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8701.
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8702.
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8709.
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8711.
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Mutations in SEPT9 cause hereditary neuralgic amyotrophy. [electronic resource] by
- Kuhlenbäumer, Gregor
- Hannibal, Mark C
- Nelis, Eva
- Schirmacher, Anja
- Verpoorten, Nathalie
- Meuleman, Jan
- Watts, Giles D J
- De Vriendt, Els
- Young, Peter
- Stögbauer, Florian
- Halfter, Hartmut
- Irobi, Joy
- Goossens, Dirk
- Del-Favero, Jurgen
- Betz, Benjamin G
- Hor, Hyun
- Kurlemann, Gert
- Bird, Thomas D
- Airaksinen, Eila
- Mononen, Tarja
- Serradell, Adolfo Pou
- Prats, José M
- Van Broeckhoven, Christine
- De Jonghe, Peter
- Timmerman, Vincent
- Ringelstein, E Bernd
- Chance, Phillip F
Producer: 20051220
In:
Nature genetics vol. 37
Availability: No items available.
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8712.
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8713.
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8714.
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8715.
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Modeling axonal degeneration within the anterior visual system: implications for demonstrating neuroprotection in multiple sclerosis. [electronic resource] by
- Frohman, Elliot M
- Costello, Fiona
- Stüve, Olaf
- Calabresi, Peter
- Miller, David H
- Hickman, Simon J
- Sergott, Robert
- Conger, Amy
- Salter, Amber
- Krumwiede, Kimberly H
- Frohman, Teresa C
- Balcer, Laura
- Zivadinov, Robert
Producer: 20080214
In:
Archives of neurology vol. 65
Availability: No items available.
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