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1 effect for the development of MAV-1-induced encephalitis.
2 patients admitted to an ICU with anti-NMDAR encephalitis.
3 cally suspected antibody-mediated autoimmune encephalitis.
4 role of IL-1 signaling during MAV-1-induced encephalitis.
5 ected in brain tissue of five cases of human encephalitis.
6 h anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis.
7 permeability, and neuroimaging damage during encephalitis.
8 rove aetiological diagnosis in children with encephalitis.
9 nst neuronal antigens, leading to autoimmune encephalitis.
10 and increases susceptibility to lethal viral encephalitis.
11 otizing stromal keratitis and herpes simplex encephalitis.
12 on when animals are no longer suffering from encephalitis.
13 an also cause blindness and life-threatening encephalitis.
14 ctivated Bak is bound to p53 during reovirus encephalitis.
15 similar to those for human survivors of NiV encephalitis.
16 ith the virus spreading to the brain causing encephalitis.
17 rmed in brain samples from patients with HIV encephalitis.
18 nosed as stroke or as noninfectious forms of encephalitis.
19 ed and SIV-infected macaques with or without encephalitis.
20 lex virus 1 (HSV-1) infections, usually from encephalitis.
21 d be investigated as adjunctive treatment in encephalitis.
22 ithout classic presentation of toxoplasmosis encephalitis.
23 of the leading etiologies of sporadic viral encephalitis.
24 serious human diseases such as arthritis and encephalitis.
25 iscuss the concept of a specific Ebola virus encephalitis.
26 increased in infected brains during reovirus encephalitis.
27 cits are important long-term sequelae of the encephalitis.
28 nia (NMT), Morvan syndrome (MoS), and limbic encephalitis.
29 the host cellular factors leading to lethal encephalitis.
30 se of a 62-year-old female with seizures and encephalitis.
31 itions, including corneal blindness or fatal encephalitis.
32 distinguishing HSE from non-HSE causes of TL encephalitis.
33 el system to study the pathogenesis of virus encephalitis.
34 a superimposed antibody-mediated autoimmune encephalitis.
35 es upon induction of experimental autoimmune encephalitis.
36 ase, neonatal infection, and, in rare cases, encephalitis.
37 en with signs and symptoms of meningitis and encephalitis.
38 dies is the leading cause of immune-mediated encephalitis.
39 itted flavivirus that can cause debilitating encephalitis.
40 everity from periodic "cold sores" to lethal encephalitis.
41 most prevalent astrovirus in cases of human encephalitis.
42 proven to have antibody-positive autoimmune encephalitis.
43 most universally fatal granulomatous amoebic encephalitis.
44 (MRI) alterations in patients with anti-LGI1 encephalitis.
45 V infection (6%) died (1 with GBS and 1 with encephalitis), 18 (51%) had chronic pain, and the median
47 axonal, and 1 Miller Fisher syndrome), 5 had encephalitis (3 with concomitant acute neuromuscular dis
48 0% Brighton level 1 certainty), 7 (18%) with encephalitis, 3 (8%) with transverse myelitis, and 1 (3%
53 uninfected and SIV-infected animals without encephalitis, a trend that was also confirmed in brain s
54 Serum samples were tested for autoimmune encephalitis Abs as well as thyroperoxidase (TPO) and gl
59 lular infiltrate found in the CNS during WNV encephalitis, although the molecular cues involved in th
60 ith symptoms suggestive of autoimmune limbic encephalitis, although they can be paucisymptomatic or m
61 mice suffering from experimental autoimmune encephalitis ameliorates the severity of the clinical sy
64 Balamuthia infection in donors with possible encephalitis and also assess donors carefully for signs
65 tribute to tissue-specific diseases, such as encephalitis and dementia in brain and pneumonia in lung
66 n the progression and outcome of VSV-induced encephalitis and demonstrated a significant decrease in
69 ll populations from two patients with limbic encephalitis and faciobrachial dystonic seizures associa
70 morphologically distinct from prototypic SIV encephalitis and human immunodeficiency virus encephalit
72 hese include the relevance of herpes simplex encephalitis and of epilepsy to AD, the action of IFN, a
73 rome-based diagnostic approach to autoimmune encephalitis and providing guidelines to navigate throug
75 ntly emerged as a causative agent of febrile encephalitis and severe respiratory disease in humans.
