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41.
Flinn, L.* et al.: Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio). Brain 132, Part 6, 1613-1623 (2009)
42.
Asmus, F.* et al.: Genomic deletion size at the epsilon-sarcoglycan locus determines the clinical phenotype. Brain 130, 2736-2745 (2007)
43.
Gempel, K.* et al.: The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene. Brain 130, 2037-2044 (2007)
44.
Horvath, R.* et al.: Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene. Brain 129, 1674-1684 (2006)
45.
Berg, D.* et al.: Type and frequency of mutations in the LRRK2 gene in familial ans sporadic Parkinson's disease. Brain 128, 3000-3011 (2005)
46.
Kamm, C.* ; Illig, T. & Wichmann, H.-E.: The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: Data from the EMSA study group. Brain 128, 1855-1860 (2005)