstay of treatment in eos
144                           Rationale: Inhaled corticosteroids (ICS) are key treatments for controlling
145 uctive pulmonary disease (COPD) with inhaled corticosteroids (ICS) is controversial, because it can r
146             In patients on high-dose inhaled corticosteroids (ICS) with type 2-high asthma (subgroups
147 n for the use of triple therapy with inhaled corticosteroids (ICS)/LABA/LAMA over dual therapy with L
148                                      Inhaled corticosteroids (ICSs) are widely used in COPD, but the
149 e anti-inflammatory maintenance with inhaled corticosteroids (ICSs) has been reserved for patients wi
150 r-level medication: medium/high-dose inhaled corticosteroids (ICSs) or ICSs + add-on medication (long
151 mized to observation in the Standard Care vs Corticosteroid in Retinal Vein Occlusion Study.
152 ich could be suppressed by the addition of a corticosteroid in vitro.
153 imab, tacrolimus, mycophenolate mofetil, and corticosteroids in 80% of patients, whereas 20% received
154 eitis, and concomitant use of other forms of corticosteroids in a time-updated fashion, treatment wit
155    They consider the indications for inhaled corticosteroids in COPD, when inhaled corticosteroids sh
156                                   Proper use corticosteroids in general type patients did not delay v
157 reveal an association, but reported doses of corticosteroids in included studies were high (mostly >
158           Although our results using topical corticosteroids in mice are highly promising for recover
159 rescribing of potent and very potent topical corticosteroids in non-white ethnicities and people of l
160 endation against the use of maintenance oral corticosteroids in patients with COPD and a history of s
161                To analyze the application of corticosteroids in patients with severe pneumonia.
162 eview updates the current evidence regarding corticosteroids in the treatment of influenza and examin
163       We examined the role of the endogenous corticosteroids in vivo and ex vivo in sea lamprey (Petr
164 c interventions for inpatients refractory to corticosteroids, in reducing risk of colectomy, (6) opti
165 zation, requiring a short course of systemic corticosteroids; in 4 cases, this occurred within 72 hou
166                                   Intranasal corticosteroids (INCS) remain the preferred monotherapy
167 atients with CRSwNP refractory to intranasal corticosteroids (INCS) significantly improved endoscopic
168 mbined plasmapheresis, HDIVig, and high-dose corticosteroids induced the complete remission of neurol
169 costeroids and omalizumab to regular inhaled corticosteroid inhalation failed to relieve symptoms.
170 or PARDS: continuous neuromuscular blockade, corticosteroids, inhaled nitric oxide (iNO), prone posit
171                                              Corticosteroids inhibited Interleukin-6(IL-6) production
172 costeroid prescription or code for an ocular corticosteroid injection within 120 days of the uveitis
173 d to < 4 mm when assessed after six weeks of corticosteroid injection.
174 bronchodilators, whereas the role of inhaled corticosteroids is less clear.
175                               Treatment with corticosteroids is recommended for Duchenne muscular dys
176                    We predict that increased corticosteroid levels activate the glucocorticoid recept
177 f there is a progressive increase in inhaled corticosteroid/long-acting beta(2) agonist therapy to a
178                    Application of lower dose corticosteroids (&lt;= 2 mg/kg day) could inhibit IL-6 prod
179 nsight as to how adding a LABA to an inhaled corticosteroid may improve clinical outcomes in asthma.
180                                              Corticosteroids may be beneficial in sepsis, but uncerta
181 ostoperative NSAIDs alone, which may suggest corticosteroid-mediated outflow obstruction distal to th
182 anasal Sinuses (TEMPS) is developed with the corticosteroid mometasone furoate.
183 ents in some motor outcomes as compared with corticosteroid-naive individuals over an 18-month treatm
184 tly different between vamorolone-treated and corticosteroid-naive participants (p = 0.088; least squa
185 ficant improvement compared to group-matched corticosteroid-naive participants for run/walk 10 meters
186 in the CINRG Duchenne Natural History Study (corticosteroid-naive, n = 19; corticosteroid-treated, n
187                                         Oral corticosteroid (OCS) treatment for severe asthma is asso
188   Despite reports of visual improvement with corticosteroids, optic canal decompression, and medical
189 al or ocular H(1)-antihistamines, intranasal corticosteroids or a fixed combination of intranasal H(1
190 ssessment of clinical status, and the use of corticosteroids or antiangiogenics.
191 findings suggest that children using inhaled corticosteroids or inhaled beta-agonists might be at inc
192 utic domains, for example, antiviral agents, corticosteroids, or immunoglobulin.
193 aft rejection, CMV infection, higher dose of corticosteroids, or prolonged neutropenia.
