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1                                              Multidrug resistant A. baumannii has risen rapidly in Vi
2                    In multivariate analysis, multidrug-resistant A. baumannii (odds ratio, 4.78; 95%
3 analyse the protein interaction network of a multidrug-resistant A. baumannii clinical strain (AB5075
4 ic agents used to treat infections caused by multidrug-resistant A. baumannii.
5 increased transmission risk; however, having multidrug-resistant-A. baumannii and specific healthcare
6 a potential selective advantage possessed by multidrug-resistant-A. baumannii in this environment and
7 n-resistant Staphylococcus aureus (MRSA) and multidrug-resistant Acinetobacter baumannii (MDR-AB) wer
8                                              Multidrug-resistant Acinetobacter baumannii presents a g
9 ion therapy is deployed for the treatment of multidrug-resistant Acinetobacter baumannii, as it can r
10 ycin-resistant enterococci, C difficile, and multidrug-resistant Acinetobacter.
11 y-onset infections; 66 isolates (50.0%) were multidrug resistant and, of 33 isolates tested for carba
12  The regimen could be effective against both multidrug-resistant and drug-susceptible tuberculosis in
13                                              Multidrug-resistant and epidemic strains are a large pro
14 ull gyrA and gyrB open reading frames in 240 multidrug-resistant and extensively drug-resistant tuber
15 utic options, particularly for patients with multidrug-resistant and extensively drug-resistant tuber
16 es in the world, and the increased number of multidrug-resistant and extremely drug-resistant strains
17                       The global increase of multidrug-resistant and pan-resistant Acinetobacter isol
18  frequent cause of such infections, is often multidrug resistant, and chronically colonizes a sizable
19 s, we characterize l(2)03659 as a Drosophila multidrug resistant-associated ABC transporter.
20  transient hypoxia and the appearance of the multidrug resistant bacteria Staphylococcus simulans in
21 over new antibiotics or strategies to combat multidrug resistant bacteria, especially Gram-negative b
22  veterinary medicine causes the emergence of multidrug resistant bacteria.
23                                     Emerging multidrug-resistant bacteria are a challenge for modern
24                                              Multidrug-resistant bacteria are responsible for substan
25                             The emergence of multidrug-resistant bacteria emphasizes the urgent need
26                       The rapid emergence of multidrug-resistant bacteria has renewed interest in dev
27  to ameliorate the development and spread of multidrug-resistant bacteria in cirrhosis.
28 ion imbalance in living cells while fighting multidrug-resistant bacteria is a paramount topic.
29                            Infections due to multidrug-resistant bacteria represent a major global he
30 ntions, including drugs and vaccines against multidrug-resistant bacteria such as Neisseria gonorrhoe
31 lator-associated pneumonia, and infection by multidrug-resistant bacteria were independently associat
32                      With rapid emergence of multidrug-resistant bacteria, there is often a need to p
33 sesses potent antibacterial activity towards multidrug-resistant bacteria.
34                                              Multidrug resistant bacterial pathogens have become a se
35  quantum dots (QDs) can kill a wide range of multidrug-resistant bacterial clinical isolates, includi
36                                              Multidrug-resistant bacterial infections are an ever-gro
37                             The incidence of multidrug-resistant bacterial infections is increasing g
38 min antibiotics are used clinically to treat multidrug-resistant bacterial infections, but their poor
39 , and have been proposed to be used to treat multidrug-resistant bacterial infections.
40 ed rational drug design approach to treating multidrug-resistant bacterial infections.
41 could serve as adjunctive treatments against multidrug-resistant bacterial infections.
42             The risk of infections caused by multidrug-resistant bacterial pathogens increases with h
43 chanism when combined with AgNPs against the multidrug-resistant bacterium Salmonella typhimurium DT
44 ith the industrial production of eggs and of multidrug-resistant, bloodstream-invasive infection in A
45  more active in vitro than paclitaxel in the multidrug resistant breast cancer cell line LCC6-MDR.
