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1  30% IOP reduction and no pain (without oral acetazolamide).
2 Hg and an IOP reduction of 30% (without oral acetazolamide).
3 relate to the reported beneficial effects of acetazolamide.
4  carbonic anhydrase (CA) inhibitors, such as acetazolamide.
5 ree-fold by the carbonic anhydrase inhibitor acetazolamide.
6 lpha-CA deletion mutant and the CA inhibitor acetazolamide.
7  symmetric blood flow and normal response to acetazolamide.
8 edly low blood flow and abnormal response to acetazolamide.
9 c paralysis and the patient's worsening from acetazolamide.
10 ding pilocarpine, epinephrine compounds, and acetazolamide.
11 is formation is increased in the presence of acetazolamide.
12 ertigo and ataxia that are not responsive to acetazolamide.
13  (n = 7) was injected intravenously with 1 g acetazolamide.
14 te levels alter the decongestive response to acetazolamide.
15 rzolamide and an additional 5 months of oral acetazolamide.
16  to 12.56; P < .001) were also observed with acetazolamide.
17 f interaction between carbonic anhydrase and acetazolamide.
18 s of dilation despite pretreatment with oral acetazolamide.
19 ne order of magnitude better than the parent acetazolamide 1 were also identified in this study, toge
20 The mean improvement in PMD was greater with acetazolamide (1.43 dB, from -3.53 dB at baseline to -2.
21      Mean improvements in papilledema grade (acetazolamide: -1.31, from 2.76 to 1.45; placebo: -0.61,
22 In addition, under the conditions used here, acetazolamide (100 microM) did not have a significant ef
23 lication of the carbonic anhydrase inhibitor acetazolamide (100 microM) in the presence of CO2/HCO3-
24  occurred in 59% of rats receiving high-dose acetazolamide (200 mg/kg).
25  rats (n = 100) were randomized to either IP acetazolamide, 200 mg/kg (high-dose), or IP saline twice
26                                              Acetazolamide (222 g/mol) binding to carbonic anhydrase
27                                          The acetazolamide (3.6 mum) and placebo (2.1 mum) groups sho
28  but was reversed by reacidifying the blood (acetazolamide; 3% FiCO2).
29 d by acetazolamide (day 3: placebo 74.8% vs. acetazolamide 41.3%, P < 0.001).
30                                     Low-dose acetazolamide (50 mg/kg) produced a pH (7.22 +/- 0.07) t
31                                              Acetazolamide (50 microM) doubled the size of the dendri
32  of acidosis induced by intraperitoneal (IP) acetazolamide (50 or 200 mg/kg) or saline.
33 n rats (n = 75) were randomized to either IP acetazolamide, 50 mg/kg (low-dose), or IP saline twice d
34 per milliliter to receive either intravenous acetazolamide (500 mg once daily) or placebo added to st
35 c peptide) >250 ng/mL to receive intravenous acetazolamide (500 mg once daily) or placebo in addition
36                                              Acetazolamide (500 mg twice daily) was administered for
37 olume overload in a 1:1 ratio to intravenous acetazolamide (500 mg/day) or matching placebo on top of
38                              Dorzolamide and acetazolamide (500 microM) did not show additive inhibit
39                                              Acetazolamide (500-1000 mg, twice daily) vs placebo admi
40 - 1-2.3 +/- 1; P = 0.02) and the use of oral acetazolamide (61%-11%; P < 0.01) were also reduced.
