Opposite Roles of NMDA Receptors in Relapsing and Primary Progressive Multiple Sclerosis

Rossi S, Studer V, Moscatelli A, Centonze D (2013)
PLoS ONE 8(6): e67357.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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DOI
Autor*in
Rossi, Silvia; Studer, Valeria; Moscatelli, AlessandroUniBi ; Centonze, Diego
Einrichtung
Fakultät für Biologie > Kognitive Neurowissenschaften
Center of Excellence - Cognitive Interaction Technology CITEC
Erscheinungsjahr
2013
Zeitschriftentitel
PLoS ONE
Band
8
Ausgabe
6
Art.-Nr.
e67357
ISSN
1932-6203
eISSN
1932-6203
Page URI
https://pub.uni-bielefeld.de/record/2616932

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Rossi S, Studer V, Moscatelli A, Centonze D. Opposite Roles of NMDA Receptors in Relapsing and Primary Progressive Multiple Sclerosis. PLoS ONE. 2013;8(6): e67357.
Rossi, S., Studer, V., Moscatelli, A., & Centonze, D. (2013). Opposite Roles of NMDA Receptors in Relapsing and Primary Progressive Multiple Sclerosis. PLoS ONE, 8(6), e67357. doi:10.1371/journal.pone.0067357
Rossi, Silvia, Studer, Valeria, Moscatelli, Alessandro, and Centonze, Diego. 2013. “Opposite Roles of NMDA Receptors in Relapsing and Primary Progressive Multiple Sclerosis”. PLoS ONE 8 (6): e67357.
Rossi, S., Studer, V., Moscatelli, A., and Centonze, D. (2013). Opposite Roles of NMDA Receptors in Relapsing and Primary Progressive Multiple Sclerosis. PLoS ONE 8:e67357.
Rossi, S., et al., 2013. Opposite Roles of NMDA Receptors in Relapsing and Primary Progressive Multiple Sclerosis. PLoS ONE, 8(6): e67357.
S. Rossi, et al., “Opposite Roles of NMDA Receptors in Relapsing and Primary Progressive Multiple Sclerosis”, PLoS ONE, vol. 8, 2013, : e67357.
Rossi, S., Studer, V., Moscatelli, A., Centonze, D.: Opposite Roles of NMDA Receptors in Relapsing and Primary Progressive Multiple Sclerosis. PLoS ONE. 8, : e67357 (2013).
Rossi, Silvia, Studer, Valeria, Moscatelli, Alessandro, and Centonze, Diego. “Opposite Roles of NMDA Receptors in Relapsing and Primary Progressive Multiple Sclerosis”. PLoS ONE 8.6 (2013): e67357.

13 Zitationen in Europe PMC

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Safety and efficacy of ADS-5102 (amantadine) extended release capsules to improve walking in multiple sclerosis: A randomized, placebo-controlled, phase 2 trial.
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Combining evidence from four immune cell types identifies DNA methylation patterns that implicate functionally distinct pathways during Multiple Sclerosis progression.
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Heart rate variability is differentially altered in multiple sclerosis: implications for acute, worsening and progressive disability.
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Intercepting virtual balls approaching under different gravity conditions: evidence for spatial prediction.
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HIV-1 protein Tat produces biphasic changes in NMDA-evoked increases in intracellular Ca2+ concentration via activation of Src kinase and nitric oxide signaling pathways.
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AUTHOR UNKNOWN, 1979
MDM2 SNP309 and TP53 Arg72Pro interact to alter therapy-related acute myeloid leukemia susceptibility.
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Analysis of multiple candidate genes in association with phenotypes of multiple sclerosis.
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