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Rebecca Schüle

Showing results (1-10 of 165) with videos related to

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Brain : a Journal of Neurology|November 8, 2017
Reply: Complicated hereditary spastic paraplegia due to ATP13A2 mutations: what's in a name?Rebecca Schüle
Seminars in Neurology|January 24, 2012
Genetics of hereditary spastic paraplegiasRebecca Schüle, Ludger Schöls
Movement Disorders : Official Journal of the Movement Disorder Society|February 15, 2017
Overcoming the divide between ataxias and spastic paraplegias: Shared phenotypes, genes, and pathwaysMatthis Synofzik, Rebecca Schüle
Annals of Neurology|April 29, 2016
ReplyRebecca Schüle, Sarah Wiethoff, Ludger Schöls
Neurology|December 13, 2006
Cerebrotendinous xanthomatosisLudger Schöls, Thomas Nägele, Rebecca Schüle, et al.
Handbook of Clinical Neurology|February 22, 2023
Ataxia and spastic paraplegia in mitochondrial diseaseMatthis Synofzik, Elena Rugarli, Evan Reid, et al.
Stem Cell Research|November 24, 2016
Generation of induced pluripotent stem cells (iPSCs) from a hereditary spastic paraplegia patient carrying a homozygous R486C mutation in CYP7B1 (SPG5)Philip Höflinger, Yvonne Theurer, Rebecca Schüle, et al.
Brain : a Journal of Neurology|March 9, 2019
Reply: Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesisMartina Minnerop, Delia Kurzwelly, Holger Wagner, et al.
Journal of Neurology|March 20, 2008
"Pseudodominant inheritance" of ataxia with ocular apraxia type 2 (AOA2)Ludger Schöls, Larissa Arning, Rebecca Schüle, et al.
Stem Cell Research|November 8, 2020
Generation of the CRISPR/Cas9-mediated KIF1C knock-out human iPSC line HIHRSi003-A-1Maike Nagel, Sandra Müßig, Philip Höflinger, et al.
Pageof 17

Showing results (1-10 of 165) with videos related to

Sort By:
Pageof 17
Brain : a Journal of Neurology|November 8, 2017
Reply: Complicated hereditary spastic paraplegia due to ATP13A2 mutations: what's in a name?Rebecca Schüle
Seminars in Neurology|January 24, 2012
Genetics of hereditary spastic paraplegiasRebecca Schüle, Ludger Schöls
Movement Disorders : Official Journal of the Movement Disorder Society|February 15, 2017
Overcoming the divide between ataxias and spastic paraplegias: Shared phenotypes, genes, and pathwaysMatthis Synofzik, Rebecca Schüle
Annals of Neurology|April 29, 2016
ReplyRebecca Schüle, Sarah Wiethoff, Ludger Schöls
Neurology|December 13, 2006
Cerebrotendinous xanthomatosisLudger Schöls, Thomas Nägele, Rebecca Schüle, et al.
Handbook of Clinical Neurology|February 22, 2023
Ataxia and spastic paraplegia in mitochondrial diseaseMatthis Synofzik, Elena Rugarli, Evan Reid, et al.
Stem Cell Research|November 24, 2016
Generation of induced pluripotent stem cells (iPSCs) from a hereditary spastic paraplegia patient carrying a homozygous R486C mutation in CYP7B1 (SPG5)Philip Höflinger, Yvonne Theurer, Rebecca Schüle, et al.
Brain : a Journal of Neurology|March 9, 2019
Reply: Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesisMartina Minnerop, Delia Kurzwelly, Holger Wagner, et al.
Journal of Neurology|March 20, 2008
"Pseudodominant inheritance" of ataxia with ocular apraxia type 2 (AOA2)Ludger Schöls, Larissa Arning, Rebecca Schüle, et al.
Stem Cell Research|November 8, 2020
Generation of the CRISPR/Cas9-mediated KIF1C knock-out human iPSC line HIHRSi003-A-1Maike Nagel, Sandra Müßig, Philip Höflinger, et al.
Pageof 17