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David Neary

Showing results (71-80 of 73) with videos related to

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Parkinsonism & Related Disorders|May 10, 2005
The effect of tau genotype on clinical features in FTDP-17Yasuhiko Baba, Yoshio Tsuboi, Matthew C Baker, et al.
The Lancet. Neurology|September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiativeRosa Rademakers, Matt Baker, Jennifer Gass, et al.
Neuron|September 28, 2011
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDAlan E Renton, Elisa Majounie, Adrian Waite, et al.
Pageof 8

Showing results (71-80 of 73) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 73 results.
Parkinsonism & Related Disorders|May 10, 2005
The effect of tau genotype on clinical features in FTDP-17Yasuhiko Baba, Yoshio Tsuboi, Matthew C Baker, et al.
The Lancet. Neurology|September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiativeRosa Rademakers, Matt Baker, Jennifer Gass, et al.
Neuron|September 28, 2011
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDAlan E Renton, Elisa Majounie, Adrian Waite, et al.
Pageof 8