46 illus fumigatus and emerging threats such as multidrug resistant Candida auris are also alarming.
47 losis cases and the second highest number of multidrug resistant cases worldwide.
48 criminate isoniazid-monoresistant cases from multidrug-resistant cases within 2 days.
49 ream, or surgical site infection caused by a multidrug-resistant (cases) or -sensitive (controls) mic
50 mal-Pgp utilization enhances cytotoxicity to multidrug-resistant cells.
51 icrobial peptides displayed activity against multidrug-resistant clinical isolates of Escherichia col
52 le 9b and 9c were highly active also against multidrug-resistant clinical isolates.
53                                Two different multidrug-resistant, clinical MRSA isolates were grown o
54 cterium tuberculosis CNCTC My 331/88 and six multidrug-resistant clinically isolated strains of M. tu
55 with accurate identification of the pandemic multidrug-resistant clonal subgroup ST131-H30.
56  of sequence type 131 (ST131) are a pandemic multidrug resistant clone associated with urinary tract
57 bial resistance was evaluated in an epidemic multidrug-resistant clone of K. pneumoniae (ST258).
58 e of serotype 35B disease and emergence of a multidrug-resistant clone reported in this issue of the
59 R genes associated with clinically important multidrug-resistant clones and epidemic plasmids, in Ame
60                       The expansion of these multidrug-resistant clones suggests that the treatment o
61  especially with the emergence and spread of multidrug-resistant clones.
62 thin the outbreak (4.7%), including within a multidrug-resistant cluster that carried a rare rpoB mut
63 munity-based, commensal population underlies multidrug-resistant E. cloacae infections within hospita
64 tudy, we analysed a systematic collection of multidrug-resistant E. cloacae isolated between 2001 and
65 n testing of fosfomycin was performed on 649 multidrug-resistant E. coli clinical isolates collected
66 tion or induction of UhpT but are rare among multidrug-resistant E. coli clinical strains.
67                   Preventing colonization by multidrug-resistant E. faecalis could therefore be a val
68 l envelope; these include metallopeptidases, multidrug-resistant efflux (MDR) pumps, TonB-dependent r
69 mycin has become a front-line antibiotic for multidrug-resistant Enterococcus faecium bloodstream inf
70 iotics reduced selective pressures favouring multidrug-resistant epidemic ribotypes and was associate
71 iotics reduced selective pressures favouring multidrug-resistant epidemic ribotypes and was associate
72 ly used antibiotics, with 18 % ESBL and 36 % multidrug resistant Escherichia coli strains.
73                 A draft genome, annotated as multidrug resistant Escherichia coli, was retrieved from
74                                 As a result, multidrug-resistant, extensively drug-resistant, and pan
75                 Candida auris is an emerging multidrug-resistant fungal pathogen causing nosocomial a
76 s in health care caused by the prevalence of multidrug resistant Gram-negative pathogens.
77 s using efflux pump inhibitors for combating multidrug resistant Gram-negative pathogens.
78  CI, 0.32-1.40), bacteriuria associated with multidrug-resistant gram-negative bacilli (9 vs 24 episo
79 r detection of known resistance genes in 108 multidrug-resistant Gram-negative bacilli.
80 efficacy of strategies for the prevention of multidrug-resistant gram-negative bacteria (MDR-GNB) in
81 olderia cepacia complex (Bcc) are a group of multidrug-resistant gram-negative bacteria rarely report
82 line of defence in serious infections due to multidrug-resistant Gram-negative bacteria, but their us
83 yse the cell, is the last-line treatment for multidrug-resistant Gram-negative infections.
84 he last-resort antibiotics used for treating multidrug-resistant Gram-negative pathogens.
85 valuated against panels of tetracycline- and multidrug-resistant Gram-positive and Gram-negative path
86 Acinetobacter pittii are a frequent cause of multidrug-resistant, healthcare-associated infections.
87  sub-Saharan Africa, and are associated with multidrug resistant HIV-1.
