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231224s2015 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2015.01.010
|2 doi
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|a pubmed24n0820.xml
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|a (DE-627)NLM245995749
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|a (NLM)25656641
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|a (PII)S1521-6616(15)00029-7
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Ichinose, Kunihiro
|e verfasserin
|4 aut
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|a Distinguishing the cerebrospinal fluid cytokine profile in neuropsychiatric systemic lupus erythematosus from other autoimmune neurological diseases
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|c 2015
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 29.06.2015
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|a Date Revised 18.03.2022
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2015 Elsevier Inc. All rights reserved.
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|a Neuropsychiatric systemic lupus erythematosus (NPSLE) is a serious complication in SLE. Although the mechanism of NPSLE remains unclear, cytokines and chemokines are considered to be involved in their pathogenesis. Here we used Bio-Plex Pro assays to examine 27 types of cytokines and chemokines in the cerebrospinal fluid (CSF) of 32 NPSLE patients. We used the CSF of 20 patients with multiple sclerosis (MS) and 22 patients with neuromyelitis optica (NMO) as a disease control group. Fourteen of 27 cytokines/chemokines were significantly higher in the NPSLE patients compared to the MS/NMO patients. We could identify six "minimum predictive markers" by using a weighted-voting algorithm that could distinguish NPSLE from MS and NMO: interleukin (IL)-17, IL-2, interferon (IFN)-γ, IL-5, basic fibroblast growth factor (FGF)-basic and IL-15. The determination of various types of CSF cytokine profiles may contribute to the diagnosis of NPSLE and may help elucidate the mechanisms underlying this disease
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Cerebrospinal fluid
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|a Cytokine profiles
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|a Neuropsychiatric systemic lupus erythematosus
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|a Weighted-voting algorithm
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|a Cytokines
|2 NLM
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|a IL15 protein, human
|2 NLM
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|a IL2 protein, human
|2 NLM
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|a IL5 protein, human
|2 NLM
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|a Interleukin-15
|2 NLM
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|a Interleukin-17
|2 NLM
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|a Interleukin-2
|2 NLM
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|a Interleukin-5
|2 NLM
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|a Fibroblast Growth Factor 2
|2 NLM
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|a 103107-01-3
|2 NLM
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|a Interferon-gamma
|2 NLM
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|a 82115-62-6
|2 NLM
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|a Arima, Kazuhiko
|e verfasserin
|4 aut
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|a Ushigusa, Takeshi
|e verfasserin
|4 aut
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|a Nishino, Ayako
|e verfasserin
|4 aut
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|a Nakashima, Yoshikazu
|e verfasserin
|4 aut
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|a Suzuki, Takahisa
|e verfasserin
|4 aut
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|a Horai, Yoshiro
|e verfasserin
|4 aut
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|a Nakajima, Hideki
|e verfasserin
|4 aut
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|a Kawashiri, Shin-Ya
|e verfasserin
|4 aut
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|a Iwamoto, Naoki
|e verfasserin
|4 aut
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|a Tamai, Mami
|e verfasserin
|4 aut
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|a Nakamura, Hideki
|e verfasserin
|4 aut
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|a Origuchi, Tomoki
|e verfasserin
|4 aut
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|a Motomura, Masakatsu
|e verfasserin
|4 aut
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|a Kawakami, Atsushi
|e verfasserin
|4 aut
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 157(2015), 2 vom: 07. Apr., Seite 114-20
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:157
|g year:2015
|g number:2
|g day:07
|g month:04
|g pages:114-20
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|u http://dx.doi.org/10.1016/j.clim.2015.01.010
|3 Volltext
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|a GBV_ILN_350
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|a AR
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|d 157
|j 2015
|e 2
|b 07
|c 04
|h 114-20
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