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1 mors, including those that are classified as drug resistant.
2 hylococcus aureus, are becoming increasingly drug-resistant.
3 haracterized to determine the percentages of drug-resistant ALDH+ cells, MDR-1/ABCG2 overexpressing c
4  examine dose-dependent cytotoxic effects on drug-resistant and drug-sensitive cancer cell lines.
5 profiling and functional characterization of drug-resistant and engineered cell lines.
6 n 2000 experimentally supported circulating, drug-resistant and prognosis-related lncRNA biomarkers;
7                His cytomegalovirus was multi-drug resistant, and was treated with maribarir, intravit
8 ociated with brain malformations, tend to be drug-resistant, and have been linked to an increased ris
9    Pancreatic cancer is usually advanced and drug resistant at diagnosis.
10  antibiotics for combination therapy against drug resistant bacteria can be realized on an integrated
11 e a prototype for point-of-care diagnosis of drug resistant bacteria with visual signal output.
12  on macrophage function and killing of multi-drug resistant bacteria.
13 ntial new class of antibiotics against multi-drug resistant bacteria.
14 antimicrobials are urgently needed to combat drug-resistant bacteria and to overcome the inherent dif
15                              Surveillance of drug-resistant bacteria is essential for healthcare prov
16 iotics against two clinically isolated multi-drug-resistant bacteria strains (including carbapenem-re
17  against multidrug-resistant and extensively drug-resistant bacteria, including ESBL, carbapenem- and
18  shown in-vivo and in-vitro efficacy against drug-resistant bacteria.
19 ing approach for detection of live, dead and drug-resistant bacteria.
20  a purulent animal wound model infected with drug-resistant bacteria.
21 reat severe infections caused by extensively drug-resistant bacteria.
22 biotic of last resort used in treating multi-drug resistant bacterial infections in humans.
23 biotic use has led to increased isolation of drug resistant bacterial strains from respiratory sample
24 re urgently needed because the rapid rise in drug-resistant bacterial infections in recent decades ha
25 bacteriophages (phages) for the treatment of drug-resistant bacterial infections is one approach that
26 rtant combination therapies for treatment of drug-resistant bacterial infections.
27 ion, which is essential for the treatment of drug-resistant bacterial infections.
28 ead to novel approaches for the treatment of drug-resistant bacterial infections.
29                          More and more multi-drug-resistant bacterial strains cause life-threatening
30                       The emergence of multi-drug-resistant bacterial strains further complicates pat
31 l-acquired infections (HAIs) attributed to a drug-resistant bacterium in the United States, and resis
32 e therapy for individuals with CF and highly drug-resistant Bcc and B. gladioli infections.
33 sine kinase inhibitors (TKIs) may select for drug-resistant BCR-ABL1 kinase domain (KD) mutants.
34 s partially explained by microbes adopting a drug-resistant biofilm mode of growth during infection.
35 ll molecules for antifungal activity against drug-resistant C. albicans.
36 mors established from drug-sensitive but not drug-resistant cancer cell lines.
37 present work thus reveals a chemotherapeutic drug-resistant cancer cell vulnerability in PERK and sug
38 hat following initial response to treatment, drug-resistant cancer cells frequently evolve and, event
39 erapy less effective due to proliferation of drug-resistant cancer cells when using very long inducti
40 carcinogenesis and offer a novel approach to drug-resistant cancer therapy.
41  to serve as tumor killers for late-stage or drug-resistant cancers.
42 ncer therapy, specifically in the context of drug-resistant cancers.
43 t only demonstrated the competing effects of drug-resistant cell expansion versus overall tumor regre
44 bclones could be comprised of metastatic and drug resistant cells.
45 rug-sensitive cells increasing but growth of drug-resistant cells decreasing effective drug inhibitio
46 ional chemotherapy has not been effective as drug-resistant cells escape lethal DNA damage effects by
47 its restored expression impaired survival of drug-resistant cells, sensitized them to TKIs in vitro,
48 and -time course experiments showed that the drug-resistant cells, which express lower expression and
49  cancer and particularly in chemotherapeutic drug-resistant cells.
50                         The alarming rise in drug-resistant clinical cases of tuberculosis (TB) has n
51 acious antimalarials to address the emerging drug-resistant clinical cases.
52 ssible driver of myeloma cell evolution in a drug-resistant clone.
