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Browsing by Author Koppers, M.

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Full TextIssue DateTitleAuthor(s)
2012VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patientvan Blitterswijk, M.; Van Es, M.A.; Koppers, M.; van Rheenen, W.; Medic, J., et al
2012UNC13A is a modifier of survival in amyotrophic lateral sclerosis.Diekstra, F.P.; Vught, P.W. van; Rheenen, W. van; Koppers, M.; Pasterkamp, R.J., et al
2012VCP mutations in familial and sporadic amyotrophic lateral sclerosis.Koppers, M.; Blitterswijk, M.M. van; Vlam, L.; Rowicka, P.A.; Vught, P.W. van, et al
2011Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis.Es, M.A. van; Schelhaas, H.J.; Vught, P.W. van; Ticozzi, N.; Andersen, P.M., et al
2010A large genome scan for rare CNVs in amyotrophic lateral sclerosis.Blauw, H.M.; Al-Chalabi, A.; Andersen, P.M.; Vught, P.W. van; Diekstra, F.P., et al
Showing results 1 to 5 of 5

 

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