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Scientific Reports
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March 24, 2022
DNA methylation in Friedreich ataxia silences expression of frataxin isoform E
Layne N Rodden, Kaitlyn M Gilliam, Christina Lam, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 12, 2010
Communication via gap junctions underlies early functional and beneficial interactions between grafted neural stem cells and the host
Johan Jäderstad, Linda M Jäderstad, Jianxue Li, et al.
Brain : a Journal of Neurology
|
January 7, 2005
A new clinical and molecular form of Unverricht-Lundborg disease localized by homozygosity mapping
Samuel F Berkovic, Aziz Mazarib, Simri Walid, et al.
The Lancet. Neurology
|
June 20, 2025
Friedreich's ataxia-a rare multisystem disease
Kathrin Reetz, Stella A Lischewski, Imis Dogan, et al.
Annals of Neurology
|
August 13, 2014
Deferiprone in Friedreich ataxia: a 6-month randomized controlled trial
Massimo Pandolfo, Javier Arpa, Martin B Delatycki, et al.
Human Molecular Genetics
|
January 2, 2015
Unveiling a common mechanism of apoptosis in β-cells and neurons in Friedreich's ataxia
Mariana Igoillo-Esteve, Ewa Gurgul-Convey, Amélie Hu, et al.
European Journal of Human Genetics : EJHG
|
February 28, 2008
Associations of apolipoprotein E gene with ischemic stroke and intracranial atherosclerosis
Shérine Abboud, Leena E Viiri, Dieter Lütjohann, et al.
Annals of Neurology
|
December 14, 2011
A gene expression phenotype in lymphocytes from Friedreich ataxia patients
Giovanni Coppola, Ryan Burnett, Susan Perlman, et al.
Pharmacogenomics
|
March 3, 2012
Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions
Mark McCormack, Thomas J Urban, Kevin V Shianna, et al.
Neurology
|
August 12, 2018
Nonataxia symptoms in Friedreich Ataxia: Report from the Registry of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS)
Kathrin Reetz, Imis Dogan, Christian Hohenfeld, et al.
Page
of 17
Search research articles
Search
Showing results (91-100 of 163) with videos related to
Sort By:
Page
of 17
Scientific Reports
|
March 24, 2022
DNA methylation in Friedreich ataxia silences expression of frataxin isoform E
Layne N Rodden, Kaitlyn M Gilliam, Christina Lam, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 12, 2010
Communication via gap junctions underlies early functional and beneficial interactions between grafted neural stem cells and the host
Johan Jäderstad, Linda M Jäderstad, Jianxue Li, et al.
Brain : a Journal of Neurology
|
January 7, 2005
A new clinical and molecular form of Unverricht-Lundborg disease localized by homozygosity mapping
Samuel F Berkovic, Aziz Mazarib, Simri Walid, et al.
The Lancet. Neurology
|
June 20, 2025
Friedreich's ataxia-a rare multisystem disease
Kathrin Reetz, Stella A Lischewski, Imis Dogan, et al.
Annals of Neurology
|
August 13, 2014
Deferiprone in Friedreich ataxia: a 6-month randomized controlled trial
Massimo Pandolfo, Javier Arpa, Martin B Delatycki, et al.
Human Molecular Genetics
|
January 2, 2015
Unveiling a common mechanism of apoptosis in β-cells and neurons in Friedreich's ataxia
Mariana Igoillo-Esteve, Ewa Gurgul-Convey, Amélie Hu, et al.
European Journal of Human Genetics : EJHG
|
February 28, 2008
Associations of apolipoprotein E gene with ischemic stroke and intracranial atherosclerosis
Shérine Abboud, Leena E Viiri, Dieter Lütjohann, et al.
Annals of Neurology
|
December 14, 2011
A gene expression phenotype in lymphocytes from Friedreich ataxia patients
Giovanni Coppola, Ryan Burnett, Susan Perlman, et al.
Pharmacogenomics
|
March 3, 2012
Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions
Mark McCormack, Thomas J Urban, Kevin V Shianna, et al.
Neurology
|
August 12, 2018
Nonataxia symptoms in Friedreich Ataxia: Report from the Registry of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS)
Kathrin Reetz, Imis Dogan, Christian Hohenfeld, et al.
Page
of 17