41 termine the effects of three dosages of oral acetazolamide (62.5, 125, and 250 mg, all twice daily) i
42 mide also experienced a reduction in weight (acetazolamide: -7.50 kg, from 107.72 kg to 100.22 kg; pl
43            At altitude, patients either took acetazolamide (750 mg/d) or placebo in addition to autoC
44 asured by the National Eye Institute VFQ-25 (acetazolamide: 8.33, from 82.97 to 91.30; placebo: 1.98,
45 and its 10-item neuro-ophthalmic supplement (acetazolamide: 9.82, from 75.45 to 85.27; placebo: 1.59,
46 to have previous treatment with an oral CAI (acetazolamide), a topical CAI (brinzolamide/dorzolamide)
47     We found that systemic administration of acetazolamide, a CA inhibitor, immediately after the ext
48 f motor coordination that was ameliorated by acetazolamide, a carbonic anhydrase inhibitor that minim
49                                      Whether acetazolamide, a carbonic anhydrase inhibitor that reduc
50 c-PHC-102 is a (99m)Tc-labeled derivative of acetazolamide, a high-affinity small organic ligand of c
51                                              Acetazolamide, a membrane-permeable CA inhibitor, was us
52                                              Acetazolamide, a proximal tubule diuretic, delivers more
53 in this study, consisting of a derivative of acetazolamide, a spacer, and a peptidic (99m)Tc chelator
54 drase isoforms I, II, IX, XII, and XIV using acetazolamide (AAZ) as reference compound.
55                                  Infusion of acetazolamide abolished the positive PD in the later seg
56 in the presence and absence of HCO(3)(-) and acetazolamide (ACTZ) using tissue treated with siRNA spe
57  substance associated with doping in sports: acetazolamide (ACTZ).
58 h and without niflumic acid (MCT inhibitor), acetazolamide (ACTZ, a CA inhibitor), 5-(N-Ethyl-N-isopr
59  determine whether the beneficial effects of acetazolamide (ACZ) in improving vision at 6 months cont
60                                              Acetazolamide (ACZ) is used to prevent acute mountain si
61  Administration-approved small-molecule drug acetazolamide (ACZ).
62 al trial, study eyes of subjects assigned to acetazolamide (ACZ, n = 44) or placebo (PLB, n = 43) had
63 owing metabolic acidosis (via 2 days of oral acetazolamide; ACZ) with and without acute restoration o
64  obstructive sleep apnoea (OSA).However, how acetazolamide affects the key traits causing OSA remains
65 show that SLC-149 is a better inhibitor than acetazolamide against CAIX.
66 F); others were treated with weight loss and acetazolamide alone.
67  She was first treated by intravenous 250 mg acetazolamide along with maximal pressure-lowering drops
68                     Participants assigned to acetazolamide also experienced a reduction in weight (ac
69 reasing distal volume delivery elicited with acetazolamide also led to increases in renal interstitia
70 ha-CA knockout mutant and in the presence of acetazolamide, although UreI and urease remained fully f
71 ated HCO(3)(-) secretion was not affected by acetazolamide, an inhibitor of carbonic anhydrase.
72 he high-power LFOs are decreased markedly by acetazolamide and 4-aminopyridine, the primary treatment
73                                              Acetazolamide and autoCPAP resulted in better control of
74 derately elevated altitude, a combination of acetazolamide and autoCPAP therapy, compared with autoCP
75                                              Acetazolamide and autoCPAP treatment was associated with
76                                         Both acetazolamide and DIDS reduced chloride effluxes.
77    Treatment of algae with the CA inhibitors acetazolamide and ethoxyzolamide decreased photosyntheti
78 e 33-fold lower than reference drugs such as acetazolamide and gabapentin.
79                                              Acetazolamide and glucose infusion resulted in a negativ
80 /- 0.4 ms, S.E., n = 11 mice) and blocked by acetazolamide and increasing external pH (to decrease CO
81         Inhibition of total CA activity with acetazolamide and inhibition of extracellular-facing mem
82       The carbonic anhydrase (CA) inhibitors acetazolamide and its structurally similar analogue meth
83 avoided, and proximally acting agents (e.g., acetazolamide and loop diuretic agents) are preferred.
84 the right eye even under treatment with oral acetazolamide and maximal tolerated doses of topical ant
85 free conditions, DIDS, and the CA inhibitors acetazolamide and methazolamide but not by the Na-H exch
86 ated with cGMP production and is enhanced by acetazolamide and raloxifene.