76 The findings highlight the complex nature of encephalitis and suggests that IL-1 has a protective eff
77 of TLR3 mutations to varicella-zoster virus encephalitis and support the role of TLR3 genetic defect
78 clinical picture in keeping with autoimmune encephalitis and very high VGKC-complex/LGI1 antibodies.
81 as those that cause Zika, dengue, West Nile encephalitis, and chikungunya, have become endemic or ha
82 reduced severity of experimental autoimmune encephalitis, and defective immune responses to lymphocy
83 ighly debilitating and lethal herpes simplex encephalitis, and generalized infections that can lead t
85 transmission and disease, such as keratitis, encephalitis, and neurodegeneration, have been linked to
87 ith Japanese encephalitis, Venezuelan equine encephalitis, and Rift Valley fever viruses; and urbaniz
88 antibodies described in patients with limbic encephalitis, and the subsequent seminal paper describin
89 e mice is a tractable small-animal model for encephalitis, and the virus causes disruption of the BBB
90 revents the pathogenic effects of anti-NMDAR encephalitis antibodies on memory and behavior, levels o
91 s and treatment of infectious meningitis and encephalitis are critical to minimize morbidity and mort
93 However, existing criteria for autoimmune encephalitis are too reliant on antibody testing and res
94 ive adult patients diagnosed with anti-NMDAR encephalitis at the French National Reference Centre, ad
96 consecutively diagnosed as having anti-NMDAR encephalitis between May 1, 2008, and January 31, 2013.
97 lt patients (>/=18 years) with meningitis or encephalitis by International Classification of Diseases
101 c anaplasmosis, an emerging disease, and the encephalitis-causing Langat virus, and a population stru
102 al analysis revealed signs of meningitis and encephalitis, characteristic of severe human disease.
105 from 0.32 to 0.009) and admissions for mumps encephalitis decreased by 98% (from 0.60 to 0.01) after
108 iological information for patients with POWV encephalitis diagnosed at 2 hospitals in Massachusetts f
109 neurosciences center, studied patients with encephalitis diagnosed by brain biopsy from January 1, 1
112 ts, including one death (treatment-unrelated encephalitis due to influenza B infection), one life-thr
117 we show that during La Crosse Virus-induced encephalitis, egress of iMOs was surprisingly independen
120 (CASPR2), are found in patients with limbic encephalitis, faciobrachial dystonic seizures, Morvan's
122 nalysis of hospital admission statistics for encephalitis for individuals aged 0-19 years using natio
123 mmon presenting feature in antibody-mediated encephalitis, for which prompt recognition and treatment
128 t common causes of infectious meningitis and encephalitis have the potential for high clinical impact
130 y of acyclovir (ACV) therapy, herpes simplex encephalitis (HSE) continues to cause substantial morbid
135 ded encephalomyelitis in 23 (40%), brainstem encephalitis in 20 (35%), encephalitis in 6 (11%), acute
137 3 (40%), brainstem encephalitis in 20 (35%), encephalitis in 6 (11%), acute flaccid paralysis in 4 (7
138 ose an unusual and fatal case of progressive encephalitis in an immunocompromised adult presenting at
141 vere hand, foot, and mouth disease and viral encephalitis in children across the Asia-Pacific region,
142 is (JE) virus (JEV) is an important cause of encephalitis in children of South and Southeast Asia.
143 trated pathological findings consistent with encephalitis in control and knockout mice; however, intr
147 ed to estimate admission rates for childhood encephalitis in England over 33 years (1979-2011), to de
148 (VEEV), which elicits flu-like symptoms and encephalitis in humans, with an estimated 14% of cases r
154 when injected into the brain leads to lethal encephalitis in Irf2(-/-) mice after peripheral inoculat
160 euroinvasive properties (SVNI) causes lethal encephalitis in mice, and its replication in cultured ce
164 arly recognition and treatment of autoimmune encephalitis in patients receiving immune checkpoint blo
166 nsmitted by insects and cause meningitis and encephalitis in subsets of individuals in the Americas.