88 examined the evolutionary history of leading multidrug resistant hospital pathogens, the enterococci,
89  representative bacterial strains, including multidrug-resistant hospital isolates.
90 pe 258 (ST258) are among the most widespread multidrug-resistant hospital-acquired pathogens.
91 omial pneumonia, is a versatile and commonly multidrug-resistant human pathogen for which further ins
92 th or without reduced ejection fraction, and multidrug-resistant hypertension (RHT) are major worldwi
93                                              Multidrug-resistant infection was associated with prior
94 w therapeutic targets are required to combat multidrug resistant infections, such as the iron-regulat
95 opment and hold promise for the treatment of multidrug resistant infections.
96 eatment of several human diseases, including multidrug-resistant infections and genetic disorders.
97 nfective strategy has the potential to treat multidrug-resistant infections and limit the emergence o
98 s used in the last line of defense to combat multidrug-resistant infections by Gram-negative bacteria
99 sistance mutations shape the pathobiology of multidrug-resistant infections has the potential to driv
100                                              Multidrug-resistant infections were associated with rece
101 is a significant contributor to recalcitrant multidrug-resistant infections, especially in immunocomp
102 ealthcare worldwide as an important cause of multidrug-resistant infections.
103 ted bacterial pneumonia (HABP/VABP) is often multidrug-resistant infections.
104 am provides a carbapenem alternative against multidrug-resistant infections.
105  the treatment of tuberculosis, particularly multidrug-resistant infections.
106 y profiling their antiviral efficacy against multidrug-resistant influenza A viruses, in vitro drug r
107                             The existence of multidrug-resistant influenza viruses, coupled with the
108 nya, and Tanzania (both sites combined), and multidrug-resistant iNTS was isolated in Burkina Faso (b
109                        A clinical pathogenic multidrug-resistant isolate, E. coli 381, isolated from
110                      The recent emergence of multidrug-resistant isolates has raised public health co
111                        The identification of multidrug-resistant isolates highlights the need for add
112 sticity and speed of evolutionary changes in multidrug-resistant K. pneumoniae, demonstrating the hig
113 sing on the virulent, globally disseminated, multidrug-resistant lineage ST131.
114  to human cell lines, and are active against multidrug-resistant M. tuberculosis strains, indicating
115 public health efforts to limit the spread of multidrug-resistant malaria.
116  much superior to that of doxorubicin in the multidrug resistant MCF-7/ADR xenografted nude mice.
117 ests are urgently needed for the analysis of multidrug resistant (MDR) and extensively drug resistant
118 d significantly reduced drug efflux by model multidrug resistant (MDR) breast cancer cell lines (MCF-
119 ponsible for decreasing drug accumulation in multidrug resistant (MDR) cells.
120 ne in the core and pooled siRNAs that target multidrug resistant (MDR) genes in the shell.
121 ted for their antibacterial activity against multidrug resistant (MDR) Gram-positive and Gram-negativ
122 ange of therapeutic agents required to treat multidrug resistant (MDR) infections.
123 77.7% (28/36) of clinical isolates indicated multidrug resistant (MDR) patterns, 50% (18/36) indicate
124 is, resistance categories were predefined as multidrug resistant (MDR), isoniazid resistant, rifampic
125  of ceftolozane-tazobactam resistance during multidrug resistant (MDR)-Pseudomonas aeruginosa infecti
