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231224s2017 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2017.05.019
|2 doi
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|a pubmed24n0908.xml
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|a (DE-627)NLM272583812
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|a (NLM)28578025
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|a (PII)S1521-6616(16)30700-8
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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 Fernández-Paredes, Lidia
|e verfasserin
|4 aut
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|a Multimarker risk stratification approach at multiple sclerosis onset
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|c 2017
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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 28.08.2017
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|a Date Revised 06.02.2018
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2017 Elsevier Inc. All rights reserved.
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|a Delay in the diagnosis of multiple sclerosis (MS) stems from the lack of specific clinical and analytical markers to assist in the early diagnosis and prediction of progressive course. We propose a decision-tree model that better defines early at onset MS patients and those with the progressive form by analysing a 12-biomarkers panel in serum and CSF samples of patients with MS, other neurological diseases (OND) and healthy contols. Thus, patients at onset of neurological disease were first classified by serum IL-7 levels <141pg/ml (OR=6.51, p<0.001). Combination of IL-7 and CXCL10 indicated risk for a specific MS clinical form, where IL-7<141 and CXCL10<570pg/ml were associated with the highest risk for PP-MS (OR=22, p=0.01). Unexpectedly, both PP-MS and RR-MS patients shared significantly decreased prototypical biomarkers of inflammation and tissue regeneration in CSF than OND suggesting a defective intrinsic immune response playing a role at the beginning of the 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 Biomarkers
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|a Diagnostic
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|a Innate immunity deregulation
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|a Prognostic
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|a Biomarkers
|2 NLM
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|a CCL11 protein, human
|2 NLM
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650 |
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|a CCL2 protein, human
|2 NLM
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650 |
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|a CCL4 protein, human
|2 NLM
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650 |
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|a CCL5 protein, human
|2 NLM
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650 |
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|a CXCL10 protein, human
|2 NLM
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650 |
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|a CXCL9 protein, human
|2 NLM
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|a Chemokine CCL11
|2 NLM
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650 |
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|a Chemokine CCL2
|2 NLM
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|a Chemokine CCL4
|2 NLM
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650 |
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|a Chemokine CCL5
|2 NLM
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650 |
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|a Chemokine CXCL10
|2 NLM
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650 |
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|a Chemokine CXCL9
|2 NLM
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650 |
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|a HGF protein, human
|2 NLM
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650 |
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|a IL1RN protein, human
|2 NLM
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650 |
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|a IL7 protein, human
|2 NLM
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650 |
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7 |
|a Interleukin 1 Receptor Antagonist Protein
|2 NLM
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650 |
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|a Interleukin-7
|2 NLM
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650 |
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|a Fibroblast Growth Factor 2
|2 NLM
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650 |
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|a 103107-01-3
|2 NLM
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650 |
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|a Epidermal Growth Factor
|2 NLM
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650 |
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|a 62229-50-9
|2 NLM
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650 |
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|a Hepatocyte Growth Factor
|2 NLM
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650 |
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7 |
|a 67256-21-7
|2 NLM
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650 |
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|a DPP4 protein, human
|2 NLM
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650 |
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|a EC 3.4.14.5
|2 NLM
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650 |
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7 |
|a Dipeptidyl Peptidase 4
|2 NLM
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650 |
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7 |
|a EC 3.4.14.5
|2 NLM
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700 |
1 |
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|a Casrouge, Armanda
|e verfasserin
|4 aut
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1 |
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|a Decalf, Jérémie
|e verfasserin
|4 aut
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|a de Andrés, Clara
|e verfasserin
|4 aut
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|a Villar, Luisa Maria
|e verfasserin
|4 aut
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|a Pérez de Diego, Rebeca
|e verfasserin
|4 aut
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1 |
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|a Alonso, Bárbara
|e verfasserin
|4 aut
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1 |
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|a Álvarez Cermeño, José Carlos
|e verfasserin
|4 aut
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1 |
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|a Arroyo, Rafael
|e verfasserin
|4 aut
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1 |
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|a Tejera-Alhambra, Marta
|e verfasserin
|4 aut
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1 |
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|a Navarro, Joaquín
|e verfasserin
|4 aut
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1 |
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|a Oreja-Guevara, Celia
|e verfasserin
|4 aut
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|a López Trascasa, Margarita
|e verfasserin
|4 aut
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|a Seyfferth, Ansgar
|e verfasserin
|4 aut
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1 |
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|a García Martínez, Maria Angel
|e verfasserin
|4 aut
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700 |
1 |
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|a Álvarez Lafuente, Roberto
|e verfasserin
|4 aut
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1 |
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|a Albert, Matthew L
|e verfasserin
|4 aut
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|a Sánchez-Ramón, Silvia
|e verfasserin
|4 aut
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 181(2017) vom: 01. Aug., Seite 43-50
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
|
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|g volume:181
|g year:2017
|g day:01
|g month:08
|g pages:43-50
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|u http://dx.doi.org/10.1016/j.clim.2017.05.019
|3 Volltext
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|a AR
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|d 181
|j 2017
|b 01
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|h 43-50
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