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1 (eg, meningitis, encephalitis, acute flaccid myelitis).
2 is), Guillain-Barre syndrome, and transverse myelitis).
3 omes, including encephalitis, meningitis and myelitis.
4 nd increased cases of nonpolio acute flaccid myelitis.
5 sporadically in patients with acute flaccid myelitis.
6 ren met our case definition of acute flaccid myelitis.
7 IFN signaling is protective during reovirus myelitis.
8 nalyzed a cohort of 22 patients with SLE and myelitis.
9 -IgG and its application to acute transverse myelitis.
10 e useful prognostic indicators in transverse myelitis.
11 n evolving understanding of acute transverse myelitis.
12 setting of a paraneoplastic acute transverse myelitis.
13 es in inflammatory non-infectious transverse myelitis.
14 rience with West Nile virus encephalitis and myelitis.
15 therapy of West Nile virus encephalitis and myelitis.
16 aracterized by attacks of optic neuritis and myelitis.
17 ad MOGAD, 21 had MS, and 46 had seronegative myelitis.
18 ing paralytic disease known as acute flaccid myelitis.
19 nd has recently been linked to Acute Flaccid Myelitis.
20 ere respiratory infections and acute flaccid myelitis.
21 the ventral posterior nucleus (VPN), due to myelitis.
22 apsing episodes of severe optic neuritis and myelitis.
23 tis, Guillain-Barre syndrome, and transverse myelitis.
24 tis, Guillain-Barre syndrome, and transverse myelitis.
25 n to MS in patients presenting with isolated myelitis.
26 eases such as poliomyelitis or acute flaccid myelitis.
27 ger Guillain-Barre syndrome, neuropathy, and myelitis.
28 me (GBS), meningoencephalitis, or transverse myelitis.
29 tacks of acute optic neuritis and transverse myelitis.
30 diagnosed as NMOSD or idiopathic transverse myelitis.
31 io-like neurological disorder, acute flaccid myelitis.
32 PE/IA may increase recovery in isolated myelitis.
35 med encephalitis, 6 meningitis, 1 transverse myelitis, 1 nonhemorrhagic leukoencephalopathy), stroke
36 before we truly understand acute transverse myelitis: (1) What are the various triggers for the infl
37 tients seropositive for isolated MOG-IgA was myelitis (11/17 [65%]), followed by more frequent brains
40 ADEM (22 [19%]), optic neuritis (20 [17%]), myelitis (13 [11%]), neuromyelitis optica spectrum disor
41 ), less common among those with seronegative myelitis (20 of 46 children [43%]), and rare in children
42 d spinal cord lesions (46.3% long transverse myelitis, 36.1% short transverse myelitis), 37.1% satisf
43 emorrhage (34%, 20-50%), encephalitis and/or myelitis (37%, 17-60%) and myopathy (72%, 67-77%) were h
44 transverse myelitis, 36.1% short transverse myelitis), 37.1% satisfied 2010 McDonald criteria, and n
45 ations to be associated with ZIKV, including myelitis (4) , meningoencephalitis (5) and fatal encepha
47 lthough VPN was not smaller in patients with myelitis (674.3+/-67.5 mm(3)) than controls (679.7+/-68.
48 tcomes than typical patients with transverse myelitis/acute disseminated encephalomyelitis, and these
49 h concerns due to outbreaks of acute flaccid myelitis (AFM) and encephalomyelitis in North America an
57 ovirus D68 (EV-D68)-associated acute flaccid myelitis (AFM) is a devastating neurological disease for
59 /fall 2014, pediatric cases of acute flaccid myelitis (AFM) occurred in the United States, coincident
61 al spikes in EV-D68-associated acute flaccid myelitis (AFM) that have left hundreds of children paral
63 a cause of recent outbreaks of acute flaccid myelitis (AFM), a poliomyelitis-like spinal cord syndrom
64 d spikes in pediatric cases of acute flaccid myelitis (AFM), which is a poliomyelitis-like paralytic
69 rategies for the optimal management of acute myelitis after CAR T-cell therapy and draw insights from
70 ent ON or recurrent longitudinally extensive myelitis alone are also often positive for AQP4-antibody
73 4 of 9 (44%) developed recurrent transverse myelitis and 1 of 9 (11%) developed optic neuritis (p =
74 equency of longitudinal extensive transverse myelitis and a favourable clinical outcome in contrast t
76 She then presented with recurrent transverse myelitis and a vesicobullous rash over her arms and feet
81 MOSD) and related syndromes (optic neuritis, myelitis and brainstem encephalitis), but rarely in MS.
82 a is a member of the Apicomplexa that causes myelitis and encephalitis in horses but normally cycles
83 assessed for neurologic variables related to myelitis and for clinical and serologic features of SLE.