167 in turn may contribute to BBB disruption and encephalitis in susceptible mice.IMPORTANCE RNA and DNA
168 e adenovirus type 1 (MAV-1) infection causes encephalitis in susceptible strains of mice and alters t
170 osuppressive therapy in suspected autoimmune encephalitis in the setting of immune checkpoint inhibit
172 s, and outcomes of adults with meningitis or encephalitis in the United States (US) are lacking.
173 are the most common cause of meningitis and encephalitis in the United States and are treated with a
177 ry of HAstV-VA1/HMO-C-UK1(a) as the cause of encephalitis in this case provides further evidence that
178 ice.IMPORTANCE RNA and DNA viruses can cause encephalitis; in some cases, this is accompanied by MMP-
179 fluid (n = 37) specimens from patients with encephalitis, including 17 with disease due to HSV infec
180 urologic complications associated with viral encephalitis, including seizures and cognitive impairmen
181 0 per month to 5.6 per month, admissions for encephalitis increased from 0.4 per month to 1.4 per mon
184 Anti-N-methyl D-aspartate receptor (NMDAR) encephalitis is a severe neuropsychiatric disorder that
186 Leucine-rich glioma-inactivated1 (LGI1) encephalitis is an antibody-associated inflammation of t
190 though the role of acyclovir in treating HSV encephalitis is clear, the role of antiviral therapy in
194 ugh several different flaviviruses may cause encephalitis, Japanese encephalitis virus is the most si
200 neurotropic ssRNA flavivirus that can cause encephalitis, meningitis, and death in humans and mice.
201 appears broader as cases of encephalopathy, encephalitis, meningitis, myelitis, and seizures have al
202 the vesicular stomatitis virus (VSV)-induced encephalitis model, the replication, caudal penetration,
203 n = 1,433) meningitis or with herpes simplex encephalitis (n = 115), who were alive 1 year after diag
206 Selectivity was validated using Japanese Encephalitis NS1, a homologous and potentially cross-rea
207 ed whether IL-1 signaling contributes to the encephalitis observed in mouse adenovirus type 1 (MAV-1)
211 al fluid (CSF) from patients with anti-NMDAR encephalitis or controls, with or without ephrin-B2, wer
217 the performance of the FilmArray meningitis/encephalitis panel compared to conventional methods.
219 Data from this largest cohort of anti-NMDAR encephalitis patients that underwent extensive multimoda
220 is crucial to the survival of herpes simplex encephalitis patients; however, many survivors suffer fr
221 diagnosis, levels of evidence for autoimmune encephalitis (possible, probable, or definite) are achie
224 prognosis of adult patients with anti-NMDAR encephalitis requiring intensive care is good, especiall
226 measles and rubella, yellow fever, Japanese encephalitis, rotavirus, and invasive bacterial diseases
227 hat antibodies from patients with anti-AMPAR encephalitis selectively eliminate surface and synaptic
228 se in CD68+Ki-67+ cells in macaques with SIV encephalitis (SIVE) compared to uninfected and SIV-infec
231 h anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis suffer from persistent memory impairment de
232 s are not readily regenerated, recovery from encephalitis suggests that mature neurons utilize unique
234 n has been previously reported in Toxoplasma encephalitis (TE)-susceptible model, our current work de
235 ecipients from donors with signs of possible encephalitis to facilitate early diagnosis and targeted
236 ody titres from a prior inactivated Japanese encephalitis vaccination enhanced yellow fever (YF) immu
237 s of CpG oligodeoxynucleotides or tick-borne encephalitis vaccine, which occurred in an S1PR4-depende
238 domesticated animals, as seen with Japanese encephalitis, Venezuelan equine encephalitis, and Rift V
240 thogenic phenotype.IMPORTANCE Eastern equine encephalitis virus (EEEV) is one of the most pathogenic
