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Now showing items 1461-1470 of 1576
Genetic mechanisms in idiopathic epilepsies
Weber, Yvonne G.; Lerche, Holger (2008)
Wissenschaftlicher Artikel
A novel presenilin1 mutation (Q223R) associated with early onset Alzheimer's disease, dysarthria and spastic paraparesis and decreased Abeta levels in CSF
Uttner, Ingo et al. (2010)
Wissenschaftlicher Artikel
TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease
Lee, Ji-Hyun et al. (2012)
Wissenschaftlicher Artikel
Neuroimaging in amyotrophic lateral sclerosis
Turner, Martin R. et al. (2012)
Wissenschaftlicher Artikel
Detection and Differentiation of Threonine- and Tyrosine-Monophosphorylated Forms of ERK1/2 by Capillary Isoelectric Focusing-Immunoassay
Kraus, Inga et al. (2015)
Wissenschaftlicher Artikel
Different aspects of Alzheimer's disease-related amyloid beta-peptide pathology and their relationship to amyloid positron emission tomography imaging and dementia
Thal, Dietmar Rudolf et al. (2019)
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NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis
Blauw, Hylke M. et al. (2012)
Wissenschaftlicher Artikel
Mutant superoxide dismutase-1 indistinguishable from wild-type causes ALS
Synofzik, Matthis et al. (2012)
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Quantifying change in individual subjects affected by frontotemporal lobar degeneration using automated longitudinal MRI volumetry
Frings, Lars et al. (2012)
Wissenschaftlicher Artikel
Microglial Activation Correlates with Disease Progression and Upper Motor Neuron Clinical Symptoms in Amyotrophic Lateral Sclerosis
Brettschneider, Johannes et al. (2012)
Wissenschaftlicher Artikel