53 atment failure resulting from persistence of drug-resistant clones after conventional chemotherapy tr
54 persister" tumor cells underlie emergence of drug-resistant clones and contribute to relapse and dise
55 ctivity, but after initial therapy response, drug-resistant clones restore myosin II activity to incr
56 mivudine at Met184Val, and when at least one drug-resistant codon was detected in a participant's pre
57 loxacin heteroresistance and the presence of drug resistant colony forming units (CFUs) at 1 per 1000
58                  The liver metastasis showed drug-resistant CSC- and EMT-like phenotype with aerobic
59 ssays and expanded clones with wild-type and drug-resistant defective proviruses.
60                                              Drug-resistant dormant myeloma cells that reside in spec
61               Most clonal groups were highly drug resistant due to the presence of multiple antimicro
62 tous discovery of inhibitors that target the drug resistant EGFR(L858R/T790M/C797S) mutant with nanom
63 a potential therapeutic strategy to overcome drug-resistant EGFR mutations that emerge within the ATP
64 ients who underwent total callosotomy due to drug-resistant epilepsy (CPs; two females), in three non
65 eizures (odds ratio [OR] = 0.21, p = 0.032), drug-resistant epilepsy (OR = 0.23, p = 0.022), and infa
66 ve stimulation (VNS) is widely used to treat drug-resistant epilepsy and depression.
67 xtensively used to find the seizure focus in drug-resistant epilepsy and is of growing importance in
68 n a retrospective cohort of 28 patients with drug-resistant epilepsy implanted with intracranial elec
69 be epilepsy (TLE) is the most common type of drug-resistant epilepsy in adults, with an unknown etiol
70                 Sleep fragmentation in focal drug-resistant epilepsy is associated with ictal and int
71                                Patients with drug-resistant epilepsy often require surgery to become
72 wall and in neocortical parenchyma of young, drug-resistant epilepsy patients (18-28 years old) who u
73 s placed on the cortex, is typically used in drug-resistant epilepsy patients, and is increasingly be
74 electroencephalographic (SEEG) recordings in drug-resistant epilepsy patients, to qualitatively and q
75 d epileptic bursts in 36 patients with focal drug-resistant epilepsy who underwent combined stereo-el
76  previously collected from 123 patients with drug-resistant epilepsy who underwent resective epilepsy
77 tual resection predicts surgical outcome for drug-resistant epilepsy' by Kini et al. (doi:10.1093/bra
78 as these individuals can experience lifelong drug-resistant epilepsy, cerebral palsy, feeding difficu
79 al lobe epilepsy represents a major cause of drug-resistant epilepsy.
80 , we measured the "escape time" required for drug-resistant Escherichia coli populations to eclipse a
81  induce therapeutic hypothermia for treating drug-resistant fever, and for improving glucose and ener
82 anted device in adults (age >=18 years) with drug-resistant focal epilepsy followed at 35 centres acr
83                                              Drug-resistant focal epilepsy is a large-scale brain net
84 of the presurgical evaluation, patients with drug-resistant focal epilepsy were instructed to overtly
85       In kainic-acid-induced mouse models of drug-resistant focal epilepsy, electric-field changes in
86                            For patients with drug-resistant focal epilepsy, excision of the epileptog
87 ry is a widely accepted treatment option for drug-resistant focal epilepsy.
88  seizures from nine patients with unilateral drug-resistant focal epilepsy.
89    Temporal lobe epilepsy is the most common drug-resistant form of epilepsy in adults.
90                         Patients with highly drug-resistant forms of tuberculosis have limited treatm
91 in a high percentage of patients with highly drug-resistant forms of tuberculosis; some associated to
92 tro and mouse-model efficacy toward multiple-drug-resistant fungal pathogens, exhibits a wide safety
93                          Global outbreaks of drug-resistant fungi such as Candida auris are thought t
94 ed to counter the escalating threat posed by drug-resistant fungi.
95 a wide range of KIT mutants in patients with drug-resistant GISTs.
96 identification and detection of new forms of drug-resistant gonorrhoea.
97 ug target against the rising threat of multi-drug-resistant Gram-negative bacteria.
98 or novel antibiotics is especially acute for drug-resistant Gram-negative pathogens(1,2).
99 perties make it a key agent for treatment of drug-resistant Gram-positive infections.
100  is characterized by colonization with multi-drug-resistant healthcare-associated pathogens.