126    WHO estimates 480,000 cases of these were multidrug resistant (MDR).
127             An increase in the proportion of multidrug-resistant (MDR) 35B isolates has recently been
128                                              Multidrug-resistant (MDR) Acinetobacter baumannii is one
129                                              Multidrug-resistant (MDR) and extensively drug-resistant
130 he highest incidences of DR-TB, particularly multidrug-resistant (MDR) and extensively drug-resistant
131                                              Multidrug-resistant (MDR) and extensively drug-resistant
132 s are threatened by the increasing burden of multidrug-resistant (MDR) and extensively drug-resistant
133 onsumption, incidence density of Candida and multidrug-resistant (MDR) bacteria bloodstream infection
134 s known about the excess mortality caused by multidrug-resistant (MDR) bacterial infection in low- an
135                                              Multidrug-resistant (MDR) bacterial infections are a ser
136                                Prevention of multidrug-resistant (MDR) bacterial infections relies on
137  of antibiotic resistance (AR) and spread of multidrug-resistant (MDR) bacterial pathogens.
138 re are more cases of isoniazid-resistant and multidrug-resistant (MDR) disease than are identified.
139 unctional CRISPR-Cas systems are absent from multidrug-resistant (MDR) Enterococcus faecalis, which o
140 um of activity of these antibiotics includes multidrug-resistant (MDR) gram-negative bacteria (GNB),
141                                              Multidrug-resistant (MDR) gram-negative bacteria have in
142 se for the treatment of infections caused by multidrug-resistant (MDR) Gram-negative bacteria.
143                                              Multidrug-resistant (MDR) infections are on the increase
144 in the Shigellae, particularly as a specific multidrug-resistant (MDR) lineage of Shigella sonnei (li
145 Is have been complicated by the emergence of multidrug-resistant (MDR) pathogens.
146 ntial association between TTSS genotypes and multidrug-resistant (MDR) profiles, and how this interac
147           Therapeutic interventions to treat multidrug-resistant (MDR) Pseudomonas aeruginosa infecti
148 nd die from tuberculosis (TB) each year, and multidrug-resistant (MDR) strains of TB are increasingly
149 ion model to follow a hypothetical cohort of multidrug-resistant (MDR) TB patients under different be
150 ar-negative, retreatment smear-positive, and multidrug-resistant (MDR) TB.
151 sis that were due to inadequate treatment of multidrug-resistant (MDR) tuberculosis (i.e., acquired r
152 erculosis (LTBI) after contact to infectious multidrug-resistant (MDR) tuberculosis (TB) are lacking
153 rove treatment outcomes for individuals with multidrug-resistant (MDR) tuberculosis (TB).
154 al approach to assess recent transmission of multidrug-resistant (MDR) tuberculosis and identify pote
155        The projected long-term prevalence of multidrug-resistant (MDR) tuberculosis depends upon the
156  efficacy and safety in drug-susceptible and multidrug-resistant (MDR) tuberculosis during the first
157    Globally, >30 000 children fall sick with multidrug-resistant (MDR) tuberculosis every year.
158               The transcontinental spread of multidrug-resistant (MDR) tuberculosis is poorly charact
159 A novel, shorter-course regimen for treating multidrug-resistant (MDR) tuberculosis was recently reco
160                                              Multidrug-resistant (MDR) tuberculosis, "Ebola with wing
161                      In 31 patients with non-multidrug-resistant (MDR) tuberculosis, viability and qu
162                     As treatment options for multidrug-resistant (MDR) uropathogens are limited, clin
163 g-sensitive (MIC = 0.012 muM; SI >/= 16000), multidrug-resistant (MDR), and extensively drug-resistan
164 phenicol, and trimethoprim-sulfamethoxazole (multidrug resistant [MDR]) was limited to Typhi isolates
165 otgun sequencing of all stools, we find that multidrug-resistant members of the genera Escherichia, K
166 st planktonic and biofilm forms of different multidrug resistant microorganisms, we present here the
167 a significantly increased proportion of rare multidrug-resistant molds.
168 ted complete growth inhibition in vitro of 2 multidrug-resistant MRSA strains.
169 cond-line antitubercular drug used to combat multidrug-resistant Mtb strains.
170 ts inactive variant PRD25N, and an extremely multidrug-resistant mutant, PR20.
171 osis treatments, particularly in the case of multidrug-resistant Mycobacterium tuberculosis (Mtb).