85 ysis, and was diagnosed as having transverse myelitis and membranous glomerulonephritis secondary to
89 r anaphylaxis and death; 0.04 for transverse myelitis and pancreatitis; and 0.009 for motor neuron di
90 unopathogenic mechanisms in acute transverse myelitis and related inflammatory disorders of the spina
92 on between enterovirus D68 and acute flaccid myelitis and the contention that acute flaccid myelitis
93 by disabling relapses of optic neuritis and myelitis and the presence of aquaporin 4 antibodies (AQP
94 s, 36 women, 25 with prior ON, 36 with prior myelitis) and 37 healthy controls (age: 47.8 +/- 12.5 ye
95 %) with encephalitis, 3 (8%) with transverse myelitis, and 1 (3%) with newly diagnosed chronic inflam
96 ute neuromuscular disease), 2 had transverse myelitis, and 1 had chronic inflammatory demyelinating p
97 lpox, which include encephalitis, transverse myelitis, and acute disseminated encephalomyelitis among
100 phalomyelitis, optic neuritis, or transverse myelitis, and is less commonly associated with cerebral
101 ine coronavirus) causes meningoencephalitis, myelitis, and optic neuritis followed by axonal loss and
102 Dawson fingers, presence of long transverse myelitis, and presence of periependymal lesions along la
104 ding meningitis, encephalitis, acute flaccid myelitis, and seizures) and enterovirus detected from an
107 oses included multiple sclerosis, transverse myelitis, and unspecified neurodegenerative myelopathy.
108 lammatory syndrome, Bell's palsy, transverse myelitis, appendicitis, pulmonary embolism, and encephal
109 who had relapsing optic neuritis, transverse myelitis, AQP4-IgG seropositivity, and recurrent myalgia
111 euritis, longitudinally extensive transverse myelitis, area postrema attacks and less common brainste
112 ders associated with inflammatory transverse myelitis, as well as a greater appreciation of its diver
116 sed risk of relapse compared with transverse myelitis at onset (hazard ratio [HR], 2.66; 95% CI, 1.01
117 ovirus D68 (EV-D68)-associated acute flaccid myelitis at the same hospital between 2013 and 2018.
119 as follows: (1) AQP4-IgG seropositivity, (2) myelitis attack and (3) MRI spinal cord demonstrating ri
121 differences in the frequencies of transverse myelitis, brainstem involvement, cerebellar signs and se
122 nterovirus D68 with those with acute flaccid myelitis but negative for enterovirus D68 using the two-
125 hildren with EV-D68-associated acute flaccid myelitis, children with EV-A71-associated acute flaccid
126 ally and geographically linked acute flaccid myelitis clusters at the height of the 2014 outbreak, an
127 ncluding longitudinally extensive transverse myelitis), contributes to an evolving understanding of a
128 initial longitudinally extensive transverse myelitis, delay to diagnosis/treatment was greater when
130 al fluid from 14 patients with acute flaccid myelitis did not reveal evidence of an alternative infec
132 enterovirus D68 infection and acute flaccid myelitis during the 2014 enterovirus D68 respiratory out
133 hildren with EV-A71-associated acute flaccid myelitis during the study period with these findings in
136 1996 and 2015 with SCS or NMOSD whose first myelitis episode was accompanied by a spinal cord lesion
138 g-enhancement accompanies one-third of NMOSD myelitis episodes and distinguishes NMOSD from other cau
139 xial images in 36 of 43 (84%) ring enhancing myelitis episodes and extended a median of two vertebral
140 e clinical characteristics of ring-enhancing myelitis episodes did not differ from non-ring-enhancing
141 -enhancement was detected in 50 of 156 (32%) myelitis episodes in 41 patients (83% single; 17% multip
