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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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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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Cognitive function in bulbar- and spinal-onset amyotrophic lateral sclerosis - A longitudinal study in 52 patients
Schreiber, H et al. (2005)
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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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A dynein mutation attenuates motor neuron degeneration in SOD1(G93A) mice
Teuchert, M et al. (2006)
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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)
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Peripheral nerve hyperexcitability due to dominant-negative KCNQ2 mutations
Wuttke, T. V. 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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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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FKRP (826C > A) frequently causes limb-girdle muscular dystrophy in German patients
Walter, Maggie C. et al. (2004)
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