87 rong inhibition of hCA IX/XII, outperforming acetazolamide and SLC-0111.
88 ngestion of the carbonic anhydrase inhibitor acetazolamide and the ion exchange inhibitor DIDS (4,4'-
89 hdrawal, to the carbonic anhydrase inhibitor acetazolamide and to H2DIDS inhibition.
90 observed between the effect of allocation to acetazolamide and UNa on decongestion (P = 0.007).
91                                      In IIH, acetazolamide and weight loss effectively improve RNFL t
92 eated with anticoagulation and 100% required acetazolamide and/or lumbar puncture.
93 t additive to unselective CA inhibition with acetazolamide, and independent of extracellular potassiu
94            Whether the beneficial effects of acetazolamide are consistent across the entire range of
95 lowing metabolic acidosis via 2 days of oral acetazolamide at 250 mg every 8 h (ACZ; pH: -0.07 0.04 a
96 ce interval (CI), 1.03-3.79) and use of oral acetazolamide at baseline (HR, 1.74; 95% CI, 1.13-2.70),
97              Asian ethnicity and use of oral acetazolamide at baseline were associated with greater f
98      Finally, the blockade of water entry by acetazolamide attenuated ballooning in vitro and markedl
99  contributes to lithium-NDI development, and acetazolamide attenuates lithium-NDI development in mice
100 arbonic buffer was increased again by adding acetazolamide (ATZ), a membrane permeant carbonic anhydr
101 wed by the carbonic anhydrase (CA) inhibitor acetazolamide (ATZ).
102                                              Acetazolamide-augmented blood oxygenation level-dependen
103 ased computational framework for analysis of acetazolamide-augmented BOLD imaging can be used to meas
104 hronic steno-occlusive disease who underwent acetazolamide-augmented BOLD imaging for recurrent minor
105 emonstrate comprehensive characterization of acetazolamide-augmented BOLD MRI response in chronic ste
106 luorescent derivative of the CA IX inhibitor acetazolamide (AZ).
107 se IX (CAIX) overexpression and inhibited by acetazolamide (AZA) administration.
108 rbonic anhydrase II (CaII) and its inhibitor acetazolamide (AZM) into E. coli cell lysate as a model
109                          The clinically used acetazolamide (AZM) is a sulfonamide that binds with hig
110 c carbonic anhydrase (CA) inhibitors with an acetazolamide backbone.
111 l, we demonstrate a successful example of an acetazolamide-based lead compound with in vivo therapeut
112 ith AE2, these latter two being sensitive to acetazolamide because of their association with the cyto
113 e assessed the uptake of 10 pharmaceuticals (acetazolamide, beclomethasone, carbamazepine, diclofenac
114  failure, administration of a single dose of acetazolamide before sleep improves central sleep apnea
115 x with five CA sulfonamide-based inhibitors (acetazolamide, benzolamide, chlorzolamide, ethoxzolamide
116            Variability in the quality of the acetazolamide binding responses was likely a product of
117                         Although we detected acetazolamide binding to immobilized CA II and specific
118                    Our findings suggest that acetazolamide can improve OSA, probably due to reduction
119 pe 1 diabetes and preserved kidney function, acetazolamide caused an acute, reversible reduction in m
120 sessment of cerebrovascular reserve by using acetazolamide challenge in patients with intracranial va
121 tric blood flow and abnormal response to the acetazolamide challenge test may require a revasculariza
122 mography (CT) in the resting state and after acetazolamide challenge.