142 In AQP4-IgG-positive STM cases, subsequent myelitis episodes were longitudinally extensive in 92%.
143 nge, 1-12); in 21 of 48 (44%) ring enhancing myelitis episodes, the ring extended greater than or equ
148 nts had a relapsing course and more frequent myelitis, findings compatible with neuromyelitis optica
149 D68 sequences associated with acute flaccid myelitis grouped into a clade B1 strain that emerged in
150 biomarkers associated with acute transverse myelitis has led to a better understanding of the spectr
153 features associated with distinct causes of myelitis in children is essential to guide investigation
156 neurologic toxicity consisting of transverse myelitis in five patients, CNS toxicity in three, and se
158 river of epidemic outbreaks of acute flaccid myelitis in recent years(4), yet not much is known about
159 he central nervous system; necrotizing focal myelitis in the cervical spinal cord; radiculitis; neuri
160 ive myelopathy of other cause (n=66) and (2) myelitis in the context of a concurrent or subsequent di
161 his work contributes to our understanding of myelitis in these conditions and highlights the clinical
163 stigate innate immune responses during viral myelitis, including the activation of glia (microglia an
166 elitis and the contention that acute flaccid myelitis is a rare yet severe clinical manifestation of
168 owever, nonlongitudinal extensive transverse myelitis lesions were also observed frequently (105 of 2
169 es were more common (27% vs 4%; p=0.021) and myelitis less common (21% vs 50%; p=0.012) in Japanese t
170 nts with longitudinally extensive transverse myelitis (LETM) behave differently from those with AQP4-
172 ation of longitudinally extensive transverse myelitis (LETM) predicts relapse of myelitis or developm
173 a (NMO), longitudinally extensive transverse myelitis (LETM), multiple sclerosis with a history of op
174 n 25 of 77 patients (32%) with short-segment myelitis (longest lesion spanning <3 vertebral segments
176 uding microcephaly, Guillain-Barre syndrome, myelitis, meningoencephalitis, and fatal encephalitis.
177 ay be complicated by postherpetic neuralgia, myelitis, meningoencephalitis, and VZV vasculopathy.
180 (NMOSD, n=10), idiopathic AQP4-IgG-negative myelitis (n=4), idiopathic AQP4-IgG-negative optic neuri
183 nded fever, seizure, meningitis/encephalitis/myelitis, nonanaphylactic serious allergic reaction, ana
184 e flaccid paralysis associated with anterior myelitis noted in the United States from 2012 to 2015.
185 rger-scale cohort studies have revealed that myelitis occurring in the idiopathic demyelinating disea
190 lomyelitis (ADEM), one episode of transverse myelitis or optic neuritis, multiple sclerosis (MS), ant
192 s ratio [OR] = 0.97, p = 0.011), presence of myelitis (OR = 0.38, p = 0.002), CR from previous attack
193 event (optic neuritis, incomplete transverse myelitis, or brain-stem or cerebellar syndrome) and evid
194 ation (optic neuritis, incomplete transverse myelitis, or brain-stem/cerebellar syndrome) and at leas
196 syndromes such as optic neuritis, transverse myelitis, or isolated brainstem syndromes in whom multif
198 for isolated optic neuritis versus isolated myelitis (p < 0.001), and for unilateral versus bilatera
200 sed by a longitudinally extensive transverse myelitis (p=0.003), more often a complete resolution of
203 ratory illness in children and acute flaccid myelitis, raising concerns about its potential impact on
206 ronic pain scores, irrespective of number of myelitis relapses, lesion length and lesion burden.
208 itis and longitudinally extensive transverse myelitis [reported on at least 1 magnetic resonance imag
210 f a spinal cord biopsy during ring-enhancing myelitis revealed tissue vacuolation and loss of AQP4 im
213 ears with unilateral optic neuritis, partial myelitis, sensory disturbances, or brainstem syndromes s
214 f serious illnesses, including acute flaccid myelitis, severe respiratory complications, and hand-foo
215 alized with meningitis, encephalitis, and/or myelitis showed 92% sensitivity and 96% specificity rela
216 tudy was undertaken to determine whether SLE myelitis similarly encapsulates distinct syndromes.
218 cidated about the causes of acute transverse myelitis, tantalizing clues as to the potential immunopa
219 rteriovenous fistula is a very rare cause of myelitis that can only be treated interventionally or su
222 tis (ADEM), two with ON, one with transverse myelitis (TM) and two with clinically isolated syndrome
223 sent with optic neuritis (ON) and transverse myelitis (TM) are diagnosed with NMO and those who show
225 ggested that vaccines may trigger transverse myelitis (TM) or acute disseminated encephalomyelitis (A
226 syndromes (CIS), 27 patients with transverse myelitis (TM), 50 patients with human immunodeficiency v
228 ritis (ON); 20% bilateral ON; 15% transverse myelitis (TM); 15% simultaneous TM&ON; 10% Acute dissemi
229 atients were included: 25 with acute flaccid myelitis, two with enterovirus-associated encephalitis,
235 es in clinical presentation of acute flaccid myelitis, we also used a subgroup analysis to compare cl
238 hildren with EV-A71-associated acute flaccid myelitis were younger, showed neurological onset earlier
239 entral grey matter component to MOG-antibody myelitis, which we hypothesize could be partially respon
241 rt study, we included patients with isolated myelitis who were followed clinically and radiologically
242 We compared patients with acute flaccid myelitis who were positive for enterovirus D68 with thos
243 on-multiple sclerosis optic neuritis without myelitis will be shown to be associated with this autoan
244 uromyelitis optica spectrum disorder (NMOSD) myelitis, with no satisfactory treatment; few studies ha