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Neuroscience Letters|August 29, 2006
Screening for mutations of the HFE gene in Parkinson's disease patients with hyperechogenicity of the substantia nigraNilgün Akbas, Helmine Hochstrasser, Joelle Deplazes, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 10, 2005
Functional relevance of ceruloplasmin mutations in Parkinson's diseaseHelmine Hochstrasser, Jürgen Tomiuk, Uwe Walter, et al.
The Journal of Molecular Diagnostics : JMD|April 12, 2008
High-throughput homogeneous mass cleave assay technology for the diagnosis of autosomal recessive Parkinson's diseaseChristopher Schroeder, Michael Walter, Daniela Berg, et al.
Neurobiology of Disease|August 25, 2009
A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeatsJana Boy, Thorsten Schmidt, Ulrike Schumann, et al.
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|August 24, 2006
Spectrin mutations in spinocerebellar ataxia (SCA)Peter Bauer, Ludger Schöls, Olaf Riess
Proceedings of the National Academy of Sciences of the United States of America|April 6, 2004
Ubiquitylation of synphilin-1 and alpha-synuclein by SIAH and its presence in cellular inclusions and Lewy bodies imply a role in Parkinson's diseaseEsti Liani, Allon Eyal, Eyal Avraham, et al.
Journal of Medical Genetics|November 5, 2014
EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohortsJohanna Huttenlocher, Rejko Krüger, Philipp Capetian, et al.
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