123 on and apoptosis in PC12 cells; and (3) that acetazolamide, chlorthalidone, and the neurosteroid, all
124  invasive mechanical ventilation, the use of acetazolamide, compared with placebo, did not result in
125                                              Acetazolamide completely blocked the increase in Cl(-)/H
126  CA XIV at 2.8 A resolution and of an enzyme-acetazolamide complex at 2.9 A resolution.
127 "130's segment." The structure of the CA XII-acetazolamide complex is also reported at 1.50-A resolut
128           Additionally, the structure of the acetazolamide complex is essentially identical to that o
129  groups onto the par excellence CA inhibitor acetazolamide, compounds that may interact with the dist
130                                          The acetazolamide conjugate described in this study could be
131                          The (99m)Tc-labeled acetazolamide conjugate exhibits high tumor uptake and f
132 erties of said ligand and understand whether acetazolamide conjugates merit further development as dr
133                                              Acetazolamide consistently increased the likelihood of d
134                               The effects of acetazolamide could be mimicked by either amiloride or b
135                               The effects of acetazolamide could be mimicked by removal of HCO3-/CO2
136 y questions remain regarding the efficacy of acetazolamide, CSF shunting procedures and cerebral tran
137 g the treatment phase which was prevented by acetazolamide (day 3: placebo 74.8% vs. acetazolamide 41
138         We have previously described a novel acetazolamide derivative, a carbonic anhydrase ligand wi
139                                              Acetazolamide did not affect the cotransport stoichiomet
140  unclear whether the decongestive effects of acetazolamide differ across the spectrum of left ventric
141                             We conclude that acetazolamide does not function as either a nitrous anhy
142 ups 72 hrs after administration of the first acetazolamide dose (31.8 +/- 4.9-25.3 +/- 3.8 mEq/L, p <
143                                              Acetazolamide dose was lower in bariatric patients, star
144 inhaled sodium nitrite were not increased by acetazolamide during alveolar hypoxia.
145                The efficacy and safety of an acetazolamide-eluting biodegradable tubular stent (AZ-BT
146 atients with symmetric blood flow and normal acetazolamide-enhanced challenge test results will do we
147 nic anhydrase inhibitor (CAI); however, CAIs acetazolamide, ethoxyzolamide, dichlorphenamide, chlorth
148 inically used carbonic anhydrase inhibitors, acetazolamide, ethoxzolamide, and dorzolamide, have prom
149 r inhibitors, among which are methazolamide, acetazolamide, ethoxzolamide, dorzolamide, brinzolamide,
150                                              Acetazolamide facilitates decongestion in acute decompen
151               Simultaneous administration of acetazolamide fully prevented the procognitive effects o
152                                      For the acetazolamide group (n = 187), compared with the placebo
153 ccurred in 76 of 256 patients (29.7%) in the acetazolamide group and in 72 of 259 patients (27.8%) in
154 curred in 108 of 256 patients (42.2%) in the acetazolamide group and in 79 of 259 (30.5%) in the plac
155                             At 6 months, the acetazolamide group had greater reduction than the place
156  < .001) decreased significantly more in the acetazolamide group.
157  potency series of thiazide diuretic action (acetazolamide &gt; chlorothiazide > metolazone) differed si
158                                However, only acetazolamide has been explored for in vivo efficacy in
159                         An inhibitor of CAs, acetazolamide has been reported to inhibit invasion.
160             The carbonic anhydrase inhibitor acetazolamide has been used as a treatment for hypokalae
161                                              Acetazolamide has been used for decades as a respiratory
162                         With the addition of acetazolamide, however, acid-base balance as well as ENa
163 roup previously showed the 1,3,4-thiadiazole acetazolamide human carbonic anhydrase inhibitor scaffol
164 d a higher proportional treatment effect for acetazolamide if baseline HCO3 >= 27 mmol/l.
165         Moreover, systemic administration of acetazolamide immediately after the extinction training
166 reas d-phenylalanine potentiated extinction, acetazolamide impaired extinction also when infused loca
167                          In the ADVOR trial, acetazolamide improved decongestion in acute decompensat
168                        Randomization towards acetazolamide improved decongestive response over the en
169                                              Acetazolamide improved prothrombin time, factor X, and a
170                                              Acetazolamide improved subjective perception of overall
171                                              Acetazolamide improves decongestive response over the en
172 ics in patients with acute decompensated HF, acetazolamide improves the incidence of successful decon
173 , double-masked, placebo-controlled study of acetazolamide in 165 participants with IIH and mild visu
174 ngly related to successful decongestion with acetazolamide in ADHF.