172                                 Treatment of multidrug-resistant Mycobacterium tuberculosis is a chal
173                                              Multidrug-resistant Neisseria gonorrhoeae is a top threa
174 s with Mycobacterium abscessus, a species of multidrug-resistant nontuberculous mycobacteria, are eme
175 istance in patients with drug-susceptible or multidrug-resistant (nonXDR) tuberculosis strains.
176 broad range of bacterial species, especially multidrug resistant ones.
177  compliance with prevention bundles impacted multidrug-resistant organism (MDRO) infections in Thai h
178 m difficile (OR 1.02, 95% CI 0.34-3.01), and multidrug-resistant organism (OR 1.06, 95% CI 0.42-2.71)
179 2 weeks' gestation or younger; prevalence of multidrug-resistant organism colonisation; and length of
180   Mycobacterium abscessus is a fast-growing, multidrug-resistant organism that has emerged as a clini
181 SA) is the most common healthcare-associated multidrug-resistant organism.
182  have been implicated in the transmission of multidrug-resistant organisms (MDRO).
183                  The emergence and spread of multidrug-resistant organisms (MDROs) across global heal
184                                Infections by multidrug-resistant organisms (MDROs) are a global threa
185           The emergence and dissemination of multidrug-resistant organisms (MDROs) is a global threat
186  bacterial infections including those due to multidrug-resistant organisms (MDROs).
187    Patients admitted to hospital can acquire multidrug-resistant organisms and Clostridium difficile
188                                              Multidrug-resistant organisms caused 56% of bacterial in
189 ect storm" for sustained endemicity of these multidrug-resistant organisms in Colombia.
190 h the aim to decrease selective pressure for multidrug-resistant organisms in order to preserve the u
191  strategies, may help mitigate the effect of multidrug-resistant organisms in the future.
192 day mortality, and mortality associated with multidrug-resistant organisms were significantly lower i
193 f clinical cultures that tested positive for multidrug-resistant organisms, blood culture contaminati
194 he ability of bacterial pathogens, including multidrug-resistant organisms, to colonize and subsequen
195 m were identified, including infections with multidrug-resistant organisms.
196 on therapy are common and frequently involve multidrug-resistant organisms.
197 awback, the development of infections due to multidrug-resistant organisms.
198 e therapy, neutropenia, or bacteremia due to multidrug-resistant organisms.
199               Although C auris is inherently multidrug resistant, other strains typically develop res
200 countering the emergence and transmission of multidrug-resistant P. falciparum malaria.
201  evaluated for antimalarial activity against multidrug-resistant P. yoelii in mice in the dose range
202 iparum malaria due to their activity against multidrug resistant parasites.
203                  Genetic tools to detect the multidrug-resistant parasites are needed.
204 eptibility testing (AFST) of the potentially multidrug-resistant pathogen Candida glabrata against an
205          Candida auris is an emerging, often multidrug-resistant pathogen with important public healt
206 r empiric antimicrobial therapy against this multidrug-resistant pathogen.
207 n "out of the box" therapeutic treatment for multidrug resistant pathogenic bacterial infections.
208                                 The emerging multidrug-resistant pathogenic yeast Candida auris repre
209 s were used (P= .002), and in the absence of multidrug-resistant pathogens (P< .05).
210                 We will focus on 3 important multidrug-resistant pathogens that are notoriously probl
211                                 However, for multidrug-resistant pathogens, demonstration of superior
212 ts with cIAI, including infections caused by multidrug-resistant pathogens.
213 ibit potent antimicrobial activities against multidrug-resistant pathogens.
214 e shown that induction of MarA can lead to a multidrug resistant phenotype at the population level.
