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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)
Wissenschaftlicher Artikel
Global cerebral atrophy in early stages of Huntington's disease: quantitative MRI study
Kassubek, J et al. (2004)
Wissenschaftlicher Artikel
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
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)
Wissenschaftlicher Artikel
Peripheral nerve hyperexcitability due to dominant-negative KCNQ2 mutations
Wuttke, T. V. et al. (2007)
Wissenschaftlicher Artikel
IgG Antibodies against Measles, Rubella, and Varicella Zoster Virus Predict Conversion to Multiple Sclerosis in Clinically Isolated Syndrome
Brettschneider, Johannes et al. (2009)
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X-linked bulbospinal neuronopathy - Kennedy disease
Sperfeld, Anne-Dorte et al. (2002)
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Vacuolization correlates with spin-spin relaxation time in motor brainstem nuclei and behavioural tests in the transgenic G93A-SOD1 mouse model of ALS
Bucher, Selina et al. (2007)
Wissenschaftlicher Artikel