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Facioscapulohumeral muscular dystrophy - Phenotype-genotype correlation in patients with borderline D4Z4 repeat numbers
Butz, Miriam et al. (2003)
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Enhancement of Chemokine Expression by Interferon Beta Therapy in Patients With Multiple Sclerosis
Cepok, Sabine et al. (2009)
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Extended pathoanatomical studies point to a consistent affection of the thalamus in spinocerebellar ataxia type 2
Rub, U et al. (2005)
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Spinocerebellar ataxias types 2 and 3: degeneration of the precerebellar nuclei isolates the three phylogenetically defined regions of the cerebellum
Rub, U et al. (2005)
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A dynein mutation attenuates motor neuron degeneration in SOD1(G93A) mice
Teuchert, M et al. (2006)
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Grey-matter abnormalities in boys with Tourette syndrome: magnetic resonance imaging study using optimised voxel-based morphometry
Ludolph, AG et al. (2006)
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Frontotemporal cognitive function in X-linked spinal and bulbar muscular atrophy (SBMA): a controlled neuropsychological study of 20 patients
Soukup, Georg Ruediger et al. (2009)
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Neutralization of a negative charge in the S1-S2 region of the K(V)7.2 (KCNQ2) channel affects voltage-dependent activation in neonatal epilepsy
Wuttke, Thomas V. et al. (2008)
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Peripheral nerve hyperexcitability due to dominant-negative KCNQ2 mutations
Wuttke, T. V. et al. (2007)
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Are amygdalar volume alterations in children with Tourette syndrome due to ADHD comorbidity?
Ludolph, Andrea G. et al. (2008)
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