101                                              Drug resistant HIV variants, including minority variants
102 that RPV LA will not inhibit transmission of drug-resistant HIV-1 and may select for drug-resistant v
103               The presence of high-abundance drug-resistant HIV-1 jeopardizes success of antiretrovir
104 ations, the clinical impact of low-abundance drug-resistant HIV-1 variants (LA-DRVs) at levels <15%-2
105           Candida auris is an emerging multi-drug-resistant human fungal pathogen.
106 TAMs to not only eradicate highly aggressive drug-resistant human lung and pancreas cancers in mice,
107 stantial percentage of patients suffer from "drug-resistant" hypertension, a condition associated wit
108                                              Drug resistant infections represent one of the most chal
109                                       Highly drug-resistant infections are disproportionally caused b
110 d, ten million people will die annually from drug-resistant infections by 2050.
111           Current studies suggest that human drug-resistant infections can be either environmentally
112 nisms of action that are capable of treating drug-resistant infections(1).
113 biotic resistance in the treatment of severe drug-resistant infections.
114 ears could reduce disease burden and prevent drug-resistant infections.
115 unds showed better activity profiles against drug-resistant influenza A strains, as well as influenza
116 gal indicator strains, notably against multi-drug resistant Klebsiella pneumoniae ATCC 700603 while i
117 shortening regimens for drug-susceptible and drug-resistant latent and active M. tuberculosis infecti
118 or ALL in general and may suppress incurable drug-resistant leukemia forms.
119 c GSK3alpha inhibition profoundly sensitized drug-resistant leukemias to asparaginase.
120                                              Drug resistant M. tuberculosis is an emerging threat for
121                                    Combating drug-resistant malaria urgently requires the development
122 ologies in reporting the clinically relevant drug-resistant markers, including full gene deletions.
123  rates of AMR with 51.9% (28/54) being multi-drug resistant (MDR) and 53.6% of these (15/28) being ex
124                        15% of isolates multi-drug resistant (MDR) to first-line antibiotics and 60% w
125 found that PDAC consists of ALDH+/CD133+ and drug-resistant (MDR1+) subtypes of CSCs with specific me
126            Moreover, our analysis revealed a drug-resistant mechanism through which overexpression of
127 y patients and help to better understand the drug-resistant mechanism to TKIs.
128  genetic analysis is important to understand drug-resistant mechanisms; however, the clinical signifi
129 ,10-phenanthroline-5,6-dione [phendione]) in drug-resistant melanoma.
130 of prostate phenotypes from normal tissue to drug-resistant metastases.
131 ved outcomes for breast cancer patients with drug-resistant metastatic disease.
132                                          The drug-resistant metastatic state was dependent on histone
133  have investigated the clinical relevance of drug resistant minority variants, but the level at which
134 proved chemotherapeutic response in a highly drug-resistant mouse model of NSCLC.
135 ed metabolic reprogramming in the context of drug-resistant Mtb infection, previous literature examin
136 gy and differences in the immune response to drug-resistant Mtb provides significant insights into ho
137 e drug-susceptible (MIC = 0.0039 mug/mL) and drug-resistant Mtb strains (MIC = 0.0078 mug/mL).
138 eral independent acquisitions of extensively drug-resistant/multidrug-resistant-inducing plasmids, pr
139 atment is initiated, cancers already contain drug-resistant mutant cells.
140                                              Drug-resistant mutant kinases are valuable tools in drug
141 replication inhibitors, but the emergence of drug-resistant mutants is observed frequently, highlight
142 a paradigm, we have developed kinase-active, drug-resistant mutants of ERK5.
143  pandemics by reassortment and generation of drug-resistant mutants, which render antivirals and curr
144  This led to the identification of the novel drug-resistant mutation L46P located outside the drug-bi
145         Phylogenetic and network inferences, drug resistant mutations (DRMs), subtypes and HIV-1 dive
146                                         Most drug-resistant mutations are located near the ethambutol
147                                              Drug-resistant mutations cluster near loops that lay on
148 <400 copies per mL), and none had multiclass drug-resistant mutations detected.
149 within expanded clones, including those with drug-resistant mutations.
150 ral load, CD4 cell count, and antiretroviral drug-resistant mutations.
