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Now showing items 451-460 of 473
NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis
Blauw, Hylke M. et al. (2012)
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MRI allows for longitudinal quantitative analysis of body fat composition in rats: An analysis of sibutramine-associated changes at the group level
Mueller, Hans-Peter et al. (2013)
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The use of P300-based BCIs in amyotrophic lateral sclerosis: from augmentative and alternative communication to cognitive assessment
Cipresso, Pietro et al. (2012)
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FUS Mislocalization and Vulnerability to DNA Damage in ALS Patients Derived hiPSCs and Aging Motoneurons
Higelin, Julia et al. (2016)
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Camptocormia in Parkinson's Disease: A Review of the Literature
Ponfick, Matthias et al. (2011)
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Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic?
Felbecker, Ansgar et al. (2010)
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Genotypes of amyotrophic lateral sclerosis in Mongolia
Daria, Tselmen et al. (2019)
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Polyneuropathy in type 1 and type 2 diabetes: do we need different examinations?
Gdynia, Hans-Juergen; Ludolph, Albert C. (2010)
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H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis
van Rheenen, Wouter et al. (2013)
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A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany
Weishaupt, Jochen H. et al. (2013)
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