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Cognitive function in bulbar- and spinal-onset amyotrophic lateral sclerosis - A longitudinal study in 52 patients
Schreiber, H et al. (2005)
Wissenschaftlicher Artikel
Facioscapulohumeral muscular dystrophy - Phenotype-genotype correlation in patients with borderline D4Z4 repeat numbers
Butz, Miriam et al. (2003)
Wissenschaftlicher Artikel
Early diagnosis of rhinocerebral mucormycosis by cerebrospinal fluid analysis and determination of 16s rRNA gene sequence
Bengel, Dietmar et al. (2007)
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Global cerebral atrophy in early stages of Huntington's disease: quantitative MRI study
Kassubek, J et al. (2004)
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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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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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GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak
Weber, Yvonne G. et al. (2008)
Wissenschaftlicher Artikel
Are amygdalar volume alterations in children with Tourette syndrome due to ADHD comorbidity?
Ludolph, Andrea G. et al. (2008)
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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)
Wissenschaftlicher Artikel