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Authors: Mathieu Barbier
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Journal Article
SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration Free
Mathieu Barbier and others
Brain, Volume 144, Issue 9, September 2021, Pages 2798–2811, https://doi.org/10.1093/brain/awab171
Published: 21 October 2021
Journal Article
Reply: Two heterozygous progranulin mutations in progressive supranuclear palsy Free
Vincent Huin and others
Brain, Volume 144, Issue 3, March 2021, Page e28, https://doi.org/10.1093/brain/awaa456
Published: 11 January 2021
Journal Article
Reply: Early-onset phenotype of bi-allelic GRN mutations Free
Vincent Huin and others
Brain, Volume 144, Issue 2, February 2021, Page e23, https://doi.org/10.1093/brain/awaa415
Published: 22 December 2020
Journal Article
EDITOR'S CHOICE
Homozygous GRN mutations: new phenotypes and new insights into pathological and molecular mechanisms Free
Vincent Huin and others
Brain, Volume 143, Issue 1, January 2020, Pages 303–319, https://doi.org/10.1093/brain/awz377
Published: 19 December 2019
Journal Article
Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex Free
Livia Parodi and others
Brain, Volume 141, Issue 12, December 2018, Pages 3331–3342, https://doi.org/10.1093/brain/awy285
Published: 23 November 2018
Journal Article
Reply: Age-dependent penetrance among females with X-linked adrenoleukodystrophy
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Marc Engelen and others
Brain, Volume 138, Issue 2, February 2015, Page e326, https://doi.org/10.1093/brain/awu233
Published: 22 August 2014
Journal Article
X-linked adrenoleukodystrophy in women: a cross-sectional cohort study
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Marc Engelen and others
Brain, Volume 137, Issue 3, March 2014, Pages 693–706, https://doi.org/10.1093/brain/awt361
Published: 29 January 2014
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