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Anna Sailer

Showing results (1-10 of 8) with videos related to

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Current Neurology and Neuroscience Reports|April 25, 2012
Recent advances in the genetics of cerebellar ataxiasAnna Sailer, Henry Houlden
The Journal of Vascular Access|May 13, 2014
Long segment recanalization and dedicated central venous stenting in an ultimate attempt to restore vascular access central vein outflowRick de Graaf, Jorinde van Laanen, Anna Sailer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 11, 2012
Identical twins with Leucine rich repeat kinase type 2 mutations discordant for Parkinson's diseaseGeorgia Xiromerisiou, Henry Houlden, Anna Sailer, et al.
Neurology|June 8, 2012
Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseasesAnna Sailer, Sonja W Scholz, J Raphael Gibbs, et al.
Cell Reports|June 11, 2013
NDUFA4 mutations underlie dysfunction of a cytochrome c oxidase subunit linked to human neurological diseaseRobert D S Pitceathly, Shamima Rahman, Yehani Wedatilake, et al.
American Journal of Human Genetics|January 22, 2013
Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticityMonia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, et al.
Neurology|November 8, 2014
LRRK2 exonic variants and risk of multiple system atrophyMichael G Heckman, Lucia Schottlaender, Alexandra I Soto-Ortolaza, et al.
Neurology|September 16, 2016
A genome-wide association study in multiple system atrophyAnna Sailer, Sonja W Scholz, Michael A Nalls, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Current Neurology and Neuroscience Reports|April 25, 2012
Recent advances in the genetics of cerebellar ataxiasAnna Sailer, Henry Houlden
The Journal of Vascular Access|May 13, 2014
Long segment recanalization and dedicated central venous stenting in an ultimate attempt to restore vascular access central vein outflowRick de Graaf, Jorinde van Laanen, Anna Sailer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 11, 2012
Identical twins with Leucine rich repeat kinase type 2 mutations discordant for Parkinson's diseaseGeorgia Xiromerisiou, Henry Houlden, Anna Sailer, et al.
Neurology|June 8, 2012
Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseasesAnna Sailer, Sonja W Scholz, J Raphael Gibbs, et al.
Cell Reports|June 11, 2013
NDUFA4 mutations underlie dysfunction of a cytochrome c oxidase subunit linked to human neurological diseaseRobert D S Pitceathly, Shamima Rahman, Yehani Wedatilake, et al.
American Journal of Human Genetics|January 22, 2013
Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticityMonia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, et al.
Neurology|November 8, 2014
LRRK2 exonic variants and risk of multiple system atrophyMichael G Heckman, Lucia Schottlaender, Alexandra I Soto-Ortolaza, et al.
Neurology|September 16, 2016
A genome-wide association study in multiple system atrophyAnna Sailer, Sonja W Scholz, Michael A Nalls, et al.
Pageof 1