1-8 of 8
Authors: Melanie Bahlo
Journal Article
Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40
Brain, Volume 146, Issue 12, December 2023, Pages 5086–5097, https://doi.org/10.1093/brain/awad314
Published: 18 November 2023
Journal Article
Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy
Brain, Volume 145, Issue 7, July 2022, Pages 2313–2331, https://doi.org/10.1093/brain/awac082
Published: 04 July 2022
Journal Article
Atypical development of Broca’s area in a large family with inherited stuttering
Brain, Volume 145, Issue 3, March 2022, Pages 1177–1188, https://doi.org/10.1093/brain/awab364
Published: 23 November 2021
Journal Article
CYLD is a causative gene for frontotemporal dementia – amyotrophic lateral sclerosis
Brain, Volume 143, Issue 3, March 2020, Pages 783–799, https://doi.org/10.1093/brain/awaa039
Published: 23 March 2020
Journal Article
Dorsal language stream anomalies in an inherited speech disorder
Brain, Volume 142, Issue 4, April 2019, Pages 966–977, https://doi.org/10.1093/brain/awz018
Published: 23 February 2019
Journal Article
‘North Sea’ progressive myoclonus epilepsy: phenotype of subjects with GOSR2 mutation Get access
Brain, Volume 136, Issue 4, April 2013, Pages 1146–1154, https://doi.org/10.1093/brain/awt021
Published: 28 February 2013
Journal Article
Autosomal dominant congenital spinal muscular atrophy: a true form of spinal muscular atrophy caused by early loss of anterior horn cells Get access
Brain, Volume 135, Issue 6, June 2012, Pages 1714–1723, https://doi.org/10.1093/brain/aws108
Published: 23 May 2012
Journal Article
Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20 Get access
Brain, Volume 127, Issue 5, May 2004, Pages 1172–1181, https://doi.org/10.1093/brain/awh139
Published: 01 May 2004