215 ne artemisinin combination therapy (ACT) for multidrug-resistant Plasmodium falciparum malaria in Cam
216                        Due to development of multidrug-resistant Plasmodium falciparum new antimalari
217 ons, antibiotic resistance, and particularly multidrug-resistant profiles, is certainly of paramount
218                                Infections by multidrug-resistant Pseudomonas aeruginosa (MDRPa) are a
219 ith the adhesin MAM7 to a burn infected with multidrug-resistant Pseudomonas aeruginosa substantially
220   Falling 4C use predicted rapid declines in multidrug-resistant ribotypes R001 and R027.
221                                              Multidrug-resistant S Typhi was isolated in Ghana, Kenya
222  The case illustrates clinical challenges of multidrug-resistant S.
223 eus, methicillin-resistant S. aureus (MRSA), multidrug-resistant S. aureus (MDRSA), absence of scn (p
224                            In areas of Asia, multidrug-resistant Salmonella enterica serovar Typhi (S
225          With the worldwide emergence of the multidrug-resistant species Candida auris, identificatio
226                                Children with multidrug-resistant sporadic disease show better renal s
227 ers a novel strategy for attenuating current multidrug resistant staphylococcal infections.
228 an eight residue beta-sheet peptide) against multidrug resistant staphylococci.
229 otic resistance spreads among bacteria, with multidrug-resistant staphylococci and streptococci infec
230 h antibacterial activity against an array of multidrug-resistant staphylococci.
231 iance often leads to therapeutic failure and multidrug resistant strain development.
232 irds and, in one case, identical to a highly multidrug resistant strain isolated from a human child.
233  compounds possess potent activity against a multidrug resistant strain of P. falciparum and arrest p
234 ones, beta-lactam/beta-lactamase inhibitors, multidrug resistant strains and carbapenem-resistant Ent
235 be lethal due to the global dissemination of multidrug resistant strains.
236                             The emergence of multidrug-resistant strains is an increasing danger to p
237 ns are a large proportion of HAI agents, and multidrug-resistant strains of Klebsiella pneumoniae, a
238 creasingly complicated with the emergence of multidrug-resistant strains of Mycobacterium tuberculosi
239 ed by the HIV/AIDS pandemic and emergence of multidrug-resistant strains of Mycobacterium tuberculosi
240 t in antimicrobial activity observed against multidrug-resistant strains of Pseudomonas aeruginosa an
241  multiple M. tuberculosis strains (including multidrug-resistant strains).
242 gainst Mycobacterium tuberculosis, including multidrug-resistant strains, and some species of nontube
243 its over monotherapy, it may also select for multidrug-resistant strains, particularly during long-te
244 s of function was observed exclusively among multidrug-resistant strains.
245 azole drugs, resulting in difficult-to-treat multidrug-resistant strains.
246 s steadily increased, with a predominance of multidrug-resistant strains.
247 uctions into Africa, all from Asia, involved multidrug-resistant sublineages that replaced antibiotic
248 erial specific antibiotics, and treatment of multidrug resistant TB is longer.
249                        Tuberculosis (TB) and multidrug-resistant TB (MDR-TB) are major health problem
250                                              Multidrug-resistant TB and HIV coinfection represent sev
251 ansmission of Mtb in the largest outbreak of multidrug-resistant TB in South America to date.
252  have great potential to limit the spread of multidrug-resistant tuberculosis (MDR-TB) and extensivel
253 It is estimated that 33,000 children develop multidrug-resistant tuberculosis (MDR-TB) each year.
254  patients successfully treated for pulmonary multidrug-resistant tuberculosis (MDR-TB) in Tomsk, Russ
255                                              Multidrug-resistant tuberculosis (MDR-TB) is an importan
256                             Less than 30% of multidrug-resistant tuberculosis (MDR-TB) patients are c
257 antibiotics recommended for the treatment of multidrug-resistant tuberculosis (MDR-TB) patients.
