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Authors: Guntram Borck
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Journal Article

Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations Free

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David Brenner and others
Brain, Volume 142, Issue 12, December 2019, Page e67, https://doi.org/10.1093/brain/awz306
Published: 15 October 2019
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Hot-spot KIF5A mutations cause familial ALS Open Access

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David Brenner and others
Brain, Volume 141, Issue 3, March 2018, Pages 688–697, https://doi.org/10.1093/brain/awx370
Published: 12 January 2018
Journal Article

NEK1 mutations in familial amyotrophic lateral sclerosis Free

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David Brenner and others
Brain, Volume 139, Issue 5, May 2016, Page e28, https://doi.org/10.1093/brain/aww033
Published: 05 March 2016
Journal Article

Screening for CHCHD10 mutations in a large cohort of sporadic ALS patients: no evidence for pathogenicity of the p.P34S variant Free

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Nicolai Marroquin and others
Brain, Volume 139, Issue 2, February 2016, Page e8, https://doi.org/10.1093/brain/awv218
Published: 11 September 2015
Journal Article

Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood Open Access

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Joanne Ng and others
Brain, Volume 137, Issue 4, April 2014, Pages 1107–1119, https://doi.org/10.1093/brain/awu022
Published: 10 March 2014