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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)
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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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Lehrbuch Prävention und Gesundheitsförderung
Altgeld, Thomas et al.; Hurrelmann, Klaus; Klotz, Theodor; Haisch, Jochen (2007)
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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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