241 ne encephalitis virus (VEEV), eastern equine encephalitis virus (EEEV), and western equine encephalit
242 encephalitis virus (VEEV) and Eastern equine encephalitis virus (EEEV), which have demonstrated poten
243 presumptive serodiagnosis of acute Japanese encephalitis virus (JEV) and West Nile virus (WNV) infec
245 ns against neurotropic flaviviruses.Japanese encephalitis virus (JEV) is a Flavivirus responsible for
246 and efficacy of the live-attenuated Japanese encephalitis virus (JEV) SA14-14-2 vaccine are attribute
247 g EIIIs from Koutango virus (KOUV), Japanese encephalitis virus (JEV), St. Louis encephalitis virus (
248 three flaviviruses, DENV, WNV, and Japanese encephalitis virus (JEV), using a high-content immunoflu
250 Japanese encephalitis virus (JEV), St. Louis encephalitis virus (SLEV), and Bagaza virus (BAGV) were
253 encephalitic alphaviruses Venezuelan equine encephalitis virus (VEEV) and Eastern equine encephaliti
258 nfectious titer of WNV and Venezuelan equine encephalitis virus (VEEV) TC83 in the brains of Asyn-kno
259 ve the assembly of vRCs of Venezuelan equine encephalitis virus (VEEV), and G3BPs were shown to funct
260 Valley fever virus (RVFV), Venezuelan equine encephalitis virus (VEEV), and herpes simplex virus 1 (H
262 currently unavailable for Venezuelan equine encephalitis virus (VEEV), which elicits flu-like sympto
263 ate that Tc bovine-derived Venezuelan equine encephalitis virus (VEEV)-specific TcPAbs are highly eff
264 ncephalitis virus (EEEV), and western equine encephalitis virus (WEEV) are arthropod-borne positive-s
265 phalitic arboviruses, such as eastern equine encephalitis virus and West Nile virus, underscore the n
266 tron microscopy structure of mature Japanese encephalitis virus at near-atomic resolution, which reve
267 mino-terminal subdomain of Venezuelan equine encephalitis virus capsid protein, SD1, plays a critical
268 sed plasmid VRC5288 (Zika virus and Japanese encephalitis virus chimera), and the VRC 320, done in on
269 an enzootic member of the Venezuelan Equine Encephalitis Virus complex and belongs to the New World
271 laviviruses may cause encephalitis, Japanese encephalitis virus is the most significant, being respon
272 with the corresponding region from Japanese encephalitis virus NS1 to create chimeric DJ NS1 protein
273 presence of dengue virus (DENV) and Japanese encephalitis virus NS1s in the blood of infected interfe
274 -vectored vaccine (Kp47/47-Venezuelan equine encephalitis virus replicon particle) for safety, immuno
275 avirus 229E), Togaviridae (Venezuelan equine encephalitis virus), and Hepeviridae (HEV), indicating t
276 other NT human arbovirus (Venezuelan equine encephalitis virus), which is also poorly understood.
278 alphavirus infection with Venezuelan equine encephalitis virus, and this was associated with greater
280 de viral (for example, HIV, rabies, Japanese encephalitis virus, herpes simplex virus, varicella zost
281 of neurovirulence and stability in Japanese encephalitis virus, opening up new avenues for therapeut
282 bunyaviruses La Crosse virus and California encephalitis virus, suggesting a conserved role for Wnt
286 uses include dengue, West Nile, and Japanese encephalitis viruses, and the nonpathogenic flaviviruses
289 Using a mouse model of West Nile virus (WNV) encephalitis, we show that RIPK3 restricts WNV pathogene
293 d LGI1 VGKC-complex antibody-mediated limbic encephalitis were investigated using in vivo ultra-high
295 of the most frequent variants of autoimmune encephalitis with antibodies targeting neuronal surface
297 should be aware of Balamuthia as a cause of encephalitis with high rate of fatality, and should noti
299 are associated with a subtype of autoimmune encephalitis with prominent limbic involvement and seizu
300 egated squirrels (Sciurus variegatoides) had encephalitis with similar clinical signs and died 2 to 4
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