194                                   The use of corticosteroids (P: 0.007) and history of chronic respir
195 s randomized to implant or systemic therapy (corticosteroid plus immunosuppression in >90%) were foll
196 d contrast agents (GBCAs) that occur despite corticosteroid premedication (breakthrough reactions) ar
197 hen compared with use of the same agent with corticosteroid premedication (P = .10).
198 pectively) from the observed rate when using corticosteroid premedication and the same GBCA (36%; 95%
199 , 95%; four of five administrations) without corticosteroid premedication, which did not differ (P =
200    For the alternative outcome definition, a corticosteroid prescription or code for an ocular cortic
201                         We compared systemic corticosteroid prescriptions before and after CSC diagno
202                     Comedications containing corticosteroids, quetiapine, or antithrombotic agents we
203 levels in the blood, adherence rates to oral corticosteroids ranged from 47% to 92%, although the per
204 e, lampreys express only a single, ancestral corticosteroid receptor (CR).
205                     Antibiotics and systemic corticosteroids reduce treatment failure in adults with
206                      Although mechanisms for corticosteroid refractory asthma are likely to be numero
207  a new model for treating some patients with corticosteroid refractory asthma.
208 b was recently approved for the treatment of corticosteroid-refractory acute GVHD in adult and pediat
209 timal second-line treatment of patients with corticosteroid-refractory acute GVHD.
210 the ERBB receptor and ligand family to drive corticosteroid-refractory inflammation should enhance th
211 e asthma: on the one hand driving pathologic corticosteroid-refractory mixed granulocytic inflammatio
212                                  The topical corticosteroid regimen used in this study was significan
213 ey and that receptor-mediated discriminative corticosteroid regulation of hydromineral balance is an
214 ed improvements were similar in magnitude to corticosteroid-related improvements.
215 s of psoriasis, topical therapies, primarily corticosteroids, remain the mainstay of treatment to red
216 us radiotherapy, no neurological symptoms or corticosteroid requirement, and Eastern Cooperative Onco
217  can drive both corticosteroid-sensitive and corticosteroid-resistant responses.
218 tification of sputum eosinophilia indicating corticosteroid responsiveness in subjects with severe as
219 onse was explored in participants undergoing corticosteroid responsiveness testing with intramuscular
220 der how to reconcile the negative effects of corticosteroids revealed by Liu and Zhang et al. with th
221 pro-allergic cytokine, IL-13, can drive both corticosteroid-sensitive and corticosteroid-resistant re
222 nhaled corticosteroids in COPD, when inhaled corticosteroids should be withdrawn, and what other trea
223 ther and how osmoregulation is controlled by corticosteroid signaling in the phylogenetically basal v
224  starting oxygenation index of each therapy; corticosteroids started at the lowest oxygenation index
225                            Swallowed topical corticosteroids (STC) belong to the therapeutic cornerst
226 eatment consisted of various combinations of corticosteroids (systemic, intravitreal, and topical), a
227 and PIIRS were treated with adjunctive pulse corticosteroid taper therapy (PCT) consisting of intrave
228 challenge and risk of relapse of irAE-N, and corticosteroid taper, which are not specifically address
229                            Administration of corticosteroids that permitted higher levels of bacteria
230 o percent had red flagged PDDIs (mostly with corticosteroids), the same as in the 2008 survey.
231 nse prompted us to examine the role of early corticosteroid therapy in patients with moderate to seve
232                       Compared with placebo, corticosteroid therapy reduced the risk of persistent or
233 l II study and 6 level III studies) explored corticosteroid therapy that did not have uniformly bette
234                                     Systemic corticosteroid therapy was associated with improved visu
235                   Eyes treated with systemic corticosteroid therapy were identified for further analy
236 articularly following exposure cessation and corticosteroid therapy, but the time course to improveme
237  60 eyes in 40 patients who received topical corticosteroid therapy, there was a dose-dependent incre
238                            When treated with corticosteroids, this resolved or regressed at follow-up
239  We further determined the impact of topical corticosteroids to reactivate Borrelia locally in the sk
240 uspended and intensive treatment with potent corticosteroids (topical, subtenon, intravitreal, or sys
241                                              Corticosteroid-treated participants showed stunting of g
242 History Study (corticosteroid-naive, n = 19; corticosteroid-treated, n = 68) over a similar 18-month
243                             However, chronic corticosteroid treatment causes significant morbidities.
244                     Although the efficacy of corticosteroid treatment in controlling asthma is widely
245  benefit based on inputs from the Adjunctive Corticosteroid Treatment in Critically Ill Patients with
246 at a dose of 200 mg/d for 7 d for Adjunctive Corticosteroid Treatment in Critically Ill Patients with
247 omes were aggregate data from the Adjunctive Corticosteroid Treatment in Critically Ill Patients with
248                               Per Adjunctive Corticosteroid Treatment in Critically Ill Patients with
249 ter monetized benefit of $10,658 (Adjunctive Corticosteroid Treatment in Critically Ill Patients with
250 t studies reporting corticosteroid versus no corticosteroid treatment in individuals with influenza.