151                                              Drug-resistant mycobacteria are a rising problem worldwi
152 ree-phage cocktail to treat a patient with a drug-resistant Mycobacterium abscessus suggests that pha
153                      Automated genotyping of drug-resistant Mycobacterium tuberculosis (MTB) directly
154 health concern and the growing prevalence of drug-resistant Mycobacterium tuberculosis is making dise
155 H-MYCN mice; (ii) orthotopic xenografts of a drug-resistant NB line SK-N-BE(2)C (mutated TP53); (iii)
156  (mutated TP53); (iii) flank xenografts of a drug-resistant NB-PDX; and (iv) xenografts of Ewing sarc
157                  The conservation of hypoxic drug-resistant niches in bacterial and fungal biofilms i
158 -LC-07-48 which exhibited greater potency in drug-resistant NSCLC cells (IC(50) = 17 nM) and in mice
159 vated c-Myc-miR-137-EZH2 pathway in platinum drug-resistant or recurrent ovarian cancer patients.
160     We discuss novel therapeutic options for drug-resistant or refractory CMV infection, including ma
161                  Implementing an extensively drug-resistant organism registry reduced CRE spread, eve
162 tibiotic prescribing can contribute to multi-drug resistant organisms (MDRO) and Clostridioides diffi
163 ted effect of ASP on rates of infection with drug-resistant organisms.
164 iveness to reduce infections of high-profile drug-resistant organisms.
165 is review, we have outlined the evidence for drug-resistant Orientia tsutsugamushi, assessed the evid
166 also markedly extended survival of mice with drug-resistant, orthotopic NB and it caused long-term (6
167 actam over polymyxins or aminoglycosides for drug-resistant P. aeruginosa infections.
168 ycoside-based regimens for infections due to drug-resistant P. aeruginosa.
169                                Prevalence of drug-resistant P. falciparum highlights the need to unde
170 of PfCRT, explaining the impaired fitness of drug-resistant parasites.
171    Mycobacterium abscessus is an extensively drug-resistant pathogen that causes pulmonary disease, p
172         Acinetobacter baumannii is a feared, drug-resistant pathogen, characterized by its ability to
173 both aminoglycoside-producing and clinically drug-resistant pathogenic bacteria.
174 ons (HAI) resulting from the transmission of drug-resistant pathogens affect hundreds of millions of
175                                           As drug-resistant pathogens erode the effectiveness of the
176 klace 1 against both standard and clinically drug-resistant pathogens implies that the presence of Cu
177 nd can inform efforts to limit the spread of drug-resistant pathogens in hospitals.
178 the group of three "critical priority" multi-drug-resistant pathogens listed by WHO and is responsibl
179 his paves the way for selective targeting of drug-resistant pathogens without disrupting or selecting
180 itical to combating the growing emergence of drug-resistant pathogens.
181 of the misuse of antibiotics and the rise in drug-resistant pathogens.
182 ignificance of horine and verine in fighting drug-resistant pathogens.
183 ost extensively drug-resistant (XDR) and pan-drug-resistant (PDR) Gram-negative pathogens.
184  the tumor develops into a more invasive and drug-resistant phenotype and ultimately recurs.
185 wn kinase network topologies associated with drug-resistant phenotypes or specific genetic mutations.
186                  The emergence and spread of drug-resistant Plasmodium falciparum impedes global effo
187 ual blood stages of both sensitive and multi-drug-resistant Plasmodium falciparum strains.
188 ol-2-yl)ethyl sulfide (BPTES) selected for a drug-resistant population with increased endogenous GLS2
189  c-Myc in several lung cancer cell lines and drug-resistant primary lung cancer cells.
190 ere also used to quickly identify the highly drug-resistant profile of these outbreak-associated C. j
191 beta) signals to TICs, inducing invasive and drug-resistant properties and further upregulating IL-33
192 n-Darby canine kidney transfected with multi-drug resistant protein 1 (MDCK-MDR1), and human U251 GBM
193 e formulations for the treatment of multiple-drug-resistant pulmonary infections is gaining attention
194 olic pathways, with particular relevance for drug resistant, relapsed FL.
195 e initially restricted to clinical settings, drug resistant S. aureus is now one of the key causative
196 ng the last 3 years with large proportion of drug resistant S. Typhi cases.
197 s have a limited duration of activity due to drug-resistant secondary KIT mutations that arise (or th
198                                              Drug-resistant seizures are common in patients with leuc
199     Affected individuals exhibit early onset drug-resistant seizures, developmental delay, and cognit
200         Notably, the emergence of additional drug-resistant species, such as Candida auris and Candid
201                              Susceptible and drug resistant Staphylococcus aureus strains were deposi
202                                        Multi-drug resistant Staphylococcus aureus, including methicil
203 s (SAGN) cases increased owing to a surge in drug-resistant Staphylococcus aureus infections, both in
204 d stabilizes the ribosome in an inactive and drug-resistant state.