175 mented NO generation by CA from nitrite with acetazolamide in anaesthetized pigs during alveolar hypo
176                                             (Acetazolamide in Decompensated Heart Failure with Volume
177 tion and improved decongestion in the ADVOR (Acetazolamide in Decompensated Heart Failure with Volume
178                     Patients from the ADVOR (Acetazolamide in Decompensated Heart Failure with Volume
179 ludes all 519 patients from the ADVOR trial (Acetazolamide in Decompensated Heart Failure With Volume
180 tested the effect of the CA-specific blocker acetazolamide in lithium-NDI.
181 inical outcomes and decongestive response to acetazolamide in patients with acute decompensated heart
182 Trial (IIHTT) reported beneficial effects of acetazolamide in patients with mild visual loss.
183             The kidney effects and safety of acetazolamide in persons with type 1 diabetes have not b
184                                              Acetazolamide in Persons with Type 1 Diabetes, NCT054733
185 scans show more extensive hypoperfusion than acetazolamide in the two cases.
186                                              Acetazolamide increased the odds of successful decongest
187                Acidosis induced by high-dose acetazolamide, independent of hyperoxemia or hypoxemia,
188                 Studies in mice treated with acetazolamide indicated that increased bicarbonate and f
189  study, the following hypothesis was tested: acetazolamide-induced acidosis is associated with preret
190          It can be assessed by measuring the acetazolamide-induced change in regional cerebral blood
191                                              Acetazolamide induces a metabolic acidosis via an altern
192   Carbonic anhydrase (CA) inhibitors such as acetazolamide inhibit hypoxic pulmonary vasoconstriction
193                                              Acetazolamide inhibited the carbonic anhydrase activity
194                                              Acetazolamide inhibited the short-circuit current throug
195                                              Acetazolamide inhibits proximal tubular sodium and bicar
196                                              Acetazolamide inhibits proximal tubular sodium reabsorpt
197 increased more after dipyridamole than after acetazolamide injection in two patients.
198 However, current measurement methods require acetazolamide injection or hypercapnia challenge, prompt
199                                              Acetazolamide is a mild diuretic and a respiratory stimu
200                                              Acetazolamide is associated with a higher rate of succes
201                                              Acetazolamide is commonly used to treat idiopathic intra
202     AZATAX was designed to establish whether acetazolamide is safe and improves cerebellar syndrome i
203                                              Acetazolamide is well tolerated and effective for motor
204  in complex with a nonspecific CA inhibitor, acetazolamide, is available in Protein Data Bank.
205  species, reducing aqueous humor inflow with acetazolamide lowered IOP and administering water intrap
206       There is some evidence to suggest that acetazolamide may improve obstructive sleep apnoea (OSA)
207 al of HCO(3)(-)/CO(2) was inhibited by DIDS, acetazolamide, methazolamide, and low-chloride buffer.
208                           Furosemide but not acetazolamide (n = 6 each) increased medullary oxygenati
209  0.06, P < 0.001); however, neither low-dose acetazolamide nor saline induced preretinal neovasculari
210  examine the prolonged duration of action of acetazolamide observed in this study as well as the effe
211 erved in this study as well as the effect of acetazolamide on clinical end points, such as duration o
212 ween serum chloride levels and the effect of acetazolamide on death or heart failure readmissions was
213 is study sought to investigate the effect of acetazolamide on natriuresis in ADHF and its relationshi
214        We aimed to investigate the effect of acetazolamide on the traits contributing to OSA and its
215 zed to receive intravenous administration of acetazolamide, one dose of 500 mg or 250 mg every 6 hrs
216 dependent chloride/bicarbonate exchange with acetazolamide or chlorthalidone.
