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Neurogenetics
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April 15, 2009
Recent origin and spread of a common Welsh MAPT splice mutation causing frontotemporal lobar degeneration
Roberto Colombo, Daniela Tavian, Matthew C Baker, et al.
Neurogenetics
|
March 25, 2009
Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain
Ignacio F Mata, Carolyn M Hutter, María C González-Fernández, et al.
Neurogenetics
|
February 3, 2009
Interaction of the SPG21 protein ACP33/maspardin with the aldehyde dehydrogenase ALDH16A1
Michael C Hanna, Craig Blackstone
Neurogenetics
|
August 16, 2008
Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease
Jung Mi Choi, Myoung Soo Woo, Hyeo-Il Ma, et al.
Neurogenetics
|
September 7, 2007
The molecular genetics and neuropathology of frontotemporal lobar degeneration: recent developments
Ian R A Mackenzie, Rosa Rademakers
Neurogenetics
|
May 4, 2010
Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindred
Guido J Breedveld, Giovanni Fabbrini, Ben A Oostra, et al.
Neurogenetics
|
April 15, 2010
Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish
Laura Southgate, Dimitra Dafou, Jacqueline Hoyle, et al.
Neurogenetics
|
May 6, 2009
Autosomal recessive spastic paraplegia (SPG45) with mental retardation maps to 10q24.3-q25.1
Umut Dursun, Cigdem Koroglu, Elif Kocasoy Orhan, et al.
Neurogenetics
|
June 1, 2010
Age at onset in Huntington's disease: replication study on the associations of ADORA2A, HAP1 and OGG1
Elahe Taherzadeh-Fard, Carsten Saft, Stefan Wieczorek, et al.
Neurogenetics
|
September 15, 2006
Pin1 levels are downregulated during ER stress in human neuroblastoma cells
Yolanda S Kap, Jeroen J M Hoozemans, Adee J Bodewes, et al.
Page
of 108
Search research articles
Search
Showing results (141-150 of 1,080) with videos related to
Sort By:
Page
of 108
Neurogenetics
|
April 15, 2009
Recent origin and spread of a common Welsh MAPT splice mutation causing frontotemporal lobar degeneration
Roberto Colombo, Daniela Tavian, Matthew C Baker, et al.
Neurogenetics
|
March 25, 2009
Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain
Ignacio F Mata, Carolyn M Hutter, María C González-Fernández, et al.
Neurogenetics
|
February 3, 2009
Interaction of the SPG21 protein ACP33/maspardin with the aldehyde dehydrogenase ALDH16A1
Michael C Hanna, Craig Blackstone
Neurogenetics
|
August 16, 2008
Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease
Jung Mi Choi, Myoung Soo Woo, Hyeo-Il Ma, et al.
Neurogenetics
|
September 7, 2007
The molecular genetics and neuropathology of frontotemporal lobar degeneration: recent developments
Ian R A Mackenzie, Rosa Rademakers
Neurogenetics
|
May 4, 2010
Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindred
Guido J Breedveld, Giovanni Fabbrini, Ben A Oostra, et al.
Neurogenetics
|
April 15, 2010
Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish
Laura Southgate, Dimitra Dafou, Jacqueline Hoyle, et al.
Neurogenetics
|
May 6, 2009
Autosomal recessive spastic paraplegia (SPG45) with mental retardation maps to 10q24.3-q25.1
Umut Dursun, Cigdem Koroglu, Elif Kocasoy Orhan, et al.
Neurogenetics
|
June 1, 2010
Age at onset in Huntington's disease: replication study on the associations of ADORA2A, HAP1 and OGG1
Elahe Taherzadeh-Fard, Carsten Saft, Stefan Wieczorek, et al.
Neurogenetics
|
September 15, 2006
Pin1 levels are downregulated during ER stress in human neuroblastoma cells
Yolanda S Kap, Jeroen J M Hoozemans, Adee J Bodewes, et al.
Page
of 108