205 , methicillin-resistant S. aureus (MRSA; the drug resistant strain) is able to grow on gel modified e
206 lving 14 patients infected by an extensively drug-resistant strain of Pseudomonas aeruginosa was dete
207 eric pathogens, including recalcitrant multi-drug resistant strains.
208 ough the mechanisms remain poorly clarified, drug-resistant strains are widely believed to be less in
209 causes of death worldwide, and the number of drug-resistant strains is increasing.
210 t Mtb provides significant insights into how drug-resistant strains of Mtb differentially impact immu
211       Recent evidence has shown that certain drug-resistant strains of Mtb modulate host metabolic re
212  new antibiotics, particularly because multi-drug-resistant strains of this bacterium cause serious n
213 lated to introduction of relatively virulent drug-resistant strains or movements of vulnerable popula
214 clinical presentation, the growing spread of drug-resistant strains, and policy and economic ramifica
215 ve bacteria, anaerobes, atypicals, and other drug-resistant strains, like methicillin-resistant Staph
216                           In particular, for drug-resistant strains, limited medication is available.
217 blood- stage Plasmodium parasites, including drug-resistant strains.
218 tive interactions between drug-sensitive and drug-resistant subclones.
219 antibiotic efficacy when communities include drug-resistant subpopulations, leading to a wide range o
220        In the face of the global threat from drug-resistant superbugs, there remains an unmet need fo
221 ntralizing this important test for combating drug-resistant superbugs.
222 bal spread of beta-lactamase-producing multi-drug-resistant "superbugs" has caused increased alarm wi
223 rifampicin (RIF), pyrazinamide (PZA)], multi-drug resistant TB (MDR-TB) and pan-susceptible TB (PANS-
224 olates, we report the geospatial patterns of drug resistant TB, particularly the dispersion of Lisboa
225 smission in settings with high incidences of drug-resistant TB are poorly understood.
226  in ensuring that all persons diagnosed with drug-resistant TB are started on an appropriate treatmen
227  tuberculosis sequencing data on extensively drug-resistant TB cases in KwaZulu-Natal, South Africa,
228 ) and dynamic changes, and characterized the drug-resistant TB clustering risk using routine microbio
229 ding infectious cause of death globally, and drug-resistant TB strains pose a serious threat to contr
230  found that almost half of the patients with drug-resistant TB were cough aerosol culture-positive.
231 ized that lower proportions of patients with drug-resistant TB would have culturable Mycobacterium tu
232 f HIV coinfection, high preexisting rates of drug-resistant TB, human migration, and pathoadaptive ev
233 n more effective therapeutics against TB and drug-resistant TB.
234 ypothesized that the cognitive impairment in drug-resistant temporal lobe epilepsy could be due to pe
235  the hippocampus and temporal lobe cortex of drug-resistant temporal lobe epilepsy patients who under
236 se may contribute to cognitive impairment in drug-resistant temporal lobe epilepsy.
237 etic resonance images from 121 patients with drug-resistant TLE across 3 independent epilepsy centers
238 the prevalence of the MDR-TB and extensively drug resistant tuberculosis (XDR-TB) cases, there is an
239 (DLM) in treatment regimen for patients with drug-resistant tuberculosis (DR-TB) and limited therapeu
240                               In generalized drug-resistant tuberculosis (DR-TB) HIV epidemics, ident
241                      Individuals treated for drug-resistant tuberculosis (DR-TB) with aminoglycosides
242 eat individuals presumed to be infected with drug-resistant tuberculosis (DR-TB).
243 ent sputum samples for clinical diagnosis of drug-resistant tuberculosis (DR-TB).
244 s new practice guideline on the treatment of drug-resistant tuberculosis (DR-TB).