217                No effects were observed when acetazolamide or d-phenylalanine was infused locally int
218 lated by 7,8-benzoquinoline and inhibited by acetazolamide or HCO3-/CO2 removal can be said to repres
219 omized 519 patients with ADHF to intravenous acetazolamide or matching placebo on top of intravenous
220  Volume Overload), randomized to intravenous acetazolamide or matching placebo on top of intravenous
221 n 18 to 55 years of age with IIH were taking acetazolamide or methazolamide in 2018 (6828 / 0.25 = 27
222 age with IIH diagnoses and prescriptions for acetazolamide or methazolamide in 2018 were identified,
223 iaries with IIH, 6828 had a prescription for acetazolamide or methazolamide.
224                This effect is not blocked by acetazolamide or MK-801, indicating that permeability of
225  structures of CrCAH3 in complex with either acetazolamide or phosphate ions were determined at 2.6-
226 ion for more 24 hours were randomized to the acetazolamide or placebo group and 380 were included in
227 d to a double-blind cross-over protocol with acetazolamide or placebo, taken 1 h before bedtime for s
228 CO(2) did not change after administration of acetazolamide or progesterone.
229           Treatment of lithium-NDI mice with acetazolamide or thiazide/amiloride induced similar anti
230 tic agents (loop diuretic agents, thiazides, acetazolamide) or mechanical devices.
231 al dorzolamide, oral dosing of eplerenone or acetazolamide, or some combination thereof.
232 y dilation was enhanced by administration of acetazolamide (oral or intra-arterial) and oral raloxife
233 s intermediate between high-dose (200 mg/kg) acetazolamide (P < 0.001) and saline controls (7.42 +/-
234 chloride, which was effectively prevented by acetazolamide (P<0.001).
235 o-plus-diet or maximally tolerated dosage of acetazolamide-plus-diet.
236                                We found that acetazolamide prevents HPV in anaesthetized pigs, as in
237 3 exhibited a significant higher response to acetazolamide [primary endpoint: no vs. elevated HCO3; O
238         A total of 17 patients received oral acetazolamide prior to surgery to acutely lower IOP.
239                                    High-dose acetazolamide produced a severe acidosis (pH 7.13 +/- 0.
240 pupillary dilation with tropicamide and oral acetazolamide prophylaxis.
241 and analyzed an identical dilution series of acetazolamide (ranging from 4.1 to 1000 nM).
242                  In the intact eye, DIDS and acetazolamide reduced AH secretion by 25% and 44%, respe
243 d mice with the carbonic anhydrase inhibitor acetazolamide reduced lung inflammatory pathology withou
244                                              Acetazolamide reduced measured GFR by 15% (95% confidenc
245                             Preblocking with acetazolamide reduced more than 80% uptake of (18)F-AmBF
246           In collecting duct (mpkCCD) cells, acetazolamide reduced the cellular lithium content and a
247                                              Acetazolamide reduced the median [interquartile range] L
248                            Preventive use of acetazolamide reduced the relative risk of SHAI by 44%.
249                                              Acetazolamide reduces HPV in pigs without evidence of an
250 s of complexes of HpalphaCA with a family of acetazolamide-related sulfonamides have been determined.
251 ixty-seven per cent of patients treated with acetazolamide reported a good neuromuscular response.
252                                              Acetazolamide resulted in improved diuretic response mea
253     We conclude that a single 500-mg dose of acetazolamide reverses nonchloride responsive metabolic
254                                     Low-dose acetazolamide reversibly lowered GFR in persons with typ
255      Diffusion coefficients are obtained for acetazolamide, riboflavin, sodium fluorescein, and theop
256 ng of contraction alkalosis (eg, addition of acetazolamide), second agent with alternate mechanism of
257 igh selectivity against CA II (605-fold than acetazolamide selectivity).
