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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

Cognitive function in bulbar- and spinal-onset amyotrophic lateral sclerosis - A longitudinal study in 52 patients 
Schreiber, H et al. (2005)
Wissenschaftlicher Artikel

Enhancement of Chemokine Expression by Interferon Beta Therapy in Patients With Multiple Sclerosis 
Cepok, Sabine et al. (2009)
Wissenschaftlicher Artikel

A dynein mutation attenuates motor neuron degeneration in SOD1(G93A) mice 
Teuchert, M et al. (2006)
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

Peripheral nerve hyperexcitability due to dominant-negative KCNQ2 mutations 
Wuttke, T. V. 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

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)
Wissenschaftlicher Artikel

FKRP (826C > A) frequently causes limb-girdle muscular dystrophy in German patients 
Walter, Maggie C. et al. (2004)
Wissenschaftlicher Artikel

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Institut für Anatomie und Zellbiologie (4)Institut für Angewandte Physiologie (3)... View MorePersonSchreiber, Herbert (17)Ludolph, Albert C. (11)Lehmann-Horn, Frank (3)... View MoreResource type
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