245                                        Multi-drug-resistant tuberculosis (MDR-TB) is simultaneously r
246 r AMR pathogens, both historical and ongoing drug-resistant tuberculosis (TB) epidemics are character
247                  Patterns of transmission of drug-resistant tuberculosis (TB) remain poorly understoo
248                     A burgeoning epidemic of drug-resistant tuberculosis (TB) threatens to derail glo
249                                              Drug-resistant tuberculosis (TB), one of the leading cau
250                    Patients with extensively drug-resistant tuberculosis (XDR-TB) are also resistant
251 the most recent years, notification rates of drug-resistant tuberculosis among new tuberculosis cases
252 on for 26 weeks in patients with extensively drug-resistant tuberculosis and patients with multidrug-
253       Several key new developments regarding drug-resistant tuberculosis are outlined in this Commiss
254 ve led WHO to recommend all-oral therapy for drug-resistant tuberculosis for the first time ever in 2
255                           The recent rise of drug-resistant tuberculosis has complicated the choice o
256 iline treatment in multidrug and extensively drug-resistant tuberculosis HIV might be compromised by
257                                              Drug-resistant tuberculosis is a major public health con
258 ome (cure, dropout, death, or development of drug-resistant tuberculosis or treatment failure) was re
259                                              Drug-resistant tuberculosis persists as a major public h
260                                              Drug-resistant tuberculosis represents a global emergenc
261                        Notification rates of drug-resistant tuberculosis showed diverse trends, with
262 ant tuberculosis and over 90% of extensively drug-resistant tuberculosis strains are also PZA resista
263 treatment, the patient developed extensively drug-resistant tuberculosis, highlighting the importance
264        Bedaquiline, a potent new therapy for drug-resistant tuberculosis, results in improved surviva
265 lamanid and pretomanid as new drugs to treat drug-resistant tuberculosis, there is now a renewed inte
266  specifically to isoniazid, leading to multi-drug-resistant tuberculosis.
267 d not on ART, and 1749 (15%) had extensively drug-resistant tuberculosis.
268 gence of multidrug-resistant and extensively drug-resistant tuberculosis.
269 ens) has demonstrated activity against multi-drug-resistant tuberculosis.
270  HIV patients with multidrug and extensively drug-resistant tuberculosis.
271 e of the size and dynamics of a preexisting, drug-resistant tumor cell population versus a slow-growi
272 d suggest a mechanism for the development of drug-resistant tumors and a target for overcoming resist
273 ERD), which degrades the ERalpha receptor in drug-resistant tumors and has been approved for the trea
274 st various malignant solid tumors, including drug-resistant tumors and metastatic tumors.
275 antiapoptotic protein often overexpressed in drug-resistant tumors, as a cis-DDP-binding protein.
276               The recent rise of extensively drug-resistant typhoid bears the biosocial footprint of
277 d conjugate vaccine rollouts and extensively drug-resistant typhoid.
278 ors that are broadly effective against known drug-resistant variants are needed, although such compou
279 d by seven major bacterial species and their drug-resistant variants in a network of 357 hospital war
280                        Viremia, emergence of drug-resistant variants, and quasispecies diversificatio
281  efficacy is compromised by the emergence of drug-resistant variants.
282 retains efficacy against a broad spectrum of drug-resistant variants.
283                             The emergence of drug-resistant viral strains and uncertain vaccine prosp
284 mal treatment adherence and the emergence of drug-resistant viral variants, thereby limiting future t
285 n of drug-resistant HIV-1 and may select for drug-resistant virus.
286  of available compounds and the emergence of drug-resistant viruses.
287          Infections with MDR and extensively drug resistant (XDR) E. coli, XDR K. pneumoniae, and MDR
288 itive for S. Typhi, and all were extensively drug resistant (XDR) S. Typhi.
289 reported multidrug resistant and extensively drug resistant (XDR) TB cases, driven predominantly by t
290 atG was associated with baseline extensively drug resistant (XDR) TB, increased acquired fluoroquinol
291 and 53.6% of these (15/28) being extensively drug resistant (XDR).
292  the new agents against the most extensively drug-resistant (XDR) and pan-drug-resistant (PDR) Gram-n
293 istory of a successful strain of extensively drug-resistant (XDR) TB known as LAM4/KZN, first identif
294 tment of multidrug-resistant and extensively drug-resistant (XDR) tuberculosis.
295 of multidrug-resistant (MDR) and extensively drug-resistant (XDR) V. cholerae to identify AMR genes a
296 7 (50%) had MDR, 4 (29%) had pre-extensively drug-resistant (XDR), and 3 (21%) had XDR TB.
297 50%) had MDR, 4/14 (29%) had pre-extensively-drug-resistant (XDR), and 3/14 (21%) had XDR.
298 st-line antibiotics and 60% were extensively drug-resistant (XDR), resistant to first-line antibiotic
299 and 53.6% of these (15/28) being extensively drug-resistant (XDR).
300           Candida auris is an emerging multi-drug resistant yeast that causes systemic infections.

 
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