258 theless, purified CanB (a dimeric, anion and acetazolamide sensitive, zinc-containing type II beta-cl
259                                           An acetazolamide stress SPECT image was also obtained in tw
260                                Allocation to acetazolamide strongly and independently predicted natri
261                    In comparing placebo with acetazolamide, the hourly number of episodes of central
262  patients, with a 6-month first-phase single acetazolamide therapy group, followed by a randomized 5-
263                                       Add-on acetazolamide therapy improves decongestion across the e
264 n mutations in the CaV2.1 channel, for which acetazolamide therapy is suggested.
265          In the mutant or in the presence of acetazolamide, there was an approximately 3 log10 decrea
266 nderlie the reduced urinary PGE2 levels with acetazolamide, thereby contributing to the attenuation o
267      While WRF occurred more frequently with acetazolamide, this was not associated with adverse clin
268                  Drugs that decrease inflow (acetazolamide, timolol) or increase outflow facility (pi
269 urple (MFCP) was tested in mice treated with acetazolamide to cause urinary alkalinization, and Ceren
270 sed the FDA-approved carbonic anhydrase drug acetazolamide to design potent antienterococcal agents.
271  duct, or gave aldosterone and NaHCO(3) plus acetazolamide to increase luminal HCO(3)(-) concentratio
272                              The addition of acetazolamide to loop diuretic therapy in patients with
273 n the overall beneficial treatment effect of acetazolamide to the primary end point of successful dec
274 st clinical VRE strains from MIC = 2 mug/mL (acetazolamide) to MIC = 0.007 mug/mL (22) and 1 mug/mL (
275                     In vivo, the bladders of acetazolamide-treated mice exhibited a wavelength-depend
276 s previously observed in patients but not in acetazolamide-treated mice in this study.
277 -1)) 0.37 +/- 0.04 (control), 0.16 +/- 0.03 (acetazolamide-treated), and 1.14 +/- 0.15 (forskolin-tre
278   Only the latter group showed a significant acetazolamide treatment effect.
279                                 Furthermore, acetazolamide treatment reduced inulin clearance and cor
280                                              Acetazolamide treatment was associated with higher cumul
281  diet plus the maximally tolerated dosage of acetazolamide (up to 4 g/d) or matching placebo for 6 mo
282         Analysis was stratified according to acetazolamide use.
283 trial end points and the treatment effect of acetazolamide was assessed, as was the evolution of seru
284 eline HCO3 levels on the treatment effect of acetazolamide was assessed.
285                                              Acetazolamide was associated with a higher incidence of
286 stent with this hypothesis, the CA inhibitor acetazolamide was found to be a strong inhibitor of gluc
287                               A dose of oral acetazolamide was given before the patient left the clin
288 hese results show that the antidiuresis with acetazolamide was partially caused by a tubular-glomerul
289 21 [109.5]; IC [IC05]: 7.344 [4.591]), while acetazolamide was the second strongest (n = 51; PRR: 113
290 he use of oral glaucoma medications, such as acetazolamide, was considered a failure.
291      In the BNP-driven group, furosemide and acetazolamide were given more often and in higher doses
292 drase II and the resulting binding signal of acetazolamide were increased by a factor of 5 compared t
293                                 Low doses of acetazolamide were well tolerated in persons with type 1
294                                              Acetazolamide, which acidifies the subretinal space, had
295 lated by 7,8-benzoquinoline was sensitive to acetazolamide, which caused up to 50 % inhibition of the
296 antly associated with cancer risk, including acetazolamide, which was associated with reduced colorec
297 ts with IIH and mild visual loss, the use of acetazolamide with a low-sodium weight-reduction diet co
298  NO formation; however; combined infusion of acetazolamide with sodium nitrite inhalation did not fur
299 l, natriuresis and diuresis were higher with acetazolamide, with a higher treatment effect for patien
300 ibited by the sulfonamides ethoxzolamide and acetazolamide, yielding the lowest Ki values measured by

 
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