258                                              Multidrug-resistant tuberculosis (MDR-TB), caused by dru
259 e the etiology of "hotspots" of concentrated multidrug-resistant tuberculosis (MDR-tuberculosis) risk
260 focus on antibiotics that are active against multidrug-resistant tuberculosis and Gram-negative bacte
261 improve treatment outcomes for patients with multidrug-resistant tuberculosis and prevent the spread
262                                 Diagnosis of multidrug-resistant tuberculosis and prompt initiation o
263                      WGS diagnosed a case of multidrug-resistant tuberculosis before routine diagnosi
264 ing percentage reduction in the incidence of multidrug-resistant tuberculosis by 2024 compared with c
265  system increased referrals from presumptive multidrug-resistant tuberculosis cases by >10-fold, with
266 diagnosis was completed and discovered a new multidrug-resistant tuberculosis cluster.
267 idrug-resistant tuberculosis will be primary multidrug-resistant tuberculosis compared with only 15%
268 ovements in treatment for drug-sensitive and multidrug-resistant tuberculosis could reduce the number
269 ealthcare workers with the goal of improving multidrug-resistant tuberculosis detection.
270 en has potential to substantially lessen the multidrug-resistant tuberculosis epidemic, but this effe
271 en has potential to substantially lessen the multidrug-resistant tuberculosis epidemic, but this effe
272 rge public health and societal implications, multidrug-resistant tuberculosis has been long regarded
273 ns in the primary analysis, the incidence of multidrug-resistant tuberculosis in 2024 would be 3.3 (9
274 est number of patients with tuberculosis and multidrug-resistant tuberculosis in the world.
275  of isoniazid resistance, a 152% increase in multidrug-resistant tuberculosis incidence, a 242% incre
276 rculosis, and a 275% increase in the risk of multidrug-resistant tuberculosis infection.
277 ay, 2016, WHO endorsed a 9 month regimen for multidrug-resistant tuberculosis that is cheaper and pot
278 cal agents used to halt the progression from multidrug-resistant tuberculosis to extensively resistan
279 rld Health Organization category 5 drugs for multidrug-resistant tuberculosis using a 7H9 broth micro
280 CWs in 3 district hospitals with specialized multidrug-resistant tuberculosis wards in KwaZulu-Natal,
281                 By 2032, an estimated 85% of multidrug-resistant tuberculosis will be primary multidr
282 each of confirmed tuberculosis and suspected multidrug-resistant tuberculosis) to a randomly allocate
283 ence, a 242% increase in prevalent untreated multidrug-resistant tuberculosis, and a 275% increase in
284 Secondary outcomes were missed tuberculosis, multidrug-resistant tuberculosis, and comorbidities with
285 n settings with more ongoing transmission of multidrug-resistant tuberculosis, but results were other
286 d-resistant tuberculosis is more common than multidrug-resistant tuberculosis, it has been much less
287 ope is complicated by the high prevalence of multidrug-resistant tuberculosis, low rates of drug susc
288 he public sector contributed 87% of acquired multidrug-resistant tuberculosis, related to irregular a
289 h all-cause mortality among US patients with multidrug-resistant tuberculosis.
290 th a potential for immunotherapy in treating multidrug-resistant tuberculosis.
291 for the development of novel drugs to tackle multidrug-resistant tuberculosis.
292 ctinomycin antibiotic essential for treating multidrug-resistant tuberculosis.
293 terial, used in the treatment of adults with multidrug-resistant tuberculosis.
294 luating new agents/regimens for treatment of multidrug-resistant tuberculosis; and (3) evaluating saf
295 ensitive tuberculosis; improved treatment of multidrug-resistant tuberculosis; and expansion of acces
296  critical implications for drug-targeting in multidrug-resistant tumors where a stressful micro-envir
297     Broad-spectrum antibiotics for recurrent multidrug-resistant urinary tract infections (UTIs) disr
298                               Concerns about multidrug-resistant uropathogens have pointed to the nee
299 tion, and only two cases of infection with a multidrug-resistant virus have been reported under adequ
300                             Candida auris, a multidrug-resistant yeast that causes invasive infection

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