251                                              Corticosteroid treatment in influenza is associated with
252 e of the JCI, Liu and Zhang et al. evaluated corticosteroid treatment in more than 400 patients with
253                           Maternal antenatal corticosteroid treatment is standard care to accelerate
254 ction timing, bacteria/fungal infection, and corticosteroid treatment limit interpretation, we believ
255 cohort study, exposure to maternal antenatal corticosteroid treatment was significantly associated wi
256 nia are likely to benefit from moderate-dose corticosteroid treatment when administered relatively la
257          Of the 14 868 (2.22%; 46.1% female) corticosteroid treatment-exposed children, 6730 (45.27%)
258                           Maternal antenatal corticosteroid treatment.
259 f both diagnostic codes and documentation of corticosteroid treatment.
260 lp inform decisions about maternal antenatal corticosteroid treatment.
261 al-acquired infection in people treated with corticosteroids (unadjusted odds ratio, 2.74; 95% CI, 1.
262 actor receptor (EGFR/ERBB1) as a mediator of corticosteroid-unresponsive inflammation and bronchial h
263 ic therapies, many severe asthmatics exhibit corticosteroid-unresponsive mixed granulocytic inflammat
264 ib orally, starting at 5 mg twice daily plus corticosteroids, until treatment failure, unacceptable t
265 a history of ocular surgery (62.5%), topical corticosteroid use (35.4%), and dry eye syndrome (37.5%)
266 are utilization (r = 0.48; P = .03) and oral corticosteroid use (r = 0.43; P = .05) at baseline.
267 es a comprehensive overview of oral/systemic corticosteroid use and associated adverse events for pat
268 o assess the associations between asthma and corticosteroid use and the risk of COVID-19-related hosp
269                           Evidence regarding corticosteroid use for severe coronavirus disease 2019 (
270 the real-world extent and burden of systemic corticosteroid use in asthma.
271 nomic analyses, and surveys on oral/systemic corticosteroid use in children (>5 yr old), adolescents
272  A prospective, randomized trial of systemic corticosteroid use in endophthalmitis may be warranted.
273                 We report that oral/systemic corticosteroid use is prevalent in asthma management, an
274                                     Systemic corticosteroid use to manage uncontrolled asthma and its
275                      Long-term oral/systemic corticosteroid use was, in general, less frequent than s
276 ease severity, nasal polyposis, and systemic corticosteroid use were also associated with frequent AE
277 g-term and repeated short-term oral/systemic corticosteroid use were associated with an increased ris
278                 Poor ocular surface, topical corticosteroid use, previous ocular surgery, and/or a hi
279 zation associated with asthma and/or inhaled corticosteroid use.
280  severity, health care utilization, and oral corticosteroid use.
281  (asthma, eczema, and allergic rhinitis) and corticosteroid use.
282 , and observational cohort studies reporting corticosteroid versus no corticosteroid treatment in ind
283 tively low myelotoxicity profiles, including corticosteroids, vincristine, L-asparaginase, methotrexa
284 nstay of treatment, and they include topical corticosteroids, vitamin D analogues, calcineurin inhibi
285 on, treatment with <3 drops daily of topical corticosteroid was associated with an 87% lower risk of
286  of participants in whom the dose of inhaled corticosteroid was reduced halfway through the trial, an
287 ortion of participants whose dose of inhaled corticosteroid was reduced, or the cumulative fluticason
288                               Use of topical corticosteroids was associated with cataract formation i
289 led corticosteroids with or without systemic corticosteroids was not associated with COVID-19-related
290                                              Corticosteroids were associated with a higher rate of AR
291                       Overall, oral/systemic corticosteroids were commonly used for asthma management
292                                      Inhaled corticosteroids were measured directly in the blood in o
293             Eyes that received postoperative corticosteroids were more likely to experience an IOP sp
294                        Additionally, topical corticosteroids were prescribed in 18 eyes and tapered d
295 RSwNP with inadequate response to intranasal corticosteroids were randomized (1:1) to omalizumab or p
296                                    High-dose corticosteroids with IMT within 3 months resulted in imp
297                Similarly, the use of inhaled corticosteroids with or without systemic corticosteroids
298 eptor antagonist tocilizumab with or without corticosteroids, with questions remaining regarding the
299 xposure tacrolimus (EVR + rTAC; n = 52) with corticosteroid withdrawal at 6-month posttransplant or c
300 ncing rejection under belatacept-based early corticosteroid withdrawal following T-cell-depleting ind

 
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